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Sample records for disodium cromoglycate dscg

  1. Effect of Disodium Cromoglycate (DSCG) and Antihistamines on Postirradiation Cerebral Blood Flow and Plasma Levels of Histamine and Neurotensin

    Science.gov (United States)

    1988-01-01

    73 6 SOTI UNCLASIFIE ESCURIIY CLASSIFICATION OF Tm-S siki FUNDAMENTAL AND APPLIED TOXICOLOGY 10, 233-242 (1988) Effect of Disodium Cromoglycate (DSCG...given the mast cell stabilizer disodium cromoglycate and the antihistamines mepyramine and cimetidine before Irradiation did not exhibit an abrupt...occur ment with the mast cell stabilizer, disodium with equal frequency in all species, having cromoglycate (DSCG, cromolyn sodium), in- been reported

  2. Inhaled disodium cromoglycate (DSCG) as maintenance therapy in children with asthma: a systematic review

    NARCIS (Netherlands)

    M.J.A. Tasche (Marjolein); J.H.J.M. Uijen (Hans); R.M.D. Bernsen (Roos); J.C. de Jongste (Johan); J.C. van der Wouden (Hans)

    2000-01-01

    textabstractBACKGROUND: Disodium cromoglycate (DSCG) is included in the BTS guidelines on the treatment of asthma for use in children, but is now used only infrequently. We have identified and interpreted the findings of all published randomised, placebo controlled tria

  3. Inhaled disodium cromoglycate (DSCG) as maintenance therapy in children with asthma: a systematic review

    Science.gov (United States)

    Tasche, M; Uijen, J; Bernsen, R; de Jongste, J C; van der Wouden, J C

    2000-01-01

    BACKGROUND—Disodium cromoglycate (DSCG) is included in the BTS guidelines on the treatment of asthma for use in children, but is now used only infrequently. We have identified and interpreted the findings of all published randomised, placebo controlled trials of DSCG in the prophylactic treatment of children with asthma.
METHODS—Several databases were searched to identify trials. Studies were included if they investigated subjects with asthma aged 0-18 years old, addressed maintenance treatment with inhaled DSCG, and were published in English. The methodological quality of the studies was assessed independently by three reviewers. The 95% confidence intervals (CI) of differences in the treatment effect for cough and wheeze between placebo and treatment with DSCG were computed. The estimates were pooled and tested for homogeneity and, to assess possible publication bias, a funnel plot was made and tested for symmetry.
RESULTS—Of the 24 randomised, placebo controlled trials identified, the methodological scores varied widely. The null hypothesis of homogeneity was rejected. Under the assumption of heterogeneity the overall CI for wheeze was 0.11 to 0.26 and for cough was 0.13to 0.27. The overall tolerance intervals (-0.11 to 0.48 and -0.04 to 0.43 for wheeze and cough, respectively) both included zero, so it cannot be concluded that future studies will show an effect of DSCG compared with placebo. Older studies were more often in favour of DSCG. The funnel plots suggest publication bias; small studies with negative or equal outcomes are lacking.
CONCLUSION—Given the apparent publication bias, the small overall treatment effect, and the tolerance interval including zero, there is insufficient evidence that DSCG has a beneficial effect as maintenance treatment in children with asthma.

 PMID:11050259

  4. Effect of antihistamines, disodium cromoglycate (DSCG) or methysergide on post-irradiation cerebral blood flow and mean systemic arterial blood pressure in primates after 25 Gy, whole-body, gamma irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Cockerham, L.G.; Forcino, C.D. [Armed Forces Radiobiology Research Inst., Bethesda, MD (United States)

    1995-06-01

    Exposure to ionizing radiation causes hypotension, cerebral ischemia and release of histamine (HA) and serotonin (5-HT). To investigate the relationship among these responses, rhesus monkeys (Macaca mulatta) received physiological saline (i.v.), disodium cromoglycate (DSCG), antihistamines (AH, mepyramine and cimetidine), or methysergide (METH), then were given 25 Gy whole-body irradiation. Monkeys receiving DSCG, AH or METH had higher post-irradiation mean arterial blood pressure (MBP) than saline-treated controls. Compared to levels in controls, post-irradiation hippocampal blood flow (rCBF) levels were higher in monkeys receiving DSCG, AH or METH. Treatment with the 5-HT{sub 2} receptor antagonist methysergide was the most effective in maintaining both rCBF and MBP after irradiation. Results support the hypothesis that the irradiation-induced cerebral ischemia and, to some extent, the hypotension is mediated by serotonin through 5-HT{sub 2} receptor sites. (author) 72 refs.

  5. Effect of disodium cromoglycate (DSCG) and antihistamines on postirradiation cerebral blood flow and plasma levels of histamine and neurotensin

    Energy Technology Data Exchange (ETDEWEB)

    Cockerham, L.G.; Pautler, E.L.; Carraway, R.E.; Cochrane, D.E.; Hampton, J.D.

    1988-02-01

    In an attempt to elucidate mechanisms underlying the irradiation-induced decrease in regional cerebral blood flow (rCBF) in primates, hippocampal and visual cortical blood flows of rhesus monkeys were measured by hydrogen clearance, before and after exposure to 100 Gy, whole-body, gamma irradiation. Systemic blood pressures were monitored simultaneously. Systemic arterial plasma histamine and neurotensin levels were determined preirradiation and postirradiation. Compared to control animals, the irradiated monkeys exhibited an abrupt decline in systemic blood pressure to 23% of the preirradiation level within 10 min postirradiation, falling to 12% by 60 min. A decrease in hippocampal blood flow to 32% of the preirradiation level was noted at 10 min postirradiation, followed by a slight recovery to 43% at 30 min and a decline to 23% by 60 min. The cortical blood flow for the same animals showed a steady decrease to 29% of the preirradiation levels by 60 min postirradiation. Animals given the mast cell stabilizer disodium cromoglycate and the antihistamines mepyramine and cimetidine before irradiation did not exhibit an abrupt decline in blood pressure but displayed a gradual decrease to a level 33% below preirradiation levels by 60 min postirradiation. Also, the treated, irradiated monkeys displayed rCBF values that were not significantly different from the nonirradiated controls. The plasma neurotensin levels in the irradiated animals, treated and untreated, indicated a nonsignificant postirradiation increase above control levels. However, the postirradiation plasma histamine levels in both irradiated groups showed an increase of approximately 1600% above the preirradiation levels and the postirradiation control levels.

  6. Molecular Aggregation in Disodium Cromoglycate

    Science.gov (United States)

    Singh, Gautam; Agra-Kooijman, D.; Collings, P. J.; Kumar, Satyendra

    2012-02-01

    Details of molecular aggregation in the mesophases of the anti-asthmatic drug disodium cromoglycate (DSCG) have been studied using x-ray synchrotron scattering. The results show two reflections, one at wide angles corresponding to π-π stacking (3.32 å) of molecules, and the other at small angles which is perpendicular to the direction of molecular stacking and corresponds to the distance between the molecular aggregates. The latter varies from 35 - 41 å in the nematic (N) phase and 27 -- 32 å in the columnar (M) phase. The temperature evolution of the stack height, positional order correlations in the lateral direction, and orientation order parameter were determined in the N, M, and biphasic regions. The structure of the N and M phases and the nature of the molecular aggregation, together with their dependence on temperature and concentration, will be presented.

  7. Bronchodilator effect of disodium cromoglycate administered as a dry powder in exercise induced asthma.

    Science.gov (United States)

    Horn, C R; Jones, R M; Lee, D; Brennan, S R

    1984-01-01

    A double-blind, placebo controlled study of the effects of disodium cromoglycate (DSCG), administered as a dry powder via the spinhaler, in established exercise-induced asthma, was carried out. DSCG resulted in an increase in the rate of recovery compared with placebo. The findings confirm that DSCG has bronchodilator properties. PMID:6439234

  8. Disodium Cromoglycate, A Mast-Cell Stabilizer, Alters Postradiation Regional Cerebral Blood Flow in Primates

    Science.gov (United States)

    1986-01-01

    ranD RISEARCH INSTITUTI SCIENTIFIC REPORTTC SR86-14 ELECTE JUL0186_ _ ~D DISODIUM CROMOGLYCATE , A MAST-CELL STABILIZER, ALTERS POSTRADIATION...were given the mast-cell stabilizers disodium cromoglycate (DSCC) or BRL 22321 (Beecham Phar- maceuticals, Research Division) before exposure to 100 Gy...flow could be mitigated by the pre- radiation administration of either disodium cromoglycate (DSCG) (Fisons Corporation, ledford, Mass.) or BRL 22321

  9. Reaction of disodium cromoglycate with hydrated electrons

    Energy Technology Data Exchange (ETDEWEB)

    Carmichael, A.J.; Arroyo, C.M.; Cockerham, L.G.

    1988-01-01

    A possible mechanism by which disodium cromoglycate (DSCG) prevents a decrease in regional cerebral blood flow but not hypotension in primates following whole body gamma-irradiation was studied. Several studies have implicated superoxide radicals (O/sub 2//sup -/.) in intestinal and cerebral vascular disorders following ischemia and ionizing radiation, respectively. O/sub 2//sup -/. is formed during radiolysis in the reaction between hydrated electrons (e-aq) and dissolved oxygen. For this reason, the efficiency of DSCG to scavenge e-q and possibly prevent the formation of O/sub 2//sup -/. was studied. Hydrated electrons were produced by photolysis of potassium ferrocyanide solutions. The rate constant, k = 2.92 x 10(10) M-1s-1 for the reaction between e-aq and DSCG was determined in competition experiments using the spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). This spin trap reacts rapidly with e-aq followed by protonation to yield the ESR observable DMPO-H spin adduct. The results show that DSCG is an efficient e-aq scavenger and may effectively compete with oxygen for e-aq preventing the radiolytic formation of O/sub 2//sup -/..

  10. Effect of disodium cromoglycate on mast cell-mediated immediate-type allergic reactions.

    Science.gov (United States)

    Shin, Hye-Young; Kim, Jung-Sook; An, Nyeon-Hyoung; Park, Rae-Kil; Kim, Hyung-Min

    2004-04-23

    We investigated the effect of disodium cromoglycate (DSCG) on mast cell-mediated immediate-type hypersensitivity. DSCG inhibited systemic allergic reaction induced by compound 48/80 dose-dependently. Passive cutaneous anaphylaxis was inhibited by 71.6% by oral administration of DSCG (1 g/kg). When DSCG was pretreated at concentration rang from 0.01-1000 g/kg, the serum histamine levels were reduced in a dose dependent manner. DSCG also significantly inhibited histamine release from rat peritoneal mast cell (RPMC) by compound 48/80. We confirmed that DSCG inhibited compound 48/80-induced degranulation of RPMC by alcian blue/nuclear fast red staining. In addition, DSCG showed a significant inhibitory effect on anti-dinitrophenyl IgE-mediated tumor necrosis factor-alpha production. These results indicate that DSCG inhibits mast cell-mediated immediate-type allergic reaction.

  11. Effect of disodium cromoglycate (DSCG) and antihistamines on post-irradiation cerebral blood flow and plasma levels of histamine and neurotensin

    Energy Technology Data Exchange (ETDEWEB)

    Cockerham, L.G.; Pautler, E.L.; Carraway, R.E.; Cochrane, D.E.; Hampton, J.D.

    1988-01-01

    In an attempt to elucidate mechanisms underlying the irradiation-induced decrease in regional cerebral blood flow (rCBF) in primates, hippocampal and visual cortical blood flows of rhesus monkeys were measured by hydrogen clearance, before and after exposure to 100-Gy, whole-body, gamma irradiation. Systemic blood pressures were monitored simultaneously. Systemic arterial plasma histamine and neurotensin levels were determined preirradiation and postirradiation. Compared to control animals, the irradiated monkeys exhibited an abrupt decline in systemic blood pressure to 23% of the preirradiation level within 10-min postirradiation, falling to 12% by 60 min. A decrease in hippocampal blood flow to 32% of the preirradiation level was noted at 10-min postirradiation, followed by a slight recovery to 43% at 30 min and a decline to 23% by 60 min. The cortical blood flow for the same animals showed a steady decrease to 29% of the preirradiation levels by 60-min postirradiation. Animals given the mast-cell stabilizer disodium cromoglycate and the antihistamines mepyramine and cimetidine before irradiation did not exhibit an abrupt decline in blood pressure but displayed a gradual decrease to a level 33% below preirradiation levels by 60 min postirradiation. Also, the treated, irradiated monkeys displayed rCBF values that were not significantly different from the nonirradiated controls. The plasma neurotensin levels in the irradiated animals, treated and untreated, indicated a nonsignificant postirradiation increase above control levels.

  12. Disodium cromoglycate (DSCG) selectively inhibits IgE production and enhances IgG4 production by human B cell in vitro.

    Science.gov (United States)

    Kimata, H; Yoshida, A; Ishioka, C; Mikawa, H

    1991-01-01

    The effect of DSCG on human IgE production in vitro was studied. DSCG selectively inhibited interleukin-4 (IL-4) induced IgE production by mononuclear cells (MNC) from normal donors without affecting IgM, IgA, IgG1, IgG2 or IgG3 production. In contrast, DSCG enhanced IgG4 production. To achieve this effect, DSCG must be added to the culture at the initiation and be present throughout the entire culture period. Interferon-gamma (IFN-gamma) also inhibited IL-4-induced IgE production, but IgG4 production was not affected by IFN-gamma. Monoclonal anti-IFN-gamma antibody blocked the inhibition of IgE production by IFN-gamma, but did not block the inhibition of IgE production by DSCG. DSCG also selectively inhibited spontaneous IgE production and enhanced IgG4 production by B cells from atopic patients in the presence of T cells and monocytes. These results indicate that there is a mechanism of IgE production inhibition which is not mediated by IFN-gamma. We also found that DSCG is an excellent reagent for the study of IgE and IgG4 regulation in vitro. PMID:1904324

  13. [Disodium cromoglycate--mast cell degranulation blocker in the process of tissue remodelation].

    Science.gov (United States)

    Maxová, H; Vasilková, M; Tkaczyk, J; Vízek, M

    2010-01-01

    Disodium cromoglycate (DSCG) is a compound commonly used in the treatment of allergic diseases. The effect of DSCG is due to its ability to stabilize the mast cell membrane and to prevent release of histamine and inflammatory mediators. Mast cells are also an abundant source of tissue metalloproteinases, serine proteases and growth factors, which play an important role in the processes of the tissue remodeling. In this view the DSCG is a substance which allows us to study the mechanisms of the pulmonary vascular bed remodeling in the experimental animals exposed to chronic hypoxia and in a phase of the recovery from hypoxia.

  14. The inhibitory effect of disodium cromoglycate on the growth of Chlamydophila (Chlamydia) pneumoniae in vitro.

    Science.gov (United States)

    Yamazaki, Tsutomu; Yamaguchi, Tetsuya; Sasaki, Nozomu; Inoue, Miyuki; Sato, Kozue; Kishimoto, Toshio

    2006-04-01

    Chlamydophila (Chlamydia) pneumoniae is associated with asthma and several other respiratory illnesses. Disodium cromoglycate (DSCG) is known to inhibit both immediate and late asthmatic responses. In this study, the inhibitory effect of DSCG on the growth of C. pneumoniae was examined by minimum inhibitory concentration (MIC) and pre-inoculation minimal cidal concentration (MCC) assays using HL cells and C. pneumoniae AR-39. DSCG below the clinically relevant concentration inhibited the growth of C. pneumoniae in a dose-dependent manner in both the MCC and MIC assays. The inhibitory effect was also time-dependent in the MCC assay at 20 mg/ml of DSCG. These results warrant further clinical study on the connection between C. pneumoniae infections and use of DSCG.

  15. Modification of disodium cromoglycate passage across lung epithelium in vitro via incorporation into polymeric microparticles.

    Science.gov (United States)

    Haghi, Mehra; Salama, Rania; Traini, Daniela; Bebawy, Mary; Young, Paul M

    2012-03-01

    Two microparticle systems containing disodium cromoglycate (DSCG) alone or with polyvinyl alcohol (DSCG/PVA) were produced via spray drying and compared in terms of their physicochemical characteristics, aerosol performance and drug uptake across a pulmonary epithelial cell line (Calu-3), cultured under air interface conditions. The particle size distribution of DSCG and DSCG/PVA were similar, of spherical geometry, amorphous and suitable for inhalation purposes. Aerosolisation studies using a modified twin-stage impinger showed the DSCG/PVA to have greater aerosol performance than that of DSCG alone. Aerosol particles of DSCG and DSCG/PVA were deposited onto the surface of the Calu-3 air interface epithelium monolayer and the drug uptake from apical to basal directions measured over time. Drug uptake was measured across a range of doses to allow comparison of equivalent drug and powder mass deposition. Analysis of the data indicated that the percentage cumulative drug uptake was independent of the mass of powder deposited, but dependent on the formulation. Specifically, with the formulation containing DSCG, the diffusion rate was observed to change with respect to time (indicative of a concentration-dependent diffusion process), whilst DSCG/PVA showed a time-independent drug uptake (suggesting a zero-order depot release).

  16. Columnar molecular aggregation in the aqueous solutions of disodium cromoglycate

    Science.gov (United States)

    Agra-Kooijman, Dena M.; Singh, Gautam; Lorenz, Alexander; Collings, Peter J.; Kitzerow, Heinz-S.; Kumar, Satyendra

    2014-06-01

    Stack, chimneylike, and threadlike assemblies have previously been proposed for the structure of disodium cromoglycate (DSCG) aggregates in aqueous solutions. The results of the synchrotron x-ray scattering investigations reported here reveal the formation of simple columnar assemblies with π-π stacking at a separation of 3.4 Å between the DSCG molecules. Lateral separation between the assemblies is concentration and temperature dependent, varying from ˜35 to 42 Å in the orientationally ordered nematic (N) phase and from 27 to 32 Å in the columnar or middle (M) phase having long range lateral positional order. The assemblies' length depends on concentration and consists of ˜23 molecules in the N phase, becoming three to ten times larger in the M phase. The scission energy is concentration dependent in the N phase with values ˜7.19 ± 0.14 kBT (15 wt %), 2.73 ± 0.4 kBT (20 wt %), and 3.05 ± 0.2 kBT (25 wt %). Solutions of all concentrations undergo a spinodal decomposition at temperatures above ˜40 °C, resulting in DSCG-rich regions with the M phase and water-rich regions in the N and isotropic phases.

  17. Disodium cromoglycate attenuates hypoxia induced enlargement of end-expiratory lung volume in rats.

    Science.gov (United States)

    Maxová, H; Hezinová, A; Vízek, M

    2011-01-01

    Mechanism responsible for the enlargement of end-expiratory lung volume (EELV) induced by chronic hypoxia remains unclear. The fact that the increase in EELV persists after return to normoxia suggests involvement of morphological changes. Because hypoxia has been also shown to activate lung mast cells, we speculated that they could play in the mechanism increasing EELV similar role as in vessel remodeling in hypoxic pulmonary hypertension (HPH). We, therefore, tested an effect of mast cells degranulation blocker disodium cromoglycate (DSCG) on hypoxia induced EELV enlargement. Ventilatory parameters, EELV and right to left heart weight ratio (RV/LV+S) were measured in male Wistar rats. The experimental group (H+DSCG) was exposed to 3 weeks of normobaric hypoxia and treated with DSCG during the first four days of hypoxia, control group was exposed to hypoxia only (H), two others were kept in normoxia as non-treated (N) and treated (N+DSCG) groups. DSCG treatment significantly attenuated the EELV enlargement (H+DSCG = 6.1+/-0.8; H = 9.2+/-0.9; ml +/-SE) together with the increase in minute ventilation (H + DSCG = 190+/-8; H = 273 +/- 10; ml/min +/- SE) and RV/LV + S (H + DSCG = 0.39 +/- 0.03; H = 0.50 +/- 0.06).

  18. Disodium cromoglycate enhances ongoing immunoglobulin production in vitro in human B cells.

    Science.gov (United States)

    Kimata, H; Yoshida, A; Ishioka, C; Mikawa, H

    1991-01-01

    The effect of disodium cromoglycate (DSCG) upon human immunoglobulin (Ig) isotypes and IgG subclasses production by purified B cells was studied. DSCG enhanced IgM, IgG1, IgG2, IgG3, IgG4 and IgA production in a dose-dependent fashion, while DSCG failed to induce IgE production at any concentrations tested by purified B cells. When B cells were separated into small resting and large activated B cells, DSCG failed to induce Ig production from small resting B cells in the presence or absence of Staphylococcus aureus Cowan strain I (SAC). In contrast, in large activated B cells DSCG significantly enhanced all types of Ig production (two-to threefold), especially IgG4 production (seven-to 11-fold), except IgE, which large B cells did not produce. The enhancement of IgG subclass production was not subclass switching, since DSCG failed to enhance IgG1 production in B cells depleted of surface IgG1+ cells (sIgG1+ cells). Similarly, DSCG did not enhance IgG2, IgG3 or IgG4 production from sIgG2-, sIgG3- or sIgG4- B cells, respectively, Interleukin-4 (IL-4) or interleukin-6 (IL-6) also enhanced Ig production except IgG4 from large activated B cells. The enhancing effect of DSCG was not mediated by IL-4 or IL-6 since anti-IL-4 or anti-IL-6 antibody failed to block the DSCG-induced enhancement. DSCG also enhanced IgG2 and IgM production from human B-cell lines GM-1500 and CBL, respectively. These results suggest that DSCG directly and preferentially stimulates activated B cells which are producing Ig and, in addition, enhances their Ig production. PMID:1904400

  19. The effects of disodium cromoglycate on enhanced adherence of Haemophilus influenzae to A549 cells infected with respiratory syncytial virus.

    Science.gov (United States)

    Fukasawa, Chie; Ishiwada, Naruhiko; Ogita, Junko; Hishiki, Haruka; Kohno, Yoichi

    2009-08-01

    Nontypeable Haemophilus influenzae (NTHi) secondary infection often complicates respiratory syncytial virus (RSV) infections. Previous studies have revealed that RSV infections enhance NTHi adherence to airway epithelial cells. In this study, we investigated the effects of disodium cromoglycate (DSCG) and corticosteroids, which are frequently used for the treatment of wheezing often related to RSV infections, on the adherence of NTHi to RSV-infected A549 cells. DSCG inhibited enhanced adherence of NTHi to RSV-infected A549 cells, whereas dexamethasone (Dex) and fluticasone propionate (Fp) did not. DSCG suppressed the expression of ICAM-1, which is one of the NTHi receptors. Furthermore, DSCG exhibited an inhibitory effect on RSV infections. It is suggested that DSCG exerts an anti-RSV effect, and consequently attenuates the expression of NTHi receptors.

  20. Effect of lodoxamide and disodium cromoglycate on tear eosinophil cationic protein in vernal keratoconjunctivitis

    Science.gov (United States)

    Leonardi, A.; Borghesan, F.; Avarello, A.; Plebani, M.; Secchi, A.

    1997-01-01

    AIM—To validate the use of tear eosinophil cationic protein (ECP) as a marker for eosinophil activation, and its pharmacological modulation, in addition to evaluating the efficacy of lodoxamide and sodium cromoglycate in the treatment of vernal keratoconjunctivitis (VKC).
METHODS—Tears were collected from 30 patients affected by active mild to moderate VKC before and after therapy with disodium cromoglycate 4% (DSCG) (n=15) or lodoxamide 0.1% (n=15) for 10 days. Tear cytology and ECP measurement were performed, and ocular signs and symptoms evaluated.
RESULTS—While statistically significant changes did not occur after DSCG therapy, mean tear ECP increased from 343 (SD 363) µg/l to 571 (777) µg/l due to marked elevation in six eyes. The clinical score in DSCG eyes did not improve. After lodoxamide therapy, both clinical signs and symptoms, and tear ECP levels (560 (756) µg/l to 241 (376) µg/l) decreased significantly (p<0.0001 and p<0.01, respectively). Compared with DSCG treatment, lodoxamide was more effective in reducing signs and symptoms (p<0.005). ECP levels were significantly correlated with signs, symptoms, corneal involvement, and number of eosinophils in tears (p<0.0001).
CONCLUSIONS—In patients with VKC, lodoxamide significantly reduced ECP tear levels, and thus, eosinophil activation, and was more effective than DSCG in reducing clinical signs and symptoms.

 PMID:9135403

  1. Phases and structures of sunset yellow and disodium cromoglycate mixtures in water

    Science.gov (United States)

    Yamaguchi, Akihiro; Smith, Gregory P.; Yi, Youngwoo; Xu, Charles; Biffi, Silvia; Serra, Francesca; Bellini, Tommaso; Zhu, Chenhui; Clark, Noel A.

    2016-01-01

    We study phases and structures of mixtures of two representative chromonic liquid crystal materials, sunset yellow FCF (SSY) and disodium cromoglycate (DSCG), in water. A variety of combinations of isotropic, nematic (N ), and columnar (also called M ) phases are observed depending on their concentrations, and a phase diagram is made. We find a tendency for DSCG-rich regions to show higher-order phases while SSY-rich regions show lower-order ones. We observe uniform mesophases only when one of the materials is sparse in the N phases. Their miscibility in M phases is so low that essentially complete phase separation occurs. X-ray scattering and spectroscopy studies confirm that SSY and DSCG molecules do not mix when they form chromonic aggregates and neither do their aggregates when they form M phases.

  2. Plasma concentrations of disodium cromoglycate after various inhalation methods in healthy subjects

    Science.gov (United States)

    Kato, Y; Muraki, K; Fujitaka, M; Sakura, N; Ueda, K

    1999-01-01

    Aims To compare the plasma concentrations of disodium cromoglycate (DSCG) following various inhalation procedures in healthy volunteers. Methods Nine healthy subjects inhaled 2 mg of aerosol, 20 mg of nebuliser solution only, 20 mg of nebuliser solution mixed with isotonic saline, or 20 mg of nebuliser solution mixed with saline and procaterol, a β2-adenoceptor agonist, on separate occasions 2–3 weeks apart. Plasma concentrations of DSCG were determined by high-performance liquid chromatography (h.p.l.c.). Results The peak plasma concentrations of DSCG were 1.5±0.7 (range 0.4–2.4) ng ml−1 in the aerosol group, 8.8±6.2 (range 5.3–19.9) ng ml−1 in the nebuliser solution only group, 17.2±16.3 (range 5.0–38.6) ng ml−1 in the nebuliser solution plus isotonic saline group, and 24.5±11.9 (range 10.2–44.9) ng ml−1 in the nebuliser solution plus saline and procaterol group. Thus subjects who used the nebuliser had markedly higher plasma concentrations of DSCG than subjects who used the aerosol inhaler. Conclusions These findings may have important implications for the evaluation of inhalation treatment with DSCG for bronchial asthma. PMID:10417491

  3. Disodium cromoglycate prevents ileum hyperreactivity to histamine in Toxocara canis-infected guinea pigs.

    Science.gov (United States)

    Sá-Nunes, A; Corrado, A P; Baruffi, M D; Faccioli, L H

    2003-11-01

    The aim of this study was to investigate whether Toxocara canis infection in guinea pigs provokes changes in ileum responsiveness to histamine. Ileum segments from control and T. canis-infected groups were placed at isometric conditions and submitted to various doses of histamine. No changes were observed between controls and T. canis-infected groups at days 3, 6 and 12 after infection. However, at days 18 and 24 after infection, there was a significant increase in ileum responsiveness to histamine in T. canis-infected group. Pre-incubation of ileum segments with 1mgml(-1) disodium cromoglycate (DSCG) prevented the increased responsiveness to histamine in T. canis-infected guinea pigs and did not affect ileum contractility in non-infected animals. These results indicate that T. canis-infected guinea pigs develop increased intestinal responsiveness to histamine and that DSCG prevents alterations in smooth-muscle contractility.

  4. Oral disodium cromoglycate and ketotifen for a patient with eosinophilic gastroenteritis, food allergy and protein-losing enteropathy.

    Science.gov (United States)

    Suzuki, Junzo; Kawasaki, Yukihiko; Nozawa, Ruriko; Isome, Masato; Suzuki, Shigeo; Takahashi, Ai; Suzuki, Hitoshi

    2003-09-01

    We present a case report of a 10 years old boy with protein-losing enteropathy and eosinophilic gastroenteritis who had positive histamine release tests, increased allergen-specific IgE antibodies to some food items, and low levels of total serum protein and albumin. Upper gastrointestinal endoscopy revealed a number of polyps and diffuse gastritis. Biopsy specimens of the stomach and duodenum showed widespread eosinophilia and neutrophilia. Although a restricted diet was recommended, a diet which excluded foods with positive results to both histamine release test and allergen-specific IgE antibodies was poorly tolerated, and the patient rejected systemic administration of corticosteroids. Thus, we initiated an oral disodium cromoglycate (DSCG) and ketotifen therapy. After oral DSCG and ketotifen administration, the patient's condition improved gradually. Therefore, oral DSCG and ketotifen therapy might be considered as treatment option in patients with eosinophilic gastroenteritis and protein-losing enteropathy caused by food allergy.

  5. Binding of disodium cromoglycate to human serum albumin

    Science.gov (United States)

    Ochoa de Aspuru, Eduardo; Zatón, Ana M. L.

    1998-07-01

    The binding of several benzopiranone derivatives to human serum albumin was determined. The antiallergic drug disodium cromoglycate binds weakly to serum albumin. However, its precursors, chromones of smaller size, were able to bind in a hydrophobic pocket in the protein, and are carried by serum albumin in blood.

  6. Disodium cromoglycate inhibits S mu-->S epsilon deletional switch recombination and IgE synthesis in human B cells

    Science.gov (United States)

    1994-01-01

    IgE synthesis requires interleukin 4 (IL-4) and a T-B cell interaction that involves the B cell antigen CD40 and its ligand expressed on activated T cells. IL-4 induces epsilon germline transcription whereas ligation of CD40 results in deletional S mu-->S epsilon switch recombination, expression of mature epsilon transcripts, and IgE synthesis and secretion. We demonstrate that disodium cromoglycate (DSCG), a drug commonly used for the prophylactic treatment of allergic disease, inhibits T cell-driven IgE synthesis by human B cells at concentrations readily achievable in the course of inhaled therapy for asthma. Inhibition of IgE synthesis by DSCG was not the result of drug toxicity because DSCG did not affect the viability of T and B cells or their proliferation to mitogens. DSCG did not interfere with CD40 ligand expression by T cells but clearly targeted the B cells because it inhibited IgE synthesis induced by anti-CD40 and IL-4 in populations of highly purified B cells. DSCG had no effect on the induction of epsilon germline transcripts by IL-4 but strongly inhibited CD40 mediated S mu-->S epsilon deletional switch recombination in IL-4- treated B cells as assayed by nested primer PCR. The effect of DSCG was not specific for CD40-mediated induction of IgE isotype switching because DSCG inhibited IgE synthesis as well as S mu-->S epsilon deletional switch recombination induced by hydrocortisone and IL-4 in B cells. Moreover, the effect of DSCG was not specific for IgE isotype switching because DSCG inhibited the synthesis of IgG4 by B cells sorted for lack of surface expression of IgG4 and stimulated with anti- CD40 and IL-4. DSCG caused only minimal inhibition (< 15%) of spontaneous IgE synthesis by lymphocytes from patients with the hyper- IgE syndrome and did not affect pokeweed mitogen-induced IgG and IgA synthesis by lymphocytes suggesting that it has little effect on B cells that have already undergone isotype switching. These results indicate that DSCG

  7. Effect of amino acids on the dispersion of disodium cromoglycate powders.

    Science.gov (United States)

    Chew, Nora Y K; Shekunov, Boris Y; Tong, Henry H Y; Chow, Albert H L; Savage, Charles; Wu, James; Chan, Hak-Kim

    2005-10-01

    Modified disodium cromoglycate powders were prepared by co-spray drying with different concentrations of leucine, phenylalanine, tryptophan, methionine, asparagine, and arginine. Amorphous spherical particles of the same size and density where obtained which, however, exhibited different surface properties as measured by the inverse gas chromatography (IGC) and X-ray photoelectron spectroscopy (XPS) techniques. The surface energy parameters, such as the dispersive component of surface free energy of the sample, gammaSD, and the total solubility parameter, delta, were significantly lower in the presence of nonpolar chain amino acids, particularly with leucine and phenylalanine, than pure DSCG. However no quantitative relationship between these parameters, the additive concentrations, and the fine particle fractions, FPF, determined for different inhalers and air flow rates, was observed. The FPF significantly increased with addition of leucine and this effect was attributed to reduced intermolecular interactions between leucine and disodium cromoglycate molecules, as indicated by the difference in corresponding Hansen solubility parameters. Decrease of interparticle interactions for leucine-containing powders also led to a lesser dependence of FPF on the flow rate and inhaler type.

  8. Disodium cromoglycate, a mast-cell stabilizer, alters postradiation regional cerebral blood flow in primates

    Energy Technology Data Exchange (ETDEWEB)

    Cockerham, L.G.; Doyle, T.F.; Pautler, E.L.; Hampton, J.D.

    1986-01-01

    Early transient incapacitation (ETI) is the complete cessation of performance during the first 30 min after radiation exposure, and performance decrement (PD) is a reduction in performance at the same time. Supralethal doses of radiation have been shown to produce a marked decrease in regional cerebral blood flow in primates concurrent with systemic hypotension and a dramatic release of mast-cell histamine. In an attempt to elucidate mechanisms underlying the radiation-induced ETI/PD phenomena and the postradiation decrease in cerebral blood flow, primates were given the mast-cell stabilizers disodium cromoglycate (DSCG) or BRL 22321 before exposure to 100 Gy whole-body gamma radiation. Hypothalamic and cortical blood flows were measured by hydrogen clearance, before and after radiation exposure. Systemic blood pressures were determined simultaneously. The data indicated that DSCG was successful in diminishing postradiation decrease in cerebral blood flow. Irradiated animals pretreated with DSCG, showed only a 10% decrease in hypothalamic blood flow 60 min postradiation, while untreated, irradiated animals showed a 57% decrease. The cortical blood flow of DSCG treated, irradiated animals showed a triphasic response, with a decrease of 38% at 10 min postradiation, then a rise to 1% below baseline at 20 min, followed by a fall to 42% below baseline by 50 min postradiation. In contrast, the untreated, irradiated animals showed a steady decrease in cortical blood flow to 79% below baseline by 50 min postradiation. There was no significant difference in blood-pressure response between the treated and untreated, irradiated animals. Systemic blood pressure showed a 60% decrease at 10 min postradiation, falling to a 71% decrease by 60 min.

  9. Inhibition of methoxamine-induced bronchoconstriction by ipratropium bromide and disodium cromoglycate in asthmatic subjects.

    Science.gov (United States)

    Black, J; Vincenc, K; Salome, C

    1985-01-01

    We compared the effects of pretreatment with saline, ipratropium bromide, and disodium cromoglycate (DSCG) on bronchoconstriction induced by methoxamine--an alpha-adrenoceptor agonist, in asthmatic subjects. All 12 patients bronchoconstricted in response to methoxamine after saline. The PD20 (the dose of methoxamine causing a 20% fall in forced expiratory volume in 1 s [FEV1]) ranged from 0.3-18 mumol. Ipratropium bromide (200 micrograms administered by aerosol) significantly inhibited (P less than 0.05) the response to methoxamine in all patients without producing significant changes in the mean baseline lung function. The mean PD20 for methoxamine after saline was 6.8 mumol and 95% confidence limits (CL) were 3.6, 12.7 mumol. The mean PD20 for methoxamine after ipratropium bromide was 35.4 (95% CL 28.8, 43.6) mumol. DSCG also produced significant (P less than 0.05) shifts to the right in the methoxamine dose response curves, but did not affect resting airway calibre as measured by the FEV1. The mean PD20 for methoxamine increased from 3.3 mumol (95% CL 1.1, 10.0 mumol) after saline to 25.1 mumol (95% CL 14.1, 44.6) after DSCG pretreatment. These findings suggest that alpha-adrenoceptors in the airways of asthmatic subjects may be located at sites other than smooth muscle--possibly on mast cells but more likely on nerve endings and/or parasympathetic ganglia. PMID:2992563

  10. Hsp90 is a direct target of the anti-allergic drugs disodium cromoglycate and amlexanox.

    Science.gov (United States)

    Okada, Miki; Itoh, Hideaki; Hatakeyama, Takashi; Tokumitsu, Hiroshi; Kobayashi, Ryoji

    2003-09-01

    Hsp90 (heat-shock protein 90) alone can act to prevent protein aggregation and promote refolding in vitro, but in vivo it operates as a part of a multichaperone complex, which includes Hsp70 and cohort proteins. Since the physiological function of Hsp90 is not yet fully understood, the development of specific antagonists might open new lines of investigation on the role of Hsp90. In an effort to discover Hsp90 antagonists, we screened many drugs and found that the anti-allergic drugs DSCG (disodium cromoglycate) and amlexanox target Hsp90. Both drugs were found to bind directly wild-type Hsp90 via the N- and C-terminal domains. Both drugs strongly suppressed the in vitro chaperone activity of native Hsp90 towards citrate synthase at 1.5-3.0 microM. Amlexanox suppressed C-terminal chaperone activity in vitro, but not N-terminal chaperone activity, and inhibited the association of cohort proteins, such as cyclophilin 40 and Hsp-organizing protein, to the C-terminal domain of Hsp90. These data suggest that amlexanox might disrupt the multichaperone complex, including Hsp70 and cohort proteins, both in vitro and in vivo. Although DSCG inhibited the in vitro chaperone activity of the N-terminal domain, the drug had no effect either on the C-terminal chaperone activity or on the association of the cohort proteins with the C-terminus of Hsp90. The physiological significance of these interactions in vivo remains to be investigated further, but undoubtedly must be taken into account when considering the pharmacology of anti-allergic drugs. DSCG and amlexanox may serve as useful tools for evaluating the physiological significance of Hsp90.

  11. Disodium cromoglycate reverses colonic visceral hypersensitivity and influences colonic ion transport in a stress-sensitive rat strain.

    Science.gov (United States)

    Carroll, Siobhan Yvonne; O'Mahony, Siobhain Mary; Grenham, Susan; Cryan, John Francis; Hyland, Niall Patrick

    2013-01-01

    The interface between psychiatry and stress-related gastrointestinal disorders (GI), such as irritable bowel syndrome (IBS), is well established, with anxiety and depression the most frequently occurring comorbid conditions. Moreover, stress-sensitive Wistar Kyoto (WKY) rats, which display anxiety- and depressive-like behaviors, exhibit GI disturbances akin to those observed in stress-related GI disorders. Additionally, there is mounting preclinical and clinical evidence implicating mast cells as significant contributors to the development of abdominal visceral pain in IBS. In this study we examined the effects of the rat connective tissue mast cell (CTMC) stabiliser, disodium cromoglycate (DSCG) on visceral hypersensitivity and colonic ion transport, and examined both colonic and peritoneal mast cells from stress-sensitive WKY rats. DSCG significantly decreased abdominal pain behaviors induced by colorectal distension in WKY animals independent of a reduction in colonic rat mast cell mediator release. We further demonstrated that mast cell-stimulated colonic ion transport was sensitive to inhibition by the mast cell stabiliser DSCG, an effect only observed in stress-sensitive rats. Moreover, CTMC-like mast cells were significantly increased in the colonic submucosa of WKY animals, and we observed a significant increase in the proportion of intermediate, or immature, peritoneal mast cells relative to control animals. Collectively our data further support a role for mast cells in the pathogenesis of stress-related GI disorders.

  12. Disodium cromoglycate reverses colonic visceral hypersensitivity and influences colonic ion transport in a stress-sensitive rat strain.

    Directory of Open Access Journals (Sweden)

    Siobhan Yvonne Carroll

    Full Text Available The interface between psychiatry and stress-related gastrointestinal disorders (GI, such as irritable bowel syndrome (IBS, is well established, with anxiety and depression the most frequently occurring comorbid conditions. Moreover, stress-sensitive Wistar Kyoto (WKY rats, which display anxiety- and depressive-like behaviors, exhibit GI disturbances akin to those observed in stress-related GI disorders. Additionally, there is mounting preclinical and clinical evidence implicating mast cells as significant contributors to the development of abdominal visceral pain in IBS. In this study we examined the effects of the rat connective tissue mast cell (CTMC stabiliser, disodium cromoglycate (DSCG on visceral hypersensitivity and colonic ion transport, and examined both colonic and peritoneal mast cells from stress-sensitive WKY rats. DSCG significantly decreased abdominal pain behaviors induced by colorectal distension in WKY animals independent of a reduction in colonic rat mast cell mediator release. We further demonstrated that mast cell-stimulated colonic ion transport was sensitive to inhibition by the mast cell stabiliser DSCG, an effect only observed in stress-sensitive rats. Moreover, CTMC-like mast cells were significantly increased in the colonic submucosa of WKY animals, and we observed a significant increase in the proportion of intermediate, or immature, peritoneal mast cells relative to control animals. Collectively our data further support a role for mast cells in the pathogenesis of stress-related GI disorders.

  13. Phase behavior of chromonic liquid crystal mixtures of Sunset Yellow and Disodium Cromoglycate

    Science.gov (United States)

    Yamaguchi, Akihiro; Smith, Gregory; Yi, Youngwoo; Xu, Charles; Biffi, Silvia; Serra, Francesca; Bellini, Tommaso; Clark, Noel

    2014-03-01

    Chromonic liquid crystals (CLCs) are formed when planar molecules dissolved in water stack into rod-like aggregates that can order as liquid crystals. Isotropic, nematic, and M-phases can be observed depending on the degree of molecular orientational and positional order by variation of the CLC concentration. We focused on mixtures of two well-known CLCs, Sunset Yellow, a food dye, and disodium cromoglycate (DSCG), an asthma medication. In order to study the phase behaviors of these mixtures, we observed their textures in glass cells and capillaries using polarized light microscopy. We report here a ternary phase diagram describing the complete phase behavior of the CLC mixtures. We observed a variety of phase behaviors depending on species ratio and concentration. In the isotropic phase, no clear phase separation of the two dyes was observed, while separation did occur in many nematic and M-phase combinations. We will also describe phase observations made using a light spectroscopy and bulk centrifugal partitioning. Grant support: NSF DMR 1207606 and NSF MRSEC DMR-0820579.

  14. Intratracheal dosing with disodium cromoglycate inhibits late asthmatic response by attenuating eicosanoid production in guinea pigs.

    Science.gov (United States)

    Nabe, Takeshi; Yamamoto, Maki; Suga, Mikiko; Kohno, Shigekatsu

    2004-08-16

    Disodium cromoglycate is an anti-asthmatic drug that has mast cell-stabilizing effects and other anti-inflammatory effects. However, the mechanisms of its anti-inflammatory effects are unclear. In this study, we evaluated effects of disodium cromoglycate on eosinophilia, early and late asthmatic responses, and production of arachidonic acid metabolites in guinea pig lungs. Guinea pigs were alternately sensitized and challenged by exposure to mists of ovalbumin+Al(OH)(3) and ovalbumin, respectively. Disodium cromoglycate (0.5-2 mg/0.1 ml/animal) administered intratracheally before the fifth challenge dose-dependently inhibited asthmatic response, but early asthmatic response was not affected. Disodium cromoglycate at 2 mg/animal potently suppressed increases in cysteinyl leukotrienes (CysLTs) and thromboxane A(2) in the lung during late asthmatic response. Eosinophilia was slightly reduced by disodium cromoglycate. The inhibitory effect of disodium cromoglycate on late asthmatic response is apparently due to inhibition of the release of arachidonic acid metabolites, some of which may be derived from eosinophils that infiltrate the lung.

  15. Actions of salbutamol, disodium cromoglycate, and placebo administered as aerosols in acute asthma.

    Science.gov (United States)

    Hasham, F; Kennedy, J D; Jones, R S

    1981-01-01

    The effects on the peak expiratory flow rate of the drug sequences, placebo-salbutamol-disodium cromoglycate and placebo-disodium cromoglycate-salbutamol administered via a nebuliser were examined in 35 children with asthma. Twenty children were each examined once within 4 hours of admission to hospital with an acute attack of asthma, and the remaining 15 children were examined later in the attack on two occasions. The placebo effect of sterile water accounted for about half of the total bronchodilator action both early and late in the attack. It is suggested that this effect is due to the action of water on the surface film of surfactant, causing collapse of bubbles and strands or webs of mucoid material, thus decreasing airways resistance. At this time salbutamol is significantly more potent than disodium cromoglycate as a bronchodilator agent. PMID:6794462

  16. [Longitudinal study of children with bronchopulmonary dysplasia treated with disodium cromoglycate].

    Science.gov (United States)

    Kassur-Siemieńska, Barbara; Milewska-Bobula, Bogumiła; Dmeńska, Hanna; Idzik, Mirosława; Bauer, Anna; Marciński, Paweł; Dunin-Wasowicz, Dorota; Lipka, Bozena

    2003-01-01

    In order to improve the quality of life of children born prematurely, who developed chronic lung disease, clinical trials of drugs of different origin are undertaken. The aim of the work was the evaluation of the efficacy of disodium cromoglycate in the treatment of bronchopulmonary dysplasia in children. We retrospectively studied 15 infants with bronchopulmonary dysplasia (BPD) hospitalised in the Infant Care Department of Children's Health Memorial Institute from 01.01.1997 to 01.02.2000. All babies were premature (25-30 weeks of gestation) with LBW or VLBW A control group of 11 babies with BPD, matched for birth weight and gestational age, who did not have disodium cromoglycate therapy were also studied. Recurrent obturative bronchitis and bronchial hyperresponsiveness were stated in all cases in both groups. Disodium cromoglycate was administered in all babies in the study group. Inhaled corticosteroid (Budesonide mite) was given in 10 cases, for a short period of time, due to severe obturative bronchitis. Babies in the control group were treated with systemic and inhaled corticosteroids. Results of our trial compared with the log-rank and chi2 test show statistically, significant differences in the regression of obturative bronchitis (log-rank = 4.35, p < 0.0001) and normalization of capillary blood-gas examination (log-rank = 3.777, p < 0.0002) in favour of the studied group, treated with disodium cromoglycate.

  17. Idiopathic obstructive eosinophilic enteritis with raised IgE: response to oral disodium cromoglycate

    Science.gov (United States)

    Gilinsky, N. H.; Kottler, R. E.

    1982-01-01

    A 65-year-old man with a 20-year history of recurrent abdominal pain and vomiting was found to have eosinophilic enteritis affecting the muscularis layer of the distal ileum. Tests for malabsorption were negative. The IgE was raised but there was no evidence of an allergic predisposition. The symptoms, eosinophilia, and radiological abnormality responded to oral disodium cromoglycate. ImagesFig. 1Fig. 2Fig. 3 PMID:6810329

  18. The effect of disodium cromoglycate, budesonide, and cyclosporin A on interleukin-4, interleukin-5, and interleukin-13 secretions in Der p I-stimulated T cells from house dust mite-sensitive atopic and nonatopic individuals.

    Science.gov (United States)

    Oh, Jae-Won; Lee, Ha-Baik; Chung, Yong-Hoon; Choi, Yong

    2002-01-01

    Disodium cromoglycate (DSCG), budesonide, and cyclosporin A (CsA) were the well-known immunomodulators for the allergic and immunologic diseases clinically. In this study, we evaluated the characteristics of inhibition on cytokine synthesis of Der p I-stimulated T cells by the same inhibiting concentrations of DSCG, budesonide, and CsA in house-dust mite antigen (Der p I)-specific atopic and nonatopic healthy individuals. Seven house dust mite allergen specific patients were recruited for this study. Seven healthy volunteers were included on the basis of negative allergic manifestations and low serum immunoglobulin E values. Peripheral blood mononuclear cells (PBMCs) were cultured in the presence of recombinant interleukin (rIL)-2 with or without budesonide, DSCG, CsA, and Der p I for 48 hours. Cells were stained with anti-CD4 fluorescein isothiocyanate-conjugated monoclonal antibody, and then anti-human IL-4 phycoerythrin, IL-5, or IL-13 monoclonal antibody, respectively, was added to both blocked and stained samples. Incubation of PBMC from atopics with each immunomodulator and Der p I resulted in the reduction of IL-4 secretion compared with Der p I alone stimulation. However, IL-4 secretion in PBMC from nonatopics was not reduced with DSCG and Der p I stimulation. IL-4, IL-5, and IL-13 secretions of PBMC from atopics were significantly decreased after incubation with each immunomodulator and Der p I, compared with after incubation with Der p I alone. These results might be considered to show either that DSCG has a selective inhibiting effect on cytokine production in T cells from atopics or is a weak inhibitor of cytokine secretions compared with budesonide and CsA at even strength for the inhibition of lymphocyte proliferation in normal, healthy individuals.

  19. Periodic structures induced by director reorientation in the lyotropic nematic phase of disodium cromoglycate-water

    Science.gov (United States)

    Hui, Y. W.; Kuzma, M. R.; San Miguel, M.; Labes, M. M.

    1985-07-01

    A nonequilibrium periodic structure is induced by a magnetic field H applied to an aligned lyotropic uniaxial nematic phase of disodium cromoglycate-water. A series of parallel lines perpendicular to H represents boundaries between 180° out-of-phase regions of director reorientation. The distance between the lines decreases with increasing H. The line spacing is also directly proportional to thickness of the sample (in a limited range of thickness), and a secondary periodicity, consisting of nodes in these lines, is observed in thicker samples. An extension of a theoretical model by Guyon et al. is used to qualitatively interpret the abovementioned dependencies.

  20. Disodium cromoglycate: exploiting its properties as a NMR weak-aligning medium for small organic molecules.

    Science.gov (United States)

    Troche-Pesqueira, Eduardo; Cid, María-Magdalena; Navarro-Vázquez, Armando

    2014-03-28

    Chromonic phases are a family of lyotropic liquid crystals (LC) formed by ionic aromatic mesogens such as disodium cromoglycate (cromolyn), sunset yellow and others. It is well known that chromonic phases are oriented in the presence of external magnetic fields, leading to the observation of anisotropic NMR observables such as quadrupolar splittings or residual dipolar couplings. Despite the fact that the cromolyn nematic LC phase (N) presents important advantages like great homogeneity, small line broadening, and easy sample preparation, it has been scarcely used as a water-compatible NMR orienting medium, in part due to a too strong induced degree of alignment on the guest molecules. However, the use of cromolyn-brine mixtures led to the optimum degree of alignment allowing to record (1)H-(13)C dipolar couplings with good accuracy.

  1. Elasticity, viscosity, and orientational fluctuations of a lyotropic chromonic nematic liquid crystal disodium cromoglycate.

    Science.gov (United States)

    Zhou, Shuang; Neupane, Krishna; Nastishin, Yuriy A; Baldwin, Alan R; Shiyanovskii, Sergij V; Lavrentovich, Oleg D; Sprunt, Samuel

    2014-09-14

    Using dynamic light scattering, we study orientational fluctuation modes in the nematic phase of a self-assembled lyotropic chromonic liquid crystal (LCLC) disodium cromoglycate and measure the Frank elastic moduli and viscosity coefficients. The elastic moduli of splay (K1) and bend (K3) are in the order of 10 pN while the twist modulus (K2) is an order of magnitude smaller. The splay constant K1 and the ratio K1/K3 both increase substantially as the temperature T decreases, which we attribute to the elongation of the chromonic aggregates at lower temperatures. The bend viscosity is comparable to that of thermotropic liquid crystals, while the splay and twist viscosities are several orders of magnitude larger. The temperature dependence of bend viscosity is weak. The splay and twist viscosities change exponentially with the temperature. In addition to the director modes, the fluctuation spectrum reveals an additional mode that is attributed to diffusion of structural defects in the column-like aggregates.

  2. The effect of disodium cromoglycate and ketotifen on the excretion of histamine and N tau-methylimidazole acetic acid in urine of patients with mastocytosis.

    Science.gov (United States)

    Mallet, A I; Norris, P; Rendell, N B; Wong, E; Greaves, M W

    1989-01-01

    Treatment of four mastocytosis patients with the mast cell stabilising drugs, disodium cromoglycate and ketotifen failed to alter significantly the urinary excretion levels of histamine or N tau-methylimidazole acetic acid. No clinical improvement was noted in any subject after treatment by either drug. PMID:2495814

  3. Influence of Proton and Salt Concentration on the Chromonic Liquid Crystal Phase Diagram of Disodium Cromoglycate Solutions: Prospects and Limitations of a Host for DNA Nanostructures.

    Science.gov (United States)

    Zhang, Bingru; Kitzerow, Heinz-S

    2016-03-31

    Lyotropic chromonic liquid crystals have recently been suggested for use as a self-organized host for dispersing and aligning self-organized DNA origami nanostructures. However, an appropriate pH value and a suitable cation concentration are necessary to stabilize such nanostructures and to avoid unfolding of the DNA. The present study shows that the nematic and columnar liquid crystal phases appearing in aqueous solutions of disodium cromoglycate are robust against the replacement of deionized water by a neutral or alkaline buffer solution. However, disodium cromoglycate precipitates when an acidic buffer is used or when the concentration of magnesium cations exceeds a critical concentration of about 0.6-0.7 mmol/L.

  4. Effects of disodium cromoglycate on cationic exchange of deoxygenated sickle cells.

    Science.gov (United States)

    Bizumukama, Léonidas; Ferster, Alina; Gulbis, Béatrice; Kumps, Alain; Cotton, Frédéric

    2011-08-31

    In the present work, we explored the way in which cromoglycate, a drug used to treat allergies acts on ion movements in sickle cells. Cells were either slowly deoxygenated by overnight exposure to nitrogen or acutely deoxygenated by exposure to metabisulfite, a strong reducing agent which induces sickling of red blood sickle cells. Flushing the cells with nitrogen increased the intracellular concentration of Na(+) and decreased the intracellular concentration of K(+) and the sum of the concentrations of the two cations. One hundred nM cromoglycate inhibited the decrease of intracellular K(+) and the increase of intracellular Na(+) induced by deoxygenation (n=17). Metabisulfite (100mM) increased the intracellular concentration of Ca(2+) (measured by Fura Red) (n=15) and the shape of the cells (measured by light scattering) (n=9). One μM cromoglycate partially inhibited these two responses. In conclusion, cromoglycate partially inhibits abnormal K(+) loss, Ca(2+) entry pathways or Ca(2+) channels opened by cell deoxygenation and ensuing membrane modifications and prevents cell sickling.

  5. Disodium cromoglycate stabilizes mast cell degranulation while reducing the number of hemoglobin-induced microvascular leaks in rat mesentery.

    Science.gov (United States)

    Ginsburg, Maxwell I; Baldwin, Ann L

    2004-05-01

    Blood substitutes, such as diaspirin cross-linked Hb (DBBF-Hb), have been considered for use during blood transfusions. Unfortunately, bolus injection of modified Hb has been shown to rapidly increase the leakage of microvessels to plasma albumin. This effect may result from production of excess reactive oxygen species (ROS) and could be linked to the observed increase in degranulated mast cells (DMC). Disodium cromoglycate (cromolyn) stabilizes mast cells and therefore might minimize the venular permeability in the rat mesentery. In 10 anesthetized Sprague-Dawley rats, the mesenteric preparation was continuously suffused with cromolyn while the microvasculature was filled with DBBF-Hb solution (10 mg/ml) for 10 min. Six animals received cromolyn pretreatment [two intravascular injections over 30 min (experiment A)] and four animals received pretreatment with 2% HEPES-buffered saline (HBS)-BSA (experiment B). Two more animals were pretreated with HBS-BSA without DBBF-Hb infusion but with cromolyn suffusion (experiment C). Another set of experiments was performed on five animals without cromolyn suffusion or any pretreatment but with DBBF-Hb infusion (experiment D). All groups then received a 1-min perfusion of FITC-albumin, fixation for 60 min, and microscopic examination. Experiments A and B demonstrated a significant reduction in the number of venular leaks and DMC compared with experiment D, but not in the area of venular leaks. These results suggest mast cell degranulation is not a major contributor to microvascular leakage induced by DBBF-Hb.

  6. Dry powder aerosols generated by standardized entrainment tubes from drug blends with lactose monohydrate: 1. Albuterol sulfate and disodium cromoglycate.

    Science.gov (United States)

    Xu, Zhen; Mansour, Heidi M; Mulder, Tako; McLean, Richard; Langridge, John; Hickey, Anthony J

    2010-08-01

    The major objective of this study was: discriminatory assessment of dry powder aerosol performance using standardized entrainment tubes (SETs) and lactose-based formulations with two model drugs. Drug/lactose interactive physical mixtures (2%w/w) were prepared. Their properties were measured: solid-state characterization of phase behavior and molecular interactions by differential scanning calorimetry and X-ray powder diffraction; particle morphology and size by scanning electron microscopy and laser diffraction; aerosol generation by SETs and characterization by twin-stage liquid impinger and Andersen cascade impactor operated at 60 L/min. The fine particle fraction (FPF) was correlated with SET shear stress (tau(s)), using a novel powder aerosol deaggregation equation (PADE). Drug particles were <5 microm in volume diameter with narrow unimodal distribution (Span <1). The lowest shear SET (tau(s) = 0.624 N/m(2)) gave a higher emitted dose (ED approximately 84-93%) and lower FPF (FPF(6.4) approximately 7-25%). In contrast, the highest shear SET (tau(s) = 13.143 N/m(2)) gave a lower ED (ED approximately 75-89%) and higher FPF (FPF(6.4) approximately 15-46%). The performance of disodium cromoglycate was superior to albuterol sulfate at given tau(s), as was milled with respect to sieved lactose monohydrate. Excellent correlation was observed (R(2) approximately 0.9804-0.9998) when pulmonary drug particle release from the surface of lactose carriers was interpreted by PADE linear regression for dry powder formulation evaluation and performance prediction.

  7. Combination therapy using fexofenadine, disodium cromoglycate, and a hypoallergenic amino acid-based formula induced remission in a patient with steroid-dependent, chronically active ulcerative colitis.

    Science.gov (United States)

    Raithel, M; Winterkamp, S; Weidenhiller, M; Müller, S; Hahn, E G

    2007-07-01

    Corticosteroids and 5-aminosalicylic acid are the primary standard therapy for inflammatory bowel disease. Recent immunologic data implicate an involvement of mast cell activation followed by increased histamine secretion and elevated tissue concentrations of histamine in the pathogenesis of ulcerative colitis. In the present case, the clinical course of a 35-year-old man with steroid-dependent chronic active ulcerative colitis, who did not respond to high-dose steroids, antibiotics, or azathioprine during 3 years, is reported. Clinical disease activity and established serological markers were recorded during 6 weeks of unsuccessful therapy and during the next 6 weeks, as a new nonsedative antihistaminergic drug, a mast cell stabilizer, and an hypoallergenic diet were implemented in addition to conventional therapy. Induction of remission was achieved within 2 weeks after treatment with fexofenadine, disodium cromoglycate, and an amino acid-based formula. Clinical disease activity, stool frequency, leukocytes, c-reactive protein, and orosomucoid levels in serum decreased rapidly. Daily steroid administration could be gradually reduced along with 6 weeks of this treatment. This report suggests that histamine and mast cell activity may be important pathophysiological factors responsible for persistent clinical and mucosal inflammatory activity in ulcerative colitis despite the use of steroids. In ulcerative colitis, patients unresponsive to conventional treatment, therapeutic considerations should also include an antiallergic approach when further signs of atopy or intestinal hypersensitivity are present.

  8. DSCG binding protein and process for preparing same

    Energy Technology Data Exchange (ETDEWEB)

    Pecht, I.; Mazurek, N.

    1987-07-28

    An essentially pure protein is described consisting essentially of the protein, (CBP), present in nature in membranes of basophile cells and in mast cells, having a molecular weight of about 60,000 +- 2,000 determined by SDS polyacrylamide electrophoresis an isoelectric point of about 3.9 and an amino acid composition of about 4 units of asparagine, 3 units of threonine and serine, 3 units glycine, 2 units alanine, 2 units proline, 1 unit cysteine, 2 units valine, 1 unit methionine, 1 unit isoleucine, 2 units leucine, 1 unit tyrosine, 1 unit phenylalanine, 2 units histamine, 2 units lysine and 1 unit arginine. The protein is able to build calcium and having a calcium dependent affinity to the disodium salt of 1,2 bis(-2 carboxychromon-5-yloxy)-2-hydroxy propane (DSCG).

  9. Disodium Cromoglycate (LomudaI) in Asthma with Emphasis on ...

    African Journals Online (AJOL)

    1971-07-31

    Jul 31, 1971 ... out of 20, no change in a standardized exercise test and an improvement in ... type antibodies. ... tion, heart rate, respiratory rate and arterial oxygen saturation ..... an increase in the respiratory rate per minute during exercise ...

  10. Disodium cromoglycate protects dystrophin-deficient muscle fibers from leakiness.

    Science.gov (United States)

    Marques, Maria Julia; Ventura Machado, Rafael; Minatel, Elaine; Santo Neto, Humberto

    2008-01-01

    In dystrophin-deficient fibers of mdx mice and in Duchenne dystrophy, the lack of dystrophin leads to sarcolemma breakdown and muscle degeneration. We verified that cromolyn, a mast-cell stabilizer agent, stabilized dystrophic muscle fibers using Evans blue dye as a marker of sarcolemma leakiness. Mdx mice (n=8; 14 days of age) received daily intraperitoneal injections of cromolyn (50 mg/kg body weight) for 15 days. Untreated mdx mice (n=8) were injected with saline. Cryostat cross-sections of the sternomastoid, tibialis anterior, and diaphragm muscles were stained with hematoxylin and eosin. Cromolyn dramatically reduced Evans blue dye-positive fibers in all muscles (P<0.05; Student's t-test) and led to a significant increase in the percentage of fibers with peripheral nuclei. This study supports the protective effects of cromolyn in dystrophic muscles and further indicates its action against muscle fiber leakiness in muscles that are differently affected by the lack of dystrophin.

  11. Sodium cromoglycate in nocturnal asthma.

    OpenAIRE

    1986-01-01

    To investigate whether mast cell degranulation was important in producing nocturnal asthma, the effect of a single high dose of nebulised sodium cromoglycate on overnight bronchoconstriction, oxygen saturation, and breathing patterns in eight patients with nocturnal wheeze was examined. The study took the form of a double blind placebo controlled crossover comparison. Treatment with cromoglycate did not reduce the overnight fall in FEV1 or FVC, although it was associated with improved nocturn...

  12. 21 CFR 172.135 - Disodium EDTA.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Disodium EDTA. 172.135 Section 172.135 Food and... Preservatives § 172.135 Disodium EDTA. The food additive disodium EDTA (disodium ethylenediaminetetraace-tate... following foods at not to exceed the levels prescribed, calculated as anhydrous calcium disodium EDTA:...

  13. Sodium cromoglycate in nocturnal asthma.

    Science.gov (United States)

    Morgan, A D; Connaughton, J J; Catterall, J R; Shapiro, C M; Douglas, N J; Flenley, D C

    1986-01-01

    To investigate whether mast cell degranulation was important in producing nocturnal asthma, the effect of a single high dose of nebulised sodium cromoglycate on overnight bronchoconstriction, oxygen saturation, and breathing patterns in eight patients with nocturnal wheeze was examined. The study took the form of a double blind placebo controlled crossover comparison. Treatment with cromoglycate did not reduce the overnight fall in FEV1 or FVC, although it was associated with improved nocturnal oxygenation. This study suggests that mast cell degranulation may not be important in the pathogenesis of nocturnal asthma. PMID:3085257

  14. Radioimmunoassay of sodium cromoglycate in human plasma

    Energy Technology Data Exchange (ETDEWEB)

    Brown, K.; Gardner, J.J.; Lockley, W.J.S.; Preston, J.R.; Wilkinson, D.J. (Fisons plc, Loughborough (UK). Pharmaceutical Div.)

    1983-01-01

    A sensitive radioimmunoassay method for sodium cromoglycate in human plasma is described. The lowest quantifiable concentration of sodium cromoglycate is 0.93 nmol/l when 0.1 ml plasma samples are analysed. The range of the method is limited; both 0.01 and 0.1 ml volumes of plasma must be analysed to encompass the concentration range 0.93-139 nmol/l which may be encountered in plasma samples from patients and human volunteers. The method is specific for sodium cromoglycate as indicated by a low cross-reactivity of the anti-cromoglycate antiserum with a number of drugs.

  15. 21 CFR 573.360 - Disodium EDTA.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Disodium EDTA. 573.360 Section 573.360 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS... Listing § 573.360 Disodium EDTA. The food additive disodium EDTA (disodium ethylenediaminetetraace-...

  16. Inhaled sodium cromoglycate for asthma in children

    NARCIS (Netherlands)

    van der Wouden, Johannes C.; Uijen, Johannes H. J. M.; Bernsen, Roos M. D.; Tasche, Marjolein J. A.; de Jongste, Johan C.; Ducharme, Francine

    2008-01-01

    Background Sodium cromoglycate has been recommended as maintenance treatment for childhood asthma for many years. Its use has decreased since 1990, when inhaled corticosteroids became popular, but it is still used in many countries. Objectives To determine the efficacy of sodium cromoglycate compare

  17. Radioimmunoassay of sodium cromoglycate in human plasma

    Energy Technology Data Exchange (ETDEWEB)

    Brown, K.; Gardner, J.J.; Lockley, W.J.S.; Preston, J.R.; Wilkinson, D.J. (Fisons Ltd., Loughborough (UK). Pharmaceutical Div.)

    1983-01-01

    A sensitive radioimmunoassay method for sodium cromoglycate in human plasma is described. The lowest quantifiable concentration of sodium cromoglycate is 0.93 nmol/1 when 0.1 ml plasma samples are analysed. Direct analysis of sodium cromoglycate concentrations in plasma samples collected up to several hours after the administration of single therapeutic doses of the compound is possible. The range of the method is limited; both 0.01 and 0.1 ml volumes of plasma must be analysed to encompass the concentration range 0.93-139 nmol/1 which may be encountered in plasma samples from patients and human volunteers. The method is specific for sodium cromoglycate as indicated by a low cross-reactivity of the anti-cromoglycate antiserum with a number of drugs.

  18. Cromoglycate drugs suppress eicosanoid generation in U937 cells by promoting the release of Anx-A1.

    Science.gov (United States)

    Yazid, Samia; Solito, Egle; Christian, Helen; McArthur, Simon; Goulding, Nicolas; Flower, Roderick

    2009-06-15

    Using biochemical, epifluorescence and electron microscopic techniques in a U937 model system, we investigated the effect of anti-allergic drugs di-sodium cromoglycate and sodium nedocromil on the trafficking and release of the anti-inflammatory protein Annexin-A1 (Anx-A1) when this was triggered by glucocorticoid (GC) treatment. GCs alone produced a rapid (within 5min) concentration-dependent activation of PKCalpha/beta (Protein Kinase C; EC 2.7.11.13) and phosphorylation of Anx-A1 on Ser(27). Both phosphoproteins accumulated at the plasma membrane and Anx-A1 was subsequently externalised thereby inhibiting thromboxane (Tx) B(2) generation. When administered alone, cromoglycate or nedocromil had little effect on this pathway however, in the presence of a fixed sub-maximal concentration of GCs, increasing amounts of the cromoglycate-like drugs caused a striking concentration-dependent enhancement of Anx-A1 and PKCalpha/beta phosphorylation, membrane recruitment and Anx-A1 release from cells resulting in greatly enhanced inhibition of TxB(2) generation. GCs also stimulated phosphatase accumulation at the plasma membrane of U937 cells. Both cromoglycate and nedocromil inhibited this enzymatic activity as well as that of a highly purified PP2A phosphatase preparation. We conclude that stimulation by the cromoglycate-like drugs of intracellular Anx-A1 trafficking and release (hence inhibition of eicosanoid release) is secondary to inhibition of a phosphatase PP2A (phosphoprotein phosphatase; EC 3.1.3.16), which probably forms part of a control loop to limit Anx-A1 release. These experiments provide a basis for a novel mechanism of action for the cromolyns, a group of drugs that have long puzzled investigators.

  19. Efficacy of cromoglycate in persistently wheezing infants.

    Science.gov (United States)

    Furfaro, S; Spier, S; Drblik, S P; Turgeon, J P; Robert, M

    1994-01-01

    A prospective study was undertaken to evaluate the efficacy of (sodium) cromoglycate in the treatment of persistent wheezing in 31 children between 4 and 12 months of age. The subjects were randomised to receive either 40 mg of cromoglycate (n = 16) or physiological saline as placebo (n = 15) three times a day by wet nebulisation in a double blind fashion for a period of six weeks. The patients were evaluated with daily symptom scores and respiratory function testing measuring maximal expiratory flow at functional residual capacity (VmaxFRC) before initiating treatment and upon completion. At baseline, mean (SD) symptom scores between the two groups were comparable (cromoglycate 99.5 (29.8), placebo 104.5 (29.7)) as were VmaxFRC expressed as per cent of predicted normals (cromoglycate 48 (28), placebo 46 (20)). Upon completion of the treatment protocol, no significant difference could be found between the two groups for either symptom score (cromoglycate 67.6 (40.2), placebo 58.6 (41.4)), or VmaxFRC (cromoglycate 52 (24), placebo 60 (32)). It is concluded, therefore, that 40 mg of cromoglycate three times a day administered via facemask and wet nebulisation was no more effective than placebo in the treatment of our sample of persistently wheezing infants under 1 year of age. PMID:7979527

  20. 21 CFR 582.6290 - Disodium phosphate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Disodium phosphate. 582.6290 Section 582.6290 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Disodium phosphate. (a) Product. Disodium phosphate. (b) Conditions of use. This substance is...

  1. 21 CFR 182.6290 - Disodium phosphate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Disodium phosphate. 182.6290 Section 182.6290 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... phosphate. (a) Product. Disodium phosphate. (b) Conditions of use. This substance is generally recognized...

  2. [Study of biopharmaceutic characteristics of cromoglycate eye drops].

    Science.gov (United States)

    Klimas, Rimantas; Inkeniene, Asta Marija; Briedis, Vitalis; Gerbutaviciene, Rima Jūrate

    2003-01-01

    One of the factors influencing the release of active substance from the drug formulation is presence of polymeric substance resulting in increase of viscosity of eye drops. Diffusion of sodium cromoglycate from polyvinyl alcohol 1.4%, 3% solutions and hypromellose 1% aqueous solution was investigated using in vitro method and diffusion coefficients were evaluated. Release of sodium cromoglycate from polyvinyl alcohol 1.4%, 3% solutions and hypromellose 1% aqueous solution was slower than the release from aqueous solution of sodium cromoglycate. The sodium cromoglycate diffusion from ophthalmic vehicle process kinetics was influenced by viscosity of these solutions and nature of the used polymers. The diffusion process of sodium cromoglycate from 1.4% PVA solution was more intensive if compared to diffusion from 1% hypromellose solution. The influence of excipients on sodium cromoglycate diffusion from eye drop formulation was evaluated when polymeric solutions have been used as vehicles.

  3. 21 CFR 73.2120 - Disodium EDTA-copper.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Disodium EDTA-copper. 73.2120 Section 73.2120 Food... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2120 Disodium EDTA-copper. (a) Identity. The color additive disodium EDTA-copper is disodium ] (4-)-N,N′,O,O′,O N,O N′] cuprate (2-)....

  4. Cromoglycate and Nedocromil: Influence on Airway Reactivity

    Science.gov (United States)

    Valletta, E. A.

    1994-01-01

    Although basic mechanisms of bronchial hyper-responsiveness (BHR) are still incompletely understood, inflammation of airways is likely to play a fundamental role in modulating BHR in patients with asthma. The involvement of several inflammatory cells (eosinophils, mast cells, lymphocytes, neutrophils, macrophages and platelets) and of bioactive mediators secreted by these cells in the pathogenesis of asthma is well documented. Sodium cromoglycate and nedocromil sodium are two pharmacological agents which have anti-allergic and anti-inflammatory properties. Their clinical effectiveness in mild to moderate asthma, and the capacity to reduce BHR under different natural and experimental conditions, make them valuable drugs for maintenance therapy in patients with asthma. PMID:18475597

  5. Enhanced biological phosphorus removal employing EDTA disodium

    Energy Technology Data Exchange (ETDEWEB)

    Bojinova, D.; Velkova, R. [Higher Inst. of Chemical Technology, Sofia (Bulgaria)

    1996-12-31

    The biological phosphorus removal is a promising alternative to the conventional chemical technologies for processing of phosphate raw materials. The object of this study was the effect of EDTA disodium on the biotreatment of tunisian phosphorite with the strain of Aspergillus niger. The incubation was carried out in two nutritive mediums, with different phosphate content. The experimental results showed that the additives of EDTA disodium in the nutritive medium increased the rate of extraction of P{sub 2}O{sub 5} and shortened significantly the time for biological leaching. 5 refs., 3 figs., 2 tabs.

  6. Lysine, disodium guanylate and disodium inosinate as flavor enhancers in low-sodium fermented sausages.

    Science.gov (United States)

    Campagnol, Paulo Cezar Bastianello; dos Santos, Bibiana Alves; Terra, Nelcindo Nascimento; Pollonio, Marise Aparecida Rodrigues

    2012-07-01

    Fermented sausages were produced with 50% replacement of NaCl with KCl and with addition of lysine, disodium guanylate, and disodium inosinate. The sausage production was monitored with physical, chemical and microbiological analyses. The final products were submitted to a consumer study. The replacement of NaCl with KCl did not cause changes in the technological process. However, defects in the sensory quality were detected. Lysine at a concentration of 1% with disodium inosinate (300 mg/kg) and disodium guanylate (300 mg/kg) reduced the sensory defects caused by the replacement of 50% NaCl with KCl allowing the preparation of sensory acceptable fermented sausages with a 50% decrease in sodium.

  7. Inhaled sodium cromoglycate in angiotensin-converting enzyme inhibitor cough.

    Science.gov (United States)

    Hargreaves, M R; Benson, M K

    1995-01-07

    Cough is a frequent side-effect of angiotensin-converting enzyme (ACE) inhibitors. We examined the effects of inhaled sodium cromoglycate in 10 patients with ACE-inhibitor cough in a double-blind crossover study. After a 2-week run-in, patients were randomised to either 2 weeks' inhaled sodium cromoglycate or placebo followed by a further 2 weeks on the other treatment. Patients kept a cough diary during each study period. Cough severity was recorded on a scale from 0 to 12. At the end of each study period the cough threshold to inhaled capsaicin was measured. 9 patients reported a reduction in cough after sodium cromoglycate. Median (range) daily cough scores during run-in and placebo periods were 3.6 (1.9-6.4) and 4.1 (0.6-8.1), respectively (p > 0.05). Median daily cough score after sodium cromoglycate was 1.8 (0.4-3; p sodium cromoglycate; and cough-reflex sensitivity to inhaled capsaicin was significantly reduced. Inhaled sodium cromoglycate is an effective treatment for ACE-inhibitor cough. Its effect may be due to suppression of afferent vagal activity.

  8. Sodium cromoglycate in asthma: correlation between response and serum concentrations.

    Science.gov (United States)

    Yahav, Y; Dany, S; Katznelson, D; Farfel, Z

    1988-01-01

    The clinical response to sodium cromoglycate treatment was compared with its concentration in serum. Twenty five children with asthma entered a 10 week trial of two baseline weeks followed by eight weeks of treatment by the inhalation of 20 mg of sodium cromoglycate spincaps four times a day. Individual clinical response was determined by the differences between baseline and treatment periods of: (a) percentage of symptomless days (delta score 0); (b) diary derived daily score for four symptoms (delta DS); and (c) peak expiratory flow rate (delta PEFR). At the end of the treatment period, patients inhaled a 20 mg spincap of sodium cromoglycate and the technique of inhalation was graded. Concentrations of sodium cromoglycate in serum were measured by radioimmunoassay in samples withdrawn 5 to 120 minutes after inhalation. Delta Score 0, delta DS, and delta PEFR correlated significantly with the area under the concentration time curve. Both the area under the sodium cromoglycate concentration time curve and clinical response correlated significantly with inhalation technique score. We suggest that response of children with asthma to inhalation treatment with sodium cromoglycate is correlated to its serum concentrations. PMID:3133990

  9. Nebulised sodium cromoglycate in recurrently wheezy preschool children.

    Science.gov (United States)

    Cogswell, J J; Simpkiss, M J

    1985-01-01

    A double blind crossover study of nebulised sodium cromoglycate in 27 asthmatic preschool children was carried out over a one year period. All subjects had sufficiently severe asthma to have had at least one admission to hospital. The active treatment was sodium cromoglycate 20 mg (in 2 ml) administered by a nebuliser four times daily. Assessment was made by a diary card and clinical examination. Results were analysed in 24 subjects who completed the study. Statistical analysis allowed for order of treatment and seasonal effects. Significant results in favour of treatment with sodium cromoglycate were obtained for night cough, day activity, percentage of symptom free days, and overall severity of asthma. During active treatment there was no reduction in the rate of admissions to hospital or intravenous drugs used. The wheeze score during the week after an upper respiratory tract infection was not reduced during treatment with sodium cromoglycate. Nebulised sodium cromoglycate is a tedious prophylactic treatment for the young asthmatic child but is useful when other treatments have failed. PMID:3929698

  10. Nebulised sodium cromoglycate in infancy: airway protection after deterioration.

    Science.gov (United States)

    O'Callaghan, C; Milner, A D; Swarbrick, A

    1990-01-01

    Over a two year period 100 infants with histories of wheeze were challenged with nebulised water. They were sedated and lung function measured by total body plethysmography. Thirteen of the 53 infants who developed bronchoconstriction after challenge with nebulised water were given nebulised sodium cromoglycate and rechallenged with nebulised water. All infants were initially challenged with normal saline, after which there was no significant change in lung function. After challenge with nebulised water and sodium cromoglycate there were significant decreases in specific conductance compared with those found after challenge with normal saline. After rechallenge with nebulised water there was no deterioration in lung function. Although sodium cromoglycate caused a deterioration in lung function in these infants, it protected their airways from challenge with nebulised water. PMID:2111980

  11. Nebulised sodium cromoglycate and verapamil in methacholine induced asthma.

    Science.gov (United States)

    Boner, A L; Vallone, G; Andreoli, A; Biancotto, R; Warner, J O

    1987-01-01

    Fifteen children with asthma underwent challenges with methacholine on separate days after double blind administration by nebuliser of either verapamil (5 mg), cromoglycate (20 mg), or saline (placebo). The provocation doses that produced a 20% fall in forced expiratory volume in one second (PD20) were analysed. There was variation in the protective effects of verapamil and cromoglycate among the patients. Although cromoglycate produced an increase in PD20 in 53% of the children tested, the protection was not significant when compared with the placebo. Verapamil was partially protective, however, in 80% of children and achieved significantly better results than the placebo. We suggest that this is likely to be due to a direct effect on bronchial smooth muscle. PMID:3105472

  12. Nebulised cromoglycate, theophylline, and placebo in preschool asthmatic children.

    Science.gov (United States)

    Glass, J; Archer, L N; Adams, W; Simpson, H

    1981-01-01

    Sixteen children aged under 5 years with chronic asthma completed a double-blind crossover trial of treatment with oral choline theophyllinate (6.7 mg/kg four times daily) and nebulised sodium cromoglycate (20 mg four times daily). The trial comprised three 8-week treatment periods during which active sodium cromoglycate, active choline theophyllinate, and placebo were given in random order. Symptom scores for sleep disturbance, cough, wheeze, and daily activities were similar during the three treatment periods if results were analysed using Friedman's non-parametric analysis of variance. However the Mantel-Haenszel test showed that sodium cromoglycate was superior to placebo (P less than 0.05) in maintaining normal daily activities. Either regimen is safe and well tolerated by young children. PMID:6791596

  13. Deep inspiration increases the absorption of inhaled sodium cromoglycate.

    Science.gov (United States)

    Richards, R; Fowler, C; Simpson, S F; Renwick, A G; Holgate, S T

    1989-01-01

    The plasma concentrations of sodium cromoglycate were measured for 4 h following a single dose of 20 mg given by inhalation to six normal volunteers. A series of forced expiratory manoeuvres was performed 2 h after the dose, which resulted in a rapid and marked increase in the plasma concentrations of the drug. A similar increase was found in three volunteers who undertook a single deep inspiration at 4 h. These data indicate that the absorption of cromoglycate from the airways can be affected by manoeuvres used to assess lung function. PMID:2503020

  14. 色甘酸钠鼻吸治疗过敏性鼻炎%Allergic rhinitis with disodium cromoglycate

    Institute of Scientific and Technical Information of China (English)

    高春妮; 康小宁

    2009-01-01

    过敏性鼻炎是目前临床常见的一种过敏性疾病,典型症状有突然阵发性鼻塞、鼻痒、连续喷嚏、流清水样鼻涕等.色甘酸钠是治疗支气管哮喘的一种常用药物,通过抑制肥大细胞释放过敏介质来发挥作用.我们用鼻吸色甘酸钠治疗过敏性鼻炎,在临床上取得了一定的效果.现将结果报告如下:

  15. Effect of topical cromoglycate solution on atopic dermatitis: combined treatment of sodium cromoglycate solution with the oral anti-allergic medication, oxatomide.

    Science.gov (United States)

    Kimata, H; Hiratsuka, S

    1994-02-01

    The effect of topically applied sodium cromoglycate solution in moderate to severe atopic dermatitis (AD) in children aged 4-14 years was studied in a double-blind, placebo-controlled, randomized group-comparative trial. One group of patients was treated with topical sodium cromoglycate solution and oral oxatomide whereas the other group was treated with topical placebo solution and oral oxatomide. After 4 weeks, AD improved significantly in the group treated with the sodium cromoglycate solution and oxatomide combination while marginal improvement was noted in the placebo. In addition, spontaneous IgE production from peripheral blood mononuclear cells decreased significantly in the sodium cromoglycate group but not in the placebo group. These results suggest that sodium cromoglycate solution may be very effective in combination with anti-allergic medication in the treatment of moderate to severe AD in children.

  16. Dose-response effect of sodium cromoglycate pressurised aerosol in exercise induced asthma.

    OpenAIRE

    Tullett, W M; Tan, K. M.; Wall, R T; Patel, K R

    1985-01-01

    The effects of 2, 10, and 20 mg of sodium cromoglycate delivered by aerosol were compared with those of placebo in a double blind study in 11 patients with extrinsic and exercise induced asthma. The effect of nebulised sodium cromoglycate delivered through a Wright nebuliser (estimated dose 12 mg) was also studied. Patients exercised on a treadmill for six to eight minutes at submaximal work loads on five days, 30 minutes after inhaling placebo or sodium cromoglycate. The FEV1 was recorded be...

  17. Dose-response effect of sodium cromoglycate pressurised aerosol in exercise induced asthma.

    Science.gov (United States)

    Tullett, W M; Tan, K M; Wall, R T; Patel, K R

    1985-01-01

    The effects of 2, 10, and 20 mg of sodium cromoglycate delivered by aerosol were compared with those of placebo in a double blind study in 11 patients with extrinsic and exercise induced asthma. The effect of nebulised sodium cromoglycate delivered through a Wright nebuliser (estimated dose 12 mg) was also studied. Patients exercised on a treadmill for six to eight minutes at submaximal work loads on five days, 30 minutes after inhaling placebo or sodium cromoglycate. The FEV1 was recorded before treatment, before exercise, and up to 30 minutes after exercise. Mean baseline values of FEV1 before and after placebo or sodium cromoglycate did not differ significantly on the five days. After exercise the mean (SEM) maximal percentage fall in FEV1 after placebo; 12 mg sodium cromoglycate nebuliser solution; and 2, 10, and 20 mg sodium cromoglycate aerosol were 31.1 (3.8); 9.4 (2.1); and 19.4 (4.6), 13.7 (3.5), and 9.4 (1.9). Sodium cromoglycate inhibited exercise induced asthma at all doses used; the protective effect of the aerosol increased from 2 to 20 mg. The protective effect of 20 mg sodium cromoglycate aerosol was similar to that seen with 12 mg nebulised solution. Our results suggest that the effect of sodium cromoglycate aerosol in exercise induced asthma is dose related.

  18. Dose-response effect of sodium cromoglycate pressurised aerosol in exercise induced asthma.

    Science.gov (United States)

    Tullett, W M; Tan, K M; Wall, R T; Patel, K R

    1985-01-01

    The effects of 2, 10, and 20 mg of sodium cromoglycate delivered by aerosol were compared with those of placebo in a double blind study in 11 patients with extrinsic and exercise induced asthma. The effect of nebulised sodium cromoglycate delivered through a Wright nebuliser (estimated dose 12 mg) was also studied. Patients exercised on a treadmill for six to eight minutes at submaximal work loads on five days, 30 minutes after inhaling placebo or sodium cromoglycate. The FEV1 was recorded before treatment, before exercise, and up to 30 minutes after exercise. Mean baseline values of FEV1 before and after placebo or sodium cromoglycate did not differ significantly on the five days. After exercise the mean (SEM) maximal percentage fall in FEV1 after placebo; 12 mg sodium cromoglycate nebuliser solution; and 2, 10, and 20 mg sodium cromoglycate aerosol were 31.1 (3.8); 9.4 (2.1); and 19.4 (4.6), 13.7 (3.5), and 9.4 (1.9). Sodium cromoglycate inhibited exercise induced asthma at all doses used; the protective effect of the aerosol increased from 2 to 20 mg. The protective effect of 20 mg sodium cromoglycate aerosol was similar to that seen with 12 mg nebulised solution. Our results suggest that the effect of sodium cromoglycate aerosol in exercise induced asthma is dose related. PMID:3918356

  19. Sodium cromoglycate and doxantrazole are oxygen radical scavengers.

    Science.gov (United States)

    Sadeghi-Hashjin, G; Nijkamp, F P; Henricks, P A J; Folkerts, G

    2002-10-01

    The effects of two mast cell stabilisers, sodium cromoglycate (SCG) and doxantrazole, on the formation of reactive oxygen species (ROS) were studied. Guinea-pig alveolar macrophages (AMs) generated lucigenin-dependent chemiluminescence (LDCL). This was increased when the cells were stimulated by phorbol myristate acetate (PMA) or zymosan (by 133% and 464%, respectively, in total LDCL over 60 min). SCG decreased PMA-induced LDCL at higher concentrations (10 mM, by 55%) than doxantrazole (1 mM, by 75%). SCG decreased radical production by AMs in response to zymosan in a concentration-dependent manner by sodium cromoglycate-inhibited lucigenin-dependent chemiluminescence production by guinea-pig alveolar macrophages is due to a direct scavenging effect on reactive oxygen species. Doxantrazole is approximately 10-times more potent. Mast cell stabilisers may be effective in allergic asthma not only by preventing the allergen-induced mediator release, but also by preventing radical-induced lung damage.

  20. Effects of early intervention with inhaled sodium cromoglycate in childhood asthma.

    Science.gov (United States)

    Yoshihara, S; Kanno, N; Yamada, Y; Ono, M; Fukuda, N; Numata, M; Abe, T; Arisaka, O

    2006-01-01

    International and Japanese guidelines classify childhood asthma as mild, moderate, or severe, and recommend treatment with "as needed" bronchodilators, inhaled sodium cromoglycate, and inhaled corticosteroids, respectively. Alternatively, some investigators proposed inhaled corticosteroids as first-line therapy to prevent airway inflammatory obstruction. This article describes a clinical study assessing the effect of early intervention with inhaled sodium cromoglycate in childhood asthma. This was a retrospective study of 189 asthmatic children treated with inhaled sodium cromoglycate for five years and whose age of onset of asthma was six year of age or younger. An end-of-study questionnaire completed the examination. Children administered oral or inhaled corticosteroids simultaneously with sodium cromoglycate, were excluded. Asthma scores as defined by the Japanese Pediatric Allergic Committee, were reduced continuously during the five years after the start of sodium cromoglycate treatment. The frequency of emergency department visits and hospitalizations also decreased. Significant between-period intervention differences showed improvement of clinical outcomes for children with severe asthma during the five years of sodium cromoglycate inhalation. The early intervention regime of starting sodium cromoglycate inhalation within two years of the onset of asthma shows a large improvement in the long-term prognosis of childhood asthma, especially for children with severe asthma. It is possible that starting inhaled sodium cromoglycate earlier than the present recommendation of corticosteroids could further improve clinical outcomes, but a prospective study should be performed to verify our results.

  1. Exercise-induced urticaria and angio-oedema with relief from cromoglycate insufflation.

    Science.gov (United States)

    Hatty, S.; Mufti, G. J.; Hamblin, T. J.

    1983-01-01

    The pathogenesis of physical urticarias is unknown and the treatment is often difficult and unsatisfactory. A patient with severe exercise-induced angio-oedema and urticaria is reported who responded dramatically to cromoglycate by insufflation and not when treated with orally active cromoglycate. PMID:6415638

  2. Nebulised sodium cromoglycate in infancy: airway protection after deterioration.

    OpenAIRE

    O'Callaghan, C.; Milner, A. D.; Swarbrick, A.

    1990-01-01

    Over a two year period 100 infants with histories of wheeze were challenged with nebulised water. They were sedated and lung function measured by total body plethysmography. Thirteen of the 53 infants who developed bronchoconstriction after challenge with nebulised water were given nebulised sodium cromoglycate and rechallenged with nebulised water. All infants were initially challenged with normal saline, after which there was no significant change in lung function. After challenge with nebu...

  3. [Therapy of chronic allergic conjunctivitis with sodium cromoglycate (lecrolin)].

    Science.gov (United States)

    Polunin, G S; Makarov, I A

    1997-01-01

    The efficacy of lecrolin (2% sodium cromoglycate) eye drops was assessed in 22 patients with allergic conjunctivitis. Positive effect was attained in all the patients on day 4.0 +/- 1.2. Signs of the disease exacerbation completely disappeared in 68% of patients in 8.3 +/- 2.4 days. No side effects of any type were observed for a month of using lecrolin eye drops.

  4. Scientific Opinion on the safety and efficacy of disodium 5?-ribonucleotides, disodium 5?-guanylate, disodium 5?-inosinate for all animal species and categories

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP

    2014-03-01

    Full Text Available The flavours included in this assessment are widely present in nature as the building blocks of DNA and RNA. In the absence of any information on the microbial strains or substrates used for the production of the additives, and with little information on the manufacturing process, the FEEDAP Panel is unable to ascertain whether the manufacturing process introduces any safety concerns. Disodium 5′-guanylate and disodium 5′-inosinate and their mixture are considered to be safe for the target animals and the consumer. However, considering the lack of information on the production process, these conclusions apply only to the compounds ‘per se’ and their extrapolation to any feed additive containing these compounds is not possible. In the absence of any data related to hazard to the user, it would be prudent to regard disodium 5′-guanylate and disodium 5′-inosinate and their mixture as potentially hazardous to workers by skin or inhalation exposure. The compounds under assessment are naturally present in feed materials; therefore, no risk to the safety for the environment is foreseen. Since these compounds are used in food as flavourings, and their function in feed is essentially the same as that in food, no further demonstration of efficacy is necessary.

  5. Crystal structure and characterization of pyrroloquinoline quinone disodium trihydrate

    Directory of Open Access Journals (Sweden)

    Ikemoto Kazuto

    2012-06-01

    Full Text Available Abstract Background Pyrroloquinoline quinone (PQQ, a tricarboxylic acid, has attracted attention as a growth factor, and its application to supplements and cosmetics is underway. The product used for these purposes is a water-soluble salt of PQQ disodium. Although in the past, PQQ disodiumpentahydrates with a high water concentration were used, currently, low hydration crystals of PQQ disodiumpentahydrates are preferred. Results We prepared a crystal of PQQ disodium trihydrate in a solution of ethanol and water, studied its structure, and analyzed its properties. In the prepared crystal, the sodium atom interacted with the oxygen atom of two carboxylic acids as well as two quinones of the PQQ disodium trihydrate. In addition, the hydration water of the prepared crystal was less than that of the conventional PQQ disodium crystal. From the results of this study, it was found that the color and the near-infrared (NIR spectrum of the prepared crystal changed depending on the water content in the dried samples. Conclusions The water content in the dried samples was restored to that in the trihydrate crystal by placing the samples in a humid environment. In addition, the results of X-ray diffraction (XRD and X-ray diffraction-differential calorimetry (XRD-DSC analyses show that the phase of the trihydrate crystal changed when the crystallization water was eliminated. The dried crystal has two crystalline forms that are restored to the original trihydrate crystals in 20% relative humidity (RH. This crystalline (PQQ disodium trihydrate is stable under normal environment.

  6. 40 CFR 721.7000 - Polymer of disodium maleate, allyl ether, and ethylene oxide.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polymer of disodium maleate, allyl... New Uses for Specific Chemical Substances § 721.7000 Polymer of disodium maleate, allyl ether, and... substance identified generically as a polymer of disodium maleate, allyl ether, and ethylene oxide (P-91...

  7. NSAIDs in the Treatment of Adult Asthma: Sodium Cromoglycate and Nedocromil Sodium

    Directory of Open Access Journals (Sweden)

    Michel-Y Rouleau

    1995-01-01

    Full Text Available Among nonsteroidal anti-inflammatory drugs used in the treatment of adult asthma, sodium cromoglycate and nedocromil sodium are the most frequently prescribed. These medications have a similar efficacy profile in asthma although it has been suggested that nedocromil is more powerful than cromoglycate, particularly in its steroid sparing effects. Both drugs have been recommended as alternatives to steroids in the treatment of mild asthma. They are useful in the prevention of bronchospasm induced by exposure to allergens or to a variety of other stimuli. In comparison with theophylline or low dose inhaled steroids, cromoglycate and nedocromil have shown a similar antiasthmatic efficacy, although this is variable among patients.

  8. "Cromoglycate: A healing agent in acute Chlorine-induced lung damage "

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    "Pipelzadeh MH

    2002-09-01

    Full Text Available In the present study the effectiveness of sodium cromoglycate in treatment of alveolar damage induced by chlorine gas in rats was investigated. Chlorine was generated by chemical interaction between potassium permanganate and concentrated hydrochloric acid. The rats were exposed to sublethal dose of chlorine gas. Treatment with 2.5 mg of 1 ml nebulized sodium cromoglycate solution over 5 minutes was initiated 30 minutes after exposure followed by twice daily treatment for 21 days. Results of this study show that cromoglycate reduced alveolar thickness, septal rupture, hemorrhage and detachment of the epithelial lining of the bronchioles induced by chlorine gas.

  9. Effects of sodium cromoglycate and nedocromil sodium on histamine secretion from human lung mast cells.

    Science.gov (United States)

    Leung, K B; Flint, K C; Brostoff, J; Hudspith, B N; Johnson, N M; Lau, H Y; Liu, W L; Pearce, F L

    1988-01-01

    Sodium cromoglycate and nedocromil sodium produced a dose dependent inhibition of histamine secretion from human pulmonary mast cells obtained by bronchoalveolar lavage and by enzymatic dissociation of lung parenchyma. Both compounds were significantly more active against the lavage cells than against the dispersed lung cells, and nedocromil sodium was an order of magnitude more effective than sodium cromoglycate against both cell types. Tachyphylaxis was observed with the parenchymal cells but not with the lavage cells. Nedocromil sodium and sodium cromoglycate also inhibited histamine release from the lavage cells of patients with sarcoidosis and extrinsic asthma. PMID:2462755

  10. A double-blind, placebo-controlled comparison of sodium cromoglycate and ketotifen in the treatment of childhood asthma.

    Science.gov (United States)

    Croce, J; Negreiros, E B; Mazzei, J A; Isturiz, G

    1995-06-01

    We compared three treatments: sodium cromoglycate 5 mg aerosol and placebo syrup (39 patients), placebo aerosol and ketotifen syrup (39 patients), and placebo aerosol and syrup (36 patients). The patients (mean age 11.7 years) had mostly allergic, moderately severe asthma. Treatments were added to current therapy (mostly bronchodilators only) for 3 months. Aerosols were taken four times daily and syrups twice daily. The following results were significant at a level of 5%. At the final clinic visit, the changes from baseline in lung function favored sodium cromoglycate over the other treatments. During month 3, sodium cromoglycate was superior to ketotifen for night symptoms, morning tightness, daytime symptoms, and cough. Bronchodilator use decreased more with sodium cromoglycate than ketotifen. Patients' and clinicians' overall opinions of treatment effectiveness favored sodium cromoglycate over ketotifen and placebo. In these patients, sodium cromoglycate was both effective and superior to ketotifen.

  11. Determination of the antiulcer properties of sodium cromoglycate in pylorus-ligated albino rats

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    Srivastava Vivek

    2010-01-01

    Full Text Available Objectives : To study the ulcer protective property of sodium cromoglycate in pylorus-ligated rats and the biochemical role in ulcer protection by various biochemical tests. Materials and Methods : The ulcer protective effect of sodium cromoglycate was studied using a Pyloric Ligation Model using Wistar albino rats. The antiulcer effect of sodium cromoglycate 40 mg/kg b.w., i.p., was compared with the reference drug ranitidine 27 mg/kg b.w., i.p. The ulcer index was calculated and other biochemical parameters like free acidity, total acidity, pH, mucin, pepsin and volume of gastric juice were determined. Results : Pylorus ligation showed a significant (P < 0.01 reduction in gastric volume, free acidity, total acidity and ulcer index as compared to the control. Conclusion : Sodium cromoglycate has activity equipotent to ranitidine.

  12. Contrast of the Effect of Alomide and Sodium Cromoglycate in the Treatment of Allergic Eye Diseases

    Institute of Scientific and Technical Information of China (English)

    Wenlan Zhang; Zhende Lin

    2000-01-01

    Purpose: To observe the clinical effect of alomide and sodium cromoglycate eyedrops in the treatment of atopic conjunctivitis, vernal conjunctivitis and giant papillary conjunctivitis.Methods: Randomized control study was used. Alomide and sodium cromoglycate eyedrops used to treat two groups of patients for two weeks. The effects of the two groups were compared.Results: With respect of comprehensive therapeutic effect, the effectiveness rate was 83.6% in alomide group, and 63.3% in sodium cromoglycate group, which was not significantly different statistically. With respect of itching alleviation, alomide is more effective than sodium cromoglycate. No adverse effects were found in both groups.Conclusion: Our study suggests that alomide is a safe and effective drug in the treatment of allergic conjunctivitis.

  13. The effect of cromoglycate on time-dependent histamine and serotonin concentrations in stored blood products.

    Science.gov (United States)

    Konca, Kamuran; Tiftik, E Naci; Aslan, Gönül; Kanik, Arzu; Yalçin, Atilla

    2006-04-01

    Biogenic amines, having vascular and inflammatory effects, are accepted as a potential threat for some non-hemolytic transfusion reactions. The aim of this study was to investigate time-dependent histamine/serotonin levels in stored blood products and to see whether cromoglycate has any effect on these mediators. Either for platelet or whole blood, 10-fold concentrations of cromoglycate (1 microg ml(-1), 10 microg ml(-1), 100 microg ml(-1)) with controls prepared as pairs of replicate bags collected from two healthy subjects, separately. By using enzyme immunoassay, histamine and serotonin levels were determined in platelet or blood replicates. Histamine levels increased significantly with time but serotonin remained unchanged during the storage of platelet or blood specimens. Cromoglycate had no effect on these biogenic amines except an increase of serotonin in whole blood specimens containing 100 microg ml(-1) of it. So, cromoglycate cannot protect blood products against rising levels of histamine or serotonin.

  14. Betamethasone valerate compared with sodium cromoglycate in asthmatic children.

    Science.gov (United States)

    Ng, S. H.; Dash, C. H.; Savage, S. J.

    1977-01-01

    A double-blind, cross-over study was undertaken to compare inhalation of betamethasone valerate (BV, 800 microgram daily) with sodium cromoglycate (SCG, 80 mg daily) in twenty children requiring bronchodilators for perennial asthma. Each treatment period lasted 4 weeks but statistical comparisons were made only in respect of the last 14 days of each therapy. When the children were using BV they required not only less of the bronchodilator drugs but had fewer symptoms and higher daily peak expiratory flow rates when taking SCG. Statistically, all these differences were highly significant. For 2 weeks before the main trial each child was given a placebo aerosol (single-blind) to assess severity of asthma. In comparison with this period, SCG was associated with a significantly increased peak expiratory flow rate a lower symptom score by day but not by night, but their usage of bronchodilators followed a similar pattern. When the BV period was compared with the placebo period, patients had an even more significant rise in peak expiratory flow rate, less day and night symptoms, and took hardly any bronchodilators. The response to the two drugs did seem to depend upon which was given first. No monilial infections were found, nor any measurable defect in adrenal response from either treatment. Betamethasone valerate is considered to be superior to sodium cromoglycate as a treatment for childhood asthma insufficiently controlled on bronchodilators. PMID:407559

  15. Relative bioavailability of sodium cromoglycate to the lung following inhalation, using urinary excretion

    Science.gov (United States)

    Aswania, O A; Corlett, S A; Chrystyn, H

    1999-01-01

    Aims To determine if a urinary excretion method, previously described for salbutamol, could also indicate the relative bioavailability of sodium cromoglycate to the lung following inhalation from a metered dose inhaler. Method Inhaled (INH), inhaled+oral charcoal (INHC), oral (ORAL) and oral+oral charcoal (ORALC) 20 mg doses of sodium cromoglycate were given via a randomised cross-over design to 11 healthy volunteers trained on how to use a metered dose inhaler. Urine samples were collected at 0.0, 0.5, 1.0 and up to 24 h post dosing and the sodium cromoglycate urinary concentration was measured using a high performance liquid chromatographic method. Results No sodium cromoglycate was detected in the urine up to 24 h following ORALC dosing. A mean (s.d.) of 3.6 (4.3) μg, 10.4 (10.9) μg and 83.7 (71.1) μg of the ORAL dose was excreted, in the urine, during the 0.5, 1.0 and 24 h post dose collection periods, respectively. Following INH dosing, the renal excretion was significantly higher (P < 0.01) with 32.9 (14.5) μg, 61.2 (28.3) μg and 305.6 (82.3) μg excreted, respectively. The SCG excreted at 0.5, 1.0 and 24 h collection periods following INHC dosing were 26.3 (8.4) μg, 49.3 (18.1) μg and 184.9 (98.4) μg, respectively. There was no significant difference between the excretion rate of sodium cromoglycate following INHC when compared with INH dosing in the first 0.5 and 1.0 h. Conclusions The urinary excretion of sodium cromoglycate in the first 0.5 h post inhalation can be used to compare the relative lung deposition of two inhaled products or of the same product using different inhalation techniques. This represents the relative bioavailability of sodium cromoglycate to the lung following inhalation. Similar 24 h urinary excretion of sodium cromoglycate can be use to compare the total dose delivered to the body from two different inhalation products/inhalation methods. This represents the relative bioavailability of sodium cromoglycate to the body

  16. Relative lung bioavailability of generic sodium cromoglycate inhalers used with and without a spacer device.

    Science.gov (United States)

    Aswania, O; Chrystyn, H

    2001-01-01

    The relative lung bioavailability of sodium cromoglycate following inhalation has been evaluated using urinary drug excretion in nine healthly volunteers. Each inhaled four 5 mg sodium cromoglycate doses from a generic metered dose inhaler (MDI) and when it was attached to large volume spacer (MDI + VOL). A breath-actuated MDI was also evaluated either used on its own (EB) or attached to a small volume spacer tube (EBO). The mean (SD) urinary excretion of sodium cromoglycate in the first 30 min post-inhalation was 34.1 (20.2), 211.7 (123.5), 29.3 (19.5) and 52.8 (36.0) microg following MDI, MDI+VOL, EB and EBO, respectively. The cumulative mean (SD) urinary excretion of sodium cromoglycate over the 24 h post-inhalation was 364.7 (266.2), 1227.1 (459.0), 280.2 (155.4) and 429.5 (176.7) microg. A metered dose inhaler attached to a large volume spacer delivers more sodium cromoglycate to the lungs than any other inhalation method.

  17. Inhaled sodium cromoglycate to treat cough in advanced lung cancer patients.

    Science.gov (United States)

    Moroni, M; Porta, C; Gualtieri, G; Nastasi, G; Tinelli, C

    1996-07-01

    C-fibres probably represent the common final pathway in both ACE inhibitors and neoplastic cough. A recent report demonstrated that inhaled sodium cromoglycate is an effective treatment for ACE inhibitors' cough; this effect might be due to the suppression of afferent unmyelinated C-fibres. We tested the hypothesis that inhaled sodium cromoglycate might also be effective in lung cancer patients who presented with irritative neoplastic cough. Twenty non-small-cell lung cancer (NSCLC) patients complaining of cough resistant to conventional treatment were randomised to receive, in a double-blind trial, either inhaled sodium cromoglycate or placebo. Patients recorded cough severity daily, before and during treatment, on a 0 to 4 scale. The efficacy of treatment was tested with the Mann-Whitney U-test for non-parametric measures, comparing the intergroup differences in the measures of summary of symptom scores calculated in each patient before and after treatment. We report that inhaled sodium cromoglycate can reduce cough, also in NSCLC patients and that such reduction, observed in all patients treated, is statistically significant (P sodium cromoglycate appears to be a cost-effective and safe treatment for lung cancer-related cough.

  18. Attenuation of aspirin-induced bronchoconstriction by sodium cromoglycate and nedocromil sodium.

    Science.gov (United States)

    Robuschi, M; Gambaro, G; Sestini, P; Pieroni, M G; Refini, R M; Vaghi, A; Bianco, S

    1997-04-01

    The protective activity of nedocromil sodium and of sodium cromoglycate against aspirin-induced asthma has never been investigated in controlled studies. Because it has been reported that aspirin-induced platelet-mediated cytotoxic activity in vitro is inhibited after treatment in vivo with nedocromil but not with cromoglycate, we investigated whether these compounds also exhibit a different protective activity against aspirin-induced bronchoconstriction. Ten patients with aspirin-induced asthma underwent three bronchial challenges with a single dose of lysine acetylsalicylate (LASA) that caused a decrease in FEV1 of 25% or more in a preliminary dose-response test 30 min after inhalation of 4 mg nedocromil sodium, 10 mg sodium cromoglycate, or placebo. FEV1 and SRaw were recorded at intervals for 195 min. After placebo, LASA caused a maximal decrease in FEV1 of 42 +/- 4% of baseline. After cromoglycate and nedocromil the maximal decrease in FEV1 was reduced to 20 +/- 3% and 18 +/- 4%, respectively (p sodium cromoglycate and nedocromil sodium are equally effective in attenuating aspirin-induced bronchoconstriction and that it is unlikely that platelet activation participates in the pathogenesis of aspirin-induced asthma.

  19. Protective effect of sodium cromoglycate on lipopolysaccharide-induced bronchial obstruction in asthmatics.

    Science.gov (United States)

    Michel, O; Ginanni, R; Sergysels, R

    1995-11-01

    Lipopolysaccharides (LPS, the major part of endotoxins) are bacterial proinflammatory substances which can induce in asthmatic patients after inhalation a bronchial obstruction with an increase in both histamine bronchial hyperresponsiveness and blood inflammatory markers. The aim of the present study was to evaluate whether an acute inhalation of sodium cromoglycate, an anti-inflammatory and membrane-stabilizating agent, can block the LPS-induced lung function response. Using a double-blind placebo-controlled crossover method, 7 asthmatic subjects were submitted, at 4 days' interval, to a bronchial challenge test with either solvent solution or LPS (20 micrograms) preceded by inhalation of sodium cromoglycate (10 mg) or placebo. Compared to the solvent reaction, LPS induced a significant bronchial obstruction [measured by both the forced expiratory volume in 1 s (FEV1) and the airway resistances] beginning at the 60th minute and lasting more than 300 min (p sodium cromoglycate significantly inhibited the LPS-induced bronchial obstruction. The total lung capacity did not change significantly after LPS inhalation. Thus, this study showed that in asthmatics the LPS-induced FEV1 response is blocked by acute treatment with sodium cromoglycate. Sodium cromoglycate could be an active treatment in asthmatics exposed to house dust containing endotoxin.

  20. Duration of action of sodium cromoglycate on exercise induced asthma: comparison of 2 formulations.

    Science.gov (United States)

    Bar-Yishay, E; Gur, I; Levy, M; Volozni, D; Godfrey, S

    1983-01-01

    Thirteen asthmatic children aged 9-14 years participated in a double blind randomised trial to compare the effectiveness and duration of action of 2 formulations of sodium cromoglycate; one a 20 mg capsule of powdered sodium cromoglycate delivered by turbo inhaler (spinhaler), and the other 1 mg of aerosolised sodium cromoglycate delivered by pressurised cannister inhaler (aerosol). The children performed exercise tests on each of 3 days in a 10 day period--15 minutes, 2 hours, and 6 hours after inhalation of powder, aerosol, or a placebo. Two patients were not protected from exercise induced asthma by either formulation of sodium cromoglycate. Among the remaining patients both formulations gave good protection from exercise induced asthma 15 minutes after inhalation, and the effect of both wore off steadily over the next 6 hours. The spinhaler gave appreciably better protection than the aerosol at 15 minutes after inhalation, and was the only formulation to provide good protection at 2 hours and 6 hours. The more limited effectiveness of the aerosol may be explained by the lower dose of sodium cromoglycate and the more complicated inhalation technique required. PMID:6412638

  1. Inhaled sodium cromoglycate to treat cough in advanced lung cancer patients.

    Science.gov (United States)

    Moroni, M.; Porta, C.; Gualtieri, G.; Nastasi, G.; Tinelli, C.

    1996-01-01

    C-fibres probably represent the common final pathway in both ACE inhibitors and neoplastic cough. A recent report demonstrated that inhaled sodium cromoglycate is an effective treatment for ACE inhibitors' cough; this effect might be due to the suppression of afferent unmyelinated C-fibres. We tested the hypothesis that inhaled sodium cromoglycate might also be effective in lung cancer patients who presented with irritative neoplastic cough. Twenty non-small-cell lung cancer (NSCLC) patients complaining of cough resistant to conventional treatment were randomised to receive, in a double-blind trial, either inhaled sodium cromoglycate or placebo. Patients recorded cough severity daily, before and during treatment, on a 0 to 4 scale. The efficacy of treatment was tested with the Mann-Whitney U-test for non-parametric measures, comparing the intergroup differences in the measures of summary of symptom scores calculated in each patient before and after treatment. We report that inhaled sodium cromoglycate can reduce cough, also in NSCLC patients and that such reduction, observed in all patients treated, is statistically significant (P < 0.001). Inhaled sodium cromoglycate appears to be a cost-effective and safe treatment for lung cancer-related cough. PMID:8688342

  2. Forskolin versus sodium cromoglycate for prevention of asthma attacks: a single-blinded clinical trial.

    Science.gov (United States)

    González-Sánchez, R; Trujillo, X; Trujillo-Hernández, B; Vásquez, C; Huerta, M; Elizalde, A

    2006-01-01

    To determine the efficacy of forskolin in preventing asthma attacks, we performed a single-blinded clinical study in children and adult out-patients at a public hospital in Mexico. Forty patients of either sex with mild persistent or moderate persistent asthma were assigned randomly to 6 months of treatment with forskolin at 10 mg/day orally (capsules) or with two inhalations of sodium cromoglycate every 8 h, i.e. three times a day. The number of patients who had asthma attacks during the treatment period was significantly lower among those receiving forskolin (8/20, 40%) than among those receiving sodium cromoglycate (17/20, 85%). Values of forced expiratory volume in 1 s and forced expiratory flow, mid-phase, A similar in the two groups during the treatment period. We conclude that forskolin is more effective than sod cromoglycate in preventing asthma attacks in patients with mild persistent or moderate persistent asthma.

  3. Effect of verapamil and sodium cromoglycate on leukotriene D4 induced bronchoconstriction in patients with asthma.

    Science.gov (United States)

    Roberts, J A; Rodger, I W; Thomson, N C

    1986-01-01

    Leukotriene D4 (LTD4) may be an important mediator in asthma. The effect of verapamil and sodium cromoglycate on LTD4 induced bronchoconstriction has been examined in seven patients with asthma. The bronchoconstrictor response to increasing concentrations of inhaled LTD4 (0.0032-50 micrograms/ml) was assessed by measuring changes in FEV1, specific airways conductance, and flow rate at 30% of vital capacity (V30(p)). Results were expressed as the provocation concentration (PC) producing a 10% fall in FEV1 (PC10FEV1), a 35% fall in specific airways conductance (PC35SGaw), and a 30% fall in flow at 30% of vital capacity (PC30 V30(p)). Neither verapamil nor cromoglycate inhibited LTD4 induced bronchoconstriction in asthmatic subjects. These results suggest that in asthmatic patients LTD4 induced bronchoconstriction is not mediated via verapamil or cromoglycate sensitive mechanisms. PMID:3097863

  4. Dose-response study of sodium cromoglycate in exercise-induced asthma.

    Science.gov (United States)

    Patel, K R; Berkin, K E; Kerr, J W

    1982-01-01

    Ten patients with exercise-induced asthma participated in a single-blind dose-response study comparing the protective effect of inhaled sodium cromoglycate in increasing concentrations from 2 to 40 mg/ml. Saline was used as a control. Effects were assessed from the mean maximal percentage fall in forced expiratory volume in one second (FEV1) after the patients had run on a treadmill for eight minutes. There was slight bronchodilation evident from the increase in baseline FEV1 after inhalation of sodium cromoglycate, the difference reaching statistical significance with the highest concentration (5.7%, p less than 0.05). After exercise the maximal percentage falls in FEV1 (means and SEM) after saline and after sodium cromoglycate at 2, 10, 20, and 40 mg/ml were 37.3 +/- 4.7, 17.3 +/- 4.1, 10 +/- 3.3, 7.6 +/- 2.4, and 12 +/- 2.9. Sodium cromoglycate inhibited the exercise-induced fall in FEV1 at all the concentrations used in the study (p less than 0.001) and its inhibitory effect increased from 2 to 20 mg/ml. The mean FEV1 returned to baseline values within 15 minutes at higher concentrations of sodium cromoglycate (20 and 40 mg/ml) and a small bronchodilator effect was noted at 30 minutes. The findings suggest that the protective effect of sodium cromoglycate in exercise asthma is dose related. At higher concentration the drug suppresses chemical mediator release from the lung mast cells and may also modify the bronchial reactivity to release mediators. PMID:6818707

  5. Monosodium glutamate, disodium inosinate, disodium guanylate, lysine and taurine improve the sensory quality of fermented cooked sausages with 50% and 75% replacement of NaCl with KCl.

    Science.gov (United States)

    dos Santos, Bibiana Alves; Campagnol, Paulo Cezar Bastianello; Morgano, Marcelo Antônio; Pollonio, Marise Aparecida Rodrigues

    2014-01-01

    Fermented cooked sausages were produced by replacing 50% and 75% of NaCl with KCl and adding monosodium glutamate, disodium inosinate, disodium guanylate, lysine and taurine. The manufacturing process was monitored by pH and water activity measurements. The sodium and potassium contents of the resulting products were measured. The color values (L*, a* and b*), texture profiles and sensory profiles were also examined. Replacing 50% and 75% NaCl with KCl depreciated the sensory quality of the products. The reformulated sausages containing monosodium glutamate combined with lysine, taurine, disodium inosinate and disodium guanylate masked the undesirable sensory attributes associated with the replacement of 50% and 75% NaCl with KCl, allowing the production of fermented cooked sausages with good sensory acceptance and approximately 68% sodium reduction.

  6. Capsaicin inhalation in man and the effects of sodium cromoglycate.

    Science.gov (United States)

    Collier, J. G.; Fuller, R. W.

    1984-01-01

    The inhalation of capsaicin for 1 min, delivered as an aerosol by nebulising solutions of capsaicin at concentrations of 2-65 mumol 1(-1), caused dose-dependent coughing in normal volunteers and subjects with mild asthma. Capsaicin did not cause a feeling of breathlessness, and had no effect on forced expiratory volume in 1 s (FEV1) measured at the 1st, 5th and 9th min after the challenge was completed. Coughing started within seconds of applying the face mask, continued throughout the minute of capsaicin inhalation, and stopped within seconds of the mask being removed. In any one subject the number of coughs was reproducible when repeated on the same day or after an interval of several days. Experiments using local anaesthesia applied to the buccal mucosa or larynx indicated that the cough was caused by the stimulation of capsaicin-sensitive nerve terminals situated in the larynx. Cough response was not altered by the prior inhalation of sodium cromoglycate. PMID:6423016

  7. The effect of topical sodium cromoglycate on intranasal histamine challenge in allergic rhinitis.

    Science.gov (United States)

    Birchall, M A; Henderson, J C; Studham, J M; Pride, N B; Fuller, R W

    1994-12-01

    Topical sodium cromoglycate is used to treat allergic diseases of the upper and lower airways. To investigate its mechanisms of action, intranasal histamine challenge was used in nine subjects with perennial allergic rhinitis. After a preliminary day where subjects' reactivity thresholds (D100) for histamine were determined, intranasal sodium cromoglycate was administered in a double-blind, placebo-controlled fashion. Graded (D100/3, D100, D100X3), sequential challenges were performed on days 1 and 21 of each course, and responses measured by changes in nasal airway resistance, sneezes, secretion volume and secretion content: total protein, lysozyme and mucin. After a single dose of sodium cromoglycate, there was no change in resistance, but secretion volumes fell significantly (3.12 ml/5 min c.i. 2.83-3.4; placebo 3.61, c.i. 3.32-3.90: P = 0.026). After a 3-week-course, there was a significant fall in resistance (4.29 cm H2O/l/s, c.i. 3.85-4.72; placebo 5.45, c.i. 5.01-5.88: P sodium cromoglycate has both short- and long-term effects on nasal reactivity to histamine challenge. Acutely, there is a reduction in nasal lavage fluid volume which may be the result of reduced irritant receptor activity. After a 3-week course, there is a reduction in nasal resistance responses, a possible anti-inflammatory effect.

  8. Relative lung and systemic bioavailability of sodium cromoglycate inhaled products using urinary drug excretion post inhalation.

    Science.gov (United States)

    Aswania, Osama; Chrystyn, Henry

    2002-05-01

    The relative lung and systemic bioavailability of sodium cromoglycate following inhalation by different methods have been determined using a urinary excretion pharmacokinetic method. On three separate randomised study days, 7 days apart, subjects inhaled (i) 4x5 mg from an Intal metered dose inhaler (MDI), (ii) 4x5 mg from an MDI attached to a large volume spacer (MDI+SP) and (iii) 20 mg from an Intal Spinhaler (DPI). Urine samples were provided at 0, 0.5, 1, 2, 5 and 24 h post dose. The mean (S.D.) amount of sodium cromoglycate excreted in the urine during the first 30 min post inhalation was 38.1 (27.5), 222.3 (120.3) and 133.1 (92.2) microg following MDI, MDI+SP and DPI, respectively. The mean ratio (90% confidence interval) of these amounts excreted in the urine over the first 30 min for MDI+SP vs. MDI, DPI vs. MDI and MDI+SP vs. DPI was 801.0 (358.0, 1244; psodium cromoglycate excreted over the 24 h post inhalation the ratios were 375.4 (232.9, 517.9; psodium cromoglycate from a metered dose inhaler attached to a large volume spacer.

  9. Inhaled sodium metabisulphite induced bronchoconstriction: inhibition by nedocromil sodium and sodium cromoglycate.

    Science.gov (United States)

    Dixon, C M; Ind, P W

    1990-01-01

    1. The effects of nedocromil sodium and sodium cromoglycate on bronchoconstriction induced by inhaled sodium metabisulphite have been studied in eight atopic subjects, three of whom had mild asthma. 2. Nedocromil sodium (4 mg, 7.8 X 10(-6) M), sodium cromoglycate (10 mg, 24.1 X 10(-6) M) and matched placebo were administered by identical metered dose inhalers 30 min before a dose-response to sodium metabisulphite (5-100 mg ml-1) was performed. 3. Maximum fall in sGaw after placebo pre-treatment was -43.9 +/- 3.3% baseline (mean +/- s.e. mean). At the same metabisulphite concentration maximum fall in sGaw after sodium cromoglycate was -13.0 +/- 3.6% and after nedocromil sodium was +4.3 +/- 6.8%. Nedocromil sodium prevented any significant fall in sGaw even after higher concentrations of metabisulphite. 4. Both nedocromil sodium, 4 mg, and sodium cromoglycate, 10 mg, inhibited sodium metabisulphite induced bronchoconstriction but nedocromil sodium was significantly more effective. Relative in vivo potency of the two drugs is broadly in line with other in vivo and in vitro studies. PMID:2171616

  10. Inhaled histamine increases the rate of absorption of sodium cromoglycate from the lung.

    Science.gov (United States)

    Richards, R; Fowler, C; Simpson, S; Renwick, A G; Holgate, S T

    1992-01-01

    Since many factors may alter lung epithelial permeability (LEP) to water soluble molecules, the effect of histamine on the absorption and clearance of inhaled sodium cromoglycate was examined in seven mildly asthmatic patients with hyperresponsive airways and eight normal subjects. The subjects underwent histamine challenge to determine the provocative concentration of histamine required to reduce the forced expiratory volume in one second (FEV1) by 20% (PC20) from baseline. On two further visits they inhaled either saline placebo or histamine and 5 min later inhaled an aerosol containing sodium cromoglycate. Measurements of FEV1 were made and blood samples taken for analysis of plasma sodium cromoglycate concentration at intervals for 3 h. In the asthmatic group histamine inhalation led to a 24 +/- 4% reduction in FEV1 but had no effect on the normal subjects. When compared with inhaled saline, histamine increased the initial pulmonary absorption of SCG without influencing the total amount of drug absorbed in both asthmatics and normals. These observations suggest that the pharmacokinetics of inhaled sodium cromoglycate may be altered significantly by inflammatory mediators present at the site of drug absorption from the airways. PMID:1576060

  11. Bradykinin-induced bronchoconstriction: inhibition by nedocromil sodium and sodium cromoglycate.

    Science.gov (United States)

    Dixon, C M; Barnes, P J

    1989-01-01

    1. The effects of inhaled nedocromil sodium and sodium cromoglycate on bradykinin-induced bronchoconstriction have been studied in a double-blind, placebo controlled study, in eight mild asthmatic subjects. 2. The subjects attended on four occasions. Fifteen minutes after drug pre-treatment a bradykinin challenge was performed. Increasing concentrations were inhaled until a greater than 40% fall in expiratory flow at 30% of vital capacity from a partial flow volume manoeuvre (V p30) was demonstrated. 3. Inhaled bradykinin (0.06-8.0 mg ml-1) caused dose-related bronchoconstriction with the geometric mean cumulative dose causing a 40% fall in V p30 (PD40) of 0.035 (95% CI: 0.02-0.07) mumol, after placebo inhalation, which was similar to that measured before the trial (0.04: 0.02-0.09 mumol). 4. Both nedocromil sodium (4 mg) and sodium cromoglycate (10 mg) gave significant protection (P less than 0.05) against bradykinin-induced bronchoconstriction (PD40 0.37: 0.19-0.72 mumol after nedocromil sodium and 0.22: 0.11-0.49 after sodium cromoglycate). 5. Since bradykinin-induced bronchoconstriction is probably neurally mediated we conclude that both nedocromil sodium and sodium cromoglycate have an action on neural pathways which may be useful in the control of asthma symptoms. PMID:2547408

  12. Comparative study of the efficacy and safety of olopatadine eyedrops and sodium cromoglycate in clinical practice: a prospective study

    Directory of Open Access Journals (Sweden)

    Scandashree K

    2016-10-01

    Conclusions: Olopatadine ophthalmic solution is better than sodium cromoglycate ophthalmic solution in reducing the ocular signs and symptoms in allergic conjunctivitis. [Int J Basic Clin Pharmacol 2016; 5(5.000: 1764-1769

  13. Effect of lignocaine, sodium cromoglycate, and ipratropium bromide in exercise-induced asthma

    Science.gov (United States)

    Tullett, WM; Patel, KR; Berkin, KE; Kerr, JW

    1982-01-01

    Eight patients with exercise-induced asthma participated in a single-blind trial comparing the protective effects of inhaled lignocaine (estimated dose 48 mg), sodium cromoglycate (estimated dose 12 mg), and ipratropium bromide (estimated dose 120 μg). Saline was used as control. Effects were assessed from the mean maximal percentage fall in forced expiratory volume in one second (FEV1) and maximal mid-expiratory flow rates (MMFR) after they had run on a treadmill for eight minutes. There was no significant change in baseline FEV1 or MMFR before each agent was given. Saline, lignocaine, and sodium cromoglycate did not alter the mean baseline FEV1 or MMFR significantly. Ipratropium caused bronchodilatation with an increase of 16·3% in the mean FEV1 (p<0·001) and of 43·4% in the mean MMFR (p<0·05). After exercise the maximal percentage falls in FEV1 (means and SEM) after saline, lignocaine, sodium cromoglycate, and ipratropium bromide were 38·1% (5·0), 34·5% (6·1), 11·3% (3·7), and 19·3% (7·4) respectively. Similarly, the mean maximal falls in MMFR after saline, lignocaine, sodium cromoglycate, and ipratropium bromide were 54·4% (5·2), 52·9% (7·7), 23·6% (6·6), and 32·1% (10·5) respectively. The inhibitory effects of sodium cromoglycate and ipratropium bromide were significant whereas lignocaine failed to produce an effect. These results suggest that mediator release is an important factor in exercise-induced asthma and that in some patients the effects of the mediators may be on the postsynaptic muscarinic receptors. Local anaesthesia of sensory vagal receptors, on the other hand, does not prevent exercise asthma and these receptors do not appear to have any important role in exercise-induced bronchoconstriction. PMID:6218645

  14. Troubleshooting arterial-phase MR images of gadoxetate disodium-enhanced liver

    Energy Technology Data Exchange (ETDEWEB)

    Huh, Ji Mi; Kim, So Yeon; Lee, Seung Soo; Kim, Kyoung Won [Dept. of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Seoul (Korea, Republic of); Yeh, Benjamin M.; Wang, Z. Jane [Dept. of Radiologyand Biomedical Imaging, University of California San Francisco, San Francisco (United States); Wu, En Haw [Dept. of Medical Imaging and Intervention, Chang Gung Memorial Hospital, Linkou and Chang Gung University College of Medicine, Taoyuan (China); Zhao, Li Qin [Beijing Friendship Hospital, Capital Medical University, Beijing (China); Chang, Wei Chou [Tri-Service General Hospital and National Defense Medical Center, Taipei (China)

    2015-12-15

    Gadoxetate disodium is a widely used magnetic resonance (MR) contrast agent for liver MR imaging, and it provides both dynamic and hepatobiliary phase images. However, acquiring optimal arterial phase images at liver MR using gadoxetate disodium is more challenging than using conventional extracellular MR contrast agent because of the small volume administered, the gadolinium content of the agent, and the common occurrence of transient severe motion. In this article, we identify the challenges in obtaining high-quality arterial-phase images of gadoxetate disodium-enhanced liver MR imaging and present strategies for optimizing arterial-phase imaging based on the thorough review of recent research in this field.

  15. Effect of oral sodium cromoglycate and ketotifen in fish-induced bronchial asthma.

    Science.gov (United States)

    Ellul-Micallef, R

    1983-01-01

    The effects of sodium cromoglycate and ketotifen were studied in a group of 20 patients in whom fish repeatedly provoked an attack of wheezing and dyspnoea within one hour of its being eaten. Fish ingestion resulted in a fall in forced expiratory volume in one second (FEV1) of at least 15%. All patients had a weal greater than 4 mm in response to fish antigen in the skinprick test and most had blood eosinophilia and raised serum IgE levels. Administration of drugs and placebos was carried out under double-blind conditions, in a randomised fashion, on different days. Cromoglycate blocked the fall in FEV1 either completely or significantly in 16 patients. Ketotifen did not appear to have any significant effect in the group as a whole. PMID:6412384

  16. Platelet activation during exercise induced asthma: effect of prophylaxis with cromoglycate and salbutamol.

    Science.gov (United States)

    Johnson, C E; Belfield, P W; Davis, S; Cooke, N J; Spencer, A; Davies, J A

    1986-01-01

    Peak expiratory flow (PEF) and plasma concentrations of platelet factor 4 and beta thromboglobulin were measured before and after exercise in nine asthmatic patients and 12 non-asthmatic volunteers. Exercise was preceded by administration in random order of either placebo, salbutamol 200 micrograms, or sodium cromoglycate 2 mg from a pressurised inhaler. In control subjects there were minimal changes in PEF and plasma concentrations of platelet factor 4 and beta thromboglobulin. In the asthmatic patients the typical changes in PEF were seen on exercise; plasma concentrations of platelet factor 4 and beta thromboglobulin rose significantly in parallel, the rise preceding the fall in PEF. The changes in peak flow and platelet activation induced by exercise were attenuated by prior administration of salbutamol or cromoglycate. These results indicate that exercise induced asthma is associated with a rise in platelet release products similar to that observed in antigen induced asthma. PMID:2943049

  17. Effects of nebulized sodium cromoglycate on adult patients with severe refractory asthma.

    Science.gov (United States)

    Sano, Yasuyuki; Adachi, Mitsuru; Kiuchi, Takahiro; Miyamoto, Terumasa

    2006-03-01

    Many patients with severe refractory asthma, which is insufficiently controlled by additional high-dose of inhaled corticosteroids, require oral corticosteroids and/or immunosuppressant. Clinicians should seek for suitable medications, for its' chronic use may induce high risk of side effects. The purpose of this study was to evaluate the efficacy and safety of nebulized sodium cromoglycate (3-4 times/day) in adult severe asthmatic patients with poorly controlled asthmatic symptoms, despite treatments with high-dose inhaled corticosteroids. Adult patients with severe asthma (n=251) were enrolled in a randomized clinical trial at 30 medical centers in Japan. Isotonic saline was used as placebo. The study was conducted for 10 weeks; with initial 2 weeks of observation followed by 8 weeks of treatments. Efficacy was primarily evaluated based on improvements in morning peak expiratory flow after treatment. All patients who applied inhalation of nebulized sodium cromoglycate (SCG group) or saline (Controls) were treated with high-dose of inhaled corticosteroids (median of beclomethasone dipropionate equivalent dose: 1600 microg/days) and second-line control therapy including oral corticosteroids. There was no significant difference in morning peak expiratory flow between SCG group and controls. However, when patients were stratified into atopic and non-atopic groups, morning peak expiratory flow had significantly improved in the atopic SCG group compared to atopic Controls. Additional inhalation of nebulized sodium cromoglycate with inhaled corticosteroids is effective even in patients with severe atopic asthma. This finding shows that nebulized sodium cromoglycate is expected to be new second-line therapeutic option in severe asthma.

  18. Inhibition of neutrophil and eosinophil induced chemotaxis by nedocromil sodium and sodium cromoglycate.

    Science.gov (United States)

    Bruijnzeel, P. L.; Warringa, R. A.; Kok, P. T.; Kreukniet, J.

    1990-01-01

    1. Neutrophils and eosinophils infiltrate the airways in association with the allergen-induced late phase asthmatic reaction. Mobilization of these cells takes place via lipid-like and protein-like chemotactic factors. In this study platelet-activating factor (PAF), leukotriene B4 (LTB4), zymosan-activated serum (ZAS) and N-formyl-methionyl-leucyl-phenylalanine (FMLP) were used as illustrative examples of both groups. Chemotaxis was studied in human neutrophils and eosinophils. The inhibitory effects of nedocromil sodium and sodium cromoglycate were evaluated. 2. All chemotactic factors tested attracted neutrophils with the following rank order of activity: ZAS greater than PAF identical to FMLP identical to LTB4. Eosinophils were only mobilized by PAF, LTB4 and ZAS with the following rank order of activity: ZAS greater than PAF greater than LTB4. 3. Nedocromil sodium and sodium cromoglycate were equally active as the PAF antagonist BN 52021 in inhibiting the PAF-induced chemotaxis of neutrophils (IC50 approximately 10(-8) M). Both drugs were also equally active in inhibiting the chemotaxis of neutrophils induced by ZAS (IC50 approximately 10(-7)-10(-6) M), FMLP (IC50 approximately 10(-7) M) and LTB4 (IC50 approximately 10(-6) M). 4. Nedocromil sodium significantly inhibited the chemotaxis of eosinophils induced by PAF (IC50 approximately 10(-6) M) and LTB4 (IC50 approximately 10(-7) M). The inhibitory potency of BN 52021 was similar to that of nedocromil sodium on the PAF-induced chemotaxis of eosinophils. Sodium cromoglycate was incapable of eliciting significant inhibition of these chemotactic responses. However, sodium cromoglycate significantly inhibited the chemotaxis of eosinophils induced by ZAS (IC50 approximately 10(-7) M), whereas nedocromil sodium was ineffective. PMID:2163279

  19. Sodium cromoglycate as a replacement for inhaled corticosteroids in mild-to-moderate childhood asthma.

    Science.gov (United States)

    Petersen, W; Karup-Pedersen, F; Friis, B; Howitz, P; Nielsen, F; Strömquist, L H

    1996-12-01

    We investigated whether sodium cromoglycate 10 mg three times daily, delivered as an aerosol via Nebuhaler (in addition to terbutaline 0.5 mg three times daily), could replace inhaled steroid in children with mild-to-moderate asthma. Children (mean age 10.3 years) were randomly allocated to 12-week treatment with sodium cromoglycate 10 mg plus terbutaline 0.5 mg (group A; n = 30) or placebo plus terbutaline 0.5 mg (group B; n = 32), both taken three times a day. The daily steroid dose was reduced by 50 microg/week for 4 weeks from a starting dose of 200 microg. Fewer patients withdrew owing to worsening asthma from group A (n = 1) than group B (n = 11). Symptom scores, morning and evening peak flows, and additional beta2-agonist usage, recorded on diary cards, were better in group A than group B. Lung function measured at clinic visits was unchanged in either group. Overall opinions of efficacy favoured Group A. Adverse events were similar in the groups. Sodium cromoglycate plus terbutaline substituted effectively for inhaled steroid therapy.

  20. The influence of ipratropium bromide and sodium cromoglycate on benzalkonium chloride-induced bronchoconstriction in asthma.

    Science.gov (United States)

    Miszkiel, K A; Beasley, R; Holgate, S T

    1988-01-01

    1. Benzalkonium chloride, an antibacterial preservative that is added to nebuliser solutions, has been shown to cause bronchoconstriction when inhaled by asthmatic subjects. 2. To investigate the potential role of reflex and mast cell-dependent mechanisms in the pathogenesis of bronchoconstriction produced by benzalkonium chloride we examined the effects of ipratropium bromide and sodium cromoglycate on this response in both concentration-response and time-course studies in nine asthmatic subjects. 3. Pretreatment with inhaled ipratropium bromide (1 mg) and sodium cromoglycate (40 mg) displaced the benzalkonium chloride concentration-response curves to the right by a mean 2.2 fold and 3.1 fold respectively. 4. Ipratropium bromide and sodium cromoglycate markedly attenuated the airway response to benzalkonium chloride throughout the 45 min time course period, inhibiting the overall response by 56% and 78% respectively. 5. We conclude that benzalkonium chloride provokes bronchoconstriction in asthmatic subjects through a combination of mast cell activation and stimulation of peripheral and central neural pathways. PMID:2972308

  1. Sodium cromoglycate and atropine block the fall in FEV1 but not the cough induced by hypotonic mist.

    Science.gov (United States)

    Fuller, R W; Collier, J G

    1984-01-01

    In a group of patients with mild asthma the inhalation of mist derived from ultrasonically nebulised distilled water caused an increase in cough and a fall in FEV1. Double blind administration for five minutes of sodium cromoglycate (from an original solution containing 30 mg/ml) or atropine (2 mg/ml) by inhalation from a Minineb nebuliser, 30 minutes before the mist challenge, caused a significant reduction in the fall in FEV1 (p less than 0.05), but not in cough, by comparison with the protection afforded by placebo (saline). In a second study the fall in FEV1 caused by the inhalation of distilled water was not significantly different from that seen in response to hypotonic sodium chloride (1.7 g/l, 58 mmol/l), but both produced a significantly greater fall than did a similar mist containing sodium cromoglycate at an original concentration of 10 mg/ml (58 mmol/l). The results show that both atropine and sodium cromoglycate can block the fall in FEV1 due to mist and that protection by sodium cromoglycate is immediate. These results suggest that sodium cromoglycate blocks the nervous reflexes concerned in the response to mist, probably in the afferent limb of the reflex. PMID:6437001

  2. Combretastatin A4 disodium phosphate-induced myocardial injury

    Science.gov (United States)

    Tochinai, Ryota; Nagata, Yuriko; Ando, Minoru; Hata, Chie; Suzuki, Tomo; Asakawa, Naoyuki; Yoshizawa, Kazuhiko; Uchida, Kazumi; Kado, Shoichi; Kobayashi, Toshihide; Kaneko, Kimiyuki; Kuwahara, Masayoshi

    2016-01-01

    Histopathological and electrocardiographic features of myocardial lesions induced by combretastatin A4 disodium phosphate (CA4DP) were evaluated, and the relation between myocardial lesions and vascular changes and the direct toxic effect of CA4DP on cardiomyocytes were discussed. We induced myocardial lesions by administration of CA4DP to rats and evaluated myocardial damage by histopathologic examination and electrocardiography. We evaluated blood pressure (BP) of CA4DP-treated rats and effects of CA4DP on cellular impedance-based contractility of human induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs). The results revealed multifocal myocardial necrosis with a predilection for the interventricular septum and subendocardial regions of the apex of the left ventricular wall, injury of capillaries, morphological change of the ST junction, and QT interval prolongation. The histopathological profile of myocardial lesions suggested that CA4DP induced a lack of myocardial blood flow. CA4DP increased the diastolic BP and showed direct effects on hiPS-CMs. These results suggest that CA4DP induces dysfunction of small arteries and capillaries and has direct toxicity in cardiomyocytes. Therefore, it is thought that CA4DP induced capillary and myocardial injury due to collapse of the microcirculation in the myocardium. Moreover, the direct toxic effect of CA4DP on cardiomyocytes induced myocardial lesions in a coordinated manner. PMID:27559241

  3. Crystal structure studies on plate/shelf like disodium ditungstate

    Indian Academy of Sciences (India)

    Dragana J Jovanović; Ivana Lj Validžić; Miodrag Mitrić; Jovan M Nedeljković

    2013-02-01

    The structure of plate/shelf like disodium ditungstate (Na2W2O7) synthesized by newmethod in the process of ultrasonic spray pyrolysis using acidified aqueous solutions of tungsten (VI) oxide clusters as a precursor was refined down to the -factor of 8.9%. X-ray diffraction analysis undoubtedly confirmed formation of orthorhombic Na2W2O7 and refinement of the diffraction data showed that Na2W2O7 powder belongs to the base-centred orthorhombic type of structure with 64 space group, . The structure of Na2W2O7 can be described as infinite chains formed from tetrahedral (WO4) and octahedral (WO6) building units joined together. It was found that the basic units of the precursor complexes exist in the structure of Na2W2O7. Scanning electron microscopy confirmed formation of plate/shelf like Na2W2O7 particles with an average thickness of about 1.2 m.

  4. [HPLC-MS/MS method for determination of sodium cromoglycate concentration in human plasma and its pharmacokinetics].

    Science.gov (United States)

    Xu, Xiao-yan; Zhang, Rui; Yuan, Gui-yan; Wang, Ben-jie; Liu, Xiao-yan; Guo, Rui-chen

    2008-09-01

    The study established an HPLC-MS/MS method for determining the concentrations of sodium cromoglycate in human plasma and evaluated the pharmacokinetics of nasal drops and nasal spray. A C18 column was used to separate sodium cromoglycate in plasma with a mobile phase of a mixture of ammonium-methanol (involves 50% acetonitrile) (15:85) at a flow rate of 0.4 mL x min(-1). Electronic spray ionization (ESI) and multiple-reaction monitoring (MRM) were used for the determination of sodium cromoglycate in human plasma. The linear range of the standard curve of sodium cromoglycate was from 0.3 to 20 ng x mL(-1), and the minimum concentration of detection was 0.3 ng x mL(-1). The extraction recovery was more than 94.1%, intra-day and inter-day RSD were less than 14.3%. After a single dose of sodium cromoglycate, the main pharmacokinetic parameters of nasal spray and nasal drops were as follows, T(1/2)(1.82 +/- 0.54) h, (1.59 +/- 0.52) h; Tmax (0.47 +/- 0.12) h, (0.44 +/- 0.15) h; Cmax, (9.79 +/- 4.66) ng x mL(-1), (10.88 +/- 4.05) ng x mL(-1); AUC(0-5 h)(11.52 +/- 3.46) ng x mL(-1) x h x h, (12.63 +/- 4.23) ng x mL(-1) x h, Fr(93.6 +/- 13.8)%. The method is sensitive, rapid and accurate. It is suitable for therapeutic drug monitoring and human pharmacokinetic study of sodium cromoglycate.

  5. Blockade of mast cell activation reduces cutaneous scar formation.

    Science.gov (United States)

    Chen, Lin; Schrementi, Megan E; Ranzer, Matthew J; Wilgus, Traci A; DiPietro, Luisa A

    2014-01-01

    Damage to the skin initiates a cascade of well-orchestrated events that ultimately leads to repair of the wound. The inflammatory response is key to wound healing both through preventing infection and stimulating proliferation and remodeling of the skin. Mast cells within the tissue are one of the first immune cells to respond to trauma, and upon activation they release pro-inflammatory molecules to initiate recruitment of leukocytes and promote a vascular response in the tissue. Additionally, mast cells stimulate collagen synthesis by dermal fibroblasts, suggesting they may also influence scar formation. To examine the contribution of mast cells in tissue repair, we determined the effects the mast cell inhibitor, disodium cromoglycate (DSCG), on several parameters of dermal repair including, inflammation, re-epithelialization, collagen fiber organization, collagen ultrastructure, scar width and wound breaking strength. Mice treated with DSCG had significantly reduced levels of the inflammatory cytokines IL-1α, IL-1β, and CXCL1. Although DSCG treatment reduced the production of inflammatory mediators, the rate of re-epithelialization was not affected. Compared to control, inhibition of mast cell activity caused a significant decrease in scar width along with accelerated collagen re-organization. Despite the reduced scar width, DSCG treatment did not affect the breaking strength of the healed tissue. Tryptase β1 exclusively produced by mast cells was found to increase significantly in the course of wound healing. However, DSCG treatment did not change its level in the wounds. These results indicate that blockade of mast cell activation reduces scar formation and inflammation without further weakening the healed wound.

  6. Blockade of mast cell activation reduces cutaneous scar formation.

    Directory of Open Access Journals (Sweden)

    Lin Chen

    Full Text Available Damage to the skin initiates a cascade of well-orchestrated events that ultimately leads to repair of the wound. The inflammatory response is key to wound healing both through preventing infection and stimulating proliferation and remodeling of the skin. Mast cells within the tissue are one of the first immune cells to respond to trauma, and upon activation they release pro-inflammatory molecules to initiate recruitment of leukocytes and promote a vascular response in the tissue. Additionally, mast cells stimulate collagen synthesis by dermal fibroblasts, suggesting they may also influence scar formation. To examine the contribution of mast cells in tissue repair, we determined the effects the mast cell inhibitor, disodium cromoglycate (DSCG, on several parameters of dermal repair including, inflammation, re-epithelialization, collagen fiber organization, collagen ultrastructure, scar width and wound breaking strength. Mice treated with DSCG had significantly reduced levels of the inflammatory cytokines IL-1α, IL-1β, and CXCL1. Although DSCG treatment reduced the production of inflammatory mediators, the rate of re-epithelialization was not affected. Compared to control, inhibition of mast cell activity caused a significant decrease in scar width along with accelerated collagen re-organization. Despite the reduced scar width, DSCG treatment did not affect the breaking strength of the healed tissue. Tryptase β1 exclusively produced by mast cells was found to increase significantly in the course of wound healing. However, DSCG treatment did not change its level in the wounds. These results indicate that blockade of mast cell activation reduces scar formation and inflammation without further weakening the healed wound.

  7. The ability of single-chain surfactants to emulsify an aqueous-based liquid crystal oscillates with odd-even parity of alkyl-chain length.

    Science.gov (United States)

    Varghese, Nisha; Shetye, Gauri S; Yang, Sijie; Wilkens, Stephan; Smith, Robert P; Luk, Yan-Yeung

    2013-12-15

    The physical properties of many organic molecules often oscillate when the number of carbons in their aliphatic chains changes from odd to even. This odd-even effect for single-chain surfactants in solution is rarely observed. Here, we report the ability of single-chain surfactants to emulsify a class of non-amphiphilic organic salts, disodium cromoglycate (5'DSCG) oscillates as a function of the odd or even number of the aliphatic carbons. This system provides a water-in-oil-in-water emulsion, in which aqueous droplets of 5'DSCG in liquid crystal phases are coated with single-chain surfactants in a bulk carrying aqueous solution. For both surfactants of [Formula: see text] and CH3(CH2)nCOO(-)Na(+), the ability to emulsify 5'DSCG molecules in water is stronger for surfactants with an odd number of sp(3)-hybridized carbon atoms in the aliphatic chains than those with an even number. This observed odd-even effect is consistent with the notion that conventional micelles possess a core of randomly arranged surfactant hydrocarbon tails. However, this water-in-oil-in-water resembles a vesicle system in which the surfactants assemble in a highly ordered structure that separates two aqueous systems. These new self-assembled phases have potential application in the formulation and design of new organic soft materials.

  8. Effects of Sodium Cromoglycate on Iranian Asthmatic Subjects Without Exposure to any Bronchoconstrictor agent.

    Science.gov (United States)

    Mombeini, Tajmah; Zahedpoure-Anaraki, Mohammad Reza; Dehpour, Ahmad Reza

    2012-01-01

    Cromolyn sodium, a mast cell stabilizing agent, provides an immediate protective effect against the exercise-induced bronchoconstriction while being used before the exercise. However, cromolyn is ineffective in reversing asthmatic bronchospasm; it is used as a maintenance therapy and has a prophylactic role in chronic asthma. The purpose of this study was to determine the extent of change in baseline lung function tests following a single dose of cromolyn sodium in adult asthmatics. Forty volunteers (33 women and 7 men) with moderate to severe persistent asthma were randomly assigned to receive 20 mg cromolyn, 40 mg cromolyn or cromolyn-placebo. The percent of improvement in lung function parameters was compared among the groups, during 1 h of inhalation. Low dose of cromolyn induced more improvement in most lung function parameters such as forced expiratory flow volume in one second, forced vital capacity and peak expiratory flow compared with other groups. After 15 min, the improvement percentage of baseline forced expiratory flow volume in one second was 3.35 ± 1.5, for sodium cromoglycate-20 mg group compared with 0.98 ± 1.43 and - 0.68 ± 1.2 for sodium cromoglycate-placebo and sodium cromoglycate-40 mg, groups respectively. However, the differences between means were not significant. Furthermore, based on the definition of American Thoracic Society (ATS) for a "significant post-bronchodilator response" developed in a few patients 15 min after the inhalation of 20 mg cromolyn sodium. It is suggested that probably the inhalation of 20 mg of cromolyn sodium could immediately improve the lung function in few adults with asthma.

  9. Ameliorative potential of sodium cromoglycate and diethyldithiocarbamic acid in restraint stress-induced behavioral alterations in rats.

    Science.gov (United States)

    Manchanda, Rajneet K; Jaggi, Amteshwar S; Singh, Nirmal

    2011-01-01

    The present study was designed to investigate the ameliorative effects of sodium cromoglycate and diethyldithiocarbamic acid in acute stress-induced behavioral alterations in rats subjected to restraint stress. The rats were placed in the restrainer (5.5 cm in diameter and 18 cm in length) for 3.5 h. Restraint stress-induced behavioral alterations were assessed using the hole-board, social interactions and open field tests. Restraint stress resulted in a decrease in the frequency of head dips, rearing in the hole board, line crossings and rearings in the open field, and an increase in avoidance behaviors in the social interaction tests. Sodium cromoglycate (25 mg/kg and 50 mg/kg, ip), a mast cell stabilizer, and diethyldithiocarbamic acid (75 mg/kg and 150 mg/kg, ip), a selective NF-κB inhibitor, were employed to modulate restraint stress-induced behavioral changes. The administration of sodium cromoglycate and diethyldithiocarbamic acid significantly attenuated the restraint stress-induced behavioral changes. The noted beneficial effects of sodium cromoglycate and diethyldithiocarbamic acid may possibly be attributed to mast cell stabilization and inhibition of NF-κB activity, respectively.

  10. Randomised placebo-controlled trial of inhaled sodium cromoglycate in 1-4-year-old children with moderate asthma

    NARCIS (Netherlands)

    M.J.A. Tasche (Marjolein); J.C. van der Wouden (Hans); J.H.J.M. Uijen (Hans); B.P. Ponsioen (Ben); R.M.D. Bernsen (Roos); L.W.A. van Suijlekom-Smit (Lisette); J.C. de Jongste (Johan)

    1997-01-01

    textabstractAbstract BACKGROUND: Inhalation therapy with sodium cromoglycate is recommended as the first-line prophylactic treatment for moderate asthma in children. The availability of spacer devices with face-masks has extended the applicability of metered-dose inhalers to younger children. We st

  11. Effect of sodium cromoglycate on light racehorses with elevated metachromatic cell numbers on bronchoalveolar lavage and reduced exercise tolerance.

    Science.gov (United States)

    Hare, J E; Viel, L; O'Byrne, P M; Conlon, P D

    1994-06-01

    Some young horses with clinical signs of small airway disease demonstrate increased metachromatic cell numbers on bronchoalveolar lavage. The purpose of this study was to determine the effect of sodium cromoglycate treatment on clinical signs, bronchoalveolar lavage cytology and bronchoalveolar lavage histamine parameters in these horses. Twelve racehorses (age: 3.4 +/- 1.6 years) with a history of respiratory embarrassment at exercise, clinical signs of obstructive airway disease and bronchoalveolar lavage metachromatic cell differential greater than 2% were selected. Horses were randomly assigned to receive either 200 mg sodium cromoglycate or saline placebo nebulized twice daily for 7 days. A clinical respiratory score was assigned and bronchoalveolar lavage was performed on each animal on days 0 and 7. Measurements were made of the following bronchoalveolar lavage fluid parameters: total nucleated cell concentration, differential cell percentage and concentration, supernatant and lysate histamine concentration, lysate: supernatant histamine ratio and metachromatic cell histamine content. Between the two evaluation periods, sodium cromoglycate treated horses demonstrated an improvement in respiratory score (P = 0.01) and a stabilizing of metachromatic cell histamine content (P = 0.04) when compared with placebo treated horses. We concluded that sodium cromoglycate is effective for the treatment of small airway disease in this population of young racehorses although the pharmacodynamics of this drug in the horse require further investigation.

  12. The effect of nedocromil sodium and sodium cromoglycate on antigen-induced bronchoconstriction in the Ascaris-sensitive monkey.

    Science.gov (United States)

    Eady, R. P.; Greenwood, B.; Jackson, D. M.; Orr, T. S.; Wells, E.

    1985-01-01

    Nedocromil sodium inhibited the bronchoconstriction caused by antigen challenge in Ascaris-sensitive monkeys and in addition it prevented the release of histamine from mast cells lavaged from sensitive monkeys. Sodium cromoglycate was relatively inactive in both these systems. It is suggested that nedocromil sodium can stabilize both mucosal and connective tissue mast cells and may represent a new type of drug. PMID:2992657

  13. Inhibitory effect of sodium cromoglycate on pulmonary responses to histamine administered after indomethacin in anaesthetized guinea-pigs.

    Science.gov (United States)

    Mitchell, H. W.

    1988-01-01

    1. Histamine (2-4 micrograms kg-1 i.v.) increased airways resistance (Raw) and decreased dynamic lung compliance (Cdyn) in urethane-anaesthetized guinea-pigs. The effects on Raw were almost abolished by atropine (0.1 mg kg-1 i.v.) and reduced by vagal cooling (11-16 degrees C). 2. Histamine-induced changes in Raw and Cdyn were significantly (P less than 0.05) enhanced by indomethacin (1 mg kg-1 i.v.). 3. In animals not treated with indomethacin, exposure to an aerosol containing sodium cromoglycate (0.01-2% for 30 s) failed to affect subsequent (3 min) histamine-induced bronchoconstriction. 4. Administration of an aerosol containing low (0.01-0.2%) concentrations of sodium cromoglycate had no effect on the enhanced responses (i.e. hyperreactivity) seen after indomethacin. However, more concentrated sodium cromoglycate aerosols (greater than 0.2%) reduced or abolished the hyperreactivity to histamine seen after indomethacin. 5. It was concluded that sodium cromoglycate can prevent the development of hyperreactivity to histamine, possibly by interacting with some mechanism utilized by both histamine and indomethacin in this model. PMID:3134970

  14. 40 CFR 721.3820 - L-Glutamic acid, N-(1-oxododecyl)-, disodium salt.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false L-Glutamic acid, N-(1-oxododecyl... Specific Chemical Substances § 721.3820 L-Glutamic acid, N-(1-oxododecyl)-, disodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as...

  15. SYNTHESIS AND PHYSICAL-PROPERTIES OF HIGHLY CA2+- TOLERANT DISODIUM 2-(SULFATOMETHYL)-1-ALKYLSULFATE SURFACTANTS

    NARCIS (Netherlands)

    KOOREMAN, PA; ENGBERTS, JBFN

    1994-01-01

    The synthesis, critical micelle concentrations (CMC) and Krafft temperatures (T(Krafft)) of a series of disodium 2-(sulfatomethyl)-1-alkylsulfates (2a-d) are presented, with alkyl being n-tetradecyl (C-14), n-hexadecyl (C-16), n-octadecyl (C18) and n-eicosyl(C20). The surfactants exhibit a large Ca2

  16. A double-blind group comparative study of ophthalmic sodium cromoglycate, 2% four times daily and 4% twice daily, in the treatment of seasonal allergic conjunctivitis.

    Science.gov (United States)

    Leino, M; Montan, P; Njå, F

    1994-03-01

    In a multicenter, double-blind, single-dummy, group-comparative study, 169 patients received ophthalmic sodium cromoglycate 2% four times daily, and 170 patients received 4% ophthalmic sodium cromoglycate twice daily, together with placebo eye-drops twice daily, for the treatment of seasonal allergic conjunctivitis (SAC) to birch pollen. The treatment period was 4 weeks during the birch pollen season. Daily pollen counts were used to identify the peak 14-d period. Clinical examinations were made before the start of treatment, after 1 week of treatment, and at the end of the treatment period. Patients kept daily diary record cards of eye symptom severity and concomitant therapy. Symptoms were generally mild and, except for chemosis (week 4) and soreness (weeks 2 and 3), which were less in the 4% group (P sodium cromoglycate eye-drops twice daily is as effective and well tolerated as 2% sodium cromoglycate four times daily in the treatment of birch-pollen conjunctivitis.

  17. Inhibition by sodium cromoglycate of bronchoconstriction stimulated by respiratory heat loss: comparison of pressurised aerosol and powder.

    Science.gov (United States)

    Latimer, K M; Roberts, R; Morris, M M; Hargreave, F E

    1984-01-01

    The protective effect was examined of three doses (2, 10, and 20 mg) of sodium cromoglycate inhaled from a pressurised metered dose inhaler on the response to isocapnic hyperventilation of cold dry air in 10 asthmatic subjects. This was compared with the effect of cromoglycate powder (20 mg) inhaled from a Spincap and with placebo given on two occasions. The medications were inhaled on separate days, in random order and with the use of a double blind double dummy technique, 20 minutes before isocapnic hyperventilation of two fold increasing volumes of air (-15 degrees C, 0% humidity) to produce a 20% fall in the post-treatment FEV1. The response was expressed as the provocative dose of respiratory heat loss required to cause a fall in FEV1 of 15% (PD15, kcal/min). The mean baseline spirometric indices exceeded 85% of predicted normal values on each test day; both placebo treatments reduced the baseline FEV1 by comparison with all active treatments (p less than 0.0001). Comparison of the PD15 on the two placebo days confirmed excellent reproducibility. All doses of cromoglycate shifted the respiratory heat loss dose-response curve to the right of the placebo curve; PD15 after all active treatments exceeded PD15 after placebo (p less than 0.0001). There was no cromoglycate dose-response relationship between the three doses of aerosol (p greater than 0.05), or between any dose of aerosol and powder (p greater than 0.05). It is concluded that cromoglycate aerosol inhaled from a pressurised inhaler in a dose of 2 mg gives the same magnitude of protection against bronchoconstriction stimulated by airway cooling as 20 mg of pressurised aerosol or powder from a Spincap. PMID:6426073

  18. [Sodium cromoglycate in the treatment of food hypersensitivity in children under 3 years of age].

    Science.gov (United States)

    Zur, E; Kaczmarski, M

    2001-09-01

    Dietary elimination is a treatment of first choice in food hypersensitivity. Such therapy is not always enough to stop the disease and introduction of pharmacological treatment is necessary. In prevention and long term treatment antiallergic drugs are recommended. The aim of the study was to assess efficacy and safety of oral sodium cromoglycate in treatment of food hypersensitivity in the youngest children. In our study we examined: the group of 25 children aged 6 months-3 years treated with oral cromolyn sodium during the period 4-20 weeks and 29 children aged 6 months-3 years treated with ketotifen. Symptoms from skin, digestive and respiratory tract, behaviour status were evaluated for drugs efficacy. Cromolyn and ketotifen effected a significant decrease in total symptoms score. The treatment was well tolerated. No serious side effects were noted. The incidents of skin rash, disquiet during the night, diarrhoea and urticaria were only 8 percent. Sodium cromoglycate is safe and effective drug in treatment of food allergy in children; specially in symptoms from gastrointestinal tract and multi-organs allergy.

  19. The pharmacokinetics of sodium cromoglycate in man after intravenous and inhalation administration.

    Science.gov (United States)

    Neale, M G; Brown, K; Hodder, R W; Auty, R M

    1986-01-01

    The pharmacokinetics of sodium cromoglycate in four healthy volunteers after slow intravenous infusion have been evaluated following measurement of plasma concentrations by radioimmunoassay. The results confirm earlier findings that sodium cromoglycate is rapidly eliminated from the body and that the data can be fitted to a two compartment open model. The pharmacokinetic parameters derived from the intravenous administration were used to evaluate the pharmacokinetics after inhalation administration via the Spinhaler. A model for absorption from the lungs is described which involves absorption at two different rates; this gives a better fit to the observed data than a single absorption rate. A fast absorption rate constant with a mean value of 0.54 min-1 and a slower rate constant with a mean value of 0.0097 min-1 were found. Of a mean total of 2.84 mg absorbed from a 20 mg inhaled dose, 0.68 +/- 0.15 (s.e. mean) mg were absorbed at the fast rate and 2.17 +/- 0.37 mg at the slower rate. These rates probably reflect absorption from different sites within the lungs. The results may have important implications for interpretation of clinical findings. PMID:3094571

  20. Respiratory motion artefacts in dynamic liver MRI: a comparison using gadoxetate disodium and gadobutrol

    Energy Technology Data Exchange (ETDEWEB)

    Luetkens, Julian A.; Kupczyk, Patrick A.; Doerner, Jonas; Willinek, Winfried A.; Schild, Hans H.; Kukuk, Guido M. [University of Bonn, Department of Radiology, Bonn (Germany); Fimmers, Rolf [University of Bonn, Department of Medical Biometry, Informatics, and Epidemiology, Bonn (Germany)

    2015-11-15

    Our aim was to retrospectively evaluate the occurrence of respiratory motion artefacts in patients undergoing dynamic liver magnetic resonance (MR) either with gadoxetate disodium or gadobutrol. Two hundred and thirty liver MR studies (115 with gadobutrol, 115 with gadoxetate disodium) were analysed. Respiratory motion artefacts on dynamic 3D T1-weighted MR images (pre-contrast, arterial, venous, and late-dynamic phase) were assessed using a five-point rating scale. Severe motion was defined as a score ≥ 4. Mean motion scores were compared with the Mann-Whitney-U-test. The chi-squared-test was used for dichotomous comparisons. Mean motion scores for gadoxetate disodium and gadobutrol showed no relevant differences for each phase of the dynamic contrast series (pre-contrast: 1.85 ± 0.70 vs. 1.88 ± 0.57, arterial: 1.85 ± 0.81 vs. 1.87 ± 0.74, venous: 1.82 ± 0.67 vs. 1.74 ± 0.64, late-dynamic: 1.75 ± 0.62 vs. 1.79 ± 0.63; p = 0.469, 0.557, 0.382 and 0.843, respectively). Severe motion artefacts had a similar incidence using gadoxetate disodium and gadobutrol (11/460 [2.4 %] vs. 7/460 [1.5 %]; p = 0.341). Gadoxetate disodium is associated with equivalent motion scores compared to gadobutrol in dynamic liver MRI. In addition, both contrast agents demonstrated a comparable and acceptable rate of severe respiratory motion artefacts. (orig.)

  1. Effect of Cromoglycate on Gas Changes, During Bronchial Challenge by UNCDW in Children with Asthma

    Science.gov (United States)

    Bavaro, S.; Moramarco, G.; Torio, D.; Falciatore, D.; Ciccarone, G.; Cicciomessere, L.; Rigillo, N.

    1994-01-01

    Eighteen asthmatic children were challenged with ultrasonically nebulized cold distilled water (UNCDW). Blood gas composition was monitored transcutaneously (tcpO2 and tcpCO2) during and after the challenge. Assuming as basal the response to this UNCDW test, nine children (Group A) were then chosen at random to inhale cromoglycate by aerosol delivery for 8 days. Nine children (Group B), acting as a control, inhaled saline for 8 days. At the end of this therapy, each child repeated the UNCDW test. Statistical analysis with t-test for paired data was used to compare the results of each child to both tests. Mean basal tcpO2 and tcpCO2 were all within the expected normal range. In all children, both mean tcpO2 and tcpCO2 were reduced during and after UNCDW inhalation. Mean tcpCO2 values during the challenge were significantly (p < 0.001) lower than the corresponding steady state 2 rain after the UNCDW challenge, with a mean drop of −7% (2.1 S.D.). Mean tcpO2 values remained significantly decreased (p < 0.001) from the fifth mitt of the UNCDW challenge to the end of the observation period, with a mean drop of −20% (15.5 S.D.). After treatment with cromoglycate (Group A), the mean tcpCO2 values during UNCDW did not change significantly from those ofsteady state conditions: −0.8% (0.5 S.D.); whereas mean tcpO2 values decreased by −4% (4.9 S.D.). The control children treated with saline (Group B) showed mean tcpCO2 and tcpO2 values which were significantly different (p < 0.001) from those of the steady state conditions: mean drop of tcpCO2, −6% (4.2 S.D.); mean drop of tcpO2, −20% (4.7 S.D.). In conclusion, it emerges that: UNCDW induces nonspecific broncho-constriction in asthmatic children with a typical drop of tcpCO2 and tcpO2; the treatment with cromoglycate normalizes the time course of tcpCO2 (hyper-reactivity) and reduces dramatically the drop of tcpO2 time course (hyper-responsivity) during and after the UNCDW test. PMID:18475603

  2. Equilibrium and kinetic aspects of sodium cromoglycate adsorption on chitosan: mass uptake and surface charging considerations.

    Science.gov (United States)

    de Lima, C R M; Pereira, M R; Fonseca, J L C

    2013-09-01

    Chitosan has more and more been suggested as a material for use as adsorbent in the treatment of effluents as well as in the synthesis of drug-loaded nanoparticles for controlled release. In both cases, a good understanding of the process of adsorption, both kinetically and in terms of equilibrium, has an importance of its own. In this manuscript we study the interaction between sodium cromoglycate, a drug used in asthma treatment, and chitosan. Equilibrium experiments showed that Sips (or Freundlich-Langmuir) isotherm described well the resultant data and adsorption possibly occurred as in multilayers. A model based on ordinary reaction-rate theory, compounded of two processes, each one with a correlated velocity constant, described the kinetics of sorption. Kinetic and equilibrium data suggested the possibility of surface rearrangement, favored by the increase of temperature.

  3. Determination of Sodium Cromoglycate by a New Kinetic Spectrophotometric Method in Biological Samples

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2013-01-01

    Full Text Available A new kinetic spectrophotometric method is described for the determination of ultratrace amounts of sodium cromoglycate (SCG. The method based on catalytic action of SCG on the oxidation of amaranth with periodate in acidic and micellar medium. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of the amaranth at 518 nm, for the first 4 min from initiation of the reaction. Calibration curve was linear in the range of 4.0−36.0 ng mL−1 SCG. The limit of detection is 2.7 ng mL−1 SCG. The relative standard deviation (RSD for ten replicate analyses of 12, 20, and 28 ng mL−1 SCG was 0.40%, 0.32%, and 0.53%, respectively. The proposed method was used for the determination of SCG in biological samples.

  4. Vernal keratoconjunctivitis in an Israeli group of patients and its treatment with sodium cromoglycate.

    Science.gov (United States)

    Baryishak, Y R; Zavaro, A; Monselise, M; Samra, Z; Sompolinsky, D

    1982-01-01

    Vernal keratoconjunctivitis (VKC) is usually considered as an allergic eye disorder of type I, and in most therapeutic trials it has been shown to yield to topical treatment with sodium cromoglycate. This has been confirmed in the present study of VKC patients from Israel. However, some of the cases seemed not to benefit from this treatment. In a survey of IgE levels in VKC patients in Israel tear IgE levels were significantly increased in 63.5%, but in 29% of the patients both tear and blood IgE levels were normal to low. The possibility that some of the cases diagnosed as VKC might have another cause than IgE-mediated atopy is discussed. Images PMID:6800400

  5. Development and validation of an ion-pair liquid chromatographic method for the quantitation of sodium cromoglycate in urine following inhalation.

    Science.gov (United States)

    Aswania, O A; Corlett, S A; Chrystyn, H

    1997-03-07

    An ion-pair liquid high-performance chromatography method with solid-phase extraction for measuring urinary concentrations of sodium cromoglycate following inhalation has been developed and validated. Sodium cromoglycate was extracted from urine on a 100-mg phenyl cartridge (Isolute, Jones Chromatography) and then quantified on a 25-cm C8 Spherisorb 5 microns stationary phase with a mobile phase of methanol-0.045 M phosphate buffer-0.05 M dodecyl triethyl ammonium phosphate (550:447.6:2.4, v/v) pH 2.3, at 0.85 ml min-1 using nedocromil sodium as an internal standard and UV detection at 238 nm. The inter- and intra-day reproducibilities were 8.33 and 13.63%, respectively, at 0.25 mg l-1. The limit of determination for sodium cromoglycate was 0.25 mg l-1 (with a signal-to-noise ratio of greater than 10:1). Following oral and inhaled administration of 20 mg of sodium cromoglycate to eight healthy volunteers, the mean and S.D. of sodium cromoglycate excreted in the urine at 0.5, 1 and 24 h post-dose were 0.02, 0.05 and 0.33%, and 0.16, 0.30 and 1.55% of the dose, respectively. The urinary recovery of sodium cromoglycate at 0.5 and 1 h following inhalation can therefore be used to compare the amount of drug reaching the respiratory tract using different sodium cromoglycate inhaled products or inhalation methods.

  6. Improvement in sodium cromoglycate delivery from a spacer device by use of an antistatic lining, immediate inhalation, and avoiding multiple actuations of drug.

    Science.gov (United States)

    O'Callaghan, C; Lynch, J; Cant, M; Robertson, C

    1993-01-01

    BACKGROUND--Aerosols generated from metered dose inhalers may be highly charged. The aim of this study was to determine whether lining the walls of a polycarbonate spacer device with an antistatic agent would result in an increase in drug output. The effects of multiple actuations of drug into the spacer device and increasing residence time of drug within the spacer were also determined. METHODS--The amount of sodium cromoglycate contained in particles of various size available for inhalation (per 5 mg actuation) from a 750 ml polycarbonate spacer was determined by impinger measurement and spectrophotometric assay. RESULTS--Lining the spacer with an antistatic agent increased the mean (SD) amount of sodium cromoglycate in particles < 5 microns available for inhalation (per 5 mg actuation) by 244% from (0.59 (0.03) to 1.44 (0.2) mg). When there was a 20 second interval between actuation into the spacer device and inhalation, sodium cromoglycate available for inhalation in particles < 5 micrograms decreased by 67% (from 0.59 (0.03) mg to 0.2 (0.01) mg). Use of the spacer device increased sodium cromoglycate available for inhalation in respirable particles (< 5 microns) by 18% compared with direct delivery by metered dose inhaler. Multiple actuations into the spacer decreased the amount of sodium cromoglycate available for inhalation in particles < 5 microns by 31% after two actuations and 56% after three acutations. CONCLUSIONS--Multiple actuations of sodium cromoglycate into a spacer device before inhalation should be avoided, and inhalation from spacer devices should take place immediately after actuation to ensure maximum dose. Lining of a standard spacer device with an antistatic agent significantly increased output of sodium cromoglycate. This may have implications for improved therapeutic response and drug cost. Images PMID:8346488

  7. Nedocromil sodium versus sodium cromoglycate in treatment of exercise-induced bronchoconstriction: a systematic review.

    Science.gov (United States)

    Kelly, K D; Spooner, C H; Rowe, B H

    2001-01-01

    The objective of this review was to compare the effects of prophylactic doses of nedocromil sodium (NCS) and sodium cromoglycate (SCG) on postexercise lung function, in persons diagnosed with exercise-induced bronchoconstriction. Randomized controlled trials were identified from the Cochrane Airways Review Group Asthma Register, plus hand searching for trials in journals, bibliographies of relevant studies and review articles. Randomized controlled trials comparing NCS to SCG in prophylactic treatment of exercise-induced bronchoconstriction were eligible. Studies were pooled using odds ratios (OR) for dichotomous outcomes or weighted mean differences (WMD) with 95% confidence intervals (95% CI) for continuous outcomes. No significant differences were noted between NCS and SCG with respect to the maximum per cent decrease in forced expiratory volume in one second (WMD=-0.88; 95% CI -4.50-2.74), complete protection (OR=0.95; 95% CI 0.50-1.81), clinical protection (OR=0.71; 95% CI 0.36-1.39), unpleasant taste (OR=6.85; 95% CI 0.77-60.73), or sore throat (OR=3.46; 95% CI 0.32-37.48). Subgroup analyses based on age, dosages of medications and timing of exercise postinhalation were consistent with the overall pooled analyses. No significant differences were evident between the effects of nedocromil sodium and sodium cromoglycate during the immediate postexercise period in adults and children with exercise-induced bronchoconstriction, with regards to maximum per cent decrease in forced expiratory volume in one second, complete protection, or clinical protection. Side-effect profiles were similar.

  8. Determination of sodium cromoglycate in human plasma by liquid chromatography with tandem mass.

    Science.gov (United States)

    Liu, Xiao-yan; Qu, Ting-ting; Wang, Ben-jie; Wei, Chun-min; Yuan, Gui-yan; Zhang, Rui; Guo, Rui-chen

    2008-09-01

    A sensitive and selective liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the determination of sodium cromoglycate (SCG) in human plasma after a nasal dose of 10.4 mg sodium cromoglycate nasal spray, using pravastatin sodium as the internal standard. The method was validated over a linear range of 0.300-20.0 ng/mL. SCG and I.S. were extracted from 1.0 mL of heparinized plasma by C(18) solid-phase extraction cartridges using methanol as eluting solvent. The dried residue was reconstituted with 100 microL of mobile phase, and 10 microL was injected onto the LC-MS/MS system. Chromatographic separation was achieved on a C(18) column (250 x 4.6 mm i.d., 5 microm particle size) with a mobile phase of methanol-acetonitrile-water (containing 2 mmol/L ammonium acetate; 42.5:42.5:15, v/v/v) at a flow rate of 0.4 mL/min. The analytes were detected with a triple quad LC-MS/MS using ESI with positive ionization. Ions monitored in the multiple reaction monitoring mode were m/z 469.0 (precursor ion) to m/z 245.0 (product ion) for SCG and m/z 447.2 (precursor ion) to m/z327.1 (product ion) for pravastatin sodium (internal standard) The average recovery of SCG from human plasma was 94.88% and the lower limit of quantitation was 0.3 ng/mL. Results from a 3-day validation study demonstrated excellent precision and accuracy across the calibration range of 0.3-20 ng/mL. The method was successfully applied to the pharmacokinetic study of SCG in healthy Chinese volunteers.

  9. Pemetrexed disodium in recurrent locally advanced or metastatic squamous cell carcinoma of the head and neck

    OpenAIRE

    Pivot, X; Raymond, E; Laguerre, B.; Degardin, M; Cals, L; Armand, J P; Lefebvre, J L; Gedouin, D; Ripoche, V; Kayitalire, L; Niyikiza, C; Johnson, R.; Latz, J.; Schneider, M.

    2001-01-01

    This phase II study determined response rate of patients with locally advanced or metastatic head and neck cancer treated with pemetrexed disodium, a new multitargeted antifolate that inhibits thymidylate synthase, dihydrofolate reductase and glycinamide ribonucleotide formyl transferase. 35 patients with local or metastatic relapse of squamous cell carcinoma of the head and neck (31 male, 4 female; median age 53 years) were treated with pemetrexed 500 mg m2 administered as a 10-minute infusi...

  10. Effect of ipratropium bromide and/or sodium cromoglycate pretreatment on water-induced bronchoconstriction in asthma.

    Science.gov (United States)

    Tranfa, C M; Vatrella, A; Parrella, R; Bariffi, F

    1995-04-01

    The mechanisms underlying water-induced bronchoconstriction are still not fully understood. Cholinergic reflexes and mast cell mediator release are currently believed to play an important pathogenetic role. In order to evaluate the relative contribution of each of these mechanisms, we studied the effect of ipratropium bromide (80 micrograms), a muscarinic antagonist, and sodium cromoglycate (20 mg), an inhibitor of mast cell mediator release, administered alone and in combination, in the prevention of bronchospasm induced by ultrasonic mist of distilled water (UMDW). Fifteen patients with documented atopic asthma and hyperresponsiveness to distilled water were selected for this randomized, placebo-controlled, double-blind study. Airway responses to pharmachological agents and bronchial challenge were measured by change in specific airways conductance (sGaw). Sodium cromoglycate had no effect on bronchial calibre, whilst ipratropium bromide and the combination of the two drugs produced a significant bronchodilation 30, 60 and 90 min after treatments. The maximal increase in sGaw (mean % +/- SD) was observed at 90 min: 63 +/- 28% and 58 +/- 22% after ipratropium bromide and the combined drugs respectively. UMDW (2, 4, 8, 16 ml water) caused a -36 +/- 19%, -42 +/- 19%, -49 +/- 18%, -56 +/- 15% mean % +/- SD fall in sGaw after placebo. Pretreatment with sodium cromoglycate abolished the bronchoconstriction to 2 ml (fall sGaw -5 +/- 23% NS) and significantly reduced the effect of 4 (-15 +/- 22%), 8 (-21 +/- 20%) and 16 ml (-24 +/- 18%) water.(ABSTRACT TRUNCATED AT 250 WORDS)

  11. The mast cell stabilizer sodium cromoglycate reduces histamine release and status epilepticus-induced neuronal damage in the rat hippocampus.

    Science.gov (United States)

    Valle-Dorado, María Guadalupe; Santana-Gómez, César Emmanuel; Orozco-Suárez, Sandra Adela; Rocha, Luisa

    2015-05-01

    Experiments were designed to evaluate changes in the histamine release, mast cell number and neuronal damage in hippocampus induced by status epilepticus. We also evaluated if sodium cromoglycate, a stabilizer of mast cells with a possible stabilizing effect on the membrane of neurons, was able to prevent the release of histamine, γ-aminobutyric acid (GABA) and glutamate during the status epilepticus. During microdialysis experiments, rats were treated with saline (SS-SE) or sodium cromoglycate (CG-SE) and 30 min later received the administration of pilocarpine to induce status epilepticus. Twenty-four hours after the status epilepticus, the brains were used to determine the neuronal damage and the number of mast cells in hippocampus. During the status epilepticus, SS-SE group showed an enhanced release of histamine (138.5%, p = 0.005), GABA (331 ± 91%, p ≤ 0.001) and glutamate (467%, p ≤ 0.001), even after diazepam administration. One day after the status epilepticus, SS-SE group demonstrated increased number of mast cells in Stratum pyramidale of CA1 (88%, p histamine (but not GABA and glutamate) release, lower number of mast cells (p = 0.008) and reduced neuronal damage in hippocampus. Our data revealed that histamine, possibly from mast cells, is released in hippocampus during the status epilepticus. This effect may be involved in the subsequent neuronal damage and is diminished with sodium cromoglycate pretreatment.

  12. The effect of nedocromil sodium, sodium cromoglycate and codeine phosphate on citric acid-induced cough in dogs.

    Science.gov (United States)

    Jackson, D. M.

    1988-01-01

    1. The effects of nedocromil sodium, sodium cromoglycate and codeine phosphate on citric acid-induced cough have been studied in conscious tracheostomised dogs. 2. Nedocromil sodium (approximately 15 mg given as an aerosol) and codeine phosphate (5 mg kg-1, i.v.) significantly increased the time to the first cough when dogs were challenged with citric acid aerosol. The mean number of coughs in the initial period of coughing fell after treatment of dogs with nedocromil sodium or with codeine phosphate, but this reduction in mean cough number was not statistically significant. 3. Neither sodium cromoglycate (approximately 15 mg given as an aerosol) nor saline had significant effect on a citric acid challenge. 4. It is concluded that nedocromil sodium, but not sodium cromoglycate, possesses an anti-tussive action that may result from inhibition of sensory nerve activity in the lung. Nedocromil sodium may prove useful in the treatment of unproductive cough in situations where the use of a centrally-acting antitussive is undesirable. PMID:2836011

  13. Bronchospasm induced by inhalation of substance P: effect of sodium cromoglycate.

    Science.gov (United States)

    Crimi, N; Palermo, F; Oliveri, R; Vancheri, C; Palermo, B; Polosa, R; Mistretta, A

    1988-01-01

    The aim of this study was to evaluate in vivo the effect of inhaled substance P (SP) and to determine the effect of sodium cromoglycate (SCG) on bronchospasm induced by its inhalation in 6 asthmatic patients. At the beginning of the study, all patients were asymptomatic, with an FEV1 value not less than 20%. SP was administered as aerosol, prepared in 0.9% saline to produce a dose range of 0.03-1 mg. Airway response was measured as FEV1 using a pulmonary system 47120A Hewlett-Packard instrument. The dose of SP producing a 20% change in FEV1 was calculated from the individual semi-logarithmic dose-response curve (PD20). After administration of the placebo, SP produced a dose-related bronchoconstriction with a geometric mean PD20 of 0.15 mg. After SCG, the mean PD20 value was of 0.64 mg (p less than 0.01). These results confirmed the bronchospasm induced by inhalation of SP and demonstrated that SCG is able to prevent this effect although it is impossible to define the exact mechanism of the drug.

  14. Changes induced by sodium cromoglycate in brain catecholamine turnover in morphine dependent and abstinent mice.

    Science.gov (United States)

    San-Martín-Clark, O; Cuéllar, B; De Alba, J; Leza, J C; Lorenzo, P

    1995-04-01

    The effects of sodium cromoglycate (CRO) were studied in relation to the metabolism of brain catecholamines: dopamine (DA) and noradrenaline (NA), and their metabolites 3,4-dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA) and 4-hydroxy-3-methoxyphenylethyleneglycol (MHPG). CRO was injected SC in control mice, morphine-tolerant mice (tolerance was induced by SC implantation of a 75 mg morphine pellet; CRO was administered on day 4 of addiction) and 30 min before abstinence (withdrawal was induced by SC injection of naloxone (1 mg/kg) on day 4 of addiction). Brain catecholamines and their metabolites were measured using high performance liquid chromatography coupled with electrochemical detection (HPLC-ECD), for DA, NA, DOPAC and HVA, and coupled with fluorescence detection for MHPG. The ratios of DOPAC + HVA/DA and MHPG/NA were kept as an index of DA and NA turnovers, respectively. CRO administered 30 min before naloxone-precipitated withdrawal diminished significantly NA levels in frontal cortex. CRO increased DA turnover in striatum and frontal cortex in naive animals and significantly diminished DA levels in frontal cortex and DOPAC levels in frontal cortex and midbrain in morphine-dependent mice. These findings are discussed in relation to the protective effects of CRO on opiate withdrawal and the effects of CRO on locomotor activity.

  15. Changes induced by sodium cromoglycate on brain serotonin turnover in morphine dependent and abstinent mice.

    Science.gov (United States)

    San-Martin-Clark, O; Leza, J C; Lizasoain, I; Lorenzo, P

    1993-01-01

    This study was designed to explain the action of sodium cromoglycate (CRO) on the brain serotonergic system in control, morphine tolerant (by SC implantation of a 75 mg morphine pellet), and also in morphine dependent mice just before naloxone-precipitated withdrawal. After SC injections of CRO in control mice, morphine tolerant mice (day 4 of addiction), and 1 h before abstinence (withdrawal was induced by SC injection of 1 mg/kg naloxone on day 4 of addiction), animals were decapitated and various brain areas were rapidly removed. 5HT (Serotonin) and 5HIAA (5-hydroxyindole-3-acetic acid) were measured by high performance liquid chromatography coupled with electrochemical detection (HPLC-ECD). The ratio 5HIAA/5HT provided one index by which the turnover of the indoleamine was measured. CRO increased the turnover of 5HT in most of the brain areas studied in both control and morphine dependent mice. Furthermore, previous administration of CRO prior to naloxone challenge induced a significant increase in the 5HIAA/5HT ratio in the hypothalamus and striatum. These results are discussed as the reason for the preventive effect of CRO on jumping behaviour in morphine abstinent mice.

  16. Sodium cromoglycate, verapamil and nicardipine antagonism to leukotriene D4 bronchoconstriction.

    Science.gov (United States)

    Advenier, C.; Cerrina, J.; Duroux, P.; Floch, A.; Pradel, J.; Renier, A.

    1983-01-01

    1--The effects of nicardipine, verapamil and sodium cromoglycate (SCG) on the increase in pulmonary airway resistance(RAw) and decrease in pulmonary dynamic compliance (CDyn) induced by leukotriene D4 (LTD4) 0.5 micrograms kg-1 and acetylcholine (ACh) 3 micrograms kg-1 were investigated in anaesthetized guinea-pigs. The effects of these three agents on the contractile effects of LTD4 and ACh were tested on isolated tracheal preparations of the guinea-pig. 2--Nicardipine and verapamil (0.3 and 1 mg kg-1), as well as SCG (3 and 10 mg kg-1), partially but significantly inhibited the effects of LTD4 on RAw. Partial inhibition of the effect of LTD4 on CDyn was only observed with verapamil (0.3 and 1 mg kg-1). Nicardipine and verapamil had no effect on ACh-induced bronchoconstriction in vivo. 3--In concentrations higher than 10(-5) M, nicardipine and verapamil inhibited the contractile effects of LTD4 and ACh on guinea-pig isolated trachea. SCG had no effect on this preparation. 4--These results suggest that nicardipine, verapamil and SCG partially reduce the component of bronchoconstriction associated with stimulation of irritant receptors by LTD4. However, the site and mechanism of action of Ca2+-entry antagonists remain uncertain. PMID:6403095

  17. Comparative trial of sodium cromoglycate enemas with prednisolone enemas in the treatment of ulcerative colitis.

    Science.gov (United States)

    Grace, R H; Gent, A E; Hellier, M D

    1987-01-01

    A double blind multicentre study comparing sodium cromoglycate (600 mg/100 ml) by enema with prednisolone (20 mg/100 ml) by enema is reported. The study was conducted over a nine week period in the treatment of 70 patients with ulcerative colitis. Analysis of symptoms showed significant decreases in scores for patients in both groups, both at four and eight weeks; the only difference between the two groups was a significantly greater improvement in the reduction of rectal bleeding after four weeks in the prednisolone group. On sigmoidoscopy, both treatment groups showed a highly significant improvement after four and eight weeks with no significant differences being seen between the groups. Histology of the rectal biopsies showed a significant improvement in the inflammation of the mucosa for both treatment groups after four and eight weeks with no differences being observed between the groups. There were no significant changes in eosinophils from baseline and no difference between the groups at four and eight weeks. PMID:3102323

  18. Inhibition by cromoglycate and some flavonoids of nucleoside diphosphate kinase and of exocytosis from permeabilized mast cells.

    Science.gov (United States)

    Martin, M. W.; O'Sullivan, A. J.; Gomperts, B. D.

    1995-01-01

    1. The anti-allergic compound, cromoglycate, is reported to possess affinity for, and to suppress the autophosphorylation of a 72kDa protein having the sequence of nucleoside diphosphate kinase (NDPK). 2. We have tested the ability of cromoglycate, and a panel of ten structurally related flavonoids of plant origin, to inhibit the NDPK reaction and the exocytotic process of permeabilized mast cells. The conditions of permeabilization (use of an isotonic medium based on sodium glutamate) were selected to ensure that NDPK activity would be an essential component in the induction of Ca(2+)-induced exocytosis in which ATP is required for generation of GTP. For comparison, we also measured the inhibition of exocytosis induced by GTP-gamma-S; this proceeds in the absence of ATP and bypasses the need for NDPK activity. 3. We found that cromoglycate does not discriminate between Ca2+ and GTP-gamma-S-induced exocytosis and is a poor inhibitor of NDPK activity. Concentrations in the millimolar range are required for inhibition of all these functions. By comparison, many of the flavonoids are effective at concentrations in the micromolar range. 4. While we were unable to discern any systematic relationships between their ability to inhibit the three functions, two compounds, quercetin and genistein, inhibit Ca(2+)-induced, but not GTP-gamma-S-induced exocytosis. Inhibition of the late stages of the stimulus-response pathway in mast cells by these compounds is therefore likely to be due to inhibition of NDPK and the consequent failure to generate GTP. PMID:7582506

  19. Enhancement patterns and pseudo-washout of hepatic haemangiomas on gadoxetate disodium-enhanced liver MRI

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Bohyun [University of Ulsan College of Medicine, Asan Medical Center, Department of Radiology and Research Institute of Radiology, Seoul (Korea, Republic of); Ajou University School of Medicine, Department of Radiology, Suwon (Korea, Republic of); Byun, Jae Ho; Kim, Hyoung Jung; Won, Hyung Jin; Kim, So Yeon; Shin, Yong Moon; Kim, Pyo Nyun [University of Ulsan College of Medicine, Asan Medical Center, Department of Radiology and Research Institute of Radiology, Seoul (Korea, Republic of)

    2016-01-15

    To compare the enhancement patterns and prevalence of pseudo-washout between rapidly and slowly enhancing hepatic haemangiomas on gadoxetate disodium-enhanced MRI in patients with chronic liver disease (CLD) and healthy liver (HL). On gadoxetate disodium-enhanced MRI, the extent of intralesional arterial enhancement >50 % and ≤50 % of lesions was defined as rapid and slow enhancement, respectively. The enhancement patterns and presence of pseudo-washout during the portal venous phase (PVP) and transitional phase (TP) of 74 hepatic haemangiomas were retrospectively evaluated in the CLD and HL groups. Sequential changes of signal-to-noise ratio (SNR) were measured in unenhanced phase, PVP and TP. Irrespective of hepatic health status, pseudo-washout in TP was significantly more common in the rapidly enhancing haemangiomas (p ≤ 0.026). In both groups, rapidly enhancing haemangiomas showed complete or progressive incomplete enhancement in PVP, which either lasted or transformed to pseudo-washout in TP, whereas slowly enhancing haemangiomas showed progressive incomplete enhancement in PVP and TP. SNR of hepatic parenchyma continued to rise until TP, whereas that of portal vein and haemangioma falls in TP. Regardless of CLD, pseudo-washout in TP was more common in rapidly than in slowly enhancing haemangiomas, with enhancement patterns differing in the two subgroups. (orig.)

  20. 色甘酸二钠对早期断乳仔猪腹泻的作用研究%Effect of disodium cromoglycate on diarrhea of early weaned piglets

    Institute of Scientific and Technical Information of China (English)

    徐海军; 黄利权

    2000-01-01

    用2窝20头长×嘉仔猪在28日龄断乳,断乳前1 d和断乳后1周内,在试验组日粮中添加抗过敏药物色甘酸二钠;对照组的日粮不添加药物.结果:对照组仔猪在断乳当日就开始出现腹泻,腹泻持续5 d;试验组仔猪在断乳后第3 d才出现腹泻,腹泻持续3 d.结果表明,色甘酸二钠具有一定的预防仔猪早期断乳后腹泻的效果.

  1. Reduce the cytotoxic effect of mitomycin C in pterygium by disodium cromoglycate%色甘酸钠减少胬肉术中丝裂霉素影响的观察

    Institute of Scientific and Technical Information of China (English)

    杜宁静; 陈琦

    2002-01-01

    目的探讨色甘酸钠对翼状胬肉术中应用丝裂霉素C(MMC)影响的治疗方法与疗效的评定.方法翼状胬肉手术切除联合术中局部应用MMC,采用术后色甘酸钠滴眼的方法治疗一组复发性翼状胬肉22例,术后随防1~26月,平均(10.3±2.9)月.结果术后再次复发率为4.55%,手术成功率为95.45%,手术并发症,早期有轻度浅层点状角膜炎8例(36.36%),全部手术无严重并发症发生.结论术后应用色甘酸钠可减少胬肉术中应用MMC的影响,有效地防止复发性胬肉术后的再次复发.

  2. Preparation and characterisation of controlled release co-spray dried drug-polymer microparticles for inhalation 1: influence of polymer concentration on physical and in vitro characteristics.

    Science.gov (United States)

    Salama, Rania; Hoe, Susan; Chan, Hak-Kim; Traini, Daniela; Young, Paul M

    2008-06-01

    A series of co-spray dried microparticles containing di-sodium cromoglycate (DSCG) and polyvinyl alcohol (PVA - 0%, 30%, 50%, 70% and 90% w/w, respectively), were prepared as potential controlled release (CR) viscous/gelling vehicles for drug delivery to the respiratory tract. The microparticles were characterised in terms of particle size, crystal structure, density, surface morphology, moisture sorption, surface energy and in vitro aerosolisation efficiency. The co-spray dried particles were amorphous in nature and had spherical geometry. High-resolution atomic force microscopy analysis of the surfaces of the DSCG/PVA suggested no significant differences in roughness between microparticles containing 30-90% w/w PVA (ANOVA, p<0.05), while no specific trend in either size or density was observed with respect to PVA concentration. In comparison, a linear decrease in the relative moisture sorption (R2=0.997) and concurrent increase in total surface free energy (R2=0.870) were observed as PVA concentration was increased. Furthermore a linear increase in the aerosolisation efficiency, measured by inertial impaction, was observed as PVA concentration was increased (R2=0.993). In addition, the increase in aerosolisation efficiency showed good correlation with equilibrium moisture content (R2=0.974) and surface energy measurement (R2=0.905). These relationships can be attributed to the complex interplay of particle forces at the contiguous interfaces in this particulate system.

  3. Orientations of Chromonic Liquid Crystals by Imprinted or Rubbed Polymer Films

    Science.gov (United States)

    Yi, Youngwoo; McGuire, Aya; Clark, Noel

    2014-03-01

    A variety of novel alignment effects of chromonic liquid crystal phases of sunset yellow (SSY)/water, disodium cromoglycate (DSCG)/water, and their mixtures by thiol-ene polymer films topographically imprinted with linear channels are observed using polarizing optical microscopy. Nematic DSCG and SSY at low concentration and their nematic mixtures orient with the long axes of stacked chromonic aggregates on average parallel to the channels, that is, with the molecular planes normal to the channel axis. On the contrary, nematic SSY in contact with the rubbed polyimide films orients with the long axes on average in-plane perpendicular to the rubbing direction, arguably, due to a tongue-groove interaction between SSY and the stretched PI chains. Furthermore, multi-stable alignments are observed in SSY solutions of sufficiently high concentration, including preferential in-plane orientation of the long axes of the aggregates parallel to, perpendicular to, and 45° rotated from the channels. This work was supported by NSF grant DMR 1207606, NSF MRSEC grant DMR 0820579, and NSF Research Experience for Undergraduate programs.

  4. Chromones.

    Science.gov (United States)

    Edwards, Alan M

    2014-01-01

    The chromones are a class of chemical compounds characterised by the presence of the structure 5:6 benz-1:4-pyrone in their chemical make-up. The first chromone in clinical use, khellin, was extracted from the seeds of the plant Ammi visnaga, and had been used for centuries as a diuretic and as a smooth muscle relaxant. Its use in bronchial asthma was reported in 1947. In the 1950s, Benger's Laboratories embarked on a research programme to synthesise and develop modifications of khellin for the treatment of asthma. New compounds were screened using animal models to test the ability of the compound to prevent the anaphylactic release of histamine and SRS-A (leukotrienes) from sensitised guinea pig lung, and a human model to check the ability to reduce the bronchoconstriction induced by inhaled antigen bronchial challenge. For initial screening the human work was undertaken by Dr. R.E.C. Altounyan, who suffered from allergic bronchial asthma and was employed by Benger's Laboratories. After 8 years and more than 600 challenges using over 200 compounds, in 1965 Altounyan arrived at disodium cromoglycate (DSCG), the chromone that met the criteria of providing more than 6 h of protection. DSCG is still used today as a mast cell stabiliser. © 2014 S. Karger AG, Basel.

  5. Anti-allergic effects of ethanol extracts from brown seaweeds

    Institute of Scientific and Technical Information of China (English)

    Haider SAMEE; Zhen-xing LI; Hong LIN; Jamil KHALID; Yong-chao GUO

    2009-01-01

    Ethanol extracts of brown seaweeds from Pakistan and China were isolated and compared for their antiallergenic activities.They included Sargassum tennerimum (ST) and Sargassum cervicorne (SC) from Pakistan,and Sargassum graminifolium turn (SG),Sargassum thunbergii (STH),and Laminariajaponica (LJ) from China.The ethanol extracts of these brown seaweeds were optimized at 85% (v/v) ethanol for the maximum yield of phlorotannin,an inhibitor against hyaluronidase.Total phlorotannins contained in the crude extracts were measured as 1.71% (SG),0.74% (STH),0.97% (LJ),3.30% (SC),and 5.06% (ST).The 50% inhibitory concentrations (IC50) of Pakistani SC and ST were 109.5 and 21 μg/ml,respectively,lower than those of Chinese SG,STH,and LJ (134,269,and 148 μg/ml,respectively).An antiallergic drug,disodium cromoglycate (DSCG),had an IC50=39 μg/ml,and a natural inhibitor of hyaluronidase,catechin,had an IC50=20 μg/ml.The IC50 of ST extract was found similar to that of catechin (21 vs 20 μg/ml) and lower than that of DSCG (21 vs 39 μg/ml).This suggests that ST is a potent inhibitor of hyaluronidase,indicating a promising future development of natural antiallergic medicines or functional foods.

  6. A comparison of the effects of sodium cromoglycate and beclomethasone dipropionate on pulmonary function and bronchial hyperreactivity in subjects with asthma

    DEFF Research Database (Denmark)

    Svendsen, U G; Frølund, L; Madsen, F;

    1987-01-01

    After a run-in period of 2 weeks, receiving a regimen of inhaled beta 2-agonists and/or theophyllines, 38 atopic patients with asthma with perennial symptoms were randomly allocated to receive an 8-week treatment of additional inhalation treatment with either sodium cromoglycate (SCG), 2 mg four...

  7. Comparison of the efficacy and tolerability of topical levocabastine and sodium cromoglycate in the treatment of seasonal allergic rhinoconjunctivitis in children.

    Science.gov (United States)

    Vermeulen, J; Mercer, M

    1994-11-01

    Children (n = 110) with seasonal allergic rhinoconjunctivitis were randomized to receive either twice daily 0.05% levocabastine eye drops and nasal spray plus twice daily topical placebos or 2% sodium cromoglycate eye drops and nasal spray four times daily for a period of 4 weeks. Patients were required to use the nasal sprays as directed and the eye drops only when required. The results obtained suggest that topical levocabastine is at least as effective as sodium cromoglycate for the treatment of this condition. After 2 weeks treatment the effect of therapy on nasal symptoms was considered to be excellent or good in 72% of levocabastine-treated patients and 54% of patients on sodium cromoglycate (p = 0.009), with corresponding values for ocular symptoms of 81% and 57% in the two groups, respectively (p sodium cromoglycate with intergroup differences attaining statistical significance in favor of the topical antihistamine for nasal congestion (p < 0.05). Both agents were well-tolerated with no significant differences in the incidence or type of adverse reactions in the two treatment groups.

  8. A double blind placebo controlled group comparative study of ophthalmic sodium cromoglycate and nedocromil sodium in the treatment of vernal keratoconjunctivitis.

    Science.gov (United States)

    el Hennawi, M

    1994-05-01

    In a 4 week double masked comparative study, patients received 2% nedocromil sodium (48), 2% sodium cromoglycate (48), or placebo eye drops (42), four times daily, for the treatment of vernal keratoconjunctivitis (VKC). Clinical examinations of eye condition and symptom severity were made before and after a 1 week baseline before starting test treatment, and after 1, 2, and 4 weeks of treatment. Patients kept daily diary card records of symptom severity and concomitant therapy. At the clinic, significant improvements were seen with both active treatments after 2-4 weeks. During the final visit, significant benefits over placebo were recorded for five ocular signs with nedocromil sodium and three with sodium cromoglycate, bulbar and lower tarsal chemosis being better controlled by nedocromil sodium (p sodium cromoglycate). Diary card trends showed improvement with all three treatments, which was greatest with nedocromil sodium and least with placebo. Compared with placebo, both the active drugs produced statistically significant improvements in general eye condition during weeks 1-2, and nedocromil sodium significantly reduced itching within the first week. Overall, nedocromil sodium had the greatest effect on symptoms, although diary card data revealed no statistically significant differences between the two active drugs. In conclusion, both 2% nedocromil sodium and 2% sodium cromoglycate were effective in controlling VKC when administered four times daily into the eyes, while the marked anti-inflammatory activity of nedocromil sodium was apparent in its more pronounced overall therapeutic effect.

  9. Transient Severe Motion Artifact Related to Gadoxetate Disodium-Enhanced Liver MRI: Frequency and Risk Evaluation at a German Institution.

    Science.gov (United States)

    Well, Lennart; Rausch, Vanessa Hanna; Adam, Gerhard; Henes, Frank Oliver; Bannas, Peter

    2017-07-01

    Purpose Varying frequencies (5 - 18 %) of contrast-related transient severe motion (TSM) imaging artifacts during gadoxetate disodium-enhanced arterial phase liver MRI have been reported. Since previous reports originated from the United States and Japan, we aimed to determine the frequency of TSM at a German institution and to correlate it with potential risk factors and previously published results. Materials and Methods Two age- and sex-matched groups were retrospectively selected (gadoxetate disodium n = 89; gadobenate dimeglumine n = 89) from dynamic contrast-enhanced MRI examinations in a single center. Respiratory motion-related artifacts in non-enhanced and dynamic phases were assessed independently by two readers blinded to contrast agents on a 4-point scale. Scores of ≥ 3 were considered as severe motion artifacts. Severe motion artifacts in arterial phases were considered as TSM if scores in all other phases were  0.05). Conclusion We revealed a high frequency of TSM after injection of gadoxetate disodium at a German institution, substantiating the importance of a diagnosis-limiting phenomenon that so far has only been reported from the United States and Japan. In accordance with previous studies, we did not identify associated risk factors for TSM. Key Points:  · Gadoxetate disodium causes TSM in a relevant number of patients.. · The frequency of TSM is similar between the USA, Japan and Germany.. · To date, no validated risk factors for TSM could be identified.. Citation Format · Well L, Rausch VH, Adam G et al. Transient Severe Motion Artifact Related to Gadoxetate Disodium-Enhanced Liver MRI: Frequency and Risk Evaluation at a German Institution. Fortschr Röntgenstr 2017; 189: 651 - 660. © Georg Thieme Verlag KG Stuttgart · New York.

  10. Design and optimization of mucoadhesive nasal in situ gel containing sodium cromoglycate using factorial design

    Directory of Open Access Journals (Sweden)

    Riten A Shah

    2011-01-01

    Full Text Available Nasal in situ gel of sodium cromoglycate was prepared for sustained release and improvement of drug bioavailability. Carbopol 940 was used as a key ingredient which gives pH-induced sol to gel conversion of the formulations. Different formulations were prepared by varying the concentrations of carbopol 940 and different grades of Hydroxyl Propyl Methyl Cellulose (HPMC K100, HPMC K4M and HPMC K15M. These formulations were evaluated for parameters like pH, drug content, viscosity, gel strength, in vitro drug release and drug excipient compatibility. In this study, the release profile depends on the concentration of carbopol 940 and grade HPMC. A 3 2 factorial was applied to check the effect of varying the concentration of carbopol 940 (X 1 and different grades of HPMC (X 2 on the dependent variable i.e. viscosity, mucoadhesive strength, cumulative percentage drug released in 1 h (Q 1 , 4 h (Q 4 and 8 h (Q 8 as dependent variables . In vitro release data was fitted to various models to ascertain the kinetic of drug release. Regression analysis and analysis of variance were performed for dependent variables. The results of the F-statistics were used to select the most appropriate model. Formulation F6 was considered optimum which contained carbopol 940 (0.75% and HPMC K4M (0.50% and was more similar to the theoretical predicted dissolution profile (f2 =70.99. The studies indicate that the formulation was effective in providing in vitro release, in vitro permeation of drug and the mucoadhesion which increases the residence time of drug.

  11. Protective effects of nedocromil sodium and sodium cromoglycate on gastroduodenal ulcers: a comparative study in rats.

    Science.gov (United States)

    Tariq, Mohammad; Moutaery, Meshal Al; Elfaki, Ibrahim; Arshaduddin, Mohammad; Khan, Haseeb Ahmad

    2006-08-01

    Stabilization of mast cells plays a key mechanism to protect gastrointestinal tract from injury. This study presents a comparative evaluation of mast cell stabilizers nedocromil sodium (NDS) and sodium cromoglycate (SCG) in experimental gastric and duodenal ulcers in rats. Wistar rats of either sex were used in this study. Both NDS and SCG, in the doses of 10, 30 and 100 mg/kg were given intraperitoneally for gastric secretion studies and by gavage for antiulcer studies. Acid secretion studies were undertaken in pylorus-ligated rats. Gastric lesions were induced by water immersion restraint stress (WIRS), indomethacin and ethanol whereas duodenal ulcers were produced by cysteamine. The level of glutathione (GSH) and gastric wall mucus were measured in glandular stomach of rats following ethanol-induced gastric lesions. SCG was more effective than NDS in preventing WIRS- and indomethacin-induced gastric lesions whereas reverse was true in ethanol- and cysteamine-induced ulcers. All the 3 doses of SCG offered almost equal protection against WIRS-induced gastric lesions whereas only medium and high dose of NDS provided significant protection in this model of ulcer. NDS significantly inhibited cysteamine-induced duodenal ulcers whereas SCG failed to do so. Pretreatment with NDS or SCG significantly and dose-dependently protected gastric mucosa against ethanol-induced injury, while the former drug appeared to be more effective. The cytoprotective effects of these two drugs were accompanied by the attenuation of ethanol-induced depletion of gastric wall mucus and GSH. The differential effects of NDS and SCG against various gastric lesions rationalize the possible benefits of a combined therapy (NDS+SCG) for the treatment of complex gastroduodenal ulcers.

  12. Gadoxate disodium: gadolinium EOB DTPA, gadoxetic acid, Gd-EOB-DTPA.

    Science.gov (United States)

    2004-01-01

    Gadoxate disodium [gadolinium EOB DTPA, Gd-EOB-DTPA, gadoxetic acid, Eovist injection, Primovist] is a hydrophilic paramagnetic contrast agent being developed by Schering AG for hepatobiliary magnetic resonance imaging. In April 2004, gadoxate disodium (Primovist) was approved in Sweden, the reference member state for the EU registration. Following the Swedish approval, Schering will initiate a mutual recognition procedure for the EU with approvals expected in most countries during 2004. Gadoxate disodium is in phase III clinical trials in the US and has completed phase III studies in Japan. Submissions for approval in Japan and other Asian countries are planned for 2004. Schering AG plans to launch Eovist in Japan in 2005. Schering AG acquired a worldwide, royalty-bearing licence to EPIX Medical's patents covering liver-enhancing agents such as Eovist injection. These included a European patent (222886) and the US patents (4,899,755 and 4,888,008) that EPIX Medical exclusively licensed from the Massachusetts General Hospital (MGH). The MGH patents, a part of EPIX's extensive intellectual property, also covered albumin-targeted agents such as MS 325 (AngioMARK). Schering AG formally withdrew from the opposition proceedings against EPIX's EU patent 222886 following its acquisition of EPIX's intellectual property. These EU and US patents were also non-exclusively licensed by EPIX Medical to Bracco in September 2001. Apart from covering Eovist (Schering AG), the EU patent also covered gadobenate dimeglumine (MultiHance Bracco). Following the licensing agreement, Bracco withdrew its opposition to the patents in Europe and Japan, and both EPIX Medical and Bracco settled their European patent dispute. In its 2002 Annual Report, Schering predicted that Eovist has the potential to reach peak sales of euro50 million, three years after launch--at the time, launch in Europe was anticipated in 2004, followed by launch in Japan in 2005. This is down from earlier predictions

  13. Optical properties on thermally evaporated and heat-treated disodium phthalocyanine derivative thin films

    Indian Academy of Sciences (India)

    M E Sánchez-Vergara; M Rivera; R A Torres-García; C O Perez-Baeza; E A Loza-Neri

    2014-08-01

    Thin films were grown on quartz substrates and crystalline silicon wafers using disodium phthalocyanine and the organic ligands 2,6-diaminoanthraquinone, 2,6-dihydroxianthraquinone and its potassium derivative salt. The surface morphology of these films was analysed by atomic force microscopy (AFM) and scanning electron microscopy (SEM). IR spectroscopy was employed in order to investigate possible changes of the intra-molecular bonds between the powder compounds and thin films. The optical parameters have been investigated using spectrophotometric measurements of absorbance in the wavelength range of 200–1100 nm and the effects of post-deposition heat treatment were analysed. The absorption spectra recorded in the UV–Vis region for the deposited samples showed two bands, namely the Q and Soret bands. The absorption coefficient in the absorption region reveals non-direct transitions. In addition, the optical gap dependence upon the thickness of these thin films was evaluated.

  14. EMBRYOTOXIC AND TERATOGENIC EFFECT OF DISODIUM GLYCYRRHETINIC ACID HEMIPHTHALATE IN MICE

    Directory of Open Access Journals (Sweden)

    H. Marzbnn

    1998-07-01

    Full Text Available Disodium glycyrrhetinic acid hemiphthalaic (GAP was evaluated for developmental toxicity in pregnant NMRI mice. GAP was administered intrapcritoneally on days S, 9, 10, of gestation at doses of 0, 25, 50 and 75 mg/kg/dav. On gestation day of IS, after operational delivery, the fetuses were examined for soft tissue, external and skeletal defects."nIncreased absorptions, dead fetuses, and reduce fetal body weight per litter were observed at doses of 50 and 75 mg/kg/day. In addition by using different doses of GAP at different critical gestation times, developmental delay was observed as reduction in ossification centers and vertebral number in caudal region. It seems that GAP at doses of (50 and 75 mg/kg/day has a cmbiyotoxic and teratogenic potential in mice.

  15. Growth during one year of treatment with fluticasone propionate or sodium cromoglycate in children with asthma.

    Science.gov (United States)

    Price, J F; Russell, G; Hindmarsh, P C; Weller, P; Heaf, D P; Williams, J

    1997-09-01

    The aim of this study was to compare accurately measured growth over 12 months in asthmatic children treated with either fluticasone propionate (FP) 50 micrograms twice daily (b.i.d.) or sodium cromoglycate (SCG) 20 mg four times daily (q.i.d.). After a 2-week run-in, asthmatic children aged 4-10 years from 15 UK centers were randomized in a 3:4 ratio to open-label FP (n = 52) or SCG (n = 70). After 8 weeks, those whose asthma was not adequately controlled were switched from SCG to FP or withdrawn. Standing height was measured (Holtain stadiometry) at baseline, after 8 weeks and at 6 weeks intervals thereafter for 1 year. Morning peak flows (PEFam) were recorded by patients for 2 weeks during baseline, and 1 week before each visit during treatment. Urinary free cortisol (24 h) was measured at baseline, 6 months, and 1 year. After 8 weeks, 22 patients were withdrawn from SCG group (and were switched to FP), and five patients were withdrawn from the FP group due to poor asthma control. A further 21 and 11 patients were withdrawn from the SCG and FP groups, respectively, during the course of the study. There were no significant differences between patients who received FP and SCG for 1 year (n = 34 and n = 26, respectively) in terms of height velocity adjusted for age and gender (HV), or height velocity standard deviation scores adjusted for gender (HVSDS). Mean HV (mean HVSDS) were 6.0 cm/yr (0.1) and 6.5 cm/yr (0.5) for FP and SCG, respectively. There were no treatment differences in mean 24 h urinary free cortisol levels at 6 and 12 months. Mean % predicted PEFam improved over 1 year in both groups but to a greater degree in the FP group. We concluded that growth was normal in mildly asthmatic children receiving FP (50 micrograms bid) for 1 year. There were fewer withdrawals and lung function improved to a greater extent in FP treated patients than in patients receiving SCG.

  16. Molecular distribution of gold(I) in human blood plasma after treatment with the antiarthritic disodium aurothiomalate.

    Science.gov (United States)

    Rayner, M H; Grootveld, M; Sadler, P J

    1989-01-01

    On-line separation and detection of both high- and low-molecular-weight gold species in human blood plasma treated with disodium aurothiomalate were achieved by a technique incorporating a combination of fast protein liquid chromatography with continuous monitoring of absorbance at 254 nm and eluant gold concentration by flame atomic absorption spectroscopy. The fate of gold (40 microM disodium aurothiomalate) in human blood plasma was monitored over a period of 24 h. Results obtained indicated that more than 50% of the gold is associated with a peak identified as albumin after a 5 min incubation period at 37 degrees C, and by 30 min more than 90% is found to be associated with albumin. This novel analytical combination enables the rapid, selective and sensitive determination of gold(I) and its biotransformation products (both protein--and non-protein-bound) in biological fluids.

  17. Synthesis of disodium-3-amino-1-hydroxypropane-1, 1-diphosphonate-1-/sup 14/C. (APD. 2Na)

    Energy Technology Data Exchange (ETDEWEB)

    Magnien, E.; Shaikh, M.; Suh, J.T.; Jones, H. (Revlon Health Care Group, Tuckahoe, New York (USA))

    1982-10-01

    Disodium-3-amino-1-hydroxy-1, 1-diphosphonate-1-/sup 14/C (APD 2Na), a powerful calcium binding agent and potential drug for the treatment of Paget's Disease was synthesized. The reaction was carried out by reacting ..beta..-alanine (1-/sup 14/C) with phosphorus acid and phosphorus trichloride in chlorobenzene. Treatment of the resultant APD with two equivalents of sodium hydroxide gave the title compound.

  18. From khellin to sodium cromoglycate--a tribute to the work of Dr. R. E. C. Altounyan (1922-1987).

    Science.gov (United States)

    Meyer, U

    2002-01-01

    Sodium cromoglycate, which was launched in 1968 by the British company Fisons for the treatment of allergies and asthma, was an absolute novelty in chemical, pharmacological as well as therapeutic respects. The khellin derivative meanwhile did not owe its discovery to the usual strategies for finding drugs. On the contrary, the protective effect of the substance was discovered in a self trial through systematic antigen-induced provocation tests of the medicinal doctor and allergic Roger Ernest Collingwood Altounyan (1922-1987). The only subsequently formed hypothesis of a mast cell stabilising effect of Sodium cromoglcycate did not prove to be valid for the search for similar or more effective substances. A further development of this drug class could not take place because of the lack of suitable pharmacological models.

  19. Long-term Efficacy and Safety of Pamidronate Disodium in Treatment of Bone Metastases in Breast Cancer

    Institute of Scientific and Technical Information of China (English)

    Li-jun Di; Jun Ren; Ying Yan; Feng-ling Wan; Guo-gong Song; Jing Yu

    2009-01-01

    Objective: To evaluate the long-term efficacy and safety of pamidronate disodium in patients with bone lesions secondary to advanced breast carcinoma. Methods: A retrospective chart review was conducted of 62 patients receiving intravenous pamidronate disodium for metastatic breast cancer. The proportion of patients experiencing at least one skeletal related event (SRE) after 12 months of therapy was determined.Results: The proportion of patients who had an SRE was 29.00% (18 individuals) and the median time to first event was greater than 350 days. Radiotherapy(11 individuals)and pathologic fracture(6 individuals)were the most frequent type of SRE, while cord compression(1 individuals) and hypercalcaemia(0 individuals) were rare. A total of 37 individuals had transient hypocalcaemia without any clinical symptom. No significant creatinine abnormalities were encountered. There were no clinically relevant changes of calcium ,phosphate and creatinine before and after therapy.Conclusion: Long-term treatment with pamidronate disodium significantly reduces and delays skeletal morbidity from osteolytic metastases . Prolonged therapy was well tolerated. This study suggests that the rate of clinically relevant SREs is substantially lower than the event rate observed in phase III clinical trials.

  20. Determination of sodium cromoglycate in human plasma by liquid chromatography-mass spectrometry in the turbo ion spray mode.

    Science.gov (United States)

    Ozou, M L; Girault, J; Malgouyat, J M; Pasquier, O

    2001-12-25

    A highly sensitivity liquid chromatography-tandem mass spectrometry method has been developed for the quantitation of sodium cromoglycate (SCG) in human plasma. The method was validated over a linear range of 0.100-50.0 ng/ml, using 13C4 sodium cromoglycate as the internal standard. Compounds were extracted from 1.0 ml of lithium heparin plasma by methanol elution of C18 solid-phase extraction cartridges. The dried residue was reconstituted with 100 microl of 0.01 N HCl. and 30 microl was injected onto the LC-MS-MS system. Chromatographic separation was achieved on a C8 (3.5 microm) column with an isocratic mobile phase of methanol-water-0.5 M ammonium acetate (35:64.8:0.2, v/v/v). The analytes were detected with a PE Sciex API 3000 mass spectrometer using turbo ion spray with positive ionization. Ions monitored in the multiple reaction monitoring (MRM) mode were m/z 469.2 (precursor ion) to m/z 245.1 (product ion) for SCG and m/z 473.2 (precursor ion) to m/z 247.1 (product ion) for 13C4 SCG (I.S.). The average recoveries of SCG and the I.S. from human plasma were 91 and 87%, respectively. The low limit of quantitation was 0.100 ng/ml. Results from a 4-day validation study demonstrated excellent precision (C.V.% values were between 1.9 and 6.5%) and accuracy (-5.4 to - 1.2%) across the calibration range of 0.100-50.0 ng/ml.

  1. Regeneration of poly-L-lysine modified carbon electrodes in the accumulation and cathodic stripping voltammetric determination of the cromoglycate anion.

    Science.gov (United States)

    Pereira, F C; Fogg, A G; Zanoni, M V B

    2003-07-27

    Cromoglycate is accumulated on a poly-L-lysine (PLL) modified carbon electrode best from pH 4 solution, where it is anionic and the PLL is cationic, and at which pH the cromoglycate gives a good reduction peak at -0.82 V. The PLL film can be regenerated readily by washing the electrode with 3 M sodium hydroxide solution, in which the PLL is deprotonated. Regeneration of the film is not required as frequently when larger amounts of PLL are incorporated into it. This allows standard addition procedures to be carried out without regenerating the electrode. Linear calibration graphs have been obtained typically in the range 0.1-1.5 microg ml(-1). Detection limits have been calculated to be 10 ng ml(-1). The standard addition method has been applied satisfactorily to diluted urine solutions.

  2. Inhibition of platelet-activating factor- and zymosan-activated serum-induced chemotaxis of human neutrophils by nedocromil sodium, BN 52021 and sodium cromoglycate.

    Science.gov (United States)

    Bruijnzeel, P. L.; Warringa, R. A.; Kok, P. T.

    1989-01-01

    1. Inflammatory cells such as eosinophils and neutrophils are thought to contribute actively to the pathogenesis of asthma since they infiltrate into the lung tissue. These cells are mobilized by lipid-like and protein-like chemotactic factors. As illustrative examples of both groups, platelet-activating-factor (Paf) and zymosan-activated-serum (ZAS) were used in this study. The inhibitory effects of nedocromil sodium, the Paf antagonist BN 52021 and sodium cromoglycate on Paf- and ZAS-induced neutrophil chemotaxis were evaluated. 2. All tested drugs inhibited Paf-induced neutrophil chemotaxis with approximately the same potency (IC50 approximately 1 nM). 3. Nedocromil sodium and sodium cromoglycate were equally potent in inhibiting ZAS-induced neutrophil chemotaxis (IC50 = 0.1-1 microM), whereas BN 52021 was considerably less potent (IC30 = 10 microM). 4. To find out whether the drugs tested could inhibit early events in cell activation, their capacity to inhibit Paf- and ZAS-induced cytosolic free Ca2+-mobilization was investigated. BN 52021, at a concentration of 100 microM, completely inhibited Paf-induced Ca2+-mobilization and inhibited ZAS-induced Ca2+-mobilization by about 50%. Nedocromil sodium and sodium cromoglycate were ineffective. PMID:2551444

  3. Phase conjugation by degenerate four wave mixing in disodium fluorescein solution in methanol

    Science.gov (United States)

    Abdeldayem, Hossin; Sekhar, P. Chandra; Venkateswarlu, P.; Geroge, M. C.

    1989-01-01

    Organic dyes are known to show the resonant type of nonlinear optical properties, including phase conjugation. In the present work, disodium fluorescein in methanol is used as an organic nonlinear medium for degenerate four wave mixing at 532 nm to see the intensity dependence of the phase conjugate signal at different concentrations of the solution. It is observed that the maximum reflectivity of the signal occurs in a concentration range of 5 x 10(exp -3)/cu cm to 1.2 x 10(exp -2) g/cu cm. It is also observed that the intensity of the signal drops suddenly to less than half of its maximum outside the concentration range mentioned above. An investigation of the phase conjugate signal intensity by changing the delay time between probe signal and the forward pump is also examined. Briefly discussed is the possibility of population grating in dye liquids as a source of enhancing the third order susceptibility besides the other techniques mentioned in reference. The experiment is done by beam splitting the second harmonic (532 nm) of Nd:YAG laser, Q-switched at 20 pulses/sec (pulse width is approximately 8 and 200 mJ per pulse).

  4. Early Effects of Combretastatin-A4 Disodium Phosphate on Tumor Perfusion and Interstitial Fluid Pressure

    Directory of Open Access Journals (Sweden)

    Carsten D. Ley

    2007-02-01

    Full Text Available Combretastatin-A4 disodium phosphate (CA4DP is a vascular-disruptive agent that causes an abrupt decrease in tumor blood flow. The direct actions of CA4DP include increases in vascular permeability and destabilization of the endothelial cytoskeleton, which are thought to contribute to occlusion of the tumor vasculature. It has been proposed that increased permeability causes a transient increase in interstitial fluid pressure (IFP, which in turn could collapse intratumoral blood vessels. We examined the immediate effects of CA4DP on tumor IFP in C3H mammary carcinoma. Mice were treated with 100 mg/kg CA4DP by intraperitoneal injection. Tumor perfusion was recorded by laser Doppler flowmetry at separate time points, and IFP was recorded continuously by the wickin-needle method. In this study, we found that CA4DP treatment resulted in a rapid reduction in tumor perfusion, followed by a decrease in IFP; no increases in IFP were observed. This suggests that CA4DP-induced reductions in tumor perfusion are not dependent on increases in IFP.

  5. Electroacupuncture improves neuropathic pain Adenosine,adenosine 5'-triphosphate disodium and their receptors perhaps change simultaneously

    Institute of Scientific and Technical Information of China (English)

    Wen Ren; Wenzhan Tu; Songhe Jiang; Ruidong Cheng; Yaping Du

    2012-01-01

    Applying a stimulating current to acupoints through acupuncture needles-known as electroacupuncture-has the potential to produce analgesic effects in human subjects and experimental animals.When acupuncture was applied in a rat model,adenosine 5'-triphosphate disodium in the extracellular space was broken down into adenosine,which in turn inhibited pain transmission by means of an adenosine A1 receptor-dependent process.Direct injection of an adenosine A1 receptor agonist enhanced the analgesic effect of acupuncture.The analgesic effect of acupuncture appears to be mediated by activation of A1 receptors located on ascending nerves.In neuropathic pain,there is upregulation of P2X purinoceptor 3(P2X3)receptor expression in dorsal root ganglion neurons.Conversely,the onset of mechanical hyperalgesia was diminished and established hyperalgesia was significantly reversed when P2X3 receptor expression was downregulated.The pathways upon which electroacupuncture appear to act are interwoven with pain pathways,and electroacupuncture stimuli converge with impulses originating from painful areas.Electroacupuncture may act via purinergic A1 and P2X3 receptors simultaneously to induce an analgesic effect on neuropathic pain.

  6. Evaluation of the chitosan/glycerol-{beta}-phosphate disodium salt hydrogel application in peripheral nerve regeneration

    Energy Technology Data Exchange (ETDEWEB)

    Zheng Lu; Zhang Xiufang; Gong Yandao [State Key Lab Biomembrane and Membrane Biotechnology, School of Life Sciences, Tsinghua University, Beijing 100084 (China); Ao Qiang; Han Hongyan, E-mail: gongyd@tsinghua.edu.c, E-mail: aoqiang@tsinghua.edu.c [Institute of Neurological Disorders, Yuquan Hospital, Tsinghua University, Beijing 100049 (China)

    2010-06-01

    Research efforts have been devoted to evaluating the application of the chitosan (CS)/glycerol-{beta}-phosphate (GP) disodium salt hydrogel in peripheral nerve regeneration. The gelation time was determined to be 770 s using ultraviolet spectrophotometry. A standard 10 mm long rat sciatic nerve defect model was employed, followed by bridging the proximal and distal stumps with chitosan conduits injected with the Schwann cell-containing hydrogel. Injections of the blank hydrogel, Schwann cell suspension and culture medium were used as controls. Two months later, electrophysiological assessment and fluorogold retrograde tracing showed that compound muscle action potentials (CMAPs) and fluorogold-labeled neurons were only detected in the Schwann cell suspension group and culture medium group. The rats were then killed, and implanted conduits were removed for examination. There were no regenerated nerves found in groups injected with the blank hydrogel or Schwann cell-containing hydrogel, while the other two groups clearly displayed regenerated nerves across the gaps. In the subsequent histological assessment, immunohistochemistry, toluidine blue staining and transmission electron microscopy were performed to evaluate the regenerated nerves. The relative wet weight ratio, Masson trichrome staining and acetylcholinesterase staining were employed for the examination of gastrocnemius muscles in all four groups. The Schwann cell suspension group showed the best results for all these indexes; the culture medium group ranked second and the two hydrogel-injected groups showed the least optimal results. In conclusion, our data revealed that the implanted CS/GP hydrogel actually impeded nerve regeneration, which is inconsistent with former in vitro reports and general supposition. We believe that the application of the CS/GP hydrogel in nerve regeneration requires a further study before a satisfactory result is obtained. In addition, the present study also confirmed that

  7. Use of disodium pamidronate bisphosphonate in patients with bone metastases of lung cancer

    Directory of Open Access Journals (Sweden)

    Ranković Boško

    2002-01-01

    Full Text Available Disodium pamidronate (Aredia®, a drug of the bisphosphonate group, was administered to 20 patients with pains in the bones due to secondary deposits of lung cancer. The aim of the study was to investigate the analgesic effect of pamidronate to osteolytic metastases of lung cancer in the bone. In 16 (80% patients non-small-cell lung cancer was diagnosed, and in 4 (20% patients small-cell-lung cancer was confirmed. Intensive disseminated pains in the bones were present in all the patients. Metastases in the skeleton were confirmed by radiography and scintigraphy of the bones. Initial values of calcium in the plasma were determined in those patients. In 11 (55% patients, initial values of calcium in the serum were normal, and in 9 (45% patients, they were elevated. Patients with normal calcium values received 30 mg of pamidronate in 250 ml of normal saline, and patients with hypercalcaemia received 45-60 mg in 500 ml of normal saline. Analgesic effect of pamidronate was present in 12 (60% patients, and the completely painless state was achieved in 4 out of 12 patients. Evaluation of the pain was done by questionnaire, using a simple, descriptive scale. In all 9 (100% patients with hypercalcaemia, values of calcium in plasma were normalized. Pamidronate exerted favorable analgesic effect in the case of metastases of lung cancer in the bones in more than 50% patients. Satisfactory results were also achieved in the patients non-responsive to palliative therapy by irradiation This enables the use of opiates in lower doses.

  8. Extraction of protoporphyrin disodium and its inhibitory effects on HBV-DNA

    Institute of Scientific and Technical Information of China (English)

    Chao-Pin Li; Li-Fa Xu; Qun-Hong Liu; Chao Zhang; Jian Wang; Yu-Xia Zhu

    2004-01-01

    AIM: To explore an ideal method for extracting protoporphyrin disodium (PPN) from unanticoagulated animal blood, and to study the inhibitory effects of PPN on HBV-DNA duplication and its cytotoxicity to 2.2.15 cell strain.METHODS: Protoporphyrin methyl ester and other intermediate products were prepared with protoheme separated from protein hydrolysates of coagulated animal blood, which were finally made into PPN and detected quantitatively with an ultraviolet fluorescent analyzer.Ten μg/ml, 20 μg/ml, 40 μg/ml, 80 μg/ml and 160 μg/ml of PPN-aqueous solution were added into culture medium for 2.2.15 cells respectively. Eight days later, the drug concentration in supernatant from the culture medium was detected when inhibition rate of HBeAg, cell Survival rate when inhibition rate of HBeAg was 50% (ID50), and when survival cells in experimental group were 50% of those in control group (CD50), and the therapeutic index (TI) was also detected. PPN with different concentration of 10 μg/ml,20 μg/ml, 40 μg/ml, 80 μg/ml and 160 μg/ml was respectively mixed and cultivated with HepG2 2.2.15 cell suspension,and then the inhibition of PPN against HBV-DNA was judged by PCR.RESULTS: The extract of henna crystal was identified to be PPN. When the concentrations of PPN were 160 μg/ml and 80 μg/ml, the inhibition rates of HBeAg were 89.8% and 82.4%, and the cell survival rates were 98.7% and 99.2%.CONCLUSION: It is suggested that PPN can be extracted from unanticoagulated animal blood. PPN can inhibit HBV-DNA expression and duplication ih vitro, and has no cytotoxicity to liver cells. Further study and application of PPN are warranted.

  9. Antimutagenic activity of a novel ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate.

    Science.gov (United States)

    Hisama, Masayoshi; Matsuda, Sanae; Shibayama, Hiroharu; Iwaki, Masahiro

    2008-06-01

    A novel amphiphilic vitamin C derivative, disodium isostearyl 2-O-L-ascorbyl phosphate (VCP-IS-2Na) possessing an alkyl chain of C(18) to a stable ascorbate derivative sodium L-ascorbic acid 2-phosphate (VCP-Na), was synthesized and evaluated as an anti-mutagen with suppressive effect on SOS-inducing activity on mutagen in the Salmonella typhimurium TA1535/pSK1002 umu test. VCP-IS-2Na was assayed with chemical mutagens, N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide (furylfuramide) and 4-nitroquinolin 1-oxide (4NQO), which do not require liver metabolizing enzymes. VCP-IS-2Na at a concentration of 0.40 micromol/ml suppressed 66.2%, 54.7% and 60.2% of the SOS-inducing activity on MNNG, furylfuramide, and 4NQO, and the 50% inhibitory dose value (ID(50)) was 0.12 micromol/ml, 0.26 micromol/ml, and 0.17 micromol/ml, respectively. In addition, VCP-IS-2Na was assayed with 2-aminoanthracene (2AA) and 3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1), which require liver metabolizing enzymes. To study the structure-activity relationship, L-ascorbic acid (VC) and VCP-Na were also assayed with all mutagens. VCP-IS-2Na, suppressed the chemical and physical mutagens-induced SOS response greater than VC and VCP-Na in the umu test. Also, the antimutagenic activities of VCP-IS-2Na, VC, and VCP-Na against MNNG and Trp-P-1 were assayed by the Ames test using the S. typhimurium TA100 strain. In summary, this research suggests that VCP-IS-2Na showed potent antimutagenic effects against chemical mutagens and UV irradiation.

  10. Inhalation and deposition of nebulized sodium cromoglycate in two different particle size distributions in children with asthma.

    Science.gov (United States)

    Nerbrink, O L; Lindström, M; Meurling, L; Svartengren, M

    2002-11-01

    The relative deposition of two inhaled droplet size distributions of sodium cromoglycate produced by a Hudson Updraft II nebulizer was evaluated, using a setup modified from the proposed Comité Européen Normalisé (CEN) standard prEN 13544-1. The modified setup comprised an Andersen 296 impactor and a Spira Electro 2 dosimeter. The setup was characterized prior to use in children with sodium cromoglycate (SCG) and sodium fluoride as tracer aerosol. The main in vivo study was designed to allow nine children with a mean age of 10 years to inhale SCG aerosol at two different relative humidities (RH), a high RH (> 90%) and a low RH (13%), which in turn resulted in two different droplet size distributions. The nebulizer/dosimeter was set to provide 1-sec nebulization during 50 inhalations. Throughout the exposures, the children were instructed to inhale in a consistent manner with target tidal volumes (0.5 L) and inhalation flows (0.4 L/sec). Blood samples were taken at predefined time intervals, and the area under the curve (AUC) was calculated. A lung deposition program, TGLD2, was used to calculate the expected deposition, using the droplet sizes and inhalation parameters obtained during in vivo exposures. The in vivo monitoring of droplet size distribution during the exposure showed that the low, intermediate (room air), and high RHs gave a mean droplet size distribution with a mass median aerosol diameter (MMAD) of 1.2, 1.7, and 2.0 microm, respectively. The average tidal volume over all exposures was 0.51 +/- 0.12 L. The total deposition fraction was 33.4% of the estimated nebulizer output. A correlation was found between tidal volume and the calculated deposited fraction. The results indicate that there is a difference in total deposition, depending on the size of the droplet size distribution, with the larger droplet size distribution (MMAD, 2.0 microm) having a higher total deposition than the smaller droplet size distribution (MMAD, 1.2 microm). The

  11. A simple pharmacokinetic method to evaluate the pulmonary dose in clinical practice--analyses of inhaled sodium cromoglycate.

    Science.gov (United States)

    Lindström, Maria; Svensson, Jan Olof; Meurling, Lennart; Svartengren, Katharina; Anderson, Martin; Svartengren, Magnus

    2004-01-01

    When the expected effect of an inhaled drug is not achieved, the cause could be poor inhalation technique and consequently a low pulmonary dose. A simple in vivo test to evaluate the pulmonary dose would be a benefit. This study evaluates the relative and systemic bioavailability following inhalation of nebulized sodium cromoglycate (SCG) in healthy subjects. Blood samples were collected during 240 min and urine was collected in two portions, up to 6 h post-inhalation. Two exposures were performed and comparisons based on the quantification of drug in plasma and urine by a high-performance liquid chromatography (HPLC) procedure were done. In one of the exposures, a pulmonary function test was performed to study if an expected effect of increased absorption could be detected. There was a good correlation between the two exposures shown in the plasma concentrations, but not in the urine analyses. The forced exhaled volume manoeuvres were associated with a higher Cmax and plasma concentrations up to 60 min post-inhalation (P<0.01). This effect was not detected in the urine analyses. We conclude that this pharmacokinetic method with inhaled SCG and plasma analyses could be used to evaluate individual inhalation technique. The HPLC method used was rapid and had adequate sensitivity.

  12. Sensitive detection of sodium cromoglycate with glutathione-capped CdTe quantum dots as a novel fluorescence probe.

    Science.gov (United States)

    Hao, Chenxia; Liu, Shaopu; Li, Dan; Yang, Jidong; He, Youqiu

    2015-11-01

    A sensitive and simple analytical strategy for the detection of sodium cromoglycate (SCG) has been established based on a readily detectable fluorescence quenching effect of SCG for glutathione-capped (GSH-capped) CdTe quantum dots (QDs). The fluorescence of GSH-capped CdTe QDs could be efficiently quenched by SCG through electron transfer from GSH-capped CdTe QDs to SCG. Under optimum conditions, the response was linearly proportional to the concentration of SCG between 0.6419 and 100 µg/mL, with a correlation coefficient (R) of 0.9964; the detection limit (3δ/K) was 0.1926 µg/mL. The optimum conditions and the influence of coexisting foreign substances on the reaction were also investigated. The very effective and simple method reported here has been successfully applied to the determination of SCG in synthetic and real samples. It is believed that the established approach could have good prospects for application in the fields of clinical diseases diagnosis and treatment.

  13. The abnormal in vitro response to aspirin of platelets from aspirin-sensitive asthmatics is inhibited after inhalation of nedocromil sodium but not of sodium cromoglycate.

    Science.gov (United States)

    Marquette, C H; Joseph, M; Tonnel, A B; Vorng, H; Lassalle, P; Tsicopoulos, A; Capron, A

    1990-01-01

    1. Blood platelets from patients with aspirin-sensitive asthma (ASA) generated cytotoxic mediators in the presence of aspirin. This abnormal in vitro response to aspirin was abolished within 1 h after nedocromil sodium inhalation but not after sodium cromoglycate inhalation. 2. Platelets recovered this reactivity to aspirin by 12 hours after nedocromil sodium treatment of ASA-patients. 3. The in vitro reactivity to aspirin of ASA platelets isolated before inhalation was inhibited in the presence of serum isolated 15 and 60 min after nedocromil sodium inhalation. PMID:2161678

  14. [Role of sodium cromoglycate in brain protection and its effects on tumor necrosis factor-alpha and interleukin-1beta after global cerebral ischemia-reperfusion injury in gerbils].

    Science.gov (United States)

    Shen, Ning; Gan, Xiao-Liang; Pang, Hu-Yu; He, Zi-Qing

    2009-03-01

    To investigate the role of sodium cromoglycate in brain protection and its effects on brain tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) expressions after global cerebral ischemia-reperfusion (IR) injury in gerbils. Twenty-four healthy male gerbils were randomized into 3 equal groups, namely the sham-operated group with isolation of the bilateral carotid arteries but without occlusion, IR injury model group with bilateral carotid artery occlusion, and sodium cromoglycate treatment group with bilateral carotid artery occlusion and sodium cromoglycate administration at 25 mg/kg via the lingual vein as soon as the reperfusion start with another dose 1 h later. The animals were then sacrificed and the thalamus were removed, fixed in 10% formaldehyde and sliced for observation under light microscope with HE staining. The rest brain tissues were prepared into homogenate to determine the content of TNF-alpha and IL-1beta. The right hemispheres of the gerbils were measured for wet weight and dry weight to calculate the water content in the brain. The water content in the brain of the gerbils in the model group was the highest among the groups, and that in sodium cromoglycate treatment group was significantly less than that of the model group (PIR injury possibly by lowering the TNF-alpha and IL-1beta levels in the brain tissues.

  15. Effect of creatine phosphate disodium on postoperative cognitive function under combined intravenous and volatile anesthesia in geriatric patients

    Directory of Open Access Journals (Sweden)

    Bao-sen JIA

    2016-08-01

    Full Text Available Objective  To explore the relationship of perioperative INVOS cerebral oxygen saturation (rSO2 and postoperative cognition function alteration of geriatric patients under combined intravenous and volatile anesthesia with creatine phosphate disodium to provide guidance for clinical anesthesia. Methods  Sixty ASA Ⅰ-Ⅱpatients aged >60 years scheduled for selective abdominal surgeries or surgeries on lower limb were enrolled in the study. The patients were randomly divided into 3 groups of 20 patients: creatine phosphate disodium group 1 (CPD1, creatine phosphate disodium group 2 (CPD2, control group (C. All the patients were not premedicated with atropine 0.5mg until entering the operation room. Anesthesia was induced with intravenous infusion of propofol, fentanyl and cisatracurium slowly, and maintained by inhalational anesthetics sevoflurane 1 MAC plus intravenous infusion of propofol (6-8mg•kg-1•min-1 and remifentanyl (0.2-0.4μg•kg-1•min-1, and intravenous bolus cisatracurium (0.07-0.10mg•kg-1. After tracheal intubation, all the patients were mechanically ventilated with PETCO2 in the normal range. rSO2 was continuously monitored and recorded during the operation. The Mini-Mental State Examination (MMSE, Trail-making Test and Grooved Pegboard Test were used to access cognitive function 24h before surgery and 4, 8, 12, 24h after surgery. Results  (1 There were no significant differences in general status between the three groups (P>0.05. (2 The scores of MMSE, Trail-making Test and Grooved Pegboard Test were not different 24h before the operation between the three groups (P>0.05. (3 The scores of cognitive tests were higher in group CPD2 and group CPD1 than in group C (P0.05. Conclusion  CPD can reduce the occurrence of postoperative cognitive dysfunction in geriatric patients under combined intravenous and inhalational anesthesia. DOI: 10.11855/j.issn.0577-7402.2016.07.11

  16. The effect of inhaled sodium cromoglycate on cellular infiltration into the bronchial mucosa and the expression of adhesion molecules in asthmatics.

    Science.gov (United States)

    Hoshino, M; Nakamura, Y

    1997-04-01

    There is no direct evidence of the anti-inflammatory effect of inhaled sodium cromoglycate (SCG). To investigate whether inhaled SCG has any effect on cellular infiltration into the bronchial mucosa and the expression of adhesion molecules in patients with asthma, biopsies of the bronchial mucosa were taken from nine patients with atopic bronchial asthma before and after treatment with inhaled SCG (8 mg x day(-1)) from a metered-dose inhaler (MDI). Eosinophils were stained with anti-EG2, neutrophils with anti-NP57, mast cells with anti-AA1, T-lymphocytes with anti-CD4, CD8 and CD3, and macrophages with anti-CD68. Intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), endothelial leucocyte adhesion molecule-1 (ELAM-1) and P-selectin were stained at the same time as adhesion molecules expressed in vascular endothelium. The intensity of ICAM-1 expression in the bronchial epithelium was also evaluated. The numbers of eosinophils, mast cells, T-lymphocytes and macrophages were significantly reduced as a result of SCG administration, and the expression of ICAM-1, VCAM-1 and ELAM-1 was also significantly inhibited. A significant correlation was found between ICAM-1 expression and T-lymphocytes and between VCAM-1 expression and eosinophils. It was concluded that sodium cromoglycate does have an effect on the infiltration of the bronchial mucosa by inflammatory cells and also on the expression of adhesion molecules.

  17. Nasal sodium cromoglycate (Lomusol) modulates the early phase reaction of mild to moderate persistent allergic rhinitis in patients mono-sensitized to house dust mite: a preliminary study.

    Science.gov (United States)

    Lejeune, Margaux; Lefebvre, Philipe P; Delvenne, Philippe; El-Shazly, Amr E

    2015-05-01

    We evaluated the clinical improvement of patients with mild to moderate persistent allergic rhinitis (AR) due to mono-sensitization to house dust mite (HDM) allergen, by sodium cromoglycate nasal spray (Lomusol 4%). Lomusol was used as a single agent treatment, and its anti-inflammatory effects, in the early phase reaction were evaluated. Herein we showed that Lomusol significantly improved the subjective nasal symptom scores especially nasal obstruction. This was associated with significant and specific reduction in neutrophils influx in nasal cytology but had no effect on other cell types. This selective anti-inflammatory effect on nasal cytology was associated with significant reduction in the levels of platelet activating factor (PAF) and histamine in nasal secretions but had no effect on PGD2, LTC4 or CysLt levels. Lomusol was also able to induce significant reduction in eosinophil cationic protein (ECP) levels in nasal secretions without altering the percentage of eosinophil influx in nasal cytology. Taken collectively, we showed the first evidence that nasal sodium cromoglycate possesses a selective inhibition on neutrophil recruitment into nasal cytology in the early phase reaction of AR patients mono-sensitized to HDM. This may be attributed to the ability of Lomusol to significantly reduce the amount of PAF recovered in nasal secretion. These results were associated with significant improvement in subjective symptom scores especially nasal obstruction that may in addition, be due to the ability of Lomusol to down-regulate eosinophil degranulation activity as well.

  18. Sodium cromoglycate on plasma protein exudation to topically-applied substance P in the tracheal airways of rats or guinea-pigs in vivo.

    Science.gov (United States)

    O'Donnell, S R; Coulson, F R; Bigg, C S

    2000-01-01

    Sodium cromoglycate (SCG) was examined against substance P(SP)-induced plasma protein exudation in the trachea of anaesthetized rats and guinea-pigs in vivo to determine whether SCG is a tachykinin receptor antagonist in the airways. A segment of trachea was prepared in situ for continuous perfusion with normal saline. Plasma-derived protein in the perfusion fluid (airway lumen) was increased after topical application of SP (1 microM, 5 min contact). In rats, the SP response was not attenuated by iv SCG but was inhibited (29%) by topical SCG under certain experimental conditions and using a high concentration of SCG (500 microM, 5 min contact, 30 min before SP and with SP). The NK(1)receptor antagonist, RP 67 580 (67 microM) abolished the SP response in rats. Sodium cromoglycate did not inhibit the SP response in guinea-pigs (same protocol as in rats). Thus, SCG attenuates plasma protein exudation (and presumably microvascular leak) induced by SP in rat tracheal airways but, if SCG is a tachykinin receptor (NK(1)) antagonist, it not only lacks potency but is species-selective, i.e. more effective in rats than in guinea-pigs.

  19. Cromoglycate and nedocromil enhanced the reactive oxygen species-dependent suppressions with, but not without, dexamethasone in ischaemic and histamine paw oedema of mice

    Science.gov (United States)

    Oyanagui, Y.

    1997-01-01

    Anti-inflammatory actions of two anti-allergic drugs, alone or with dexamethasone (Dex) were examined in two models, because inflammation is claimed to be important for allergic events, especially for asthma. Cromoglycate and nedocromil were tested in ischaemic- and histamineinduced paw oedema models of mice. These antiallergic drugs (1–100 mg/kg, i.p.) failed to suppress these oedemata, but enhanced the suppressions by a low dose of dexamethasone (0.1 mg/kg, s.c.) at 3–8 h after Dex injection. The mode of effects by anti-allergic drugs resembled that of a natural antioxidant (α-tocopherol, β-carotene etc.), and was different from that of an immunosuppressant like FK506. The enhancing potencies of the two anti-allergic drugs were similar at 6 h after Dex in both oedemata, and were diminished by superoxide dismutase (SOD) or catalase (i.p.). Cycloheximide completely abolished suppressions. Nedocromil, but not cromoglycate, inhibits inflammatory events. Therefore, there are common unknown actions by which the two anti-allergics enhance suppression by Dex. A possible mechanism of this action was supposed to enhance the superoxide and/or hydrogen peroxide-dependent glucocorticoid receptor (GR) signalling in the target cells. PMID:18472872

  20. Cromoglycate and nedocromil enhanced the reactive oxygen species-dependent suppressions with, but not without, dexamethasone in ischaemic and histamine paw oedema of mice

    Directory of Open Access Journals (Sweden)

    Y. Oyanagui

    1997-01-01

    Full Text Available Anti-inflammatory actions of two anti-allergic drugs, alone or with dexamethasone (Dex were examined in two models, because inflammation is claimed to be important for allergic events, especially for asthma. Cromoglycate and nedocromil were tested in ischaemic- and histamineinduced paw oedema models of mice. These antiallergic drugs (1–100 mg/kg, i.p. failed to suppress these oedemata, but enhanced the suppressions by a low dose of dexamethasone (0.1 mg/kg, s.c. at 3–8 h after Dex injection. The mode of effects by anti-allergic drugs resembled that of a natural antioxidant (α-tocopherol, β-carotene etc., and was different from that of an immunosuppressant like FK506. The enhancing potencies of the two anti-allergic drugs were similar at 6 h after Dex in both oedemata, and were diminished by superoxide dismutase (SOD or catalase (i.p.. Cycloheximide completely abolished suppressions. Nedocromil, but not cromoglycate, inhibits inflammatory events. Therefore, there are common unknown actions by which the two anti-allergics enhance suppression by Dex. A possible mechanism of this action was supposed to enhance the superoxide and/or hydrogen peroxide-dependent glucocorticoid receptor (GR signalling in the target cells.

  1. The combination of nebulized sodium cromoglycate and salbutamol in the treatment of moderate-to-severe asthma in children.

    Science.gov (United States)

    Furusho, Kenshi; Nishikawa, Kiyoshi; Sasaki, Sei; Akasaka, Toru; Arita, Masahiko; Edwards, Alan

    2002-06-01

    The aim of this multi-centre prospective study was to evaluate the efficacy, tolerability, and safety of the combination of sodium cromoglycate (SCG) and salbutamol (administered as a nebulized solution), compared to SCG alone and salbutamol alone, in the management of severe, intractable asthma in childhood. The study was an open, randomized, cross-over trial of 12 weeks' duration in children with moderate-to-severe intractable asthma. All treatments were administered twice daily by powered nebulizer. The primary outcome measure was the change in asthma severity, as measured by the mean asthma score during the last 2 weeks of a baseline period and the last 2 weeks of each treatment. Secondary outcome measure was the patient's opinion of the effectiveness of treatment. The change in asthma scores from baseline values were significantly greater with the combination treatment compared to each component administered separately. The mean difference in asthma score between the combination and salbutamol was: -7.5; 95% CI, -11.70 to -3.29 (p < 0.0001). The mean difference between the combination and SCG was: -8.53; 95% CI, -14.03 to -3.25 (p < 0.0001). Patients were also significantly in favor of combination treatment (p < 0.001 vs. salbutamol; p < 0.01 vs. SCG). Two patients reported adverse effects. We concluded that regular twice-daily inhalation of a combination of SCG and salbutamol gave better control of symptoms than previous treatments in patients with severe, intractable asthma. Few adverse effects with this therapy suggest that it is extremely useful, safe, and effective.

  2. Disodium edetate as a promising interfacial material for inverted organic solar cells and the device performance optimization.

    Science.gov (United States)

    Li, Xiaodong; Zhang, Wenjun; Wang, Xueyan; Gao, Feng; Fang, Junfeng

    2014-12-10

    Disodium edetate (EDTA-Na), a popular hexadentate ligand in analytical chemistry, was successfully introduced in organic solar cells (OSCs) as cathode interfacial layer. The inverted OSCs with EDTA-Na showed superior performance both in power conversion efficiency and devices stability compared with conventional devices. Interestingly, we found that the performance of devices with EDTA-Na could be optimized through external bias treatment. After optimization, the efficiency of inverted OSCs with device structure of ITO/EDTA-Na/polymer thieno[3,4-b]thiophene/benzodithiophene (PTB7):PC71BM/MoO3/Al was significantly increased to 8.33% from an initial value of 6.75%. This work introduces a new class of interlayer materials, small molecule electrolytes, for organic solar cells.

  3. Study of apparent molal volume and viscosity of mutual citric acid and disodium hydrogen orthophosphate aqueous systems

    Indian Academy of Sciences (India)

    Man Singh

    2006-05-01

    Fundamental properties, density () and viscosity (), of citric acid (CA) and disodium hydrogen orthophosphate (DSP) at various strengths were obtained at different temperatures. The and values were used to determine apparent molal volumes and viscosity of systems. The , and values were regressed against molality for ρ0, 0 and $V^{0}_{\\phi}$f, the limiting constants at infinite dilution ( → 0) forionic and molecular interactions. The ρ0 and $V^{0}_{\\phi}$f of aq. acids are higher than those of aq. DSP and the viscosity of DSP is higher than that of aq. CA. Examination of ρ0 and $V^{0}_{\\phi}$ functions indicates that mutual compositions of CA and DSP counterbalance concentration and temperature effects on pH in bioprocesses.

  4. Disodium hydrogen citrate sesquihydrate, Na2HC6H5O7(H2O1.5

    Directory of Open Access Journals (Sweden)

    Alagappa Rammohan

    2016-07-01

    Full Text Available The crystal structure of disodium hydrogen citrate sesquihydrate, 2Na2+·C6H6O72−·1.5H2O, has been solved and refined using laboratory X-ray single-crystal diffraction data, and optimized using density functional techniques. The asymmetric unit contains two independent hydrogen citrate anions, four sodium cations and three water molecules. The coordination polyhedra of the cations (three with a coordination number of six, one with seven share edges to form isolated 8-rings. The un-ionized terminal carboxylic acid groups form very strong hydrogen bonds to non-coordinating O atoms, with O...O distances of 2.46 Å.

  5. Determination of adenosine disodium triphosphate (ATP) using norfloxacin-Tb{sup 3+} as a fluorescence probe by spectrofluorimetry

    Energy Technology Data Exchange (ETDEWEB)

    Miao Yanhong [Department of Chemistry, Shandong Normal University, Jinan 250014 (China); College of Science and Technology, Shandong Agriculture University, Taian 271000 (China); Liu Jinkai [Department of Chemistry, Shandong Normal University, Jinan 250014 (China); Hou Faju [Department of Chemistry, Shandong Normal University, Jinan 250014 (China); Jiang Chongqiu [Department of Chemistry, Shandong Normal University, Jinan 250014 (China)]. E-mail: jiangchongqiu@sdnu.edu.cn

    2006-01-15

    A new spectrofluorimetric method was developed for determination of trace amount of adenosine disodium triphosphate (ATP). Using norfloxacin (NFLX)-terbium (Tb{sup 3+}) as a fluorescent probe, in the buffer solution of pH=7.40, ATP can remarkably enhance the fluorescence intensity of the NFLX-Tb{sup 3+} complex at {lambda}=545nm and the enhanced fluorescence intensity of Tb{sup 3+} ion is in proportion to the concentration of ATP. Optimum conditions for the determination of ATP were also investigated. The dynamic range for the determination of ATP is 1.00x10{sup -6}-1.60x10{sup -5}mol/L with detection limit of 4.13x10{sup -8}mol/L. This method is simple, practical and relatively free interference from coexisting substances and can be successfully applied to determination of ATP in samples.

  6. Synthesis of Cefotetan disodium%头孢替坦二钠的合成工艺研究

    Institute of Scientific and Technical Information of China (English)

    刘秀霞; 孙元朋; 高景梅; 顾孝红

    2013-01-01

    目的:合成头孢替坦二钠.方法:以7-ACA为起始原料,经缩合、取代、加成、酰化、成盐、环合得粗品,在局部100级进行精制、冷冻干燥,得无菌头孢替坦二钠.结果:目标化合物经元素分析、质谱、核磁共振氢谱、核磁共振碳谱、红外光谱、紫外光谱等确证其化学结构,总收率为26.1%.结论:该合成路线无需特殊的原料及化学试剂,反应条件温和,操作简便,收率高,适合工业化生产.%Objective:To synthesize Cefotetan disodium.Method:The sterile Cefotetan disodium was synthesized from 7-ACA as a starting material via steps including condensation,substitution,addition,acylation,salification,cyclization to obtain crude product and purification,freeze dehydration in location of 100 grade in advance.Result:The structure of the target compound was confirmed by element,MS,1H-NMR,13C-NMR,IR and UV analysis.The yield was 26.1%.Conclusion:This procedure with the advantages such as without special ingredients or reagents,milder reaction conditions and simple operations is worthy of the further pilot manufacture.

  7. A novel model of IgE-mediated passive pulmonary anaphylaxis in rats.

    Science.gov (United States)

    Wex, Eva; Thaler, Eva; Blum, Sylvia; Lamb, David

    2014-01-01

    Mast cells are central effector cells in allergic asthma and are augmented in the airways of asthma patients. Attenuating mast cell degranulation and with it the early asthmatic response is an important intervention point to inhibit bronchoconstriction, plasma exudation and tissue oedema formation. To validate the efficacy of novel pharmacological interventions, appropriate and practicable in vivo models reflecting mast cell-dependent mechanisms in the lung, are missing. Thus, we developed a novel model of passive pulmonary anaphylaxis in rats. Rats were passively sensitized by concurrent intratracheal and intradermal (ear) application of an anti-DNP IgE antibody. Intravenous application of the antigen, DNP-BSA in combination with Evans blue dye, led to mast cell degranulation in both tissues. Quantification of mast cell degranulation in the lung was determined by (1) mediator release into bronchoalveolar lavage, (2) extravasation of Evans blue dye into tracheal and bronchial lung tissue and (3) invasive measurement of antigen-induced bronchoconstriction. Quantification of mast cell degranulation in the ear was determined by extravasation of Evans blue dye into ear tissue. We pharmacologically validated our model using the SYK inhibitor Fostamatinib, the H1-receptor antagonist Desloratadine, the mast cell stabilizer disodium cromoglycate (DSCG) and the β2-adrenergic receptor agonist Formoterol. Fostamatinib was equally efficacious in lung and ear. Desloratadine effectively inhibited bronchoconstriction and ear vascular leakage, but was less effective against pulmonary vascular leakage, perhaps reflecting the differing roles for histamine receptor sub-types. DSCG attenuated both vascular leakage in the lung and bronchoconstriction, but with a very short duration of action. As an inhaled approach, Formoterol was more effective in the lung than in the ear. This model of passive pulmonary anaphylaxis provides a tissue relevant readout of early mast cell activity and

  8. A novel model of IgE-mediated passive pulmonary anaphylaxis in rats.

    Directory of Open Access Journals (Sweden)

    Eva Wex

    Full Text Available Mast cells are central effector cells in allergic asthma and are augmented in the airways of asthma patients. Attenuating mast cell degranulation and with it the early asthmatic response is an important intervention point to inhibit bronchoconstriction, plasma exudation and tissue oedema formation. To validate the efficacy of novel pharmacological interventions, appropriate and practicable in vivo models reflecting mast cell-dependent mechanisms in the lung, are missing. Thus, we developed a novel model of passive pulmonary anaphylaxis in rats. Rats were passively sensitized by concurrent intratracheal and intradermal (ear application of an anti-DNP IgE antibody. Intravenous application of the antigen, DNP-BSA in combination with Evans blue dye, led to mast cell degranulation in both tissues. Quantification of mast cell degranulation in the lung was determined by (1 mediator release into bronchoalveolar lavage, (2 extravasation of Evans blue dye into tracheal and bronchial lung tissue and (3 invasive measurement of antigen-induced bronchoconstriction. Quantification of mast cell degranulation in the ear was determined by extravasation of Evans blue dye into ear tissue. We pharmacologically validated our model using the SYK inhibitor Fostamatinib, the H1-receptor antagonist Desloratadine, the mast cell stabilizer disodium cromoglycate (DSCG and the β2-adrenergic receptor agonist Formoterol. Fostamatinib was equally efficacious in lung and ear. Desloratadine effectively inhibited bronchoconstriction and ear vascular leakage, but was less effective against pulmonary vascular leakage, perhaps reflecting the differing roles for histamine receptor sub-types. DSCG attenuated both vascular leakage in the lung and bronchoconstriction, but with a very short duration of action. As an inhaled approach, Formoterol was more effective in the lung than in the ear. This model of passive pulmonary anaphylaxis provides a tissue relevant readout of early mast cell

  9. Graphene oxide and creatine phosphate disodium dual template-directed synthesis of GO/hydroxyapatite and its application in drug delivery.

    Science.gov (United States)

    Yao, Chengli; Zhu, Jinmiao; Xie, Anjian; Shen, Yuhua; Li, Hongying; Zheng, Bin; Wei, Yanxin

    2017-04-01

    In this study, graphene oxide and creatine phosphate disodium acted as dual template and was employed to synthesize graphene oxide (GO)/hydroxyapatite (HA) hybrids as drug carriers. In the rapid preparation of GO/HA hybrids, creatine phosphate disodium salt (CPDS) severed as a phosphorus source and graphene oxide acted as a template in aqueous solution. The effects of the reaction temperature, time and pH value of the aqueous solution on the morphology of the product were investigated. The result showed that the hydrolysis of CPDS under hydrothermal condition played an important role in the formation of hierarchical hollow GO/HA hybrids. The GO nanosheets provided reactive sites for the binding of HA nanoparticles and absorbing ibuprofen (IBU) molecules. The GO/HA hybrids had ideal sustained drug-release behavior. It indicated that the prepared GO/HA hybrids may be promising materials for applications in biomedical area. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. Toothbrush disinfection – a myth or reality? – A comparative evaluation of 4% disodium EDTA, 10% sodium perborate in the disinfection of toothbrushes: clinicomicrobiological study

    Directory of Open Access Journals (Sweden)

    Nilofer Sultan Sheikh, Nilima Rajhans, Nilkanth Mhaske, Nikesh Moolya, Sudip HM

    2014-11-01

    Full Text Available The aim of this randomized clinical trial was to evaluate the bacterial survival rate on toothbrushes and efficacy of their decontamination by4% disodium ethyl diamine acetic acid [EDTA], 10% sodium perborate and compared with control. Methods: Thirty subjects with chronic periodontitis enrolled in this randomized controlled clinical trial were provided with autoclaved toothbrushes which were free from microorganisms. Brushing instructions were given to each participant. Toothbrushes were collected from all study participants after 1 week and were placed with head down position in an autoclaved test tube containing sterile peptone water. Toothbrushes collected were sent for aerobic culture in laboratory for growth of micro-organisms. Incubation was done for 24 hours at 370C.The toothbrushes were then divided into three groups and immersed in disinfectantslike4% disodium EDTA, 10% sodium perborate and their efficacy was evaluated by aerobic culture analysis. Chi – Square test was used for statistical analysis of the data. Results: Escherichia coli, Pseudomonas Aeroginosa, Streptococci and Klebsiella species were recovered from the samples. The results obtained showed that 4% Disodium EDTA showed 100% efficacy, whereas 10% Sodium perborate showed 40% effectiveness in decontaminating the toothbrushes. Distilled water as a control showed least effectiveness in cleaning toothbrushes. Conclusion: After single brushing toothbrushes get contaminated by a wide array of bacteria’s which a major cause of concern is. As contaminated toothbrush can reintroduce microorganisms into the oral cavity, it is therefore recommended for individuals to use solutions like 4% Disodium EDTA, which proved to be an effective disinfecting agent for decontaminating toothbrushes.

  11. Effect of the Food Additives Sodium Citrate and Disodium Phosphate on Shiga Toxin-Producing Escherichia coli and Production of stx-Phages and Shiga toxin.

    Science.gov (United States)

    Lenzi, Lucas J; Lucchesi, Paula M A; Medico, Lucía; Burgán, Julia; Krüger, Alejandra

    2016-01-01

    Induction and propagation of bacteriophages along the food production chain can represent a significant risk when bacteriophages carry genes for potent toxins. The aim of this study was to evaluate the effect of different compounds used in the food industry on the growth of Shiga toxin-producing Escherichia coli (STEC) and the production of stx-phage particles and Shiga toxin. We tested the in vitro effect of lactic acid, acetic acid, citric acid, disodium phosphate, and sodium citrate on STEC growth. A bacteriostatic effect was observed in most of treated cultures. The exceptions were those treated with sodium citrate and disodium phosphate in which similar growth curves to the untreated control were observed, but with reduced OD600 values. Evaluation of phage production by plaque-based assays showed that cultures treated with sodium citrate and disodium phosphate released phages in similar o lower levels than untreated cultures. However, semi-quantification of Stx revealed higher levels of extracellular Stx in STEC cultures treated with 2.5% sodium citrate than in untreated cultures. Our results reinforce the importance to evaluate if additives and other treatments used to decrease bacterial contamination in food induce stx-phage and Stx production.

  12. Effect of the Food Additives Sodium Citrate and Disodium Phosphate on Shiga Toxin-Producing Escherichia coli and Production of stx-Phages and Shiga toxin

    Science.gov (United States)

    Lenzi, Lucas J.; Lucchesi, Paula M. A.; Medico, Lucía; Burgán, Julia; Krüger, Alejandra

    2016-01-01

    Induction and propagation of bacteriophages along the food production chain can represent a significant risk when bacteriophages carry genes for potent toxins. The aim of this study was to evaluate the effect of different compounds used in the food industry on the growth of Shiga toxin-producing Escherichia coli (STEC) and the production of stx-phage particles and Shiga toxin. We tested the in vitro effect of lactic acid, acetic acid, citric acid, disodium phosphate, and sodium citrate on STEC growth. A bacteriostatic effect was observed in most of treated cultures. The exceptions were those treated with sodium citrate and disodium phosphate in which similar growth curves to the untreated control were observed, but with reduced OD600 values. Evaluation of phage production by plaque-based assays showed that cultures treated with sodium citrate and disodium phosphate released phages in similar o lower levels than untreated cultures. However, semi-quantification of Stx revealed higher levels of extracellular Stx in STEC cultures treated with 2.5% sodium citrate than in untreated cultures. Our results reinforce the importance to evaluate if additives and other treatments used to decrease bacterial contamination in food induce stx-phage and Stx production. PMID:27446032

  13. Topical levocabastine—a review of therapeutic efficacy compared with topical sodium cromoglycate and oral terfenadine on days with high pollen counts

    Directory of Open Access Journals (Sweden)

    Marianela de Azevedo

    1995-01-01

    Full Text Available Levocabastine is a new H1-receptor antagonist specifically developed for the topical treatment of seasonal allergic rhinoconjunctivitis. Clinical experience to date clearly demonstrates that levocabastine eye drops and nasal spray are effective and well tolerated for the treatment of this allergic disorder. Analysis of data from a number of comparative trials reveals that topical levocabastine is at least as effective as sodium cromoglycate and the oral antihistamine terfenadine, even on days with high pollen counts (≥ 50 pollen particles/m3 when symptoms are severe. Coupled with a rapid onset of action and twice daily dosing, these findings make topical levocabastine an attractive alternative to other therapeutic approaches as a first-line therapy for the treatment, of this common condition.

  14. Plasma concentrations of sodium cromoglycate given by nebulisation and metered dose inhalers in patients with exercise-induced asthma: relationship to protective effect.

    Science.gov (United States)

    Patel, K R; Tullett, W M; Neale, M G; Wall, R T; Tan, K M

    1986-01-01

    Plasma sodium cromoglycate (SCG) concentrations were measured in 11 patients at regular intervals before and after exercise in a double-blind study to assess the protective effect in exercise-induced asthma (EIA) of 2, 10 and 20 mg SCG aerosol and placebo, and (on an open basis) nebulised SCG (10 g l-1). There was a dose related increase in plasma concentration and AUC (0-1 h) with the aerosol formulations; values with nebulised SCG were significantly higher than with any aerosol dose. Protection from EIA increased to a maximum of 66% at plasma concentrations of 4 ng ml-1 and above. Thus measurement of plasma concentration can allow a comparison to be made between the protective effects of SCG following different methods of inhalation. It is important to note, however, that plasma concentration per se is almost certainly not related directly to protective effect. PMID:3082347

  15. Mechanism of oxidation of 3-hydroxy-2,7-naphthalenedisulfonic acid disodium salt with oxygen in subcritical water.

    Science.gov (United States)

    Imbierowicz, Mirosław

    2017-06-01

    The article presents the results of studies on the oxidation mechanism of 3-hydroxy-2,7-naphthalenedisulfonic acid disodium salt (R-salt) with oxygen in subcritical water. To this aim, a series of experiments were carried out which showed that at a temperature of 413 K and pH > 9 the oxidation reaction of a substrate with oxygen was relatively quick and after approximately 40 min the R-salt oxidation yield exceeded 95%. In an acidic medium (pH oxidation is small. In order to identify the mechanism of R-salt oxidation, experiments were carried out at 413-569 K in solutions with pH = 10.0 and at partial oxygen pressure pO2 = 1.73 MPa. As a result of these experiments, a stable oxidation product was isolated from the reaction mixture and subjected to spectroscopic analysis. The analysis of (H)NMR of this product proved that a stable intermediate product of R-salt oxidation was 4-sulfophthalic acid sodium salt. The results of the experiments have shown that destructive oxidation of R-salt can easily be obtained at a temperature of 413 K, but satisfactory reduction of TOC in wastewater containing this substrate requires the use of very high temperature: at 569 K only 60% reduction of TOC was achieved. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Exploring the sodium storage mechanism in disodium terephthalate as anode for organic battery using density-functional theory calculations

    Science.gov (United States)

    Sk, Mahasin Alam; Manzhos, Sergei

    2016-08-01

    We present an ab initio study of sodium storage mechanism in disodium terephthalate (Na2TP) which is a very promising anode material for organic sodium (Na)-ion batteries with reported experimental capacities of ∼255 mAh g-1, previously attributed to Na attachment to the two carboxylate groups (coordinating to oxygen atoms). We show here that the inserted Na atoms prefer to bind at carboxylate sites at low Na concentrations and are dominant for insertion of up to one Na atom per molecule; for higher Na concentrations, the hexagonal sites (on the aromatic ring) become dominant. We confirm that the Na2TP crystal can store a maximum of two Na atoms per molecule, as observed in experiments. Our current results are intriguing as we reveal that the Na binding at carboxylate sites contributes to the initial part of Na2TP sodiation curve and the Na binding at hexagonal sites contributes to the second part of the curve. The inserted Na atoms donate electrons to empty states in the conduction band. Moreover, we show that the Na diffusion barriers in clean Na2TP can be as low as 0.23 eV. We also show that there is significant difference in the mechanism of Na interaction between individual molecules and the crystal.

  17. Hypophosphatemic rickets developed after treatment with etidronate disodium in a patient with generalized arterial calcification in infancy

    Directory of Open Access Journals (Sweden)

    Kentaro Miyai

    2015-12-01

    Full Text Available Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1 was originally reported as a responsible gene for generalized arterial calcification in infancy (GACI. Though the prognosis of GACI patients is poor because of myocardial infarction and heart failure in relation to medial calcification of the coronary arteries, some patients rescued by bisphosphonate treatment have been reported. Recently, ENPP1 is also reported as responsible for autosomal recessive hypophosphatemic rickets type 2. We show here a boy with homozygous ENPP1 mutations diagnosed as having GACI in early infancy. After the diagnosis, he was treated with etidronate disodium (EHDP in combination with antihypertensive drugs. The calcification of major arteries was diminished and disappeared by the age of eight months. He also showed mild hypophosphatemia (2.6–3.7 mg/dl from the age of one year. After the treatment with EHDP for five years, he showed genu valgum with hypophosphatemia (2.6 mg/dl. He was diagnosed as having hypophosphatemic rickets at the age of seven years. The findings that hyper-mineralization of the arteries and hypo-mineralization of the bone observed in the same patient are noteworthy. ENPP1 could be regarded as a controller of the calcification of the whole body at least in part.

  18. Inhibitory effects of a novel ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate on melanogenesis.

    Science.gov (United States)

    Matsuda, Sanae; Shibayama, Hiroharu; Hisama, Masayoshi; Ohtsuki, Mamitaro; Iwaki, Masahiro

    2008-03-01

    We investigated the inhibitory effects of a novel amphiphilic ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate (VCP-IS-2Na), synthesized from a hydrophilic ascorbic derivative, sodium-2-O-L-ascorbyl phosphate (VCP-Na), on melanogenesis in cultured human melanoma cells, normal human melanocytes, and three-dimensional cultured human skin models. Melanin synthesis in melanoma cells treated with VCP-IS-2Na at 300 muM and melanocytes treated with VCP-IS-2Na at 100 muM decreased to 23% and 52% of that in non-treated cells, respectively, and the cell viability was not affected. VCP-IS-2Na also significantly suppressed the cellular tyrosinase activity of melanoma cells and melanocytes. Melanin synthesis in human skin models was evaluated by macro- and microscopic observations of its pigmentation and quantitative measurements of melanin. Treatment of the human skin models with 1.0% VCP-IS-2Na did not inhibit cell viability, while melanin synthesis was decreased to 21% of that in the control. In contrast, L-ascorbic acid (VC) and VCP-Na did not seem to inhibit melanin synthesis and cellular tyrosinase activity. These results indicate that VCP-IS-2Na may be an effective whitening agent for the skin, and we expect the application of VCP-IS-2Na in the cosmetic industry.

  19. The value of gadoxetate disodium-enhanced MR imaging for predicting posthepatectomy liver failure after major hepatic resection: A preliminary study

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Seung Hyun, E-mail: shcho2405@gmail.com [Department of Radiology, Daegu Fatima Hospital, 576-31 Sinam-dong, Dong-gu, Daegu 701-600 (Korea, Republic of); Kang, Ung Rae, E-mail: tadtail@hanmail.net [Department of Radiology, Catholic University of Daegu, School of Medicine, 3056-6 Daemyung-4-dong, Nam-gu, Daegu 705-718 (Korea, Republic of); Kim, Joo Dong, E-mail: milledr@naver.com [Department of Surgery, Catholic University of Daegu, School of Medicine, 3056-6 Daemyung-4-dong, Nam-gu, Daegu 705-718 (Korea, Republic of); Han, Young Seok, E-mail: gshyskhk@hanmail.net [Department of Surgery, Catholic University of Daegu, School of Medicine, 3056-6 Daemyung-4-dong, Nam-gu, Daegu 705-718 (Korea, Republic of); Choi, Dong Lak, E-mail: dnchoi@cu.ac.kr [Department of Surgery, Catholic University of Daegu, School of Medicine, 3056-6 Daemyung-4-dong, Nam-gu, Daegu 705-718 (Korea, Republic of)

    2011-11-15

    Purpose: To investigate whether preoperative gadoxetate-disodium-enhanced MR imaging predicts posthepatectomy liver failure (PHLF) in patients who underwent major hepatic resection. Materials and methods: Twenty nine patients who underwent preoperative gadoxetate-disodium-enhanced MR imaging and following major hepatic resection were enrolled. Hepatic parenchymal signal intensity (SI) on pre-contrast T1-weighted imaging and 20 min hepatocyte phase was measured at each of the four liver segments by two observers using region of interest measurements. The mean value was calculated and used at each phase. The relative contrast enhancement index (RCEI) was calculated: (20 min hepatocyte phase SI - pre-contrast SI)/pre-contrast SI. PHLF was determined by the International Study Group of Liver Surgery 2011 guidelines. Correlation analysis was performed between preoperative liver function test and RCEI. Diagnostic accuracy of RCEI for predicting PHLF was calculated with receiver operating characteristic curve analysis. The reproducibility of the RCEI measurement was evaluated. Results: There was a significant correlation between preoperative albumin (r = 0.496, P = 0.006), T-bilirubin (r = -0.383, P = 0.041), and RCEI. Seven patients (24%) experienced PHLF, and one of these patients (3%) died. The diagnostic accuracy of RCEI was 0.838 (sensitivity 85.7%, specificity 77.3%, cut-off value: 0.7508, 95% confidence interval: 0.654, 0.947). The 95% limits of agreement and ICC between repeated RCEI measurements were 18.4% of the mean and 0.94, respectively, and between RCEI measurements by the two observers were 21.7% and 0.929, respectively. Conclusion: Our results show that preoperative gadoxetate-disodium-enhanced MR imaging can predict PHLF in patients who underwent major hepatic resection.

  20. Enhanced Molecular Recognition between Nucleobases and Guanine-5'-monophosphate-disodium (GMP) by Surfactant Aggregates in Aqueous Solution.

    Science.gov (United States)

    Liu, Zhang; Wang, Dong; Cao, Meiwen; Han, Yuchun; Xu, Hai; Wang, Yilin

    2015-07-15

    Only specific base pairs on DNA can bind with each other through hydrogen bonds, which is called the Watson-Crick (W/C) pairing rule. However, without the constraint of DNA chains, the nucleobases in bulk aqueous solution usually do not follow the W/C pairing rule anymore because of the strong competitive effect of water and the multi-interaction edges of nucleobases. The present work applied surfactant aggregates noncovalently functionalized by nucleotide to enhance the recognition between nucleobases without DNA chains in aqueous solution, and it revealed the effects of their self-assembling ability and morphologies on the recognition. The cationic ammonium monomeric, dimeric, and trimeric surfactants DTAB, 12-3-12, and 12-3-12-3-12 were chosen. The surfactants with guanine-5'-monophosphate-disodium (GMP) form micelles, vesicles, and fingerprint-like and plate-like aggregates bearing the hydrogen-bonding sites of GMP, respectively. The binding parameters of these aggregates with adenine (A), uracil (U), guanine (G), and cytosine(C) indicate that the surfactants can promote W/C recognitions in aqueous solution when they form vesicles (GMP/DTAB) or plate-like aggregates (GMP/12-3-12) with proper molecular packing compactness, which not only provide hydrophobic environments but also shield non-W/C recognition edges. However, the GMP/12-3-12 micelles with loose molecular packing, the GMP/12-3-12 fingerprint-like aggregates where the hydrogen bond sites of GMP are occupied by itself, and the GMP/12-3-12-3-12 vesicles with too strong self-assembling ability cannot promote W/C recognition. This work provides insight into how to design self-assemblies with the performance of enhanced molecule recognition.

  1. Effects of dietary pyrroloquinoline quinone disodium on growth performance, carcass yield and antioxidant status of broiler chicks.

    Science.gov (United States)

    Samuel, K G; Zhang, H J; Wang, J; Wu, S G; Yue, H Y; Sun, L L; Qi, G H

    2015-03-01

    Pyrroloquinoline quinone (PQQ), a putative essential nutrient and redox modulator in microorganisms, cell and animal models, has been recognized as a growth promoter in rodents. Growth performance, carcass yield and antioxidant status were evaluated on broiler chickens fed different levels of PQQ disodium (PQQ.Na2). A total of 784 day-old male Arbor Acres (AA) broilers were randomly allotted into seven dietary groups: negative control group (NC) fed a basal diet without virginiamycin (VIR) or PQQ.Na2; a positive control group (PC) fed a diet with 15 mg of VIR/kg diet; and PQQ.Na2 groups fed with 0.05, 0.10, 0.20, 0.40 or 0.80 mg PQQ.Na2/kg diet. Each treatment contained eight replicates with 14 birds each. The feeding trial lasted for 6 weeks. The results showed that chicks fed 0.2 mg PQQ.Na2/kg diet significantly improved growth performance comparable to those in PC group, and the feed efficiency enhancement effects of dietary PQQ.Na2 was more apparent in grower phase. Dietary addition of PQQ.Na2 had the potential to stimulate immune organs development, and low level dietary addition (<0.1 mg/kg) increased plasma lysozyme level. Broilers fed 0.2 mg PQQ.Na2/kg diet gained more carcasses at day 42, and had lower lipid peroxide malondialdehyde content and higher total antioxidant power in plasma. The results indicated that dietary PQQ.Na2 (0.2 mg/kg diet) had the potential to act as a growth promoter comparable to antibiotic in broiler chicks.

  2. Effects of disodium fumarate on ruminal fermentation and microbial communities in sheep fed on high-forage diets.

    Science.gov (United States)

    Zhou, Y W; McSweeney, C S; Wang, J K; Liu, J X

    2012-05-01

    This study was conducted to investigate effects of disodium fumarate (DF) on fermentation characteristics and microbial populations in the rumen of Hu sheep fed on high-forage diets. Two complementary feeding trials were conducted. In Trial 1, six Hu sheep fitted with ruminal cannulae were randomly allocated to a 2 × 2 cross-over design involving dietary treatments of either 0 or 20 g DF daily. Total DNA was extracted from the fluid- and solid-associated rumen microbes, respectively. Numbers of 16S rDNA gene copies associated with rumen methanogens and bacteria, and 18S rDNA gene copies associated with rumen protozoa and fungi were measured using real-time PCR, and expressed as proportion of total rumen bacteria 16S rDNA. Ruminal pH decreased in the DF group compared with the control (P sheep were fed on basal diet for 2 weeks and continuously for 4 weeks with supplementation of DF at a level of 20 g/day. Ruminal samples were collected every week to analyze fermentation parameters and microbial populations. No effects of DF were observed on pH, acetate and butyrate (P > 0.05). Populations of methanogens and R. flavefaciens decreased in the fluid samples (P clone sequences from cut-out bands appearing in both the 2nd and the 4th week were 94% to 100% similar to Prevotella-like bacteria, and four sequences showed 95% to 98% similarity to Selenomonas dianae. Another 15 sequences were obtained from bands, which appeared in the 4th week only. Thirteen of these 15 sequences showed 95% to 99% similarity to Clostridium sp., and the other two showed 95% and 100% similarity to Ruminococcus sp. In summary, the microorganisms positively responding to DF addition were the cellulolytic bacteria, R. albus, F. succinogenes and B. fibrisolvens as well as proteolytic bacteria, B. fibrisolvens, P. ruminicola and Clostridium sp.

  3. Laryngeal edema induced by disodium cantharidinate injection%斑蝥酸钠注射液致喉头水肿

    Institute of Scientific and Technical Information of China (English)

    陈小蕾; 吴立强; 赵青

    2013-01-01

      1例72岁男性患者,确诊为左肺腺癌7个月,既往有小牛血清去蛋白过敏史。治疗期间输入斑蝥酸钠注射液约30 min,患者突然烦躁,急发憋闷、喉痒、发声嘶哑、吸气性呼吸困难,口唇明显发绀,三凹征阳性等。立即停止输入,给予氧气吸入,甲强龙、异丙嗪、葡萄糖酸钙抗过敏以及其他对症治疗,约20 min后,患者症状明显改善,口唇发绀及三凹征消失。%  One 72-year-old male patient was diagnosed with left lung adenocarcinoma 7 months ago. He had a history of deproteinised calf blood serum injection allergy. About 30 minutes after the disodium cantharidinate injection was used, the patient suddenly developed dysphoria, oppressed, throat itching, voice hoarse, inspiratory dyspnea, obvious lips hematocyanosis, three depression sign positive and so on. This medicine was immediately stopped. The patient received oxygen inhalation and the therapy of antianaphylaxis by methylprednisolone, promethazine hydrochloride injection, calcium gluconate and other treatments. After about 20 minutes, the symptoms improved obviously, lips hematocyanosis and three depression sign disappeared.

  4. Influence of Combined Therapeutic Potential of Meso 2, 3-dimercaptosuccinic Acid and Calcium Disodium Edetate on Lead-induced Testicular Alterations in Rats

    Institute of Scientific and Technical Information of China (English)

    GOVINDER J.S. FLORA; USHA ARORA; ARD PRAHLAD K. SETH

    1999-01-01

    The therapeutic efficacy of a combination of meso 2,3-dimercaptosuccinic acid (DMSA) and calcium disodium EDTA in protecting testicular disorders in chronic lead intoxication was investigated. The results indicate that two five-days courses of the combined therapy produced a more effective recovery in the lead induced biochemical and histopathological disorders compared to conventional single 5 days therapy. No adverse effect of the chelators, when administered individually or in combination, was noticed in the testes of control (without lead exposure) animals.

  5. Sodium cromoglycate inhibits absorption of the major soybean allergen, Gly m Bd 30K, in mice and human intestinal Caco-2 cells.

    Science.gov (United States)

    Weangsripanaval, Thanakorn; Murota, Kaeko; Murakami, Yoko; Kominami, Masaru; Kusudo, Tatsuya; Moriyama, Tatsuya; Ogawa, Tadashi; Kawada, Teruo

    2006-11-01

    Our previous data showed that Gly m Bd 30K was absorbed from the gastrointestinal tract and circulated in blood in mice. This study was conducted to determine the mechanism and identify the inhibitor of such absorption. Using sandwich ELISA and immunoblotting, we found that intact Gly m Bd 30K was absorbed from apical to basolateral solutions and intracellularly accumulated by Caco-2 cells in a dose- and time-dependent manner. The absorption and intracellular accumulation of Gly m Bd 30K were significantly suppressed when Caco-2 cells were treated with sodium cromoglycate (SCG) (0-50 mmol/L) in a dose-dependent manner. In 24-d-old mice orally treated with SCG (10-1000 mg/kg body weight), plasma Gly m Bd 30K concentration decreased significantly 30-120 min after Gly m Bd 30K (2000 mg/kg body weight) administration. Moreover, inhibitors that suppress the clathrin-dependent endocytosis dansylcadaverine, the caveolae-dependent endocytosis nystatin and clathrin, and the caveolae-dependent endocytosis methyl-beta-cyclodextrin had inhibitory effects on the absorption and intracellular accumulation of Gly m Bd 30K by Caco-2 cells. These data indicate that Gly m Bd 30K is absorbed and intracellularly accumulated in Caco-2 cells via clathrin- or caveolae-dependent endocytosis. We propose that the absorption and intracellular accumulation of Gly m Bd 30K are inhibited by SCG via clathrin- or caveolae-dependent endocytosis.

  6. Hepatic hemangiomas: Difference in enhancement pattern on 3T MR imaging with gadobenate dimeglumine versus gadoxetate disodium

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Rajan T., E-mail: rajan.gupta@duke.edu [Duke University Medical Center, Department of Radiology, DUMC 3808, Durham, NC 27710 (United States); Marin, Daniele; Boll, Daniel T.; Husarik, Daniela B.; Davis, Drew E.; Feuerlein, Sebastian; Merkle, Elmar M. [Duke University Medical Center, Department of Radiology, DUMC 3808, Durham, NC 27710 (United States)

    2012-10-15

    Purpose: To compare intraindividual differences in enhancement pattern of hepatic hemangiomas between gadobenate dimeglumine (Gd-BOPTA) and gadoxetate disodium (Gd-EOB-DTPA)-enhanced 3T MR imaging. Materials and methods: This is a HIPAA-compliant, IRB-approved retrospective study with waiver for informed consent granted. From 10/07 to 5/09, 10 patients (2 males, 8 females; mean age, 57.3 years) with 15 hepatic hemangiomas (mean diameter, 4.4 ± 5.6 cm) underwent both Gd-BOPTA- and Gd-EOB-DTPA-enhanced 3T MR imaging (mean interval, 266 days; range, 38–462 days). Diagnosis of hemangioma was based on strict imaging criteria. MR imaging was obtained during three arterial, portal venous, and up to four delayed phases. During each phase, hemangioma-to-liver contrast-to-noise ratio (CNR) was measured for each lesion on both examinations. Statistical analysis was performed using paired Student's t-test. Results: Hemangioma-to-liver CNR peaked during the portal venous phase (Gd-BOPTA: 48.9 ± 65.8, Gd-EOB-DTPA: 0.7 ± 3.8). During all imaging phases except the first arterial phase, hemangioma-to-liver CNR was significantly lower on Gd-EOB-DTPA-enhanced compared to Gd-BOPTA-enhanced MR images (p < 0.05). Notably, Gd-EOB-DTPA yielded negative hemangioma-to-liver CNR (−2.5 ± 2.4) compared to Gd-BOPTA (40.7 ± 56.4) during the first delayed phase (7–8 min after contrast administration), remaining negative for the rest of the delayed phases (up to 26 min after contrast administration). Conclusion: The enhancement patterns of hepatic hemangiomas differs significantly between Gd-BOPTA and Gd-EOB-DTPA-enhanced 3T MR imaging. The smaller dose, shorter plasma half-life, and increased hepatobiliary uptake of Gd-EOB-DTPA leads to a negative CNR of hemangioma-to-liver on delayed phases and could create an imaging pitfall with this agent.

  7. The influence of disodium cromoglycate on the whole gastrointestinal transit time in patients with diarrhea-predominant irritable bowel syndrome%色甘酸二钠对腹泻型肠易激综合征全胃肠转运时间的影响

    Institute of Scientific and Technical Information of China (English)

    沈顺华; 陈杏林; 唐世孝; 郑凯

    2011-01-01

    目的 探讨色甘酸二钠对腹泻型肠易激综合征(D-IBS)患者全胃肠转运时间的影响.方法 30例D-IBS患者口服色甘酸二钠治疗,20mg/次,3次/d,疗程4周,比较治疗前后全胃肠转运时间(GTT)和肠易激综合征症状评分的变化.结果 与治疗前比较,D-IBS患者治疗后GTT明显延长(P0.05).腹痛或腹部不适与排便次数的评分下降明显(P<0.01).结论 色甘酸二钠能明显延长D-IBS患者GTT,并有效改善IBS症状.

  8. Final report on the safety assessment of Glycyrrhetinic Acid, Potassium Glycyrrhetinate, Disodium Succinoyl Glycyrrhetinate, Glyceryl Glycyrrhetinate, Glycyrrhetinyl Stearate, Stearyl Glycyrrhetinate, Glycyrrhizic Acid, Ammonium Glycyrrhizate, Dipotassium Glycyrrhizate, Disodium Glycyrrhizate, Trisodium Glycyrrhizate, Methyl Glycyrrhizate, and Potassium Glycyrrhizinate.

    Science.gov (United States)

    2007-01-01

    11beta -hydroxysteroid dehydrogenase-2 (11beta -OHSD2) in the kidney. Glycyrrhetinic Acid and its derivatives block gap junction intracellular communication in a dose-dependent manner in animal and human cells, including epithelial cells, fibroblasts, osteoblasts, hepatocytes, and astrocytes; at high concentrations, it is cytotoxic. Glycyrrhetinic Acid and Glycyrrhizic Acid protect liver tissue from carbon tetrachloride. Glycyrrhizic Acid has been used to treat chronic hepatitis, inhibiting the penetration of the hepatitis A virus into hepatocytes. Glycyrrhetinic Acid and Glycyrrhizic Acid have anti-inflammatory effects in rats and mice. The acute intraperitoneal LD(50) for Glycyrrhetinic Acid in mice was 308 mg/kg and the oral LD(50) was > 610 mg/kg. The oral LD(50) in rats was reported to be 610 mg/kg. Higher LD(50) values were generally reported for salts. Little short-term, subchronic, or chronic toxicity was seen in rats given ammonium, dipotassium, or disodium salts of Glycyrrhizic Acid. Glycyrrhetinic Acid was not irritating to shaved rabbit skin, but was considered slightly irritating in an in vitro test. Glycyrrhetinic Acid inhibited the mutagenic activity of benzo[a]pyrene and inhibited tumor initiation and promotion by other agents in mice. Glycyrrhizic Acid inhibited tumor initiation by another agent, but did not prevent tumor promotion in mice. Glycyrrhizic Acid delayed mortality in mice injected with Erlich ascites tumor cells, but did not reduce the mortality rate. Ammonium Glycyrrhizate was not genotoxic in in vivo and in vitro cytogenetics assays, the dominant lethal assay, an Ames assay, and heritable translocation tests, except for possible increase in dominant lethal mutations in rats given 2000 mg/kg day(-1) in their diet. Disodium Glycyrrhizate was not carcinogenic in mice in a drinking water study at exposure levels up to 12.2 mg/kg day(-1) for 96 weeks. Glycyrrhizate salts produced no reproductive or developmental toxicity in rats, mice

  9. Treatment of Allergic Rhinitis with Ectoine Containing Nasal Spray and Eye Drops in Comparison with Azelastine Containing Nasal Spray and Eye Drops or with Cromoglycic Acid Containing Nasal Spray

    Directory of Open Access Journals (Sweden)

    Nina Werkhäuser

    2014-01-01

    Full Text Available Objectives. Allergic rhinitis is a common disease with increasing prevalence and high impact on economic burden and comorbidities. As treatment with pharmacological drugs is not always satisfactory due to side effects and incomplete efficacy, alternative treatment strategies are needed. Ectoine is an osmolyte with membrane stabilizing and inflammation reducing capacities. Nasal spray and eye drops containing ectoine are promising new treatment regimens for allergic rhinitis sufferers. Design and Methods. The current two noninterventional trials evaluated the efficacy and safety of ectoine containing nasal spray and eye drops for treating allergic rhinitis in comparison with either azelastine or cromoglycic acid containing products. Nasal and ocular symptom developments as well as judgment of tolerability and efficacy were assessed both by investigators and patients over a time period of one to two weeks. Results. Both trials confirmed that ectoine containing products reduced nasal and ocular symptoms in allergic rhinitis patients. Results clearly demonstrated good safety profiles of the ectoine products comparable to those of azelastine and even better to those of cromoglycate products. Conclusion. Ectoine containing nasal spray and eye drops are interesting new treatment strategies for sufferers of allergic rhinitis, combining both good efficacy and absence of side effects.

  10. Treatment of allergic rhinitis with ectoine containing nasal spray and eye drops in comparison with azelastine containing nasal spray and eye drops or with cromoglycic Acid containing nasal spray.

    Science.gov (United States)

    Werkhäuser, Nina; Bilstein, Andreas; Sonnemann, Uwe

    2014-01-01

    Objectives. Allergic rhinitis is a common disease with increasing prevalence and high impact on economic burden and comorbidities. As treatment with pharmacological drugs is not always satisfactory due to side effects and incomplete efficacy, alternative treatment strategies are needed. Ectoine is an osmolyte with membrane stabilizing and inflammation reducing capacities. Nasal spray and eye drops containing ectoine are promising new treatment regimens for allergic rhinitis sufferers. Design and Methods. The current two noninterventional trials evaluated the efficacy and safety of ectoine containing nasal spray and eye drops for treating allergic rhinitis in comparison with either azelastine or cromoglycic acid containing products. Nasal and ocular symptom developments as well as judgment of tolerability and efficacy were assessed both by investigators and patients over a time period of one to two weeks. Results. Both trials confirmed that ectoine containing products reduced nasal and ocular symptoms in allergic rhinitis patients. Results clearly demonstrated good safety profiles of the ectoine products comparable to those of azelastine and even better to those of cromoglycate products. Conclusion. Ectoine containing nasal spray and eye drops are interesting new treatment strategies for sufferers of allergic rhinitis, combining both good efficacy and absence of side effects.

  11. Effect of ethylenediamine tetraacetic acid disodium on the corrosion of cold rolled steel in the presence of benzotriazole in hydrochloric acid

    Energy Technology Data Exchange (ETDEWEB)

    Qu, Qing [Department of Chemistry, Yunnan University, Kunming 650091 (China)]. E-mail: quqing58@yahoo.com.cn; Jiang, Shuan [Department of Chemistry, Yunnan University, Kunming 650091 (China); Bai, Wei [Department of Chemistry, Yunnan Nationalities University, Kunming 650092 (China); Li, Lei [Laboratory for Conservation and Utilization of Bio-Resources, Yunnan University, Kunming 650091 (China)

    2007-08-01

    The inhibition behavior of cold rolled steel in 0.1 M hydrochloric acid (HCl) by ethylenediamine tetraacetic acid disodium (EDTA) in the absence and presence of benzotriazole (BTA) was investigated with Tafel polarization curve and electrochemical impedance spectroscopy (EIS). The polarization curve results show that the single EDTA acts as an anodic type inhibitor while the combination of EDTA and BTA acts as mixed type inhibitor and mainly inhibits anodic reaction. All impedance spectra in EIS tests exhibit one capacitive loop which indicates that the corrosion reaction is controlled by charge transfer process. Inhibition efficiencies obtained from Tafel polarization, charge transfer resistance (R {sub t}) are consistent. The corrosion of cold rolled steel in 0.1 M HCl is obviously reduced by EDTA in combination with lower concentrations of BTA. Fourier transform infrared spectroscopy (FTIR) and atomic force microscopy (AFM) were used to characterize the corrosion surface of cold rolled steel. Probable mechanisms are present to explain the experimental results.

  12. Stability-Indicating RP-HPLC Methods for the Determination of Fluorometholone in Its Mixtures with Sodium Cromoglycate and Tetrahydrozoline Hydrochloride.

    Science.gov (United States)

    El-Bagary, Ramzia I; Fouad, Marwa A; El-Shal, Manal A; Tolba, Enas H

    2016-07-01

    Two stability-indicating reversed-phase liquid chromatographic methods were developed and validated for the determination of fluorometholone (FLU) in its mixtures with sodium cromoglycate (SCG) and tetrahydrozoline hydrochloride (THZ). The first HPLC method (Method 1) was based on isocratic elution of FLU and SCG along with their alkaline degradation products on a reversed phase C18 column (250 × 4.6 mm id)-ACE Generix 5, using a mobile phase consisting of methanol-water (70 : 30, v/v), pH adjusted to 2.5 using orthophosphoric acid at a flow rate of 1.2 mL min(-1) Quantitation was achieved with UV detection at 240 nm. The second HPLC method (Method 2) was based on isocratic elution of FLU, its alkaline degradation product and THZ on a reversed phase C8 column (250 × 4.6 mm)-ACE Generix 5, using a mobile phase consisting of acetonitrile-50 mM potassium dihydrogen orthophosphate (40 : 60, v/v) at a flow rate of 2 mL min(-1) Quantitation was achieved by applying dual-wavelength detection, where FLU and its alkaline degradation product were detected at 240 nm and THZ was detected at 215 nm at ambient temperatures. Linearity, accuracy and precision were found to be acceptable over the concentration range of 5-50 and 10-500 μg mL(-1) for FLU and SCG (Method 1) and over the concentration range of 5-80 and 5-60 μg mL(-1) for FLU and THZ (Method 2), respectively. Besides, the FLU alkaline degradation product was verified using IR, NMR and LC-MS spectroscopy. The two proposed methods could be successfully applied for the routine analysis of the studied drugs either in their pure bulk powders or in their pharmaceutical preparations without any preliminary separation step.

  13. Antigen-induced bronchial anaphylaxis in actively sensitized guinea-pigs: effect of long-term treatment with sodium cromoglycate and aminophylline.

    Science.gov (United States)

    Andersson, P.; Bergstrand, H.

    1981-01-01

    1 The effects of long-term treatment with sodium cromoglycate (SCG) and aminophylline on antigen-induced bronchoconstriction have been studied in guinea-pigs actively sensitized according to two different regimens (one producing IgE- and IgG-like antibodies and the other producing exclusively IgG-like antibodies). 2 Treatment for three weeks with SCG (10 mg/kg) and aminophylline (10, 30 or 60 mg/kg) led to a decreased bronchial response capacity which persisted even three days after treatment ceased. In this respect SCG was effective only in guinea-pigs sensitized to produce at least partly IgE-like antibodies; aminophylline was effective in guinea-pigs sensitized to produce both IgE and/or IgG antibodies. 3 The results in vivo with SCG were reflected in vitro by a reduced capacity of chopped lung tissue to release histamine at antigen challenge; lungs from animals treated with aminophylline did not show reduced histamine releasing capacity. 4 Acute treatment with atropine was shown to reduce significantly the antigen-induced bronchial contraction in guinea-pigs sensitized to produce both IgE- and IgG-antibodies. No effect of atropine was seen on an IgG-mediated anaphylaxis. 5 Increased reactivity to methacholine but not to histamine was seen in guinea-pigs sensitized to produce both IgG- and IgE-antibodies. Long-term treatment with SCG did not affect this hyperreactivity to methacholine. 6 Decreased reactivity to isoprenaline was found in isolated tracheae taken from guinea-pigs sensitized to produce both IgE- and IgG-like antibodies compared to unsensitized guinea-pigs. Long-term treatment with SCG, but not with aminophylline, reversed this decreased reactivity. PMID:6170376

  14. Morphine, but not sodium cromoglycate, modulates the release of substance P from capsaicin-sensitive neurones in the rat trachea in vitro.

    Science.gov (United States)

    Ray, N. J.; Jones, A. J.; Keen, P.

    1991-01-01

    1. Opioids have been shown to inhibit substance P (SP) release from primary afferent neurones (PAN). In addition, opioid receptors have been identified on PAN of the vagus nerves. Sodium cromoglycate (SCG) decreases the excitability of C-fibres in the lung of the dog in vivo. We have utilised a multi-superfusion system to investigate the effect of opioids and SCG on the release of SP from the rat trachea in vitro. 2. Pretreatment of newborn rats with capsaicin (50 mg kg-1 s.c. at day 1 and 2 of life) resulted in a 93.2 +/- 6.3% reduction in tracheal substance P-like immunoreactivity (SP-LI) content when determined by radioimmunoassay in the adult. 3. Exposure to isotonically elevated potassium concentrations (37-90 mM), capsaicin (100 nM-10 microM), and bradykinin (BK; 10nm-1 microM) but not des-Arg9-BK (1 microM) stimulated SP-LI release by a calcium-dependent mechanism. 4. SCG (1 microM and 100 microM) did not affect spontaneous, potassium (60 mM)- or BK (1 microM)-stimulated SP-LI release. 5. Morphine (0.1-100 microM) caused dose-related inhibition of potassium (60 mM)-stimulated SP-LI release with the greatest inhibition of 60.4 +/- 13.7% at 100 microM. The effect of morphine was not mimicked by the kappa-opioid receptor agonist, U50,488H (10 microM) or the delta-opioid receptor agonist, Tyr-(D-Pen)-Gly-Phe-(D-Pen) (DPDPE). 6. The effect of morphine was totally abolished by prior and concomitant exposure to naloxone (100 nM) which had no effect on control release values.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:1713104

  15. Inhibition of tumour necrosis factor-alpha (TNF-alpha) release from mast cells by the anti-inflammatory drugs, sodium cromoglycate and nedocromil sodium.

    Science.gov (United States)

    Bissonnette, E Y; Enciso, J A; Befus, A D

    1995-01-01

    TNF-alpha is a cytokine thought to be involved in the pathogenesis of asthma and in several other inflammatory conditions. Given recent evidence that mast cells (MC) are an important source of TNF-alpha, we investigated the effects of two anti-inflammatory drugs, nedocromil sodium (NED) and sodium cromoglycate (SCG), on rat MC-derived TNF-alpha. We established that at least 2 h pretreatment with NED or SCG followed by washing was required to inhibit TNF-alpha-dependent cytotoxicity by rat peritoneal MC (PMC). A maximum inhibition of TNF-alpha occurred after 6 h treatment. The inhibitory effect of NED and SCG (10(-5)-10(-3)M) was concentration-dependent (20-37% for NED and 16-37% for SCG). The time-course analysis and the use of cycloheximide, an inhibitor of protein synthesis, provided strong evidence that new protein synthesis by the MC is required for this inhibitory effect. Furthermore, 24 h treatment with 1 mM NED inhibited the levels of mRNA for TNF-alpha by 59-83%. In addition to the effect on TNF-alpha-dependent cytotoxicity by MC, 20 min pretreatment with 10(-4) M NED and SCG inhibited antigen-stimulated TNF-alpha release (6h) by 42% and 48%, respectively. Interestingly, the functionally distinct intestinal mucosal MC (IMMC) is unresponsive to these drugs with regard to histamine secretion. However, as with PMC, 2h pretreatment with NED or SCG inhibited TNF-alpha-dependent cytotoxicity by IMMC. These effects may be important in the action of these drugs in vivo in the late phase reaction in asthma or other inflammatory conditions. Images Fig. 6 PMID:7554404

  16. Effect of a novel ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate on human dermal fibroblasts: increased collagen synthesis and inhibition of MMP-1.

    Science.gov (United States)

    Shibayama, Hiroharu; Hisama, Masayoshi; Matsuda, Sanae; Ohtsuki, Mamitaro; Iwaki, Masahiro

    2008-04-01

    The effects of a novel amphiphilic vitamin C derivative, disodium isostearyl 2-O-L-ascorbyl phosphate (disodium 2-(1,3,3-trimethyl-n-butyl)-5,7,7-trimethyl-n-octyl-L-ascorbyl phosphate, VCP-IS-2Na), possessing a C18 alkyl chain attached to a stable sodium L-ascorbic acid 2-phosphate (VCP-Na), on the proliferation of fibroblasts and collagen synthesis, and inhibition of matrix metalloproteinase-1 (MMP-1) in normal human fibroblasts, NHDFs and NB1RGBs, were evaluated. Compared with proliferation of non-treated fibroblasts, VCP-IS-2Na at 50 microM increased proliferation to 123 and 135% of that in NHDFs and NB1RGBs. On the other hand, L-ascorbic acid (vitamin C) and VCP-Na had little effect on proliferation. At a concentration of 5.0-50 microM, VCP-IS-2Na stimulated collagen synthesis with an effectiveness comparable to that of vitamin C and VCP-Na. The amount of type I collagen in the culture medium was increased by treatment with VCP-IS-2Na for 72 h, in a concentration-dependent manner. Maximum increases of 126 and 1067% were seen with VCP-IS-2Na at 50 microM in NHDFs and NB1RGBs, respectively, whereas vitamin C and VCP-Na only had a small effect. VCP-IS-2Na had a small inhibitory effect on MMP-1, but vitamin C did not inhibit MMP-1, and VCP-Na had very little effect. VCP-IS-2Na exerted its collagen synthesis-promoting activity after being converted to vitamin C by phosphatase. This vitamin C promoted proliferation, collagen synthesis and inhibition of MMP-1, which are prolonged through sustained conversion of VCP-IS-2Na.

  17. Inhibitory effect of putranjivain A on allergic inflammation through suppression of mast cell activation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Hui-Hun; Park, Seung-Bin; Lee, Soyoung [CMRI, Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422 (Korea, Republic of); Kwon, Taeg Kyu [Department of Immunology, School of Medicine, Keimyung University, Daegu 704-701 (Korea, Republic of); Shin, Tae-Yong [College of Pharmacy, Woosuk University, Jeonju 565-701 (Korea, Republic of); Park, Pil-Hoon; Lee, Seung-Ho [College of Pharmacy, Youngnam University, Kyungsan 712-749 (Korea, Republic of); Kim, Sang-Hyun, E-mail: shkim72@knu.ac.kr [CMRI, Department of Pharmacology, School of Medicine, Kyungpook National University, Daegu 700-422 (Korea, Republic of)

    2014-02-01

    A great number of people are suffering from allergic inflammatory disease such as asthma, atopic dermatitis, and sinusitis. Therefore discovery of drugs for the treatment of these diseases is an important subject in human health. Putranjivain A (PJA), member of ellagitannin, is known to possess beneficial effects including anti-cancer and anti-viral activities. The aim of the present study was to elucidate whether PJA modulates the allergic inflammatory reaction and to study its possible mechanisms of action using mast cell-based in vitro and in vivo models. The study was performed in anaphylaxis mouse model and cultured mast cells. PJA inhibited the expression of pro-inflammatory cytokines in immunoglobulin E-stimulated mast cells. PJA reduced this expression by inhibiting nuclear factor (NF)-κB and nuclear factor of activated T cell. The oral administration of PJA reduced systemic and cutaneous anaphylaxis, the release of serum histamine, and the expression of the histamine H{sub 1} receptor. In addition, PJA attenuated the activation of mast cells. PJA inhibited the release of histamine from various types of mast cells by the suppression of intracellular calcium. The inhibitory activity of PJA on the allergic reaction was similar to that of disodium cromoglycate, a known anti-allergic drug. These results suggest that PJA can facilitate the prevention or treatment of allergic inflammatory diseases mediated by mast cells. - Highlights: • PJA reduced the degranulation of mast cells. • PJA inhibited the production of inflammatory cytokines. • The effect of PJA on allergic reaction was comparable to the DSCG. • PJA might be a candidate for the treatment of allergic inflammatory diseases.

  18. The anti-allergic activity of polyphenol extracted from five marine algae

    Science.gov (United States)

    Chen, Yu; Lin, Hong; Li, Zhenxing; Mou, Quangui

    2015-08-01

    Natural polyphenol has been widely believed to be effective in allergy remission. Currently, most of the natural polyphenol products come from terrestrial sources such as tea, grape seeds among others, and few polyphenols have been developed from algae for their anti-allergic activity. The aim of the study was to screen some commercial seaweed for natural extracts with anti-allergic activity. Five algae including Laminaria japonica, Porphyra sp., Spirulina platensis, Chlorella pyrenoidosa and Scytosiphon sp. were extracted with ethanol, and the extracts were evaluated for total polyphenol contents and anti-allergic activity with the hyaluronidase inhibition assay. Results showed that the total polyphenol contents in the ethanol extracts ranged from 1.67% to 8.47%, while the highest was found in the extract from Scytosiphon sp. Hyaluronidase inhibition assay showed that the extracts from Scytosiphon sp. had the lowest IC50, 0.67 mg mL-1, while Chlorella pyrenoidosa extract had the highest IC50, 15.07 mg mL-1. The anti-allergic activity of Scytosiphon sp. extract was even higher than the typical anti-allergic drug Disodium Cromoglycate (DSCG) (IC50 = 1.13 mg mL-1), and was similar with natural polyphenol from Epigallocatechin gallate (EGCG) (IC50 = 0.56 mg mL-1). These results indicated that the ethanol extract of Scytosiphon sp. contains a high concentration of polyphenol with high anti-allergic activity. Potentially Scytosiphon sp. can be developed to a natural anti-allergic compound for allergy remission.

  19. Taurine suppresses osteoblastic differentiation of aortic valve interstitial cells induced by beta-glycerophosphate disodium, dexamethasone and ascorbic acid via the ERK pathway.

    Science.gov (United States)

    Feng, Xiang; Li, Jian-ming; Liao, Xiao-bo; Hu, Ye-rong; Shang, Bao-peng; Zhang, Zhi-yuan; Yuan, Ling-qing; Xie, Hui; Sheng, Zhi-feng; Tang, Hao; Zhang, Wei; Gu, Lu; Zhou, Xin-min

    2012-10-01

    Aortic valve calcification (AVC) is an active process characterized by osteoblastic differentiation of the aortic valve interstitial cells (AVICs). Taurine is a free β-amino acid and plays important physiological roles including protective effect of cardiovascular events. To evaluate the possible role of taurine in AVC, we isolated human AVICs from patients with type A dissection without leaflet disease. We demonstrated that the cultured AVICs express SM α-actin, vimentin and taurine transporter (TAUT), but not CD31, SM-myosin or desmin. We also established the osteoblastic differentiation model of the AVICs induced by pro-calcific medium (PCM) containing β-glycerophosphate disodium, dexamethasone and ascorbic acid in vitro. The results showed that taurine attenuated the PCM-induced osteoblastic differentiation of AVICs by decreasing the alkaline phosphate (ALP) activity/expression and the expression of the core binding factor α1 (Cbfα1) in a dose-dependent manner (reaching the maximum protective effect at 10 mM), and taurine (10 mM) inhibited the mineralization level of AVICs in the form of calcium content significantly. Furthermore, taurine activated the extracellular signal-regulated protein kinase (ERK) pathway via TAUT, and the inhibitor of ERK (PD98059) abolished the effect of taurine on both ALP activity/expression and Cbfα1 expression. These results suggested that taurine could inhibit osteoblastic differentiation of AVIC via the ERK pathway.

  20. Randomized Double-Blind Clinical Comparison of Sodium Ibandronate and Pamidronate Disodium for Treatment of 141 Patients with Malignant Tumor Ostealgia

    Institute of Scientific and Technical Information of China (English)

    Guanghai Dai; Shunchang Jiao; Junlan Yang; Shaohao Jiang; Donggang Liu

    2007-01-01

    OBJECTIVE To evaluate the therapeutic effect and potential adverse effects of sodium ibandronate (SI) in patients with malignant tumor ostealgia. METHODS Patients were randomly classified into two groups. Group A (SI) of 68 patients who received 4 mg SI I.v., and 73 patients in Group B (pamidronate disodium [PD]) who received 60 mg PD I.v. A randomized, double-blind method, with PD as a positive drug control, was used to assess changes in bone pain and adverse effects over a three-week period. RESULTS A total of 141 patients were enrolled in the study, with 136 cases of appraisable efficacy. The effective rate was 72.3% (47/65) in Group A, and 63.4% (45/71) in Group B. There was no significant difference in efficacy or adverse effects between the 2 groups. CONCLUSION The SI injection, with a pronounced effect, can relieve bone pain caused by osseous metastasis from a malignant tumor. The curative and adverse effects were similar compared to PD.

  1. 帕米膦酸二钠引起严重低钙血症1例%Serious hypocalcemia induced by disodium in 1 case

    Institute of Scientific and Technical Information of China (English)

    徐贞; 史美祺; 汤依群

    2011-01-01

    帕米膦酸二钠用于治疗恶性肿瘤并发的高钙血症和溶骨性癌转移引起的骨痛.1例患者予帕米膦酸二钠90 mg iv,1天后出现全身麻木,呼吸急促,并有窒息感,诊断为严重低钙血症,经对症治疗后病情渐平稳.%Pamidronate is increasingly used both in the treatment of hy-percalcemia and bone pain of osteolytic metastasis in cancer. We describe a case of severe hypocalcemia following one injection of pamidronate. One day after the administration of 90 mg pamidronate, patient felt whole - body numbness, shortness of breath, suffocation or choking. Condition got stable after symptomatic treatment Prescribers should be thoroughly familiar with this risk of pamidronate disodium, and avoid the occurrence of serious side effects.

  2. Solubility of disodium cytidine 5′-monophosphate in different binary mixtures from 288.15 K to 313.15 K

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Jin [College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing (China); National Engineering Technique Research Center for Biotechnology, Nanjing (China); Ma, Tianle; Li, An [National Engineering Technique Research Center for Biotechnology, Nanjing (China); State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing (China); Chen, Xiaochun; Chen, Yong; Xie, Jingjing [College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing (China); National Engineering Technique Research Center for Biotechnology, Nanjing (China); Wu, Jinglan, E-mail: yinghanjie@njut.edu.cn [College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing (China); National Engineering Technique Research Center for Biotechnology, Nanjing (China); Ying, Hanjie [College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing (China); National Engineering Technique Research Center for Biotechnology, Nanjing (China); State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing (China)

    2013-08-10

    Highlights: • Solubility of 5′-CMPNa{sub 2} in different systems was measured the first time. • Experimental data were correlated by CNIBS/Redlich–Kister model and Apelblat model. • Good agreement has been observed between the calculated and the experimental data. • Enthalpy and entropy were calculated by the van’t Hoff equation and Gibbs equation. - Abstract: The solubility of disodium cytidine 5′-monophosphate (5′-CMPNa{sub 2}) in methanol + water and ethanol + water binary mixtures was measured experimentally at the temperatures ranging from 288.15 to 313.15 K. The results showed that the solubility of 5′-CMPNa{sub 2} increased with the increasing of temperature and the mole fraction of water in different binary mixtures. The (CNIBS)/Redlich–Kister model and the semi-empirical Apelblat model were applied for the prediction of the experimental data. Both models could give satisfactory simulation results. In addition, the thermodynamic properties of the dissolution process such as Gibbs energy, enthalpy, and entropy were calculated using the van’t Hoff equation and the Gibbs equation. The results indicated that the dissolution process was endothermic.

  3. Characterization of interactions between methoxatin disodium salt and human serum albumin by pressure-assisted capillary electrophoresis/frontal analysis and circular dichroism spectroscopy.

    Science.gov (United States)

    Zhao, Lijuan; Chen, Dongying

    2015-01-01

    Pressure-assisted capillary electrophoresis (PACE)/frontal analysis (FA) and circular dichroism spectroscopy were utilized to investigate the interactions between methoxatin disodium salt (PQQ-2Na) and human serum albumin (HSA). With the PACE/FA method, sodium phosphate buffer solution (67 mm, pH 7.4) was used as the background electrolyte. Hydrodynamic injection at 50 mbar for 50 s and external pressure of 50 mbar were applied. The binding constant and the number of primary binding sites to HSA were obtained under fixed concentration of PQQ-2Na (100 µm) and increasing HSA concentration (0~475 µm). The thermodynamic parameters characterized the main acting forces of hydrophobic and electrostatic interactions. The displacement experiments using phenylbutazone and flurbiprofen as ligand markers suggested that the binding site was the Sudlow site I of the HSA molecule. Circular dichroism spectroscopy was further employed to evaluate the conformation changes of HSA under the interaction of PQQ-2Na. This work provides comprehensive information for understanding the interactions between PQQ-2Na and HSA. Copyright © 2014 John Wiley & Sons, Ltd.

  4. 注射用帕米膦酸二钠致肌肉疼痛%Muscle pain caused by the iujectable pamidronate disodium

    Institute of Scientific and Technical Information of China (English)

    马媛; 封宇飞; 孙春华

    2011-01-01

    1例75岁男性患者,因治疗前列腺癌骨转移,静脉滴注帕米膦酸二钠60mg+0.9%氯化钠注射液500mL.14d后出现左上臂肌肉疼痛,逐渐发展至右上臂、胸部肌肉疼痛,同时两手手指发僵.考虑帕米膦酸二钠致肌肉疼痛,遂给予口服萘汀美酮每次0.5g,每日2次,持续10d,肌肉疼痛症状缓解并逐渐消失.%A 75-year-old male patient received an intravenous infusion of 60 mg pamidronate disodium, which was dissolved in 500 mL of 0.9% sodium chloride, for the treatment of bone metastasis by prostate cancer. Fourteen days later, the patient developed muscle pain of left upper arm and gradually developed into the right upper arm and chest muscle pain, while hands fingers stiflened. Nabumetone was orally given with the dose of 0.5 g each time, twice one day. Ten days later, the muscle pain symptoms relieved and disappeared gradually.

  5. Permeation and metabolism of a novel ascorbic acid derivative, disodium isostearyl 2-O-L-ascorbyl phosphate, in human living skin equivalent models.

    Science.gov (United States)

    Shibayama, H; Hisama, M; Matsuda, S; Ohtsuki, M

    2008-01-01

    A novel amphiphilic vitamin C (VC) derivative, disodium isostearyl 2-O-L-ascorbyl phosphate (VCP-IS-2Na), which possesses a C(18) alkyl chain attached to a stable ascorbate derivative, sodium L-ascorbic acid 2-phosphate (VCP-Na), was evaluated as a topical prodrug of VC with transdermal activity in human living skin equivalent (LSE) models. The permeation assay used was EPI-606X in the Franz-type diffusion cell system. VCP-IS-2Na exhibited much better permeability than VC and VCP-Na. The accumulation assays applied were EPI-200X and LSE-high by the dynamic system. The increased skin accumulation of VCP-IS-2Na was superior to that of VCP-Na and VC. VCP-IS-2Na that is susceptible to enzymatic hydrolysis by esterase and/or phosphatase released VC in the skin. Measurement of the metabolites that permeated and accumulated from the skin model suggested that VCP-IS-2Na was mainly metabolized via VCP-Na to VC in EPI-606X and EPI-200X, while it was mainly metabolized directly to VC in TESTSKIN LSE-high. Thus, these characteristics indicate that the novel VC derivative, VCP-IS-2Na, may be advantageous as a readily available source of VC for skin care applications.

  6. Effect of a novel ascorbic derivative, disodium isostearyl 2-O-L-ascorbyl phosphate, on normal human dermal fibroblasts against reactive oxygen species.

    Science.gov (United States)

    Shibayama, Hiroharu; Hisama, Masayoshi; Matsuda, Sanae; Kawase, Atsushi; Ohtsuki, Mamitaro; Hanada, Katsumi; Iwaki, Masahiro

    2008-04-01

    The novel amphiphilic vitamin C derivative disodium isostearyl 2-O-L-ascorbyl phosphate (VCP-IS-2Na), which has a C(18) alkyl chain attached to the stable ascorbate derivative sodium L-ascorbic acid 2-phosphate (VCP-Na), was evaluated for reduction of cell damage induced by oxidative stress, ultraviolet A (UVA), ultraviolet B (UVB), and H(2)O(2); stimulation of collagen synthesis against UVA irradiation; and inhibition of matrix metalloproteinase-1 (MMP-1) activity induced by UVA in human normal dermal fibroblasts. VCP-IS-2Na pretreatment resulted in significant protection against cell damage induced by UVB, UVA, and H(2)O(2). The amount of type I collagen following UVA irradiation was increased by treatment with VCP-IS-2Na in a concentration-dependent manner. These effects of VCP-IS-2Na were superior to those of L-ascorbic acid (vitamin C, VC) and VCP-Na. On the other hand, VCP-IS-2Na suppressed 65% of the excess MMP-1 irradiated UVA, and VC and VCP-Na slightly suppressed it.

  7. Therapeutic observation of the effect of combining therapy of desloratadine citrate disodium capsules and yupengfeng on chronic urticaria and effects on serum levels of ige%枸地氯雷他定胶囊联合玉屏风颗粒治疗慢性荨麻疹及对血清IgE的影响

    Institute of Scientific and Technical Information of China (English)

    田静; 黄圣波

    2015-01-01

    Objective To observe the therapeutic effect of desloratadine citrate disodium capsules combined with Yu-pengfeng in treating chronic urticaria and effects on Serum Levels of IgE. Method 172 patients with chronic urticaria were divided into two groups randomly. The treatment group were treated with desloratadine citrate disodium capsules combined with Yupengfeng. The control group were treated with desloratadine citrate disodium capsules alone. The treatment lasted for 4 weeks. Result The effective rates of the two groups were 93. 0% and 76. 7% respectively. There was statistically significant difference (P0.05)。结论 枸地氯雷他定胶囊联合玉屏风颗粒治疗慢性荨麻疹疗效好,复发率低,能明显降低血清IgE水平。

  8. Long-term betamethasone 21-phosphate disodium treatment has distinct effects in CD1 and DBA/2 mice on animal behavior accompanied by opposite effects on neurogenesis.

    Science.gov (United States)

    Aiello, Rossana; Crupi, Rosalia; Leo, Antonio; Chimirri, Serafina; Rispoli, Vincenzo; Marra, Rosario; Citraro, Rita; Cuzzocrea, Salvatore; De Sarro, Giovambattista; Russo, Emilio

    2015-02-01

    One of the most peculiar characteristics of the stress response is the pronounced inter-individual and inter-strain variability both in behavioral and neurochemical outcomes. Several studies confirm that rodents belonging to the same or different strain and/or gender, when exposed to a stressor, may show behavioral and cognitive differences. We compared the effects of long-term betamethasone 21-phosphate disodium (BTM), a widely clinically used corticosteroid, on animal behavior and neurogenesis in CD1 and DBA/2 mice. BTM treatment, in CD1 mice, increased body weight gain and anxiety parameters while having pro-depressant effects. Furthermore, BTM significantly reduced neurogenesis in the dentate gyrus of the hippocampus. Finally, BTM treatment induced a significant impairment in memory and learning performance in the Morris water maze. At odds, BTM administration, in DBA/2 mice, caused a significant reduction in the body weight while not modifying anxiety parameters. In addition, both an increased synaptogenesis and neurogenesis were found. Similarly to CD1 mice, also in DBA/2 mice, memory and learning were impaired. Our data confirm that long-term exposure to corticosteroids can generate or aggravate psychiatric/neurologic disorders such as depression, anxiety, memory and learning. Our study did not reveal significant differences between corticosterone and BTM treatment in CD1 mice. In contrast, BTM treatment in mice with an anxious phenotype (DBA/2 mice) revealed some contrasting results indicating that genetic factors can influence corticosteroids dependent effects. Finally, our data further underline the need for a re-evaluation of neurogenesis role; the increased neurogenesis observed in DBA/2 mice and behavioral effects might be distinguished phenomena.

  9. Development and Optimization of Gastro-Retentive Controlled-Release Tablet of Calcium-Disodium Edentate and its In Vivo Gamma Scintigraphic Evaluation.

    Science.gov (United States)

    Kumar, Neeraj; Soni, Sandeep; Singh, Thakuri; Kumar, Amit; Ahmad, Farhan Jalees; Bhatnagar, Aseem; Mittal, Gaurav

    2015-12-01

    Medical management of heavy metal toxicity, including radioactive ones, is a cause for concern because of their increased use in energy production, healthcare, and mining. Though chelating agents like EDTA and DTPA in parenteral form are available, no suitable oral formulation is there that can trap ingested heavy metal toxicants in the stomach itself, preventing their systemic absorption. The objective of the present study was to develop and optimize gastro-retentive controlled-release tablets of calcium-disodium edentate (Ca-Na2EDTA). Gastro-retentive tablet of Ca-Na2EDTA was prepared by direct compression method. Thirteen tablet formulations were designed using HPMC-K4M, sodium chloride, and carbopol-934 along with effervescing agents sodium bicarbonate and citric acid. Tablet swelling ability, in vitro buoyancy, and drug dissolution studies were conducted in 0.1 N HCl at 37 ± 0.5°C. Ca-Na2EDTA was radiolabeled with technetium-99m for scintigraphy-based in vivo evaluation. Formula F8 (Ca-Na2EDTA 200 mg, carbopol 100 mg, avicel 55 mg, citric acid 30 mg, NaHCO3 70 mg, NaCl 100 mg, and HPMC 95 mg) was found to be optimum in terms of excellent floating properties and sustained drug release. F8 fitted best for Korsmeyer-Peppas equation with an R (2) value of 0.993. Gamma scintigraphy in humans showed mean gastric retention period of 6 h. Stability studies carried out in accordance with ICH guidelines and analyzed at time intervals of 0, 1, 2, 4, and 6 months have indicated insignificant difference in tablet hardness, drug content, total floating duration, or matrix integrity of the optimized formulation. Gastro-retentive, controlled-release tablet of Ca-Na2EDTA was successfully developed using effervescent technique as a potential oral antidote for neutralizing ingested heavy metal toxicity.

  10. Disodium pentaborate decahydrate (DPD) induced apoptosis by decreasing hTERT enzyme activity and disrupting F-actin organization of prostate cancer cells.

    Science.gov (United States)

    Korkmaz, Mehmet; Avcı, Cigir Biray; Gunduz, Cumhur; Aygunes, Duygu; Erbaykent-Tepedelen, Burcu

    2014-02-01

    Animal and cell culture studies have showed that boron and its derivatives may be promising anticancer agents in prostate cancer treatment. Thus, DU145 cells were treated with disodium pentaborate decahydrate (DPD) for 24, 48, and 72 h in order to investigate the inhibitor effect and mechanisms of DPD. Then, cell proliferation, telomerase enzyme activity, actin polymerization, and apoptosis were detected by WST-1 assay, qRT-PCR, immunofluorescence labeling, and flow cytometry, respectively. We found that DPD inhibited the growth of human prostate cancer cell line DU145 at the concentration of 3.5 mM for 24 h. Our results demonstrated that 7 mM of DPD treatment prevented the telomerase enzyme activity at the rate of 38 %. Furthermore, DPD has an apoptotic effect on DU145 cells which were examined by labeling DNA breaks. With 7 mM of DPD treatment, 8, 14, and 41 % of apoptotic cells were detected for 24, 48, and 72 h, respectively. Additionally, immunofluorescence labeling showed that the normal organization of actin filaments was disrupted in DPD-exposed cells, which is accompanied by the alteration of cell shape and by apoptosis in targeted cells. Taken together, the results indicate that DPD may exert its cytotoxicity at least partly by interfering with the dynamic properties of actin polymerization and decreasing the telomerase activity. Eventually, for the first time, the results of this study showed that DPD suppressed the activity of telomerase in DU145 cells, and therefore, we suggested that DPD could be an important agent for its therapeutic potential in the treatment of prostate cancer.

  11. Preoperative Estimation of Future Remnant Liver Function Following Portal Vein Embolization Using Relative Enhancement on Gadoxetic Acid Disodium-Enhanced Magnetic Resonance Imaging

    Energy Technology Data Exchange (ETDEWEB)

    Sato, Yozo [Department of Radiology, Aichi Medical University, Aichi 480-1195 (Japan); Department of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya 464-8681 (Japan); Matsushima, Shigeru; Inaba, Yoshitaka [Department of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya 464-8681 (Japan); Sano, Tsuyoshi [Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya 464-8681 (Japan); Yamaura, Hidekazu; Kato, Mina [Department of Diagnostic and Interventional Radiology, Aichi Cancer Center Hospital, Nagoya 464-8681 (Japan); Shimizu, Yasuhiro; Senda, Yoshiki [Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya 464-8681 (Japan); Ishiguchi, Tsuneo [Department of Radiology, Aichi Medical University, Aichi 480-1195 (Japan)

    2015-11-01

    To retrospectively evaluate relative enhancement (RE) in the hepatobiliary phase of gadoxetic acid disodium-enhanced magnetic resonance (MR) imaging as a preoperative estimation of future remnant liver (FRL) function in a patients who underwent portal vein embolization (PVE). In 53 patients, the correlation between the indocyanine green clearance (ICG-K) and RE imaging was analyzed before hepatectomy (first analysis). Twenty-three of the 53 patients underwent PVE followed by a repeat RE imaging and ICG test before an extended hepatectomy and their results were further analyzed (second analysis). Whole liver function and FRL function were calculated on the MR imaging as follows: RE x total liver volume (RE Index) and FRL-RE x FRL volume (Rem RE Index), respectively. Regarding clinical outcome, posthepatectomy liver failure (PHLF) was evaluated in patients undergoing PVE. Indocyanine green clearance correlated with the RE Index (r = 0.365, p = 0.007), and ICG-K of FRL (ICG-Krem) strongly correlated with the Rem RE Index (r = 0.738, p < 0.001) in the first analysis. Both the ICG-Krem and the Rem RE Index were significantly correlated after PVE (r = 0.508, p = 0.013) at the second analysis. The rate of improvement of the Rem RE Index from before PVE to after PVE was significantly higher than that of ICG-Krem (p = 0.014). Patients with PHLF had a significantly lower Rem RE Index than patients without PHLF (p = 0.023). Relative enhancement imaging can be used to estimate FRL function after PVE.

  12. Probing the Interaction between a DNA Nucleotide (Adenosine-5'-Monophosphate Disodium) and Surface Active Ionic Liquids by Rotational Relaxation Measurement and Fluorescence Correlation Spectroscopy.

    Science.gov (United States)

    Roy, Arpita; Banerjee, Pavel; Dutta, Rupam; Kundu, Sangita; Sarkar, Nilmoni

    2016-10-02

    This article demonstrates the interaction of a deoxyribonucleic acid (DNA) nucleotide, adenosine-5'-monophosphate disodium (AMP) with a cationic surface active ionic liquid (SAIL) 1-dodecyl-3-methylimidazoium chloride (C12mimCl) and an anionic SAIL, 1-butyl-3-methylimidazolium n-octylsulfate ([C4mim][C8SO4]). Dynamic light scattering (DLS) measurements and 1H NMR (nuclear magnetic resonance) studies indicate that substantial interaction is taking place among the DNA nucleotide, AMP and the SAILs. Moreover, cryogenic transmission electron microscopy (cryo-TEM) suggests that SAILs containing micellar assemblies are transformed into larger micellar assemblies in presence of DNA nucleotide. Additionally, the rotational motion of two oppositely charged molecules, Rhodamine 6G perchlorate (R6G) and Fluorescein sodium salt (Fl-Na) have been monitored in these aggregates. The rotational motion of R6G and Fl-Na differs significantly between SAILs micelles, and SAILs-AMP containing larger micellar aggregates. The effect of negatively charged DNA nucleotide (AMP) addition into the cationic and anionic SAILs is more prominent for the cationic charged molecule R6G than that of anionic probe Fl-Na due to the favourable electrostatic interaction between the AMP and cationic R6G. Moreover, the influence of the anionic DNA nucleotide on the cationic and anionic SAIL micelles is monitored through the variation of the lateral diffusion motion of oppositely charged probe molecules (R6G and Fl-Na) inside these aggregates. This variation in diffusion coefficient values also suggests that interaction pattern of these oppositely charged probes are different within the SAILs-nucleotide containing aggregates. Therefore, both rotational and translational diffusion measurements confirm that the DNA nucleotide (AMP) renders more rigid microenvironment within the micellar solution of SAILs.

  13. Cromoglycate, not ketotifen, ameliorated the injured effect of warm ischemia/reperfusion in rat liver: role of mast cell degranulation, oxidative stress, proinflammatory cytokine, and inducible nitric oxide synthase

    Directory of Open Access Journals (Sweden)

    El-Shitany NA

    2015-09-01

    Full Text Available Nagla A El-Shitany,1,2 Karema El-Desoky3 1Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia; 2Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tanta University, Tanta, Egypt; 3Department of Pathology, Faculty of Medicine, Tanta University, Tanta, Egypt Abstract: Hepatic ischemia/reperfusion (ISCH/REP is a major clinical problem that is considered to be the most common cause of postoperative liver failure. Recently, mast cells have been proposed to play an important role in the pathophysiology of ISCH/REP in many organs. In contrast, the role played by mast cells during ISCH/REP-induced liver damage has remained an issue of debate. This study aimed to investigate the protective role of mast cells in order to search for an effective therapeutic agent that could protect against fatal ISCH/REP-induced liver damage. A model of warm ISCH/REP was induced in the liver of rats. Four groups of rats were used in this study: Group I: SHAM (normal saline, intravenously [iv]; Group II: ISCH/REP; Group III: sodium cromoglycate + ISCH/REP (CROM + ISCH/REP, and Group IV: ketotifen (KET + ISCH/REP (KET + ISCH/REP. Liver damage was assessed both histopathologically and biochemically. Mast cell degranulation was assessed histochemically. Lipid peroxidation (malondialdehyde [MDA] as well as the levels of glutathione (GSH, interleukin-6 (IL-6, and tumor necrosis factor alpha (TNF-α, the formation of nitric oxide (NO, and the expression of inducible NO synthase (iNOS were determined. The results of this study revealed increased mast cell degranulation in the liver during the acute phase of ISCH/REP. Moreover, CROM, but not KET, decreased the activity of alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase and maintained normal liver tissue histology. Both CROM and KET protected against mast cell degranulation in the liver. In addition, both CROM and KET decreased IL

  14. Dietary supplementation of pyrroloquinoline quinone disodium protects against oxidative stress and liver damage in laying hens fed an oxidized sunflower oil-added diet.

    Science.gov (United States)

    Wang, J; Zhang, H J; Xu, L; Long, C; Samuel, K G; Yue, H Y; Sun, L L; Wu, S G; Qi, G H

    2016-07-01

    The protective effects of dietary pyrroloquinoline quinone disodium (PQQ.Na2) supplementation against oxidized sunflower oil-induced oxidative stress and liver injury in laying hens were examined. Three hundred and sixty 53-week-old Hy-Line Gray laying hens were randomly allocated into one of the five dietary treatments. The treatments included: (1) a diet containing 2% fresh sunflower oil; (2) a diet containing 2% thermally oxidized sunflower oil; (3) an oxidized sunflower oil diet with 100 mg/kg of added vitamin E; (4) an oxidized sunflower oil diet with 0.08 mg/kg of PQQ.Na2; and (5) an oxidized sunflower oil diet with 0.12 mg/kg of PQQ.Na2. Birds fed the oxidized sunflower oil diet showed a lower feed intake compared to birds fed the fresh oil diet or oxidized oil diet supplemented with vitamin E (P=0.009). Exposure to oxidized sunflower oil increased plasma malondialdehyde (Pdiet were modulated by dietary vitamin E or PQQ.Na2 supplementation to levels comparable to the fresh oil group. Dietary supplementation with PQQ.Na2 or vitamin E increased the activities of total superoxide dismutase and glutathione peroxidase in plasma and the liver, when compared with the oxidized sunflower oil group (Pdiet induced elevation of liver weight (P=0.026), liver to BW ratio (P=0.001) and plasma activities of alanine aminotransferase (P=0.001) and aspartate aminotransferase (Pdiet. Furthermore, oxidized sunflower oil increased hepatic DNA tail length (Pdiet induced DNA tail length and tail moment to the basal levels in fresh oil diet. These results indicate that PQQ.Na2 is a potential antioxidant and is as effective against oxidized oil-related liver injury in laying hens as vitamin E. The protective effects of PQQ.Na2 against liver damage induced by oxidized oil may be partially due to its role in the scavenging of free radicals, inhibiting of lipid peroxidation and enhancing of antioxidant defense systems.

  15. Determination of disodium pamidronate for injection by HPLC pre- column derivatization with FMOC- Cl%FMOC-C1柱前衍生化HPLC法测定注射用帕米膦酸二钠的含量

    Institute of Scientific and Technical Information of China (English)

    林慧菁; 杨乐; 范梅娟; 廖瑜

    2012-01-01

    目的:建立氯甲酸-9-芴甲酯(FMOC-a)柱前衍生化HPLC法测定注射用帕米膦酸二钠的含量.方法:碱性条件下供试品与FMOC -Cl进行衍生化反应,采用Hypersil ODS2(4.6mm×250 mm,5 μm)色谱柱,流动相为乙腈-0.4%EDTA溶液(用1 mol·L-1氢氧化钠溶液调节pH至7.2)(25:75),流速1 mL·min-1,检测波长为265 nm.结果:帕米膦酸二钠浓度在0.05 ~1.00 ng·mL-1范围内与峰面积呈良好关系(r =0.9998),平均回收率为101.0%(n=9).结论:该方法专属性好,适合用于注射用帕米膦酸二钠的含量测定.%Objective:To develop an HPLC method with pre -column derivatization for the determination of disodium pamidronate for injection.Methods:Disodium pamidronate was derivatized with 9- fluorenylmethyl chloroformate (FMOC-C1) in 0.05 mol o L-1 Na2CO3 solution, the analytical column was Hypersil ODS2(4.6 mm × 250 mm, 5 μm) column.The mobile phase consisted of acetonitrile -0.4% EDTA(pH adjusted to 7.2 with 1 mol o L-1 sodium hydroxide solution)(25:75) at the flow rate of 1.0 mL o min-1 ,and the detection wavelength was 265 run.Results: The linear range was 0.05- 1.00 mg o mL-1 (r = 0.9998), and the average recovery was 101.0% (n =9).Conclusion:The method is specific and can be used for determination of disodium pamidronate for injection.

  16. The effect of carrier surface and bulk properties on drug particle detachment from crystalline lactose carrier particles during inhalation, as function of carrier payload and mixing time

    NARCIS (Netherlands)

    Dickhoff, B.H.J.; de Boer, Anne; Lambregts, D.; Frijlink, H.W.

    2003-01-01

    The effect of carrier payload and mixing time on the redispersion of drug particles from adhesive mixtures during inhalation for two different drugs (budesonide and disodium cromoglycate) has been investigated. A special test inhaler which retains carrier crystals during inhalation was used at 30 an

  17. Disodium terephthalate (Na{sub 2}C{sub 8}H{sub 4}O{sub 4}) as high performance anode material for low-cost room-temperature sodium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Liang; Hu, Yong-Sheng; Li, Hong; Armand, Michel; Chen, Liquan [Key Laboratory for Renewable Energy, Beijing Key Laboratory for New, Energy Materials and Devices, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing (China); Zhao, Junmei [Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing (China); Zhou, Zhibin [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan (China)

    2012-08-15

    In this contribution, a cheap organic material, disodium terephthalate, Na{sub 2}C{sub 8}H{sub 4}O{sub 4}, has been firstly evaluated as a novel anode for room-temperature Na-ion batteries. The material exhibits a high reversible capacity of 250 mAh/g with excellent cycleability. The average Na storage voltage is approximately 0.43 V vs. Na{sup +}/Na. A thin layer of Al{sub 2}O{sub 3} coating on the electrode surface derived from the atomic layer deposition technique is effective in further enhancing Na storage performance. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Study on bacterial endotoxins test of disodium cantharidinate and vitamin B_6 injection%斑蝥酸钠维生素B_6注射液细菌内毒素检查法研究

    Institute of Scientific and Technical Information of China (English)

    王贵英; 唐继坤; 潘正兴

    2009-01-01

    Objective:To establish a method for determination of the bacterial endotoxin test in disodium cantharidinate and vitamin B_6 injection.Method:Inhibition and bacterial endotoxin test was performed with amebcyte lysate manufactured by different companies with different specifications according to the method of bacterial endotoxin test approved by Chinese Pharmacopoeia 2005 edition.Results:The original solution had non-interference with the bacterial endotoxin test.The results of bacteria endotoxin test in six batchs all accorded with the standard of the quality control.Conclusion:The results suggested that bacteria endotoxin test can be used as an alternative method for the rabbit pyrogen test for disodium cantharidinate and vitamin B_6 injection.The limits of bacterial endotoxin was 6 EU·mg~(-1).%目的:建立斑蝥酸钠维生素B6注射液的细菌内毒素检查方法.方法:按中国药典2005年版二部附录XIE细菌内毒素检查法进行,用小同厂家不同规格的鲎试剂对小同批号的斑蝥酸钠维牛素B_6注射液进行了干扰试验和细菌内毒素检查.结果:本品原液对细菌内毒素检查无干扰作用.按拟定标准检验,该品种6批样品细菌内毒素检查结果均符合规定.结论:本品可用细菌内毒素检查法代替家兔热原检查法,其细菌内毒素的限值(L)为6 EU·mL~(-1).

  19. Hyaluronidase inhibitors (sodium cromoglycate and sodium auro-thiomalate) reduce the local tissue damage and prolong the survival time of mice injected with Naja kaouthia and Calloselasma rhodostoma venoms.

    Science.gov (United States)

    Yingprasertchai, Senee; Bunyasrisawat, Srisurat; Ratanabanangkoon, Kavi

    2003-11-01

    Experiments have been carried out to find potent inhibitors of hyaluronidases of Naja kaouthia (NK) and Calloselasma rhodostoma (CR) venoms with the aim of reducing local tissue damage and systemic toxicities caused by the venoms. Seven drugs/chemicals known to inhibit hyaluronidases were tested for their activity on venom enzymes. These were: sodium cromoglycate (SC), sodium aurothiomalate (SAT), apigenin, kaemferol, phenylbutazone, oxyphenbutazone and fenoprofen. The results showed that SC or SAT at 10 mM, completely inhibited the enzymes of both venoms. In in vivo experiments, SC or SAT, when incubated with NK venom prior to injection, significantly reduced edema and myonecrosis. In the case of CR venom, hemorrhage, in addition to edema and myonecrosis, was also significantly reduced. In the independent type experiment, SC or SAT were effective if injected within 1 min after the injection of venom. At longer time intervals of 3 and 10 min the inhibitors were effective in reducing some parameters of local tissue necrosis but the extent of inhibition was lower. SC and SAT at 256 and 195 microg/mouse, respectively, significantly prolonged the survival time of mice receiving lethal doses of NK. In the case of CR venoms, the two inhibitors not only prolonged the survival time but also prevented death of mice receiving lethal doses of the venom. The other inhibitors were poorly soluble in water and were studied only on enzyme inhibition and prolongation of survival time; they were mostly ineffective. Thus, SC and SAT when injected immediately at the sites of bites can reduce the systemic and local toxicity of NK and CR venoms. These results suggest that administration of these drugs at the site of venom injection may be useful in reducing venom-induced local tissue damage.

  20. Sodium cromoglycate attenuates experimental endometriosis in rats by regulating mast cells%色甘酸钠对子宫内膜异位症大鼠肥大细胞功能的调节作用

    Institute of Scientific and Technical Information of China (English)

    朱丽波; 林开清; 张信美; 林俊

    2015-01-01

    目的:探讨色甘酸钠干预对子宫内膜异位症大鼠肥大细胞的影响及相关机制。方法:取健康雌性未孕SD大鼠36只,采用自体子宫内膜移植法建立大鼠腹壁子宫内膜异位症模型,2周后根据每天腹腔注射不同剂量色甘酸钠将大鼠分为4组:大剂量组(色甘酸钠20 mg/kg )、小剂量组(色甘酸钠10 mg/kg )、阴性对照组(仅注射生理盐水)、空白对照组(模型不作任何处理)。两周后处死大鼠,并收集血液和病灶组织标本,测量各组子宫内膜异位症病灶的大小,并对病灶组织进行苏木素—伊红( HE)染色观察组织形态及角蛋白和波形蛋白免疫组织化学染色以鉴定造模是否成功。用甲苯胺蓝染色法检测各组病灶肥大细胞总数及其脱颗粒肥大细胞数、酶联免疫吸附试验测定血清肿瘤坏死因子α( TNF-α)水平、酶免疫分析法测定血清雌二醇水平、免疫组织化学染色法检测子宫内膜异位症病灶肥大细胞中类胰蛋白酶、神经生长因子的表达水平。结果:大剂量组活化的肥大细胞数少于阴性对照组( P<0.05),脱颗粒肥大细胞数/肥大细胞总数比值大剂量组小于阴性对照组和空白对照组(均P<0.05)。同时,该组血清TNF-α水平、病灶类胰蛋白酶表达均小于阴性对照组和空白对照组(均P<0.05);但经色甘酸钠治疗后子宫内膜异位症病灶神经生长因子表达差异并无统计学意义(均P>0.05)。结论:色甘酸钠可能通过稳定肥大细胞抑制其脱颗粒,减少TNF-α、类胰蛋白酶的释放,改善子宫内膜异位症。%Objective: To investigate the effect of sodium cromoglycate on experimental endometriosis in rats .Methods: Endometriosis model was established in 36 unpregnant female SD rats by transplanting autologous fragments of endometrium to the inner surface of the abdominal wall .The

  1. Clinical Observation of Desloratadine Citrate Disodium in the Decremental Treatment of Chronic Urticaria%枸地氯雷他定递减疗法治疗慢性荨麻疹的临床观察Δ

    Institute of Scientific and Technical Information of China (English)

    2015-01-01

    目的:观察枸地氯雷他定递减疗法治疗慢性荨麻疹的临床疗效和安全性。方法:212例慢性荨麻疹患者随机均分为递减疗法组和对照组。递减疗法组患者按递减疗法给予枸地氯雷他定胶囊:第1周17.6 mg,口服,每日1次;第2周8.8 mg,口服,每日1次;第3周8.8 mg,口服,2天1次;第4周8.8 mg,口服,3天1次。对照组患者给予枸地氯雷他定胶囊8.8 mg,口服,每日1次。两组患者疗程均为4周。观察两组患者的临床疗效,治疗前后血清免疫球蛋白E(IgE)水平、临床症状评分、复发率及不良反应发生情况。结果:两组患者总有效率、不良反应发生率比较,差异均无统计学意义(P>0.05),递减疗法组复发率显著低于对照组,差异有统计学意义(P<0.05)。治疗结束时及停药4周后,两组患者血清IgE水平均显著低于同组治疗前,且停药4周后递减疗法组低于对照组,差异均有统计学意义(P<0.01);对照组患者停药4周时IgE水平显著高于治疗结束时,差异有统计学意义(P<0.01)。治疗后,两组患者临床症状评分均显著低于同组治疗前,差异有统计学意义(P<0.01);但两组间比较,差异无统计学意义(P>0.05)。结论:枸地氯雷他定递减疗法与常规疗法治疗慢性荨麻疹的临床疗效和安全性均相当,但在改善血清IgE方面,枸地氯雷他定递减疗法优于常规疗法。%OBJECTIVE:To observe the clinical efficacy and safety of the effect of desloratadine citrate disodium in the decre-mental treatment of chronic urticaria. METHODS:212 patients with chronic urticaria were randomly divided into decremental treat-ment group and control group. Decremental treatment group was treated with Desloratadine citrate disodium capsules 17.6 mg in the first week,orally,qd;8.8 mg in the second week,orally,qd;8.8 mg in the third week,orally,qod;and 8.8 mg in

  2. 枸地氯雷他定与依匹斯汀治疗慢性荨麻疹随机对照研究%Desloratadine citrate disodium versus epinastine for the treatment of chronic urticaria: a randomized controlled trial

    Institute of Scientific and Technical Information of China (English)

    闫毅; 刘瑞珍; 徐德钢

    2015-01-01

    Objective To evaluate the efficacy and safety of desloratadine citrate disodium versus epinastine for the treatment of chronic urticaria (CU).Methods A randomized,double-blind,double-dummy controlled clinical trial was conducted.Patients with CU were divided into test group and control group to be treated by oral desloratadine citrate disodium (8.8 mg/d) and epinastine (10 mg/d) respectively once a day for 28 days.All the patients were followed up after starting treatment.Therapeutic effect was evaluated,and adverse reactions were observed.Results One hundred and fifty-seven patients were enrolled in this study,and 142 patients were valid for evaluation of efficacy and safety at the end of study.After treatment for 28 days,there was no significant difference between the test group and control group in response rate (81.16 % vs.78.08 %,P > 0.05) or incidence rate of adverse reactions (13.89 % vs.12.16 %,P> 0.05).Conclusion Desloratadine citrate disodium is effective and safe for the treatment of CU.%目的 探讨枸地氯雷他定和依匹斯汀治疗慢性荨麻疹的疗效和安全性.方法 随机、双盲、双模拟和对照研究.试验组服枸地氯雷他定胶囊每日1次,每次8.8 mg,对照组依匹斯汀胶囊每日1次,每次10 mg,均连续服用28 d.于用药后随访,观察疗效和不良反应.结果 入选病例157例,可评价疗效和安全性病例142例.经28 d治疗后,枸地氯雷他定组有效率81.16%、依匹斯汀组有效率78.08%,两组比较差异无统计学意义(P>0.05).枸地氯雷他定组和对照组药物相关性不良反应发生率分别为13.89%和12.16%,两组比较差异无统计学意义(P>0.05).结论 枸地氯雷他定治疗慢性荨麻疹安全有效.

  3. Cromoglycate, not ketotifen, ameliorated the injured effect of warm ischemia/reperfusion in rat liver: role of mast cell degranulation, oxidative stress, proinflammatory cytokine, and inducible nitric oxide synthase

    Science.gov (United States)

    El-Shitany, Nagla A; El-Desoky, Karema

    2015-01-01

    Hepatic ischemia/reperfusion (ISCH/REP) is a major clinical problem that is considered to be the most common cause of postoperative liver failure. Recently, mast cells have been proposed to play an important role in the pathophysiology of ISCH/REP in many organs. In contrast, the role played by mast cells during ISCH/REP-induced liver damage has remained an issue of debate. This study aimed to investigate the protective role of mast cells in order to search for an effective therapeutic agent that could protect against fatal ISCH/REP-induced liver damage. A model of warm ISCH/REP was induced in the liver of rats. Four groups of rats were used in this study: Group I: SHAM (normal saline, intravenously [iv]); Group II: ISCH/REP; Group III: sodium cromoglycate + ISCH/REP (CROM + ISCH/REP), and Group IV: ketotifen (KET) + ISCH/REP (KET + ISCH/REP). Liver damage was assessed both histopathologically and biochemically. Mast cell degranulation was assessed histochemically. Lipid peroxidation (malondialdehyde [MDA]) as well as the levels of glutathione (GSH), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF-α), the formation of nitric oxide (NO), and the expression of inducible NO synthase (iNOS) were determined. The results of this study revealed increased mast cell degranulation in the liver during the acute phase of ISCH/REP. Moreover, CROM, but not KET, decreased the activity of alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase and maintained normal liver tissue histology. Both CROM and KET protected against mast cell degranulation in the liver. In addition, both CROM and KET decreased IL-6 and TNF-α. However, CROM, but not KET, decreased MDA formation and increased GSH. Furthermore, KET, but not CROM, increased both NO formation and iNOS expression. In conclusion, this study clearly demonstrated mast cell degranulation in warm ISCH/REP in the liver of rats. More importantly, CROM, but not KET, ameliorated the effect of ISCH

  4. Cromoglycate, not ketotifen, ameliorated the injured effect of warm ischemia/reperfusion in rat liver: role of mast cell degranulation, oxidative stress, proinflammatory cytokine, and inducible nitric oxide synthase.

    Science.gov (United States)

    El-Shitany, Nagla A; El-Desoky, Karema

    2015-01-01

    Hepatic ischemia/reperfusion (ISCH/REP) is a major clinical problem that is considered to be the most common cause of postoperative liver failure. Recently, mast cells have been proposed to play an important role in the pathophysiology of ISCH/REP in many organs. In contrast, the role played by mast cells during ISCH/REP-induced liver damage has remained an issue of debate. This study aimed to investigate the protective role of mast cells in order to search for an effective therapeutic agent that could protect against fatal ISCH/REP-induced liver damage. A model of warm ISCH/REP was induced in the liver of rats. Four groups of rats were used in this study: Group I: SHAM (normal saline, intravenously [iv]); Group II: ISCH/REP; Group III: sodium cromoglycate + ISCH/REP (CROM + ISCH/REP), and Group IV: ketotifen (KET) + ISCH/REP (KET + ISCH/REP). Liver damage was assessed both histopathologically and biochemically. Mast cell degranulation was assessed histochemically. Lipid peroxidation (malondialdehyde [MDA]) as well as the levels of glutathione (GSH), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF-α), the formation of nitric oxide (NO), and the expression of inducible NO synthase (iNOS) were determined. The results of this study revealed increased mast cell degranulation in the liver during the acute phase of ISCH/REP. Moreover, CROM, but not KET, decreased the activity of alanine aminotransferase, aspartate aminotransferase, and lactic dehydrogenase and maintained normal liver tissue histology. Both CROM and KET protected against mast cell degranulation in the liver. In addition, both CROM and KET decreased IL-6 and TNF-α. However, CROM, but not KET, decreased MDA formation and increased GSH. Furthermore, KET, but not CROM, increased both NO formation and iNOS expression. In conclusion, this study clearly demonstrated mast cell degranulation in warm ISCH/REP in the liver of rats. More importantly, CROM, but not KET, ameliorated the effect of ISCH

  5. A double-blind, randomized, comparative study of the use of a combination of uridine triphosphate trisodium, cytidine monophosphate disodium, and hydroxocobalamin, versus isolated treatment with hydroxocobalamin, in patients presenting with compressive neuralgias

    Directory of Open Access Journals (Sweden)

    Goldberg H

    2017-02-01

    Full Text Available Henrique Goldberg,1 Marco Antonio Mibielli,2 Carlos Pereira Nunes,2 Stephanie Wrobel Goldberg,3 Luiz Buchman,4 Spyros GE Mezitis,5 Helio Rzetelna,6 Lisa Oliveira,2 Mauro Geller,2 Fernanda Wajnsztajn7 1UERJ Medical School, Rio de Janeiro, Brazil; 2UNIFESO Medical School, Teresópolis, Brazil; 3Washington University School of Medicine, St Louis, MO, USA; 4Instituto de Pós-Graduação Médica Carlos Chagas (ICC, Rio de Janeiro, Brazil; 5New York-Presbyterian Hospital/Weill-Cornell Medical Center, New York, NY, USA; 6Santa Casa da Misericórdia do Rio de Janeiro, Rio de Janeiro, Brazil; 7New York-Presbyterian Hospital/Columbia University Medical Center, Neurology, New York, NY, USA Context: This paper reports on the results of treatment of compressive neuralgia using a combination of nucleotides (uridine triphosphate trisodium [UTP] and cytidine monophosphate disodium [CMP] and vitamin B12.Objectives: To assess the safety and efficacy of the combination of nucleotides (UTP and CMP and vitamin B12 in patients presenting with neuralgia arising from neural compression associated with degenerative orthopedic alterations and trauma, and to compare these effects with isolated administration of vitamin B12. Methods: A randomized, double-blind, controlled trial, consisting of a 30-day oral treatment period: Group A (n=200 receiving nucleotides + vitamin B12, and Group B (n=200 receiving vitamin B12 alone. The primary study endpoint was the percentage of subjects presenting pain visual analog scale (VAS scores ≤20 at end of study treatment period. Secondary study endpoints included the percentage of subjects presenting improvement ≥5 points on the patient functionality questionnaire (PFQ; percentage of subjects presenting pain reduction (reduction in VAS scores at study end in relation to pretreatment; and number of subjects presenting adverse events. Results: The results of this study showed a more expressive improvement in efficacy evaluations among

  6. 枸地氯雷他定治疗过敏性鼻炎疗效观察%Efficacy of Desloratadine Citrate Disodium in the Treatment of Allergic Rhinitis

    Institute of Scientific and Technical Information of China (English)

    俞静

    2015-01-01

    Objective:To observe the clinical effect and safety of desloratadine citrate disodium in the treatment of allergic rhinitis ( AR) . Methods:Totally 80 patients were randomly divided into the control group and the observation group with 40 ones in each. There was no difference in gender, age, duration of allergic rhinitis, classification of serological specificity IgE between the two groups (P>0. 05). The observation group was treated with desloratadine citrate disodium tablets 8. 8mg, po, qd. The control group was given loratadine 10mg, po, qd. The treatment course was 12 days. All the patients were not given corticosteroids and other antihistamines. The clinical symptoms and signs integral, curative effect and adverse drug reactions during the treatment were observed. Results: In the observation group, 23 cases were markedly effective, 13 cases were effective, 3 cases were ineffective, one case didn’ t finish the study, and the total effective rate was 92. 30%. In the control group, the above index was 10 cases, 18 cases, 10 cases, 2 cases and 73. 68%, respectively. There was statistically significant difference in the total effective rate between the two groups (P0.05),观察组予以枸地氯雷他定片8.8 mg,po,qd,连续服用12 d。对照组予以氯雷他定10 mg,po, qd,连续服用12 d。所有观察患者均不使用皮质类固醇及其他抗组胺药物。观察两组患者治疗前后症状及体征积分、临床疗效及药品不良反应。结果:观察组显效23例,有效13例,无效3例,脱失1例,总有效率92.30%;对照组显效10例,有效18例,无效10例,脱失2例,总有效率73.68%;两组总有效率比较,差异有统计学意义(P<0.05)。观察组治疗后各项症状体征积分与对照组相比有明显降低,差异有统计学意义(P<0.05)。观察组药品不良反应发生率明显少于对照组。结论:枸地氯雷他定片治疗AR临床疗效优于氯雷他定,安全性好。

  7. A double-blind, randomized, comparative study of the use of a combination of uridine triphosphate trisodium, cytidine monophosphate disodium, and hydroxocobalamin, versus isolated treatment with hydroxocobalamin, in patients presenting with compressive neuralgias

    Science.gov (United States)

    Goldberg, Henrique; Mibielli, Marco Antonio; Nunes, Carlos Pereira; Goldberg, Stephanie Wrobel; Buchman, Luiz; Mezitis, Spyros GE; Rzetelna, Helio; Oliveira, Lisa; Geller, Mauro; Wajnsztajn, Fernanda

    2017-01-01

    Context This paper reports on the results of treatment of compressive neuralgia using a combination of nucleotides (uridine triphosphate trisodium [UTP] and cytidine monophosphate disodium [CMP]) and vitamin B12. Objectives To assess the safety and efficacy of the combination of nucleotides (UTP and CMP) and vitamin B12 in patients presenting with neuralgia arising from neural compression associated with degenerative orthopedic alterations and trauma, and to compare these effects with isolated administration of vitamin B12. Methods A randomized, double-blind, controlled trial, consisting of a 30-day oral treatment period: Group A (n=200) receiving nucleotides + vitamin B12, and Group B (n=200) receiving vitamin B12 alone. The primary study endpoint was the percentage of subjects presenting pain visual analog scale (VAS) scores ≤20 at end of study treatment period. Secondary study endpoints included the percentage of subjects presenting improvement ≥5 points on the patient functionality questionnaire (PFQ); percentage of subjects presenting pain reduction (reduction in VAS scores at study end in relation to pretreatment); and number of subjects presenting adverse events. Results The results of this study showed a more expressive improvement in efficacy evaluations among subjects treated with the combination of nucleotides + vitamin B12, with a statistically significant superiority of the combination in pain reduction (evidenced by VAS scores). There were adverse events in both treatment groups, but these were transitory and no severe adverse event was recorded during the study period. Safety parameters were maintained throughout the study in both treatment groups. Conclusion The combination of uridine, cytidine, and vitamin B12 was safe and effective in the treatment of neuralgias arising from neural compression associated with degenerative orthopedic alterations and trauma. PMID:28243144

  8. Safety and efficacy of a novel drug elores (ceftriaxone + sulbactam + disodium edetate in the management of multi-drug resistant bacterial infections in tertiary care centers: a post-marketing surveillance study

    Directory of Open Access Journals (Sweden)

    Manu Chaudhary

    Full Text Available Abstract Objective: In India, Elores (CSE-1034: ceftriaxone + sulbactam + disodium edetate was approved as a broad spectrum antibiotic in year 2011 and is used for management of Extended Spectrum Beta Lactamases/Metallo Beta lactamases infections in tertiary care centers. The objective of this study was to investigate the efficacy of this drug in patients with Extended Spectrum Beta Lactamases/Metallo Beta lactamases infections and identify the incidence of adverse events in real clinical settings. Methods: This Post Marketing Surveillance study was conducted at 17 centers across India and included 2500 patients of all age groups suffering from various bacterial infections and treated with Elores (CSE1034. Information regarding demographic, clinical and microbiological parameters, dosage and treatment duration, efficacy and adverse events (AEs associated with the treatment were recorded. Results: A total of 2500 patients were included in the study and efficacy was evaluated in 2487 patients. In total, 409 AEs were reported in 211 (8.4% patients. The major AEs reported were vomiting (3.0%, pain at injection site (2.5%, nausea (2.3%, redness at site (1.96%, thrombophlebitis (1.4%. Of total reported AEs, 40 (5.3% AEs were reported in pediatric, 310 (20.6% in adult, and 59 (23.6% in geriatric group. No AE belonging to grade IV or V was reported in any patient. In terms of efficacy, 1977 (79.4% patients were cured, 501 (20.1% patients showed clinical improvement and 5 (0.2% patients were complete failure. The treatment duration varied from 5 to 7 days in different patients depending on the infection type. Conclusion: In this post-marketing surveillance study, CSE-1034 was found to be an effective and safe option against Pip tazo and meropenem in management of patients with multi-drug resistant (MDR bacterial infections under routine ward settings.

  9. Safety and efficacy of a novel drug elores (ceftriaxone+sulbactam+disodium edetate) in the management of multi-drug resistant bacterial infections in tertiary care centers: a post-marketing surveillance study.

    Science.gov (United States)

    Chaudhary, Manu; Mir, Mohd Amin; Ayub, Shiekh Gazalla

    In India, Elores (CSE-1034: ceftriaxone+sulbactam+disodium edetate) was approved as a broad spectrum antibiotic in year 2011 and is used for management of Extended Spectrum Beta Lactamases/Metallo Beta lactamases infections in tertiary care centers. The objective of this study was to investigate the efficacy of this drug in patients with Extended Spectrum Beta Lactamases/Metallo Beta lactamases infections and identify the incidence of adverse events in real clinical settings. This Post Marketing Surveillance study was conducted at 17 centers across India and included 2500 patients of all age groups suffering from various bacterial infections and treated with Elores (CSE1034). Information regarding demographic, clinical and microbiological parameters, dosage and treatment duration, efficacy and adverse events (AEs) associated with the treatment were recorded. A total of 2500 patients were included in the study and efficacy was evaluated in 2487 patients. In total, 409 AEs were reported in 211 (8.4%) patients. The major AEs reported were vomiting (3.0%), pain at injection site (2.5%), nausea (2.3%), redness at site (1.96%), thrombophlebitis (1.4%). Of total reported AEs, 40 (5.3%) AEs were reported in pediatric, 310 (20.6%) in adult, and 59 (23.6%) in geriatric group. No AE belonging to grade IV or V was reported in any patient. In terms of efficacy, 1977 (79.4%) patients were cured, 501 (20.1%) patients showed clinical improvement and 5 (0.2%) patients were complete failure. The treatment duration varied from 5 to 7 days in different patients depending on the infection type. In this post-marketing surveillance study, CSE-1034 was found to be an effective and safe option against Pip tazo and meropenem in management of patients with multi-drug resistant (MDR) bacterial infections under routine ward settings. Copyright © 2017 Sociedade Brasileira de Infectologia. Published by Elsevier Editora Ltda. All rights reserved.

  10. 电解质对十二烷基二苯醚双磺酸钠与癸烷间界面张力的影响%Effect of electrolyte on interface tension between disodium dodecyl diphenyloxide disulfonate and decane

    Institute of Scientific and Technical Information of China (English)

    刘晓臣; 沈宏; 牛金平; 王晓宇

    2015-01-01

    The effect of electrolyte (NaCl, CaCl2 and MgCl2) on interfacial tension of disodium dodecyl di⁃phenyloxide disulfonate aqueous solution and decane was investigated. Addition of NaCl, CaCl2 or MgCl2 could decrease interfacial tension, and the interfacial tension could be kept in the range of 10-1 mN/m. The time re⁃quired for interfacial tension to reach equilibrium decreased with the increase of electrolyte concentration. Ef⁃fect of CaCl2 and MgCl2 concentration on equilibrium interfacial tension was almost the same. When NaCl and CaCl2 were added at the same time, effect of CaCl2 concentration on the time required for interfacial tension reaching equilibrium decreased with the NaCl concentration increasing.%研究了电解质NaCl、CaCl2和MgCl2对十二烷基二苯醚双磺酸钠水溶液/癸烷间界面张力的影响.NaCl、CaCl2和MgCl2的加入可以降低界面张力,且界面张力保持在10-1 mN/m数量级.随着电解质浓度的增加,界面张力达到平衡所需时间减少.CaCl2和MgCl2质量浓度对平衡界面张力的影响基本一致.同时加入电解质NaCl和CaCl2,当NaCl质量浓度增大时,CaCl2质量浓度对界面张力达到平衡所需时间的影响减小.

  11. 鼻舒适片联合枸地氯雷他定治疗过敏性鼻炎的临床研究%Clinical study on Bishushi Tablets combined with desloratadine citrate disodium in treatment of allergic rhinitis

    Institute of Scientific and Technical Information of China (English)

    陈阳静; 李宏慧; 赵瑞敏; 赵谦

    2016-01-01

    目的:探讨鼻舒适片联合枸地氯雷他定治疗过敏性鼻炎的临床疗效。方法选取2015年1月—2016年1月西安交通大学第一附属医院接受治疗的过敏性鼻炎患者138例,随机分为对照组和治疗组,每组各69例。对照组口服枸地氯雷他定胶囊,1粒/次,1次/d。治疗组在对照组的治疗基础上口服鼻舒适片,5片/次,3次/d。两组均连续治疗12 d。观察两组的临床疗效,同时比较两组治疗前后症状积分、白三烯 B4(LTB4)、IL-4、IL-10、IL-12、转化生长因子α(TGF-α)、γ-干扰素(IFN-γ)、IgE 的变化情况。结果治疗后,对照组和治疗组的总有效率分别为85.51%、95.65%,两组比较差异具有统计学意义(P<0.05)。治疗后,两组患者症状(包括鼻塞、鼻痒、喷嚏、流涕)评分、总分、IL-4、IL-10、TGF-α、LTB4、IgE 水平均显著降低,IL-12、IFN-γ水平显著升高,同组治疗前后差异有统计学意义(P<0.05);且治疗组这些观察指标的改善程度优于对照组,两组比较差异有统计学意义(P<0.05)。结论鼻舒适片联合枸地氯雷他定治疗过敏性鼻炎具有较好的临床疗效,可改善患者的临床症状,改善各检测因子水平,具有一定的临床推广应用价值。%Objective To explore the clinical efficacy of Bishushi Tablets combined with desloratadine citrate disodium in treatment of allergic rhinitis. Methods Patients (138 cases) with allergic rhinitis in the First Affiliated Hospital of Xi’an Jiaotong University from January 2015 to January 2016 were randomly divided into control and treatment groups, and each group had 69 cases. The patients in the control group were po administered with Desloratadine Citrate Disodium Capsules, 1 grain/time, once daily. The patients in the treatment group were po administered with Bishushi Tablets on the basis of the control group, 5 tablets/time, three times daily. The

  12. Therapeutic effect of desloratadine citrate disodium tablets combined with narrow band ultraviolet B in the treatment of pityriasis rosea%枸地氯雷他定联合窄谱中波紫外线治疗玫瑰糠疹疗效观察

    Institute of Scientific and Technical Information of China (English)

    闫锐; 徐爱国; 黄晨

    2015-01-01

    Objective To observe the clinical efficacy of desloratadine citrate disodium tablets combined with narrow band ultraviolet B in the treatment of pityriasis rosea.Methods According to the digital table,88 pityriasis rosea patients were randomly divided into the two groups.45 cases of the study group were treated by desloratadine citrate disodium tablets combined with narrow ultraviolet B,43 cases of the control group were treated by desloratadine citrate disodium tablets alone.The both two groups applied Binghuangfule cream.The therapeutic effect and safety of the two groups were compared.Results The cure rate in study group was 71.11%,which of the control group was 51.16%,the difference was not statistically significant (x2 =3.69,P > 0.05).The effective rate of the treatment group was 91.11%,which of the control group was 69.77%,the difference between the two groups was statistically significant (x2 =6.43,P < 0.05).Conclusion The result reveals that desloratadine citrate disodium tablets combined with narrow band ultraviolet B is more effective and worthy to be used in clinical practice.%目的 观察枸地氯雷他定口服联合窄谱中波紫外线(NB-UVB)照射治疗玫瑰糠疹的疗效.方法 选择88例玫瑰糠疹患者,采用随机数字表法分为两组.治疗组45例采用口服枸地氯雷他定联合NB-UVB照射,对照组43例口服枸地氯雷他定,两组均外用冰黄肤乐软膏.观察两组的治疗效果和安全性.结果 治疗组痊愈率71.11%,有效率91.11%;对照组痊愈率51.16%,有效率69.77%,治疗组痊愈率优于对照组,但差异无统计学意义(x2=3.69,P>0.05);两组有效率差异有统计学意义(x2 =6.43,P<0.05).结论 枸地氯雷他定联合NB-UVB照射治疗玫瑰糠疹安全有效,值得临床推广应用.

  13. [Color reactions for identification of sodium cromoglycate].

    Science.gov (United States)

    Görlitzer, K; Badia, G; Jones, P G

    2001-05-01

    Chromone-2-carboxylic acid (3) reacts with aminopyrazolone (2) in methanolic hydrochloric acid to yield the orange-red polymethine dye 4. Treating dimethyl cromoglicate (6) with compound 2 and perchloric acid leads to the tetraperchlorate 7 of the red azamerocyanine 8. The phenol 9, obtained from alkaline hydrolysis of sodium cromoglicate (1a), couples with diazotized sulfanilic acid to form the red azo dye 10. The chromone 6 condenses with 1,3-dimethylbarbituric acid (DMBA) in acetic anhydride/acetic acid to the red oxonole 12. Cromoglicinic acid (1b) reacts under these conditions to yield the yellow polymethine dye 14, whose structure is elucidated by X-ray analysis.

  14. Therapeutic effect between Pemetrexed disodium and Docetaxel as second line chemotherapy on advance non-small cell lung cancer%培美曲塞与多西他赛二线随机分组治疗晚期非小细胞肺癌对比分析

    Institute of Scientific and Technical Information of China (English)

    郑积华; 林金容; 谢波; 周娟; 徐志勇; 黄雪琴; 王仙赐; 张为民

    2013-01-01

    OBJECTIVE: To compare therapeutic effects between pemetrexed disodium and docetaxel as second line chemotherapy on advanced non-small cell lung cancer. METHODS: Eighty patients with advance non-small cell lung cancer resistant to first line chemotherapy were enrolled. Fifty-one cases had finished first line chemotherapy with paclitaxel and cis-platin or carboplatin (TP or TO. Twenty-one cases had finished first line chemotherapy with gemzar and cis-platin or carboplatin (GP or GO ,8 cases had carried out first line chemotherapy with nolvebin and cis-platin or carboplatin (NP or NC. A dose of 500 mg/m2 pemetrexed disodium or 75 mg/m2 docetaxel was respectively administered intravenously once every 21 days. RESULTS: The therapeutic effect rates in pemetrexed disodium group and docetaxel group were 7. 3% (3/41) and 5. 1 % (2/39) respectively (P>0. 05). Disease control rates in pemetrexed disodium group and docetaxel group were 46. 3%(19/41) and 33. 3% (13/39) respectively (P>0. 05). Overall survival in pemetrexed disodium group was 3. 1 — 15. 6 months (medium time 7. 6 months) while overall survival in docetaxel group was 4. 4 — 12. 6 months(medium time 8. 1 months). Time to progression in pemetrexed disodium group was 4. 9 months while time to progression in docetaxel group was 3. 9 months. Survival rates of one year were 26. 8%(11/41) in in pemetrexed disodium group and 2. 6% (1/39) in docetaxel group respectively. The main adverse effects in both group were slight and acceptable,which included neutropenia, rash, arthragia, alopecia, diarrhea, anorexia, nausea, vomiting, dizziness, headache, chest distress and abdominal pain. No patients showed abnormality in liver or kidney function. No patients showed abnormality in electrocardiogram. CONCLUSION; Single pemetrexed disodium or do cetaxel as second line chemotherapy in the treatment of patients with advanced refractory non-small cell lung cancer was safe and effect and both of them can be a choice of second line

  15. Patterns of responses to alternative medicines in controlling allergic conjunctivitis

    Directory of Open Access Journals (Sweden)

    Batra Deepak

    1988-01-01

    Full Text Available This analysis identifies the various patterns of the responses of the medicines in controlling allergic conjunctivitis. The mean S Deviation coefficient of variation, correlation matrix and loading of factors are worked out as stated in the tables. In the present case the Eigen values greater than 1.50 are retained. The four factors retained explain 68% of the total variations of the 16 responses. The first factor shows 23.38% of variations in total responses while first two and first three factors show 42.39% and 58.64% respectively. Thus medicine affective in controlling the symptoms are given In the descending order: oxymetazoline and sodium salicylate and Sodium cromoglycate, Oxymetazoline and Disodium CCromoglycate & Sodium Salicylate and disodium Cromoglycate.

  16. 枸地氯雷他定对慢性荨麻疹患者血清IL-18和IL-33的影响%Effects of desloratadine citrate disodium on the level of IL-18 and IL-33 in the patients with chronic urticaria

    Institute of Scientific and Technical Information of China (English)

    孟祖东; 盛晚香; 王恒; 王晶; 宋继权

    2015-01-01

    Objective:To determine the effects of desloratadine citrate disodium on the level of IL-18 and IL-33 in the patients with chronic urticaria ( CU) . Methods:Sixty patients with CU were treated with deslo-ratadine citrate disodium 8.8 mg, once a day, for 28 days. The efficacy of desloratadine citrate disodium in the treatment of CU was assessed by patients’ symptom score reducing index. Double antibody sandwich ABC-ELISA method was used to detect the serum levels of IL-18 and IL-33 in the healthy controls ( 50 persons) and the patients with CU before and after the treatment. Results: The effective rate of patients treated with desloratadine citrate disodium was 88.33%. The level of IL-18 of CU patients before the treatment was 131.93 ±60.17, which was higher than that of the healthy controls (68.61±28.58), with a significant difference (P0.05) . The levels of IL-33 before and after the treatment were 118.73±62.67 and 99.28±41.23 respectively and there was no sig-nificant difference between the patients and the healthy controls ( P>0.05) . Conclusion:Desloratadine citrate disodium is effective in the treatment of CU through reducing the level of IL-18.%目的::确定枸地氯雷他定胶囊对慢性荨麻疹患者血清IL-18和IL-33水平的影响。方法:60例患者口服枸地氯雷他定胶囊8.8 mg,每日1次,共服用28天。通过计算患者症状积分下降指数评价疗效,采用双抗体夹心ABC-ELISA法测定患者治疗前后及正常对照(50名)血清中IL-18和IL-33的水平。结果:治疗有效率88.33%。慢性荨麻疹患者IL-18治疗前水平为131.93±60.17,高于正常对照组68.61±28.58,差异有统计学意义(P0.05)。患者治疗前后IL-33水平分别为118.73±62.67和99.28±41.23,与正常对照组比较差异均无统计学意义(P>0.05)。结论:枸地氯雷他定胶囊可能通过调节IL-18治疗慢性荨麻疹。

  17. Combined Application of Gadoxetic Acid Disodium-Enhanced Magnetic Resonance Imaging (MRI and Diffusion-Weighted Imaging (DWI in the Diagnosis of Chronic Liver Disease-Induced Hepatocellular Carcinoma: A Meta-Analysis.

    Directory of Open Access Journals (Sweden)

    Xiang Li

    Full Text Available Gadoxetic acid disodium (Gd-EOB-DTPA is a magnetic resonance imaging (MRI contrast agent to target the liver cells with normal function. In clinical practice, the Gd-EOB-DTPA produces high quality hepatocyte specific image 20 minutes after intravenous injection, so DWI sequence is often performed after the conventional dynamic scanning. However, there are still some disputes about whether DWI sequence will provide more effective diagnostic information in clinical practice. This study aimed to explore the diagnostic value of combining Gd-EOB-DTPA-enhanced MRI and DWI in the detection of hepatocellular carcinoma (HCC in patients with chronic liver disease.A systematic literature search was performed in the PubMed and Cochrane library database up to March 2015. The quality assessment of diagnostic accuracy studies (QUADAS was used to evaluate the quality of studies. Heterogeneous test on the included literature was performed by using the software Review Manager 5.3. The MetaDiSc 1.4 software was used to calculate the pooled sensitivity, specificity, positive likelihood ratio and negative likelihood ratio; meanwhile the summary receiver operating characteristics (SROC curve was drawn to compare the diagnostic performance.A total of 13 literatures were included in this study. In 8 literatures regarding HCC diagnosis based on Gd-EOB-DTPA-enhanced MRI, the pooled sensitivity: 0.90 (95% confidence interval (CI: 0.88-0.93; specificity: 0.89 (95% CI: 0.85-0.92; positive likelihood ratio: 8.60 (95% CI: 6.20-11.92; negative likelihood ratio: 0.10 (95% CI: 0.08-0.14 were obtained. The area under curve (AUC and Q values were 0.96 and 0.90, respectively. In 5 literatures relating to HCC diagnosis by combination of Gd-EOB-DTPA-enhanced MRI and DWI sequence, the pooled sensitivity: 0.88 (95% CI: 0.85-0.91, specificity: 0.96 (0.94-0.97, positive likelihood ratio: 19.63 (12.77-30.16, negative likelihood ratio: 0.10 (0.07-0.14 were obtained. The AUC value was 0

  18. Role of neurotensin in radiation-induced hypothermia in rats

    Energy Technology Data Exchange (ETDEWEB)

    Kandasamy, S.B.; Hunt, W.A.; Harris, A.H. (Armed Forces Radiobiology Research Institute, Bethesda, MD (USA))

    1991-05-01

    The role of neurotensin in radiation-induced hypothermia was examined. Intracerebroventricular (ICV) administration of neurotensin produced dose-dependent hypothermia. Histamine appears to mediate neurotensin-induced hypothermia because the mast cell stabilizer disodium cromoglycate and antihistamines blocked the hypothermic effects of neurotensin. An ICV pretreatment with neurotensin antibody attenuated neurotensin-induced hypothermia, but did not attenuate radiation-induced hypothermia, suggesting that radiation-induced hypothermia was not mediated by neurotensin.

  19. Pharmacology of Nasal Medications: An Update

    OpenAIRE

    Martin, G. F.

    1988-01-01

    The author of this article reviews the pharmacology of nasal medication, focusing on the indications and side-effects. The newer group of non-sedating antihistamines proves to be a useful supplement to disodium cromoglycate and the traditional antihistamines in the treatment of allergic rhinitis. The topical steroids (flunisolide and beclomethasone dipropionate) did not produce a significant incidence of adrenal suppression, mucosal atrophy, or nasal candidiasis. The anticholinergic ipatropiu...

  20. Clinical observation of combination of disodium cantharidinate and vitamin B6 injection adjuvant chemotherapy on patients with lung cancer postoperation%斑蝥酸钠维生素B6注射液辅助肺癌术后化疗的临床观察

    Institute of Scientific and Technical Information of China (English)

    刘素艳; 卢军利

    2011-01-01

    目的 观察斑蝥酸钠维生素B6注射液辅助肺癌术后化疗的临床疗效及对化疗毒副反应的影响.方法 将64例肺癌术后患者随机分为2组,治疗组32例在常规化疗及对症处理基础上应用斑蝥酸钠维生素B6注射液;对照组32例予常规化疗及对症处理.2组均治疗2周后观察疗效和化疗毒副反应的发生情况.结果 治疗组有效率59.4%,对照组34.4%,2组有效率比较差异有统计学意义(P<0.05),治疗组疗效优于对照组.2组化疗毒副反应发生率比较差异有统计学意义(P<0.05),治疗组低于对照组.结论 斑蝥酸钠维生素B6注射液具有增强化疗疗效、改善患者症状、减少化疗毒副反应的作用.%Objective To investigate the effect of combination of disodium cantharidinate and vitamin B6 injection adjuvant chemotherapy on patients with lung cancer postoperation. Methods 64 patients with lung cancer postoperation were randomly divided into two groups. Patients in control group ( n = 32) received routine chemotherapy. 32 cases in treatment group received combination of disodium cantharidinate and vitamin B6 injection adjuvant chemotherapy. The therapeutic effect and toxic and side effect were observed after treatment of two weeks. Results The effective rate in treatment group was superior to that in control group ( P < 0. 05 ). Toxic and side effect in treatment group was less than that in control group ( P < 0.05). Conclusion Combination of disodium cantharidinate and vitamin B6 injection can reinforce effect of chemotherapy, improve symptoms of patients, and decrease toxic and side effect of chemotherapy.

  1. Disodium (2RS,3SR-tartrate

    Directory of Open Access Journals (Sweden)

    William Arbuckle

    2009-10-01

    Full Text Available The asymmetric unit of the anhydrous title compound, 2Na+·C4H4O62−, contains two sodium cations and one tartrate anion. Each sodium ion is six coordinate, with bonding to six O atoms from both the carboxylate and hydroxyl groups of the anion. A three-dimensional coordination network is formed with sodium ions stacking in layers along the c-axis direction. This network is supported by additional O—H...O hydrogen bonds.

  2. Anti-browning effect of disodium stannous citrate on fresh-cut lotus%柠檬酸亚锡二钠对鲜切莲藕护色作用的研究

    Institute of Scientific and Technical Information of China (English)

    金定樑; 夏文水

    2011-01-01

    柠檬酸亚锡二钠(DSC)是一种新型护色剂.将DSC用于鲜切莲藕预处理阶段,抑制莲藕多酚氧化酶活力及褐变,探讨影响DSC对鲜切莲藕片护色作用的因素,并与其他常用护色剂的护色效果进行对比.结果表明:DSC对鲜切藕产品低温保藏期间的褐变和多酚氧化酶活力都有很好的抑制作用,在pH 3~6条件下用0.05%~0.2% DSC浸泡液处理15 min后,鲜切藕产品可保持较低的褐变度和多酚氧化酶活力,同时在4℃、20 d内DSC的护色效果稳定;与其他常用护色剂比较,在0.1%的等量护色剂浓度下,DSC护色效果优于柠檬酸、抗坏血酸、异抗坏血畦钠,与亚硫酸氢钠效果相当.%Disodium stannous citrate(DSC)is an effective sntibrowning agent. This investigation was conducted to determine the efficacy of DSC as a browning control agent for use on fresh-cut lotus. Fresh-cut lotus products are prone to browning during the low-temperature preservation, The relative effectiveness of these antibrowning agents for inhibition of enzymatic browning in fresh-cut lotus was determined in terms of colour and enzyme activity measurements with respect to time for approximately 20 days storage period at 4 ℃. The fresh-cut lotus were dipped in treatment solutions for some time, then drained grid placed ;n containers. The resuhs showed that, DSC has good controlling browning effects on the lotus products. Including the enzymatic browning and non-enzymatic browning) The best concentration of DSC is 0. 05 % ~ 0. 2%, the processing lime for 15 min. pH range of applications from 3 to 6. And the effect of DSC in different temperatures on the color-preservation effect includes but not limited, and has the function of stability for the products during the shelf life. Compared with other ancibrowning agents commonly.The effect of 0.1%DSC has the more obvious effects, quite close to the effect of sodium bisulfite. The research has a theoretic guidance for

  3. HPLC determination of high molecular mass impurities in ticarcillin disodium and clavulanate potassium(15:1)%HPLC法测定替卡西林钠克拉维酸钾(15:1)中的高分子杂质

    Institute of Scientific and Technical Information of China (English)

    钟雅妮; 刘俊华; 林小洁; 李小婵

    2011-01-01

    目的:建立测定替卡西林钠克拉维酸钾(15:1)中高分子杂质的HPLC分析方法.方法:采用高效液相色谱法,以TSKG2500 PW(XL)(7.8mmx300mm,7μm)为色谱柱,以pH8.0磷酸盐缓冲液[0.15mol·L-1磷酸氢二钠溶液-0.15mol·L-1磷酸二氢钠溶液(95:5)]为流动相,流速0.8mL·min-1,检测波长230nm,柱温30℃.结果:高分子杂质与替卡西林及克拉维酸能较好分离;替卡西林的检测限为4.0ng,克拉维酸的检测限为3.7ng;替卡西林线性范围为0.052-0.32μg(r=0.9999),高分子杂质在进样量以替卡西林计为11.2-30.3μg范围内时,与峰面积线性关系良好(r=0.9992);重复性较好(RSD=0.52%,n=5).结论:该方法简单、快速、准确,重复性好,可用于替卡西林钠克拉维酸钾(15:1)中的高分子杂质检测.%Objective :To establish an HPLC method for the determination of high molecular mass impurities in ticarcillin disodium and clavulanate potassium ( 15 : 1 ) . Methods: The separation was performed on a TSK G2500 PWXL(7. 8 mm × 300 mm,7 μm) column;The mobile phase was composed of phosphate buffer[0. 15 mol · L-1 disodium hydrogen phosphate solution -0. 15 mol · L-1 sodium dihydrogen phosph ate solution(95: 5) , pH 8.0] at a flow rate of 0. 8 mL · min -1 ; The detection wavelength was 230 nm, and the column temperature was 30 ℃ . Results : High molecular mass impurities in ticarcillin disodium and clavulanate potassium( 15: 1) was separated completely between ticarcillin and clavulanate; The detection limit of ticarcillin was 4. 0 ng;The detection limit of clavulanate was 3. 7 ng; The linearity of ticarcillin was 0. 052 - 0. 32 μg( r =0. 9999 ) ; The peak area of high molecular mass impurities showed good linearity in the range of ticarcillin between 11. 2 - 30. 3 μg( r = 0. 9992). RSD was 0. 52% ( n = 5) . Conclusion : The method is simple, rapid, accurate and reproducible , and it can be used for quality control of ticarcillin disodium and clavulanate potassium( 15: 1) .

  4. 帕米膦酸二钠治疗累及股骨近端多发性纤维结构不良的24例报告%Pamidronate disodium for polyostotic fibrous dysplasia in the proximal femur:twenty-four cases report

    Institute of Scientific and Technical Information of China (English)

    徐明; 许宋锋; 于秀淳

    2014-01-01

    疗组:末次随访Harris评分(79.58±5.2)大于治疗前Harris评分(43.67±31.8);单纯药物治疗组:末次随访Harris评分(79.17±8.4)大于治疗前Harris评分(69.75±7.9),差异均有统计学意义(P=0.002)。除5例在首次静滴帕米膦酸二钠后次日发热外,24例均未见其它不良反应。结论帕米膦酸二钠治疗累及股骨近端多发性纤维结构不良疗效确切,能减少溶骨性破坏、预防骨折风险、缓解疼痛、改善髋关节功能,不良反应轻微、短暂。对无症状的PFD、MAS无须手术治疗,可直接应用帕米膦酸二钠治疗;对病变范围局限、溶骨性破坏者须行刮除植骨内固定术,对于股骨近端病变范围大、骨强度不佳者可单纯内固定,二者术后均须应用帕米膦酸二钠治疗,以防止植骨吸收及病情恶化。%Objective To investigate the therapeutic methods and clinical effects of pamidronate disodium for polyostotic ifbrous dysplasia in the proximal femur in different degrees. Methods From June 2009 to January 2012, 24 patients with polyostotic ifbrous dysplasia in the proximal femur were adopted and treated. There were 14 males and 10 females, whose average age was 24 years old ( range;8-61 years ). A combination of surgery and postoperative pamidronate disodium was performed on 11 patients, curettage, bone graft and internal ifxation on 8 patients, simple internal fixation on 3 patients and only pamidronate disodium on 13 patients. Pamidronate disodium was taken every 3 months after the operation or after the ifrst treatment, and the duration was 2 years. Before the treatment or before pamidronate disodium injection, bone metabolic markers were detected and the imaging examination was performed in all the patients, including osteocalcin ( OC ) and C-terminal telopeptides of type I collagen ( CTX-I ).The Visual Analogue Scale ( VAS ) was used to evaluate the preoperative and postoperative pain. The hip function was systematically assessed based on the Harris

  5. I. Enabling Single-Chain Surfactants to Form Vesicles by Nonamphiphilic Liquid Crystals in Water II. Controlling Attachment and Ligand-Mediated Adherence of Candida albicans on Monolayers

    Science.gov (United States)

    Varghese, Nisha

    This dissertation describes a fundamental study of weak noncovalent interactions and surface forces that exist at the interfaces of various interacting moieties (small molecules or microbes), and its relevance to colloidal and material chemistry. Chapter 1 presents an emulsion system that enables single-chain anionic or nonionic surfactants to sequester and encapsulate certain water-soluble organic salts, leading to the formation of vesicles in water. The water-soluble organic salt in the system comprises of disodium cromoglycate crystals that are emulsified by surfactants in water to form stable liquid crystal droplets. The work provides an exception to the rule of geometric packing factor that dictates formation of micelles by the surfactants in water. Chapter 2 shows that the odd or even number of carbon atoms present in the aliphatic chain of surfactants affect the ability of surfactants to emulsify aqueous-based liquid crystals of disodium cromoglycate. Such an odd-even effect is frequently observed for solid state properties like melting point, heat of fusion and refractive index but is rarely observed for molecules present in solution. When mixed in water, anionic single-chain surfactants with odd number of carbon atoms emulsifies disodium cromoglycate to form liquid crystal droplets, while surfactants with even number of carbon atoms fail to emulsify disodium cromoglycate. Chapter 3 Bolaamphiphiles usually form vesicles only in extreme conditions or in the presence of surfactants. Here, we explore the co-assembly system of synthesized bolaamphiphiles and disodium cromoglycate in water. The combination of the self-assembly forces of the bolaamphiphile and self-associating property of disodium cromoglycate liquid crystals act together at the interface form a unique microemulsion of liquid crystal droplets of disodium cromoglycate embedded in liquid crystal phase. Chapter 4 describes a key event (adhesion) that precedes infections caused by Candida albicans

  6. Effect of Desloratadine Citrate Disodium Injections on Ovalbumin-induced Allergic Rhinitis in Rats%枸地氯雷他定注射液对大鼠过敏性鼻炎的影响

    Institute of Scientific and Technical Information of China (English)

    揭琼; 袁馨; 陈美灵; 吴玉林

    2015-01-01

    Objective: To study the effect of desloratadine citrate disodium injections (DLC) on ovalbumin-induced allergic rhinitis in rats, including the rhinitis symptoms, PGD2 and LTC4 levels and inflammatory cell infiltration in nasal lavage fluid (NLF). Methods: Ovalbumin-induced allergic rhinitis male SD rats were randomly divided in five groups: model group, DLC low, medium and high dose groups, and chlorphenamine maleate injectlon (CHM) group as positive group. In addition, the normal rats were also recorded. From the 22nd day of being modeled, rats of the model and normal groups were given iv saline, the DLC low, medium and high dose groups were given DLC at 0.3, 0.6 and 1.2 mg·kg-1, CHM group were given CHM at 0.6 mg·kg-1, all the iv treatments were once a day for five days. Rats were topically sensitized by instilling ovalbumin solution into the bilateral nasal cavities on alternate days. Symptoms of rhinitis were observed continuously for 30 min at the last time for administration and topically sensitization, taking the scoring method to record the symptoms of rhinitis. Two hours after the intranasal challenge, NLF was collected, PGD2 and LTC4 levels and inflammatory cellular infiltration were evaluated, respectively. Results and Conclusion: DLC significantly attenuated ovalbumin-induced rhinitis symptoms and caused a significant reduction in PGD2 and LTC4 levels and inflammatory cellular infiltration.%目的:研究枸地氯雷他定注射液对卵白蛋白(OVA)致大鼠过敏性鼻炎的鼻部症状及鼻腔灌洗液PGD2、LTC4含量和炎症细胞浸润的影响。方法:采用OVA建立大鼠过敏性鼻炎模型,将造模成功的SD雄性大鼠随机分成5组:模型组、枸地氯雷他定注射液(简称枸地)低、中、高剂量组,阳性药马来酸氯苯那敏注射液(扑尔敏)组。另随机取正常大鼠设正常组。造模第22天,模型组和正常组静注生理盐水;枸地低、中、高剂量组分别静注0.3、0

  7. Influence of fluticasone Propionate and desloratadine citrate disodium on the level of EOs,CsF,IL-5 in the serum of allergic rhinitis Patients%丙酸氟替卡松联合枸地氯雷他定治疗对变应性鼻炎患者血清EOS﹑CSF和IL-5水平的影响

    Institute of Scientific and Technical Information of China (English)

    朱立新

    2016-01-01

    Objective To study the influence of fluticasone propionate and desloratadine citrate disodium on the level of EOS,CSF,IL- 5 in the serum of allergic rhinitis patients. Methods One hundred and thirty-six cases of allergic rhinitis were randomly divided into obser-vation group and control group. The observation group was given oral nasal spray and fluticasone propionate nasal spray,desloratadine citrate di-sodium tablets orally. The control group was given desloratadine citrate disodium tablets. The time of treatment was 4 weeks. After the treat-ment,the visual analogue scale(VAS)of nasal symptoms of the patients in two groups were decided. The changes of serum EOS,CSF and IL- 5 levels were compared between the two groups before and after treatment,and the correlation between the three groups was analyzed. Results The total effective rate of the observation group with fluticasone propionate and desloratadine citrate disodium after treatment was 94. 1% ,sig-nificantly higher than that of the control group(77. 9% ). The serum EOS,CSF and IL-5 levels of two groups of patients after treatment were significantly lower than those before treatment. The EOS,CSF and IL-5 levels of observation group were significantly lower than those in the control group( P < 0. 05). The correlation analysis showed that CSF and IL-5 had a positive correlation with EOS( P < 0. 01). Conclusion Fluticasone propionate and desloratadine citrate disodium for the treatment of allergic rhinitis patients can significantly reduce the serum levels of EOS,CSF and IL-5 levels. The CSF,IL-5 and EOS levels are closely related.%目的 探讨丙酸氟替卡松联合枸地氯雷他定治疗对变应性鼻炎患者血清嗜酸粒细胞(EOS)、集落刺激因子(CSF)、白介素(IL)-5水平的影响.方法 选取136例变应性鼻炎患者作为研究对象,随机分为观察组和对照组.观察组给予丙酸氟替卡松鼻喷雾剂喷鼻,枸地氯雷他定片口服,对照组给予枸地氯雷他

  8. 顺铂IL-2胸腔内灌注联合培美曲塞全身化疗治疗老年晚期肺腺癌恶性胸腔积液%Clinical Observation of Cisplatin+IL-2 Intrathoracic Perfusion Joint Pemetrexed Disodium Systemic Chemotherapy for Elderly Patients with Advanced Malignant Pleural Effusion of Lung Cancer

    Institute of Scientific and Technical Information of China (English)

    王永明; 荆丽君; 冯桂新; 李同源; 李志杰

    2012-01-01

      Objective:Observation on cisplatin and IL-2 intrathoracic perfusion combined with pemetrexed disodium systemic chemotherapy for elderly patients with advanced malignant pleural effusion of lung adenocarcinoma’s clinical efficacy and side effects.Method:The lung adenocarcinoma in elderly patients with pleural effusion a total of 51 cases,the intrathoracic injection of cisplatin(40 mg/m2)and IL-2(1.5 million U)once a week for 2 weeks were given. At the same time,pemetrexed disodium for injection(500 mg/m2),the first day,every 3 weeks repeated,two cycles. The 4th week for evaluating efficacy and side effects.Result:51 patients could be evaluated the effects,16 cases were completely alleviated,a part of the mitigation in 25 cases,6 cases ineffective. Then its effective rate of 80.39%,complete remission rate 31.37%.Conclusion:Cisplatin and IL-2 intrathoracic perfusion combined with pemetrexed disodium systemic chemotherapy is a effective treatment method for elderly lung adenocarcinoma patients with advanced malignant pleural effusion which were light toxicity and safe clinical use.%  目的:观察顺铂+IL-2胸腔内灌注联合培美曲塞全身化疗治疗老年晚期肺腺癌恶性胸腔积液的临床疗效及毒副反应.方法:老年肺腺癌并胸腔积液患者共51例,采用顺铂40 mg/m2及IL-2150万U胸腔灌注保留,每周一次,共2周,同时应用培美曲塞,第1天,每3周重复,完成2个周期.治疗第4周评价疗效及毒副作用.结果:51例患者均可评价疗效,完全缓解者16例,部分缓解者25例,无效者6例,其有效率为80.39%,完全缓解率31.37%.结论:顺铂+IL-2胸腔内灌注联合培美曲塞全身化疗治疗老年晚期肺腺癌恶性胸腔积液治疗的方法疗效显著,毒性反应轻,临床使用安全.

  9. Disodium Cantharidinate and Vitamin B6 Combined with Tegafur,Gimeracil and Oteracil Potassium for Treating Stage IV Pancreatic Cancer in 27 Cases%斑蝥酸钠维生素B6联合替吉奥治疗Ⅳ期胰腺癌27例

    Institute of Scientific and Technical Information of China (English)

    关丽云; 马静; 袁世发; 曲金荣

    2015-01-01

    Objective To observe the clinical effect of Disodium Cantharidinate and Vitamin B6 combined with tegafur,gimeracil and oteracil potassium for treating advanced pancreatic cancer.Methods Totally 54 patients with advanced pancreatic cancer were divided into the treatment group and the control group according to the random number method,27 cases in each group.The control group was given and tegafur,gimeracil oteracil potassium,while the treatment group was given Disodium Cantharidinate and Vitamin B6.The short-term effect,clinical effect and adverse reactions were evaluated after 2 courses.Results The total effective rate and the disease control rate in the treatment group was 1 1.1 1%,59.26% respectively,and 7.41%,55.56% in the control group respectively,the difference had no statistical significance(P >0.05);the adverse reavtion rate of leukopenia,abnormal liver function,nausea and vomiting in the treatment group was significantly lower than those in the control group (P <0.05);the total effective rate of KPS score was 81.48%, which was significantly higher than 59.26% in the control group(P <0.05).Conclusion Disodium Cantharidinate and Vitamin B6 can reduce the toxic and side effect caused by tegafur,gimeracil and oteracil potassium,improve the quality of life,and is worth of clinical promotion.%目的:观察斑蝥酸钠维生素B6注射液联合替吉奥胶囊治疗晚期胰腺癌的临床疗效。方法将54例晚期胰腺癌患者按随机数字表法分为治疗组和对照组,各27例。对照组患者采用替吉奥胶囊治疗,治疗组患者在此基础上加用斑螫酸钠维生素B6注射液治疗。治疗2个周期后,评价两组患者的近期疗效、临床效果及不良反应。结果治疗组总有效率和疾病控制率分别为11.11%和59.26%,对照组分别为7.41%和55.56%,组间比较,差异无统计学意义(P>0.05);治疗组不良反应发生率低于对照组(P<0.05),特别是白细胞减

  10. The changes of interleukin-18 and interleukin-33 expression level in chronic urticaria patients before and after being treated with desloratadine citrate disodium%慢性荨麻疹患者枸地氯雷他定治疗前后白细胞介素-18和33水平的变化

    Institute of Scientific and Technical Information of China (English)

    孟祖东; 盛晚香; 王恒; 王晶; 宋继权

    2015-01-01

    ObjectiveTo investigate the possible role and clinical signiifcance of interleukin (IL)-18 and IL-33 in the pathogenesis of chronic urticaria (CU).MethodsDouble-antibody sandwich immunosorbent assay (ABC-ELISA) was performed to detect the differential expression of IL-18 and IL-33 in peripheral blood in 60 CU patients and 50 normal controls, as well as the differential expression of IL-18 and IL-33 in CU patients before and after being treated with desloratadine citrate disodium, ifnally the correlation between the expression of IL-18, IL-33 and clinical efifcacy of desloratadine citrate disodium was investigated.ResultsThe level of IL-18 in serum of CU patients before treatment was signiifcantly higher than that of the healthy control group (P0.05). No signiifcant difference was observed in the level of IL-33 between the healthy control group and CU group before and after the treatment (P>0.05). The changes in the concentration of IL-18 before and after treatment in CU patients and its clinical therapeutic effect were positively correlated.ConclusionIL-18 may be involved in pathological processes in the pathogenesis of CU, but the role of IL-33 needs further study. Desloratadine citrate disodium is an ideal antihistamine to treat CU which could regulate the expression of cytokines involved in the pathogenesis of CU.%目的:探讨白细胞介素(IL)-18和IL-33在慢性荨麻疹(CU)发病机制中的可能作用和临床意义。方法采用双抗体夹心法免疫吸附试验(ABC-ELISA),检测60例CU患者和50名正常人外周血IL-18和IL-33表达水平,同时分析其差异与临床疗效的相关性。结果治疗前CU患者IL-18显著高于正常对照组(P<0.05);经枸地氯雷他定治疗28 d后,患者IL-18水平显著低于治疗前(P<0.05),且与正常对照组相比,差异无统计学意义(P>0.05);IL-33水平在治疗前、后分别与正常对照组相比,差异均无统计学意义(P>0.05

  11. Disodium Cantharidinate and Vitamin B6 Injection plus Chemotherapy for Non-Small Cell Lung Cancer: A Systematic Review%斑蝥酸钠维生素B6注射液联合化疗治疗非小细胞肺癌的系统评价

    Institute of Scientific and Technical Information of China (English)

    盛蕾; 李岩; 陈健鹏

    2012-01-01

    目的 系统评价斑蝥酸钠维生素B6注射液联合化疗治疗非小细胞肺癌( Non-small cell lung carcinoma,NSCLC)的有效性及安全性.方法 计算机检索Cochrane图书馆临床对照试验资料库、MEDLINE、EMbase、CBM、CNKI、VIP等数据库,检索时限为从1966年至2011年11月,纳入斑蝥酸钠维生素B6注射液联合化疗治疗NSCLC的随机对照试验.由2名评价者独立评价并交叉核对纳入研究质量后,对同质研究采用RevMan 5.1软件进行Meta分析.结果 经筛选,最终纳入8个RCT,共539例受试者.文献质量评价结果显示,8篇均为B级.Meta分析结果表明:与对照组相比,斑蝥酸钠维生素B6注射液能提高NSCLC化疗的有效率[RR=1.32,95%CI( 1.07,1.62)]、临床受益率[RR=1.24,95%CI (1.12,1.37)],改善患者生活质量[RR=2.23,95%CI( 1.55,3.19)]、临床症状[RR=1.55,95%CI( 1.24,1.95)],增加患者体重[RR=2.72,95%CI (1.74,4.25)],并减轻骨髓抑制毒性作用(白细胞下降率)[RR=0.36,95%CI (0.21,0.61)].结论 斑蝥酸钠维生素B6注射液对NSCLC患者接受化疗能起到增效减毒作用.为获得更佳的循证医学证据,建议开展更多大样本、多中心、长期随访的高质量临床随机对照试验.%Objective To systematically evaluate the effectiveness and safety of disodium cantharidinate and vita-rain B6 injection plus chemotherapy compared with chemotherapy alone, in the treatment of non-small cell lung cancer (NSCLC). Methods The Cochrane Library (Issue 1, 2011), MEDLINE (1966 to November 2011), EMbase (1984 to November 2011), CBM (1978 to November 2011), CNKI (1995 to November 2011) and VIP (1989 to November 2011) were searched electronically, and the randomized controlled trials (RCTs) about disodium cantharidinate and vitamin B6 injection plus chemotherapy for NSCLC were included. The quality of the included studies was assessed and crosschecked by two reviewers independently, and meta-analyses were performed for homogeneous

  12. Lyotropic chromonic liquid crystals: From viscoelastic properties to living liquid crystals

    Science.gov (United States)

    Zhou, Shuang

    Lyotropic chromonic liquid crystal (LCLC) represents a broad range of molecules, from organic dyes and drugs to DNA, that self-assemble into linear aggregates in water through face-to-face stacking. These linear aggregates of high aspect ratio are capable of orientational order, forming, for example nematic phase. Since the microscopic properties (such as length) of the chromonic aggregates are results of subtle balance between energy and entropy, the macroscopic viscoelastic properties of the nematic media are sensitive to change of external factors. In the first part of this thesis, by using dynamic light scattering and magnetic Frederiks transition techniques, we study the Frank elastic moduli and viscosity coefficients of LCLC disodium cromoglycate (DSCG) and sunset yellow (SSY) as functions of concentration c , temperature T and ionic contents. The elastic moduli of splay (K1) and bend (K3) are in the order of 10pN, about 10 times larger than the twist modulus (K2). The splay modulus K1 and the ratio K1/K3 both increase substantially as T decreases or c increases, which we attribute to the elongation of linear aggregates at lower T or higher c . The bend viscosity is comparable to that of thermotropic liquid crystals, while the splay and twist viscosities are several orders of magnitude larger, changing exponentially with T . Additional ionic additives into the system influence the viscoelastic properties of these systems in a dramatic and versatile way. For example, monovalent salt NaCl decreases bend modulus K3 and increases twist viscosity, while an elevated pH decreases all the parameters. We attribute these features to the ion-induced changes in length and flexibility of building units of LCLC, the chromonic aggregates, a property not found in conventional thermotropic and lyotropic liquid crystals form by covalently bound units of fixed length. The second part of the thesis studies a new active bio-mechanical hybrid system called living liquid crystal

  13. 枸地氯雷他定与阿伐斯汀递减疗法治疗慢性荨麻疹的疗效比较%Comparison of the Efficacy of Desloratadine Citrate Disodium and Acrivastine Decremental Therapy in the Treatment of Chronic Urticaria

    Institute of Scientific and Technical Information of China (English)

    董东; 何小亮; 杨德勇; 王晓霞

    2015-01-01

    目的:比较枸地氯雷他定与阿伐斯汀递减疗法治疗慢性荨麻疹的疗效和安全性.方法:132例慢性荨麻疹患者随机分为A组(62例)和B组(70例).A组患者第1~2周口服枸地氯雷他定片8.8 mg,每日1次;第3~4周给予8.8 mg,每2日1次;第5~6周给予8.8 mg,每3日1次;第7~8周给予8.8 mg,每4日1次;第9~10周给予8.8 mg,每5日1次.B组患者第1~2周口服阿伐斯汀胶囊8 mg,每日3次;第3~4周给予8 mg,每日2次;第5~6周给予8 mg,每日1次;第7~8周给予8 mg,每2日1次;第9~10周给予8 mg,每3日1次.两组患者疗程均为10周.观察两组患者的临床疗效,治疗前后的血浆组胺水平和症状体征总积分,并随访两组患者停药4周后的复发情况及不良反应发生情况.结果:两组患者总有效率、不良反应发生率比较,差异均无统计学意义(P>0.05).治疗后,两组患者血浆组胺水平和症状体征总积分均显著低于同组治疗前,差异均有统计学意义(P0.05).A组患者复发率显著低于B组,差异均有统计学意义(P0.05). After treatment,the total scores of signs and symptoms in 2 groups were significantly lower than before,the difference was statistically significant(P0.05). The recurrence rate in group A was significantly lower than group B,the difference was sta-tistically significant(P<0.05). CONCLUSIONS:Both efficacy and safety of desloratadine citrate disodium and acrivastine decre-mental therapy in the treatment of chronic urticaria are good,however,desloratadine citrate disodium is better than acrivastine in re-ducing recurrence rate.

  14. Moxibustion activates mast cell degranulation at the ST25 in rats with colitis

    Institute of Scientific and Technical Information of China (English)

    Yin Shi; Li Qi; Jing Wang; Ming-Shu Xu; Dan Zhang; Lu-Yi Wu; Huan-Gan Wu

    2011-01-01

    AIM: To investigate the effects of moxibustion on the morphology and function of mast cells (MC) at Tians-hu (ST25) in rats with trinitro-benzene-sulfonic acid (TNBS)-induced colitis.METHODS: A total of 53 male Sprague-Dawley rats were randomly divided into a normal group and experi-mental group. In the experimental group, a rat model of TNBS-induced colitis was established, and the rats were then randomly divided into a model group, moxi-bustion group, moxibustion plus disodium cromoglycate (M + DC) group and moxibustion plus normal saline (M + NS) group. Rats in the moxibustion group received suspended moxibustion at bilateral ST25 for 10 min, once a day for 7 d. Rats in the M + DC and M + NS groups were pretreated with disodium cromoglycate and normal saline at bilateral ST25, respectively, and were then concurrently subjected to the same treat-ment as rats in the moxibustion group. The hematoxy-lin-eosin staining method was used to observe histology of the colon and the toluidine blue-improved method was used to observe mast cells at ST25 acupoint areas.RESULTS: An improvement in colonic injury in the moxibustion group was observed and the degranula-tion ratio of MC at ST25 acupoint was markedly higher in the moxibustion group than in the model group (45.91 ± 11.41 vs 32.58 ± 8.28, P < 0.05). After inhi-bition of degranulation of MC at ST25 by disodium cro-moglycate, no improvement in colon tissue injury was observed.CONCLUSION: Moxibustion exerted its effect on heal-ing impaired colonic mucosa in rats with TNBS-induced colitis by increasing the degranulation ratio of local MC, but had little effect on the morphology of MC at ST25 acupoint.

  15. 骨髓源性肥大细胞对软骨细胞表达Ⅱ型胶原及糖胺多糖的影响%Effects of bone marrow- derived mast cells on expressions of type II collagen and glycosaminoglycan in co-cultured chondrocytes

    Institute of Scientific and Technical Information of China (English)

    欧阳晴晴; 赵进军; 杨敏

    2014-01-01

    Objective To investigate the influence of the bone marrow-derived mast cells (BMMCs) on the expression of type II collagen and glycosaminoglycan (GAG) in chondrocytes co-cultured with BMMCs. Methods Primarily cultured mouse BMMCs at 4 weeks and the second passage of chondrocytes were plated in a Transwell co-cultured system at a ratio of 1∶10 in the presence or absence of sodium cromoglycate (DSCG) or compound 48/80 (C48/80). The chondrocytes were harvested and lysed for detecting type II collagen expression with ELISA and Western blotting and GAG expression using 1,9 dimethylmethylene blue (DBM). Results After a 24-hour culture, the chondrocytes co-cultured with BMMCs showed similar expression levels of type II collagen and GAG to the control group regardless of the presence of DSCG (P>0.05). Compared with chondrocytes cultured alone or with BMMCs, the co- cultured chondrocytes in the presence of C48/80 showed significantly lower expressions of type II collagen and GAG (P0.05),C48/80组Ⅱ型胶原与GAG含量相对于对照组和BMMCs组显著降低(P0.05)。结论C48/80激活的BMMCs可降低软骨细胞Ⅱ型胶原以及GAG表达。

  16. Treatment of perennial rhinitis with 2% solution of sodium cromoglycate.

    Science.gov (United States)

    Lobaton, P; Seranno, V; Rubio, N; Gomez, D

    1975-08-01

    This trial has demonstrated that S.C.G. is significantly better than placebo and therefore that a 2% solution of S.C.G. is effective in the treatment of perennial rhinitis. It would appear that better results can be obtained in patients who have a demonstrable allergic aetiology with a nasal eosinophilia.

  17. Clinical observation of cytidine disodium triphosphate combined with mouse nerve growth factor in treatment of neonatal hypoxic ischemic encephalopathy%三磷酸胞苷二钠联合鼠神经生长因子治疗新生儿缺氧缺血性脑病的疗效观察

    Institute of Scientific and Technical Information of China (English)

    丁玉红; 闫俊梅; 闫静

    2015-01-01

    目的:探讨三磷酸胞苷二钠联合鼠神经生长因子治疗新生儿缺氧缺血性脑病的临床疗效。方法选择2013年1月—2014年1月徐州市妇幼保健院新生儿科收治的缺氧缺血性脑病患儿80例,随机分为对照组和治疗组,每组各40例。对照组在基本治疗的基础上,在患儿出生后6 h内肌肉注射注射用鼠神经生长因子,30μg/次,1次/d。治疗组在对照组的治疗基础上静脉滴注注射用三磷酸胞苷二钠,100 mg/次加入到5%葡萄糖溶液30 mL中,1次/d。中度患儿治疗14 d,重度患儿治疗21 d。观察两组的临床疗效,同时比较两组患儿症状与体征改善时间、行为神经测试(NBNA)评分、智能发育量表(CDCC)测试结果。结果治疗后,对照组和治疗组的总有效率分别为72.5%、92.5%,两组比较差异有统计学意义(P<0.05)。治疗组意识障碍恢复时间、惊厥停止时间、原始反射正常时间和肌张力正常时间均显著短于对照组,两组比较差异有统计学意义(P<0.05)。治疗后,两组患儿行为能力评分、被动肌张力评分、一般评估评分、总分均显著升高,治疗组主动肌张力评分、原始反射评分显著升高,同组治疗前后差异具有统计学意义(P<0.05);且治疗组这些观察指标的改善程度优于对照组,两组比较差异具有统计学意义(P<0.05)。两组患儿出生后6、12个月CDCC检测显示治疗组智能发育指数(MDI)、运动发育指数(PDI)均明显高于对照组,两组比较差异均具有统计学意义(P<0.05)。结论三磷酸胞苷二钠联合鼠神经生长因子治疗新生儿缺氧缺血性脑病具有较好的临床疗效,可改善患儿神经功能和生存质量,具有一定的临床推广应用价值。%Objective To observe the clinical efficacy of cytidine disodium triphosphate combined with mouse nerve growth factor in treatment of neonatal

  18. Inhibition of volume-activated chloride currents in endothelial cells by chromones.

    Science.gov (United States)

    Heinke, S.; Szücs, G.; Norris, A.; Droogmans, G.; Nilius, B.

    1995-01-01

    1. We have studied the effects of the reported chloride channel blocker, sodium cromoglycate, on volume-activated Cl- currents in endothelial cells from bovine pulmonary artery by means of the whole-cell patch clamp technique. Cl- currents were activated by challenging the cells with a hypotonic extracellular solution of 60% of the normal osmolarity. 2. Half maximal activation of the current at +95 mV occurred after exposure of the cells for 148 +/- 10 s (n = 6) to hypotonic solution (HTS). At the same membrane potential but in the presence of 100 microM sodium cromoglycate (disodium-1,3-bis (2'-carboxylate-chromone-5'-yloxy)-2-hydroxy-propane) activation was delayed (253 +/- 25 s, n = 6) and the maximal current amplitude was reduced to 63 +/- 7% of the control (n = 13). 3. In comparison, an equimolar concentration of NPPB (5-nitro-2(3-phenyl) propylamino-benzoic acid), another Cl- channel blocker, completely blocked the volume-activated current in less than 20 s. 4. Sodium cromoglycate, applied at the time when the HTS-induced current was completely activated, dose-dependently inhibited this current with a concentration for half maximal inhibition of 310 +/- 70 microM. Data for nedocromil sodium were not significantly different from those for sodium cromoglycate. 5. Sodium cromoglycate, loaded into the endothelial cells via the patch pipette in ruptured patches, resulted in a decline of the HTS activated current with a time course that was compatible with diffusion of the compound from the pipette into the cell.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:8564197

  19. Fospropofol disodium injection for the sedation of patients undergoing colonoscopy

    Directory of Open Access Journals (Sweden)

    Benjamin E Levitzky

    2008-09-01

    Full Text Available Benjamin E Levitzky1, John J Vargo21Department of Gastroenterology and Hepatology, 2Section of Therapeutic and Hepatobiliary Endoscopy, Department of Gastroenterology and Hepatology, Cleveland Clinic Foundation, Cleveland, Ohio, USAAbstract: Sedation plays a central role in making colonoscopy tolerable for patients and feasible for the endoscopist to perform. The array of agents used for endoscopic sedation continues to evolve. Fospropofol (FP, a prodrug of propofol with a slower pharmacokinetic profi le, is currently under evaluation for use during endoscopic procedures. Preliminary data suggests that FP dosed at 6.5 mg/kg is well tolerated by most patients with perineal paresthesias being the most commonly experienced adverse effect. This article will examine the current literature on the use of FP for the sedation of patients undergoing colonoscopy, highlighting the pharmacokinetics, pharmacodynamics, risks, and common adverse events associated with the novel sedative/hypnotic.Keywords: fospropofol, Aquavan, propofol, sedation, colonoscopy

  20. Fospropofol disodium injection for the sedation of patients undergoing colonoscopy.

    Science.gov (United States)

    Levitzky, Benjamin E; Vargo, John J

    2008-08-01

    Sedation plays a central role in making colonoscopy tolerable for patients and feasible for the endoscopist to perform. The array of agents used for endoscopic sedation continues to evolve. Fospropofol (FP), a prodrug of propofol with a slower pharmacokinetic profile, is currently under evaluation for use during endoscopic procedures. Preliminary data suggests that FP dosed at 6.5 mg/kg is well tolerated by most patients with perineal paresthesias being the most commonly experienced adverse effect. This article will examine the current literature on the use of FP for the sedation of patients undergoing colonoscopy, highlighting the pharmacokinetics, pharmacodynamics, risks, and common adverse events associated with the novel sedative/hypnotic.

  1. Fospropofol disodium injection for the sedation of patients undergoing colonoscopy

    OpenAIRE

    Levitzky, Benjamin E; Vargo, John J.

    2008-01-01

    Benjamin E Levitzky1, John J Vargo21Department of Gastroenterology and Hepatology, 2Section of Therapeutic and Hepatobiliary Endoscopy, Department of Gastroenterology and Hepatology, Cleveland Clinic Foundation, Cleveland, Ohio, USAAbstract: Sedation plays a central role in making colonoscopy tolerable for patients and feasible for the endoscopist to perform. The array of agents used for endoscopic sedation continues to evolve. Fospropofol (FP), a prodrug of propofol with a slower pharmacokin...

  2. 21 CFR 172.120 - Calcium disodium EDTA.

    Science.gov (United States)

    2010-04-01

    ... and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR... million) Use Cabbage, pickled 220 Promote color, flavor, and texture retention. Canned carbonated soft drinks 33 Promote flavor retention. Canned white potatoes 110 Promote color retention. Clams...

  3. Experimental study on the effect of adenosine disodium triphosphate on myocardial infarction rats%注射用三磷酸腺苷辅酶胰岛素对心肌梗死动物心功能改善作用的实验研究

    Institute of Scientific and Technical Information of China (English)

    邵明香; 王维亭; 郝春华; 赵专友; 汤立达

    2014-01-01

    目的:研究注射用三磷酸腺苷辅酶胰岛素( ADT)对心肌梗死大鼠心功能的改善作用。方法结扎大鼠冠状动脉左前降支,造成急性心肌梗死模型,造模成功大鼠按心肌缺血程度随机分组,分别给予0.9%NaCl、ADT 1,2,4 mg·( kg· d)-1以及依那普利10 mg·( kg· d)-1,另设8只大鼠作为假手术,给予0.9%NaCl。连续给药30 d,通过彩色多普勒超声心动图、血流动力学、心脏重量、肺水含量以及Ⅰ、Ⅲ型胶原的测定,研究ADT对实验大鼠的左心室功能、左心室构型、心肌肥厚程度、肺水肿、心肌梗死范围和心肌重塑等改善作用。结果与模型组比较,ADT可以改善心肌梗死大鼠的左心室功能,明显提高左心室的射血分数,降低左室舒张末压,缩小左心室腔体积,降低肺水含量,减少心肌梗死的范围,抑制心室重塑等。结论 ADT能改善心肌梗死大鼠的心功能。%Objective To investigate the effect of adenosine disodium triphosphate(ADT) on myocardial infarction in rats.Methods The a-cute myocardial infarction rat model was induced by ligation of the left anterior descending coronary artery.The model rats were divided into five groups randomly:model group, ADT 1, 2, 4 mg· (kg· d) -1 and enal-aprilat 10 mg· ( kg· d) -1 , and the other 8 rats received sham surgery.The effect of ADT on myocardial infarction rats included left ventricular of configuration , the degree of myocardial hypertrophy and pulmonary ede-ma, scope of myocardial infarction and myocardial remodeling were deter-mined by color Doppler echocardiography , hemodynamic , heart weight , lung water content and the content of collagen type ⅠandⅢafter contin-uous dosing for 30 days.Results Compared with model , ADT can im-prove left ventricular function of myocardial infarction rats , improve sig-nificantly left ventricular ejection fraction significantly , reduce left ven-tricular end

  4. Molecularly imprinted polymers for histamine recognition in aqueous environment.

    Science.gov (United States)

    Trikka, Foteini A; Yoshimatsu, Keiichi; Ye, Lei; Kyriakidis, Dimitrios A

    2012-11-01

    Molecularly imprinted polymers (MIP) for histamine using methacrylic acid were developed and recognition mechanisms were thoroughly characterized for the first time in this study. The binding affinity of imprinted polymer with structurally related compounds was studied in organic and aqueous media, at various conditions. In organic media, MIP was found to bind histamine two and six times more than ranitidine and fluoxetine, respectively, whereas higher selectivity was observed in the case of dimentidene or disodium cromoglycate. The specific binding sites of MIP recognized histamine over L-histidine in aqueous conditions, while higher affinity for histamine compared to ranitidine, disodium cromoglycate, putrescine and to a putrescine analogue was observed. A combination of NMR and UV spectroscopy analyses for investigation of imprinting and recognition properties revealed that strong specific interactions between the functional monomer and histamine in the prepolymerization and in the aqueous solutions were probably responsible for histamine recognition. The preparation of histamine MIPs and elucidation of imprinting and recognition mechanism may serve as useful insight for future application of MIPs.

  5. Planar anchoring strength and pitch measurements in achiral and chiral chromonic liquid crystals using 90-degree twist cells

    Science.gov (United States)

    McGinn, Christine K.; Laderman, Laura I.; Zimmermann, Natalie; Kitzerow, Heinz-S.; Collings, Peter J.

    2013-12-01

    Chromonic liquid crystals are formed by molecules that spontaneously assemble into anisotropic structures in water. The ordering unit is therefore a molecular assembly instead of a molecule as in thermotropic liquid crystals. Although it has been known for a long time that certain dyes, drugs, and nucleic acids form chromonic liquid crystals, only recently has enough knowledge been gained on how to control their alignment so that studies of their fundamental liquid crystal properties can be performed. In this article, a simple method for producing planar alignment of the nematic phase in chromonic liquid crystals is described, and this in turn is used to create twisted nematic structures of both achiral and chiral chromonic liquid crystals. The optics of 90-degree twist cells allows the anchoring strength to be measured in achiral systems, which for this alignment technique is quite weak, about 3×10-7 J/m2 for both disodium cromoglycate and Sunset Yellow FCF. The addition of a chiral amino acid to the system causes the chiral nematic phase to form, and similar optical measurements in 90-degree twist cells produce a measurement of the intrinsic pitch of the chiral nematic phase. From these measurements, the helical twisting power for L-alanine is found to be (1.1±0.4)×10-2 μm-1 wt%-1 for 15 wt% disodium cromoglycate.

  6. [N-acetyl-aspartylglutamic acid eye drops in allergic-type conjuctivitis. Double-blind comparative clinical study].

    Science.gov (United States)

    Bonnet, M; Ducournau, D; Lumbroso, P; Serpin, G

    1985-01-01

    Fifty patients with allergic conjunctivitis were included in a double-blind randomized clinical trial designed to compare the efficiency and tolerance of two antiallergic eye-drops: one containing NAAGA (22 patients), the other one containing disodium Cromoglycate (28 patients). Both treatments were used at a dosage of 1 drop 4 times per day. Ocular symptoms, conjunctivo-corneal signs and the subjective ocular condition assessed by the patients themselves with visual analogue scales, were all significantly improved by both eye-drops during the first month of treatment. Statistical analysis showed that patient ocular condition improved more rapidly with NAAGA eye-drops. In 25 patients (12 in the NAAGA group and 13 in the Cromoglycate group), the study was continued for an additional month according to a cross-over protocol. During the 2nd month of treatment, additional improvement of ocular symptoms and signs were observed with both eye-drops but more markedly in those patients who received NAAGA after Cromoglycate. Ocular tolerance was good for both eye-drops.

  7. 吡咯喹啉醌二钠对饲喂氧化鸭油肉仔鸡生长性能、血浆脂质代谢及抗氧化能力的影响%Effects of Pyrroloquinoline Quinine Disodium on Growth Performance, Plasma Lipid Metabolism and Antioxidant Ability in Broilers Fed Oxidized Duck Oil

    Institute of Scientific and Technical Information of China (English)

    张亚男; 齐博; 武书庚; 岳洪源; 王晶; 张海军; 齐广海

    2015-01-01

    本试验旨在研究吡咯喹啉醌二钠(PQQ·Na2)对饲喂氧化鸭油(ODO)肉仔鸡生长性能、血浆脂质代谢和抗氧化能力的影响. 选取270只健康、体重相近的1日龄爱拔益加肉仔鸡公雏,随机分成 3 个组,每个组 6 个重复,每个重复 15 只. 3 个组分别饲喂含有新鲜鸭油(FDO)、ODO和ODO+0.4 mg/kg PQQ·Na2(ODO+PQQ)的饲粮,油脂添加水平1~21 d 为3.0%,22~42 d为3.5%. 结果表明:1)与FDO组相比,ODO显著降低了肉仔鸡21 d的平均体重(P0.05). 与ODO组相比,ODO+PQQ组1~21 d和22~42 d 的平均日增重、42 d 平均体重具有增加的趋势( P<0. 10 ). 2 )与 FDO 组相比, PQQ·Na2显著提高了肉仔鸡42 d的全净膛率和21 d的胸肌率( P<0.05). 3)与FDO和ODO组相比,PQQ·Na2 显著降低了肉仔鸡42 d血浆总胆红素和21 d血浆葡萄糖含量( P<0.05).4) PQQ·Na2 显著抑制了ODO导致的21 d血浆总超氧化物歧化酶活性和21和42 d总抗氧化能力的降低( P<0.05) ,抑制ODO导致的21 d血浆丙二醛含量升高( P<0.05). 5) PQQ·Na2 显著抑制了ODO引起的21和42 d血浆甘油三酯含量的升高和21 d血浆高密度脂蛋白胆固醇含量的降低( P<0.05). 可见,PQQ·Na2 可通过调节血浆脂质代谢和提高机体的抗氧化能力,缓解ODO对肉仔鸡的不利影响.%The current study was conducted to investigate the effects of pyrroloquinoline quinine disodium ( PQQ·Na2 ) on growth performance, plasma lipid metabolism and antioxidant ability in broilers fed oxidized duck oil. A total of 270 one-day-old Arbor Acres broilers were randomly assigned to 3 groups ( with 6 repli-cates per group and 15 broilers per replicate) fed diets supplemented with fresh duck oil ( FDO group) , oxi-dized duck oil ( ODO group) and oxidized duck oil + 0.4 mg/kg PQQ·Na2( ODO+PQQ group) , respective-ly. The supplemental level of oil was 3.0% during 1 to 21 days and 3.5% during 22 to 42 days, respectively. The results showed as follows: 1) compared with FDO group

  8. 窄谱中波紫外线联合枸地氯雷他定及润燥止痒胶囊治疗老年糖尿病性瘙痒症疗效观察%Clinical obsevr ation of na rrow-ba nd ultraviolet B combined with desloratadine citrate disodium and Runzoa Zhiyang Capsule on patients with senile diabetic pruritus

    Institute of Scientific and Technical Information of China (English)

    戴洁; 陈文琦; 余洁

    2015-01-01

    Objective It is to observe the clinical efficacy and safety of narrow-band ultraviolet B combined with deslorata-dine citrate disodium ( DCD) and Runzao Zhiyang capsule ( RZC) on patients with senile diabetic pruritus.Methods 75 pa-tients were randomly divided into treatment group and control group;both groups were given DCD and RZC for oral, the treat-ment group was added with NB-UVB whole body irradiation.After 4 weeks of treatment, the degree of itching, seizure fre-quency, duration, effects on sleep, total symptom integral, clinical efficacy, recurrence rate and adverse reaction of the two groups were observed and compared.Results After the treatment, the degree of itching, seizure frequency, duration, effects on sleep, total symptom integral of the treatment group were significantly lower than that of the control group ( all P<0.05) . After 4 weeks of treatment, the effective rate was 95%in the treatment group and was 76%in the control group,there was sig-nificant difference between the both groups(P<0.05).After 8 weeks of treatment, the recurrence rate was 10%in the treat-ment group and was 36%in the control group there was significant difference between the both groups(P<0.05).There was no significant difference in adverse reaction between the both groups.Conclusion The curative effect of NB-UVB combined with DCD and RZC on patients with senile diabetic pruritus is better with high efficacy and low recurrence rate, it is safe and reliable.%目的:观察窄谱中波紫外线( NB-UVB)联合枸地氯雷他定和润燥止痒胶囊治疗老年糖尿病性瘙痒症的效果及其安全性。方法将75例老年糖尿病性瘙痒症患者随机分成治疗组38例和对照组37例,2组均给予枸地氯雷他定和润燥止痒胶囊口服,治疗组加用NB-UVB全身照射。治疗4周后,观察比较2组瘙痒程度、发作频率、持续时间、对睡眠影响程度、症状总积分、临床疗效、复发率和不良反应情况。结果治疗4

  9. Comparison of gadoxetate disodium and gadopentetate dimeglumine in dynamic contrast-enhanced liver MRI:an intra-individual comparative study%肝脏MR动态增强扫描:Gd-EOB-DTPA与Gd-DTPA的个体内对照研究

    Institute of Scientific and Technical Information of China (English)

    吴静云; 王可; 郭小超; 王霄英

    2016-01-01

    enhanced liver MR imaging by gadoxetate disodium (Gd-EOB-DTPA)and gadopentetate dimeglumine (Gd-DTPA).Methods:Twenty-five patients suspected of liver metastases from colorectal cancer underwent twice MR examinations on 3 .0T scanner using the contrast agent of Gd-EOB-DTPA (0.05mmol/kg)and Gd-DTPA (0.1mmol/kg)respectively.Pre- and post- dynamic contrast enhanced images were acquired,including arterial phase (AP),portal venous phase (PP),equilibrium phase (EP for Gd-DTPA)/transitional phase (TP for Gd-EOB-DTPA).On images of all phases,signal intensity of abdominal organs (liver and spleen)and vessels (aor-ta,inferior vena cava,portal vein,hepatic vein)were measured,and signal intensity of paravertebral muscle was measured as reference.Relative signal intensity (RS)were calculated and compared between the two groups using the two types of con-trast media.The image features of contrast enhanced images were also subjectively evaluated.Results:There was statistically significant difference in RS of liver on AP images between the two groups (t= 3.006,P= 0.005).There was no statistically significant difference in RS of liver on EP and TP images between the two groups.In Gd-EOB-DTPA group,liver RS on PP images was much higher than that on AP images (t= -3.014,P= 0.006),and on TP images,liver RS was lower than that on PP images but without statistic difference.In Gd-DTPA group,liver RS was much lower on EP images than that on PP images (t= 5.827,P= 0.000).In subjective evaluation,aorta,portal vein and hepatic vein of all patients were hyperintense on EP images in Gd-DTPA group;whereas in Gd-EOB-DTPA group,aorta,portal vein and hepatic vein were mainly hypo-or iso-intense images (84%,92%,92%).Conclusion:In Gd-EOB-DTPA dynamic contrast enhanced MRI,liver parenchyma was continuously enhanced during portal venous phase and transitional phase.The image features in equilibrium phase of Gd-DTPA enhanced scan are quite different from transitional phase of Gd-EOB-DTPA enhanced scan

  10. A Food and Drug Administration-approved asthma therapeutic agent impacts amyloid β in the brain in a transgenic model of Alzheimer disease.

    Science.gov (United States)

    Hori, Yukiko; Takeda, Shuko; Cho, Hansang; Wegmann, Susanne; Shoup, Timothy M; Takahashi, Kazue; Irimia, Daniel; Elmaleh, David R; Hyman, Bradley T; Hudry, Eloise

    2015-01-23

    Interfering with the assembly of Amyloid β (Aβ) peptides from monomer to oligomeric species and fibrils or promoting their clearance from the brain are targets of anti-Aβ-directed therapies in Alzheimer disease. Here we demonstrate that cromolyn sodium (disodium cromoglycate), a Food and Drug Administration-approved drug already in use for the treatment of asthma, efficiently inhibits the aggregation of Aβ monomers into higher-order oligomers and fibrils in vitro without affecting Aβ production. In vivo, the levels of soluble Aβ are decreased by over 50% after only 1 week of daily intraperitoneally administered cromolyn sodium. Additional in vivo microdialysis studies also show that this compound decreases the half-life of soluble Aβ in the brain. These data suggest a clear effect of a peripherally administered, Food and Drug Administration-approved medication on Aβ economy, supporting further investigation of the potential long-term efficacy of cromolyn sodium in Alzheimer disease.

  11. Spleen Tyrosine Kinase Inhibitor Fostamatinib Disodium for the Treatment of Rheumatoid Arthritis%类风湿性关节炎治疗药Fostamatinib disodium

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    @@ 脾酪氨酸激酶(spleen tyrosine kinase,SYK) 为一种非受体型酪氨酸蛋白激酶,具有广泛的生物活性,其在免疫细胞的成熟和激活中发挥着重要作用,现已被证明与类风湿性关节炎(rheumatoid arthritis,RA) 的发生、发展密切相关.

  12. Early effects of combretastatin-A4 disodium phosphate on tumor perfusion and interstitial fluid pressure

    DEFF Research Database (Denmark)

    Ley, C.D.; Horsman, Michael Robert; Kristjansen, P.E.G.

    2007-01-01

    of the tumor vasculature. It has been proposed that increased permeability causes a transient increase in interstitial fluid pressure (IFP), which in turn could collapse intratumoral blood vessels. We examined the immediate effects of CA4DP on tumor IFP in C3H mammary carcinoma. Mice were treated with 100 mg...

  13. Disodium diaqua-bis-(methyl-enedi-phos-pho-nato-κO,O')cobaltate(II) dihydrate.

    Science.gov (United States)

    van Merwe, Kina; Visser, Hendrik G; Venter, Johan A

    2011-10-01

    In the title compound, Na(2)[Co(CH(4)O(6)P(2))(2)(H(2)O)(2)]·2H(2)O, the asymmetric unit is composed of one methyl-enediphospho-nate ligand and one water mol-ecule, which both are coordinated to a Co(II) atom, as well as a non-coordinated water mol-ecule and a sodium cation. The Co(II) atom occupies a special position on a crystallographic inversion centre. The slightly distorted Co(II)O(6) octa-hedral coordination environment is composed of two bidentate methyl-enediphospho-nate ligands and two coordinated water mol-ecules in trans positions. The sodium ion is octa-hedrally coordinated to six O atoms with Na-O distances ranging from 2.3149 (12) to 2.6243 (12) Å. An extensive three-dimensional network of inter-molecular as well as intra-molecular O-H⋯O and C-H⋯O hydrogen bonding inter-acions is present.

  14. Suppression of Brain Mast Cells Degranulation Inhibits Microglial Activation and Central Nervous System Inflammation.

    Science.gov (United States)

    Dong, Hongquan; Zhang, Xiang; Wang, Yiming; Zhou, Xiqiao; Qian, Yanning; Zhang, Shu

    2017-03-01

    Brain inflammation has a critical role in the pathophysiology of brain diseases. Microglia, the resident immune cells in the brain, play an important role in brain inflammation, while brain mast cells are the "first responder" in the injury rather than microglia. Functional aspects of mast cell-microglia interactions remain poorly understood. Our results demonstrated that site-directed injection of the "mast cell degranulator" compound 48/80 (C48/80) in the hypothalamus induced mast cell degranulation, microglial activation, and inflammatory factor production, which initiated the acute brain inflammatory response. "Mast cell stabilizer" disodium cromoglycate (cromolyn) inhibited this effect, including decrease of inflammatory cytokines, reduced microglial activation, inhibition of MAPK and AKT pathways, and repression of protein expression of histamine receptor 1 (H1R), histamine receptor 4 (H4R), protease-activated receptor 2 (PAR2), and toll-like receptor 4 (TLR4) in microglia. We also demonstrated that C48/80 had no effect on microglial activation in mast cell-deficient Kit(W-sh/W-sh) mice. These results implicate that activated brain mast cells trigger microglial activation and stabilization of mast cell inhibits microglial activation-induced central nervous system (CNS) inflammation. Interactions between mast cells and microglia could constitute a new and unique therapeutic target for CNS immune inflammation-related diseases.

  15. The role of the arachidonic acid cascade in the species-specific X-ray-induced inflammation of the rabbit eye

    Energy Technology Data Exchange (ETDEWEB)

    Bito, L.Z.; Klein, E.M.

    1982-05-01

    To identify the mediator(s) of the apparently species-specific X-ray-induced inflammation of the rabbit eye, inhibitors of the synthesis and/or release of known or putative mediators of ocular inflammation were administered prior to irradiation. The X-ray-induced ocular inflammation, particularly the rise in intraocular pressure, was found to be inhibited by intravenous pretreatment of rabbits with flurbiprofen, indomethacin, or imidazole (1, 10, and 100 mg/kg i.v., respectively), or by combined intravitreal and topical administration of flurbiprofen. Systemic, intravitreal, and/or topical pretreatment with prednisolone or disodium cromoglycate or the retrobulbar injection of ethyl alcohol or capsaicin failed to block the inflammatory response, whereas vitamin E apparently exerted some protective effect. These findings show that the X-ray-induced inflammation of the rabbit eye is mediated, at least in part, by prostaglandins (PGs) and/or related autacoids. In addition, these results suggest that the unique sensitivity of the rabbit eye to X-ray-induced inflammation is due either to the presence in this species of a unique or uniquely effective triggering mechanism for the release of PG precursors or to the greater sensitivity of this species to the ocular inflammatory effects of PGs. Thus the rabbit eye may provide a unique model for studying some aspects of arachidonic acid release or ocular PG effects, but extreme caution must be exercised in generalizing such findings to other species.

  16. Aspectos farmacológicos de la terapéutica del paciente asmático

    Directory of Open Access Journals (Sweden)

    Alicia Zapata Martínez

    1998-12-01

    Full Text Available El asma bronquial es un importante problema de salud en la atención primaria. Se sabe que un tratamiento correcto de la enfermedad contribuye a mejorar la calidad de vida de estos pacientes. Se revisan los principales aspectos farmacológicos (acciones, indicaciones, efectos adversos, vía de administración y dosis de los 2 grupos de medicamentos más empleados en la terapéutica de la enfermedad que son: los broncodilatadores (salbutamol, teofilina, bromuro de ipratropio y los antiinflamatorios (cromoglicato de sodio y glucocorticoidesBronchial asthma is an important health problem in primary health care. It is known that an adequate treatment of the disease helps to improve the quality of life of these patients. The main pharmacological aspects (actions, indications, side effects, administration and dosage of the 2 most used groups of drugs in the therapeutics of the disease that are: the bronchodilators (salbutamol, theophylline, and ipratropium bromide, and the antiinflammatory drugs (disodium cromoglycate and glucocorticoids are reviewed.

  17. Chiral symmetry breaking by spatial confinement in tactoidal droplets of lyotropic chromonic liquid crystals.

    Science.gov (United States)

    Tortora, Luana; Lavrentovich, Oleg D

    2011-03-29

    In many colloidal systems, an orientationally ordered nematic (N) phase emerges from the isotropic (I) melt in the form of spindle-like birefringent tactoids. In cases studied so far, the tactoids always reveal a mirror-symmetric nonchiral structure, sometimes even when the building units are chiral. We report on chiral symmetry breaking in the nematic tactoids formed in molecularly nonchiral polymer-crowded aqueous solutions of low-molecular weight disodium cromoglycate. The parity is broken by twisted packing of self-assembled molecular aggregates within the tactoids as manifested by the observed optical activity. Fluorescent confocal microscopy reveals that the chiral N tactoids are located at the boundaries of cells. We explain the chirality induction as a replacement of energetically costly splay packing of the aggregates within the curved bipolar tactoidal shape with twisted packing. The effect represents a simple pathway of macroscopic chirality induction in an organic system with no molecular chirality, as the only requirements are orientational order and curved shape of confinement.

  18. Study of Therapeutic Mechanism of Acupuncture in Treating Bronchial Asthma

    Institute of Scientific and Technical Information of China (English)

    LI; Ji

    2001-01-01

    It has been considered by modern medicine that bronchial asthma is a chronic airway allergic inflammation (AAI) which is the major factor that induces reversible airway ventilating disturbance and bronchial hyper-responsiveness (BHR) in asthmatic patients, as well as a correlation between the delayed-phase onset of asthma and AAI is more significant than immediate-phase onset of asthma in its pathogenesis. Anti-inflammatory therapy as a fundamental principle of treatment for bronchial asthma has been brought forward during the interval phase so that a large number of anti-AAI drugs to significantly enhance the curative effect such as inhalant corticoid, disodium cromoglycate, and leukotriene receptors antagonist, etc., has been rapidly developed. Additionally, traditional Chinese medicine (TCM) and integration of TCM and western medicine (WM) therapies, including acupuncture, are gradually taken into account by the medical circle as a characteristic in our country for treatment of bronchial asthma. It is worthy of being pointed out that the curative effect of acupuncture and moxibustion in treating asthma is evident, and that its therapeutic mechanism has to a certain extent, been found along with the recent deep-going acupunctural research.……

  19. Study of Therapeutic Mechanism of Acupuncture in Treating Bronchial Asthma

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@  It has been considered by modern medicine that bronchial asthma is a chronic airway allergic inflammation (AAI) which is the major factor that induces reversible airway ventilating disturbance and bronchial hyper-responsiveness (BHR) in asthmatic patients, as well as a correlation between the delayed-phase onset of asthma and AAI is more significant than immediate-phase onset of asthma in its pathogenesis. Anti-inflammatory therapy as a fundamental principle of treatment for bronchial asthma has been brought forward during the interval phase so that a large number of anti-AAI drugs to significantly enhance the curative effect such as inhalant corticoid, disodium cromoglycate, and leukotriene receptors antagonist, etc., has been rapidly developed. Additionally, traditional Chinese medicine (TCM) and integration of TCM and western medicine (WM) therapies, including acupuncture, are gradually taken into account by the medical circle as a characteristic in our country for treatment of bronchial asthma. It is worthy of being pointed out that the curative effect of acupuncture and moxibustion in treating asthma is evident, and that its therapeutic mechanism has to a certain extent, been found along with the recent deep-going acupunctural research.

  20. Involvement of prostaglandins and histamine in radiation-induced temperature responses in rats

    Energy Technology Data Exchange (ETDEWEB)

    Kandasamy, S.B.; Hunt, W.A. (Armed Forces Radiobiology Research Institute, Bethesda, MD (USA))

    1990-01-01

    Exposure of rats to 1-15 Gy of gamma radiation induced hyperthermia, whereas exposure to 20-150 Gy produced hypothermia. Since radiation exposure induced the release of prostaglandins (PGs) and histamine, the role of PGs and histamine in radiation-induced temperature changes was examined. Radiation-induced hyper- and hypothermia were antagonized by pretreatment with indomethacin, a cyclooxygenase inhibitor. Intracerebroventricular administration of PGE2 and PGD2 induced hyper- and hypothermia, respectively. Administration of SC-19220, a specific PGE2 antagonist, attenuated PGE2- and radiation-induced hyperthermia, but it did not antagonize PGD2- or radiation-induced hypothermia. Consistent with an apparent role of histamine in hypothermia, administration of disodium cromoglycate (a mast cell stabilizer), mepyramine (H1-receptor antagonist), or cimetidine (H2-receptor antagonist) attenuated PGD2- and radiation-induced hypothermia. These results suggest that radiation-induced hyperthermia is mediated via PGE2 and that radiation-induced hypothermia is mediated by another PG, possibly PGD2, via histamine.

  1. Pharmacological modulation of IgE-dependent mast cell degranulation in experimental autoimmune uveoretinitis.

    Science.gov (United States)

    de Kozak, Y; Sakai, J; Sainte-Laudy, J; Faure, J P; Benveniste, J

    1983-01-01

    Immediate hypersensitivity phenomena have been shown previously to occur at the beginning of experimental autoimmune uveoretinitis (EAU) induced in Lewis rats by immunization with purified S-antigen from bovine retina. The onset time and severity of the disease were modified by modulating the mast cell (MC) function. Drugs blocking the release of mediators from MC, disodium cromoglycate and ketotifen, given as eyedrops, slightly delayed the onset and decreased the severity of inflammation. Compound 48/80, a drug effective in depleting MC of their inflammatory mediators, delayed significantly the onset, decreased and sometimes suppressed EAU, when given by the subconjunctival or intraperitoneal routes. No modification of the IgG and the IgE circulating anti-S-antibody level was demonstrated in both types of treatment, whereas in vitro reagin-dependent degranulation of peritoneal MC in the presence of the antigen was decreased in both cases. Identification of MC-bound reagins as IgE was strongly suggested by the blocking effect of anti-IgE antibodies on MC degranulation. These data confirm the link between MC activation and the onset and severity of EAU.

  2. Chiral symmetry breaking by spatial confinement in tactoidal droplets of lyotropic chromonic liquid crystals

    Science.gov (United States)

    Tortora, Luana; Lavrentovich, Oleg D.

    2011-01-01

    In many colloidal systems, an orientationally ordered nematic (N) phase emerges from the isotropic (I) melt in the form of spindle-like birefringent tactoids. In cases studied so far, the tactoids always reveal a mirror-symmetric nonchiral structure, sometimes even when the building units are chiral. We report on chiral symmetry breaking in the nematic tactoids formed in molecularly nonchiral polymer-crowded aqueous solutions of low-molecular weight disodium cromoglycate. The parity is broken by twisted packing of self-assembled molecular aggregates within the tactoids as manifested by the observed optical activity. Fluorescent confocal microscopy reveals that the chiral N tactoids are located at the boundaries of cells. We explain the chirality induction as a replacement of energetically costly splay packing of the aggregates within the curved bipolar tactoidal shape with twisted packing. The effect represents a simple pathway of macroscopic chirality induction in an organic system with no molecular chirality, as the only requirements are orientational order and curved shape of confinement. PMID:21402929

  3. Quercetin and Its Anti-Allergic Immune Response

    Directory of Open Access Journals (Sweden)

    Jiri Mlcek

    2016-05-01

    Full Text Available Quercetin is the great representative of polyphenols, flavonoids subgroup, flavonols. Its main natural sources in foods are vegetables such as onions, the most studied quercetin containing foods, and broccoli; fruits (apples, berry crops, and grapes; some herbs; tea; and wine. Quercetin is known for its antioxidant activity in radical scavenging and anti-allergic properties characterized by stimulation of immune system, antiviral activity, inhibition of histamine release, decrease in pro-inflammatory cytokines, leukotrienes creation, and suppresses interleukin IL-4 production. It can improve the Th1/Th2 balance, and restrain antigen-specific IgE antibody formation. It is also effective in the inhibition of enzymes such as lipoxygenase, eosinophil and peroxidase and the suppression of inflammatory mediators. All mentioned mechanisms of action contribute to the anti-inflammatory and immunomodulating properties of quercetin that can be effectively utilized in treatment of late-phase, and late-late-phase bronchial asthma responses, allergic rhinitis and restricted peanut-induced anaphylactic reactions. Plant extract of quercetin is the main ingredient of many potential anti-allergic drugs, supplements and enriched products, which is more competent in inhibiting of IL-8 than cromolyn (anti-allergic drug disodium cromoglycate and suppresses IL-6 and cytosolic calcium level increase.

  4. Deriving binary phase diagrams for chromonic materials in water mixtures via fluorescence spectroscopy: cromolyn and water.

    Science.gov (United States)

    Van Hecke, Gerald R; Karukstis, Kerry K; Rayermann, Scott

    2015-01-14

    We report here the first example of a new and novel method of determining the binary temperature-composition phase diagram of a chromonic material in water using its intrinsic fluorescence. Disodium cromoglycate, or cromolyn, is an anti-allergy medicine representative of a class of compounds known as the chromonics. We have discovered that cromolyn's fluorescence is very sensitive to the polarity, hence structure, of the phase it exhibits. The fluorescence signal shifts its wavelength maximum and its shape depending on whether the cromolyn is a single phase or in coexisting phases. Since the signal due to individual phases can be identified, the fluorescence signal can reveal the temperature-induced transitions between single phase and phase coexistence regions. By studying such fluorescence data for different compositions, an isobaric temperature-composition phase diagram may be constructed. We present here a phase diagram derived from fluorescence studies that is in agreement with previous determinations using other techniques. Our results suggest that the binary phase diagrams of other intrinsically fluorescent chromonic materials, such as perylene monoimide and bisimide derivatives used in organic optoelectronic devices, solar cells, and light-emitting diodes, can be studied in water using an analogous fluorescence approach.

  5. Comparative effects of vetiver oil, nootkatone and disodium octaborate tetrahydrate on Coptotermes formosanus and its symbiotic fauna.

    Science.gov (United States)

    Maistrello, Lara; Henderson, Gregg; Laine, Roger A

    2003-01-01

    The potential of vetiver oil and nootkatone as wood treatments against Coptotermes formosanus Shiraki was examined by assessing the effects on termite tunneling, feeding activity and survival, and the consequences on the symbiont protozoa responsible for wood digestion. Comparisons were made with non-treated wood (control), wood treated with the borate compound Tim-Bor (a commonly used lumber preservative) and absence of a food source (starved termites), using choice and no-choice tests. All wood slices were prepared at the same time using a 10 g liter(-1) solution of each substance and were tested in four different sessions over one year to investigate longevity of the effects. Termites had to tunnel through sand to exploit the food sources, consisting of two wood slices, placed on opposite sides of the experimental enclosure. No-choice tests showed that in the presence of vetiver oil or nootkatone, tunneling activity was always the lowest; wood consumption, termite survival and flagellate numbers and species distribution were significantly different from the control and similar to the results obtained for starved termites and with Tim-Bor-treated wood. Nootkatone negatively affected termites for 12 months and was longer lasting than vetiver oil. In choice tests, when vetiver oil or nootkatone were present, termites exhibited a significant preference for non-treated wood. Our results confirmed both the toxicity and absence of repellency of Tim-Bor. Vetiver oil and especially nootkatone affected Formosan subterranean termites and their protozoa, acting as arrestants, repellents and feeding deterrents, and represent a promising natural alternative for the control of this invasive pest.

  6. Crystal structure of disodium dicobalt(II iron(III tris(orthophosphate with an alluaudite-like structure

    Directory of Open Access Journals (Sweden)

    Adam Bouraima

    2015-05-01

    Full Text Available The title compound, Na2Co2Fe(PO43, was synthesized by a solid-state reaction. This new stoichiometric phase crystallizes in an alluaudite-like structure. In this structure, all atoms are in general positions except for four atoms which are located at the special positions of the C2/c space group. One Co atom, one P and one Na atom are all located on Wyckoff position 4e (2, while the second Na atom is located on an inversion centre 4a (-1. The other Co and Fe atoms occupy a general position with a statistical distribution. The open framework results from [(Co,Fe2O10] units of edge-sharing [(Co,FeO6] octahedra, which alternate with [CoO6] octahedra that form infinite chains running along the [10-1] direction. These chains are linked together through PO4 tetrahedra by the sharing of vertices so as to build layers perpendicular to [010]. The three-dimensional framework is accomplished by the stacking of these layers, leading to the formation of two types of tunnels parallel to [010] in which the Na+ cations are located, each cation being surrounded by eight O atoms.

  7. Poly[[hexa-aqua-sesqui(μ-benzene-1,2,4,5-tetra-carboxyl-ato)dicopper(II)disodium] monohydrate].

    Science.gov (United States)

    Camara, Magatte; Keita, Mohamed Fadel; Cisse, Cherif Cheikh Samsidine; Daiguebonne, Carole; Guillou, Olivier

    2014-08-01

    In the title compound, {[Cu2Na2(C10H2O8)1.5(H2O)6]·H2O} n , the Cu(2+) ion is hexa-coordinated by five O atoms from benzene-1,2,4,5-tetra-carboxyl-ate (btec(4-)) ligands and one water mol-ecule. The Na(+) ion is also hexa-coordinated, by four O atoms from btec(4-) ligands and two water mol-ecules. One of the two btec(4-) mol-ecules sits on a crystallographic inversion centre. CuO6 and NaO6 octa-hedra are connected, forming bi-dimensional layers. These layers, which extend parallel to the ac plane, are further inter-connected by μ10- or μ11-bridging btec(4-) ligands and by O-H⋯O hydrogen bonds, involving both btec(4-) ligands and water mol-ecules, forming a three-dimensional network.

  8. Lipid oxidation in fish oil enriched mayonnaise : Calcium disodium ethylenediaminetetraacetate, but not gallic acid, strongly inhibited oxidative deterioration

    DEFF Research Database (Denmark)

    Jacobsen, Charlotte; Hartvigsen, Karsten; Thomsen, Mikael Holm;

    2001-01-01

    The antioxidative effects of gallic acid, EDTA, and extra emulsifier Panodan DATEM TR in mayonnaise enriched with 16% fish oil were investigated. EDTA reduced the formation of free radicals, lipid hydroperoxides, volatiles, and fishy and rancid off-flavors. The antioxidative effect of EDTA...

  9. A co-crystal of nonahydrated disodium(II with mixed anions from m-chlorobenzoic acid and furosemide

    Directory of Open Access Journals (Sweden)

    Bianca King London

    2015-10-01

    Full Text Available In the title compound, [Na2(H2O9](C7H4ClO2(C12H10ClN2O5S {systematic name: catena-poly[[[triaquasodium(I]-di-μ-aqua-[triaquasodium(I]-μ-aqua] 3-chlorobenzoate 4-chloro-2-[(furan-2-ylmethylamino]-5-sulfamoylbenzoate]}, both the original m-chlorobenzoic acid and furosemide exist with deprotonated carboxylates, and the sodium cations and water molecules exist in chains with stoichiometry [Na2(OH29]2+ that propagate in the [-110] direction. Each of the two independent Na+ ions is coordinated by three monodentate water molecules, two double-water bridges, and one single-water bridge. There is considerable cross-linking between the [Na2(OH29]2+ chains and to furosemide sulfonamide and carboxylate by intermolecular O—H...O hydrogen bonds. All hydrogen-bond donors participate in a complex two-dimensional array parallel to the ab plane. The furosemide NH group donates an intramolecular hydrogen bond to the carboxylate group, and the furosemide NH2 group donates an intramolecular hydrogen bond to the Cl atom and an intermolecular one to the m-chlorobenzoate O atom. The plethora of hydrogen-bond donors on the cation/water chain leads to many large rings, up to graph set R44(24, involving two chains and two furosemide anions. The chlorobenzoate is involved in only one R22(8 ring, with two water molecules cis-coordinated to Na. The furan O atom is not hydrogen bonded.

  10. 40 CFR 180.1121 - Boric acid and its salts, borax (sodium borate decahydrate), disodium octaborate tetrahydrate...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Boric acid and its salts, borax... EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD Exemptions From Tolerances § 180.1121 Boric acid and its... the requirement of a tolerance is established for residues of the pesticidal chemical boric acid and...

  11. Inhibition of La-Fe-Co-Si compound corrosion in distilled water by sodium molybdate and disodium hydrogen phosphate

    Institute of Scientific and Technical Information of China (English)

    ZHANG Min; YE Rongchang; LONG Yi; CHANG Yongqin

    2011-01-01

    A comparative study of Na2MoO4·2H2O and Na2HPO4·12H2O as inhibitors for magnetic refrigeration material La-Fe-Co-Si comments were applied to study the corrosion behavior of the compound in the absence or presence of different concentrations of these inhibitors studied compounds acted as anodic inhibitors. The potential of zero charge (PZC) of La-Fe-Co-Si compound was determined in distilled water in the absence of the studied inhibitors. Corrosion inhibition mechanisms for inhibitors were proposed in this work.

  12. Lipid oxidation in fish oil enriched mayonnaise: calcium disodium ethylenediaminetetraacetate, but not gallic acid, strongly inhibited oxidative deterioration.

    Science.gov (United States)

    Jacobsen, C; Hartvigsen, K; Thomsen, M K; Hansen, L F; Lund, P; Skibsted, L H; Hølmer, G; Adler-Nissen, J; Meyer, A S

    2001-02-01

    The antioxidative effects of gallic acid, EDTA, and extra emulsifier Panodan DATEM TR in mayonnaise enriched with 16% fish oil were investigated. EDTA reduced the formation of free radicals, lipid hydroperoxides, volatiles, and fishy and rancid off-flavors. The antioxidative effect of EDTA was attributed to its ability to chelate free metal ions and iron from egg yolk located at the oil-water interface. Gallic acid reduced the levels of both free radicals and lipid hydroperoxides but promoted slightly the oxidative flavor deterioration in mayonnaise and influenced the profile of volatiles. Gallic acid may therefore promote the decomposition of lipid hydroperoxides to volatile oxidation products. Addition of extra emulsifier reduced the lipid hydroperoxide levels but did not influence the level of free radicals or the oxidative flavor deterioration in mayonnaisse; however, it appeared to alter the profile of volatiles. The effect of the emulsifier on the physical structure and rheological properties depended on the presence of antioxidants.

  13. Optimizing signal intensity correction during evaluation of hepatic parenchymal enhancement on gadoxetate disodium-enhanced MRI: Comparison of three methods

    Energy Technology Data Exchange (ETDEWEB)

    Onoda, Minori, E-mail: onoda@radt.med.kindai.ac.jp [Department of Radiological Technology, Kinki University Hospital, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan); Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, 5-11-80 Kodatsuno, Kanazawa, Ishikawa 920-0942 (Japan); Hyodo, Tomoko, E-mail: neneth@m.ehime-u.ac.jp [Department of Radiology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan); Murakami, Takamichi, E-mail: murakami@med.kindai.ac.jp [Department of Radiology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan); Okada, Masahiro, E-mail: okada777@med.u-ryukyu.ac.jp [Department of Radiology, Kinki University Faculty of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan); Uto, Tatsuro, E-mail: chuho@med.kindai.ac.jp [Department of Radiological Technology, Kinki University Hospital, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan); Hori, Masatoshi, E-mail: mhori@radiol.med.osaka-u.ac.jp [Department of Radiology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871 (Japan); Miyati, Tosiaki, E-mail: ramiyati@mhs.mp.kanazawa-u.ac.jp [Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, 5-11-80 Kodatsuno, Kanazawa, Ishikawa 920-0942 (Japan)

    2015-03-15

    Highlights: •Signal intensity is often used to evaluate hepatic enhancement with Gd-EOB-DTPA in the hepatobiliary phase. •Comparison of uncorrected signal intensity with T{sub 1} value revealed signal intensity instability. •Measurement of uncorrected liver SI or SNR often yields erroneous results on late-phase gadoxetate MRI due to shimming and other optimization techniques. •Signal intensity corrected by scale and rescale slope from DICOM data gave comparable results. -- Abstract: Objective: To compare signal intensity (SI) correction using scale and rescale slopes with SI correction using SIs of spleen and muscle for quantifying multiphase hepatic contrast enhancement with Gd-EOB-DTPA by assessing their correlation with T{sub 1} values generated from Look-Locker turbo-field-echo (LL-TFE) sequence data (ER-T{sub 1}). Materials and methods: Thirty patients underwent Gd-EOB-DTPA-enhanced magnetic resonance imaging (MRI) in this prospective clinical study. For each patient, breath-hold T{sub 1}-weighted fat-suppressed three-dimensional (3D) gradient echo sequences (e-THRIVE) were acquired before and 2 (first phase), 10 (second phase), and 20 min (third phase) after intravenous Gd-EOB-DTPA. Look-Locker turbo-field-echo (LL-TFE) sequences were acquired before and 1.5 (first phase), 8 (second phase), and 18 min (third phase) postcontrast. The liver parenchyma enhancement ratios (ER) of each phase were calculated using the SI from e-THRIVE sequences (ER-SI) and the T{sub 1} values generated from LL-TFE sequence data (ER-T{sub 1}) respectively. ER-SIs were calculated in three ways: (1) comparing with splenic SI (ER-SI-s), (2) comparing with muscle SI (ER-SI-m), (3) using scale and rescale slopes obtained from DICOM headers (ER-SI-c), to eliminate the effects of receiver gain and scaling. For each of the first, second and third phases, correlation and agreement were assessed between each ER-SI and ER-T{sub 1}. Results: In the first phase, all ER-SIs correlated weakly with ER-T{sub 1}. In the second and third phases, ER-SI-c showed a stronger linear correlation with ER-T{sub 1} (r{sup 2} = 0.71–0.72, p < 0.01) than did ER-SI-s (r{sup 2} = 0.37–0.39, p < 0.01) or ER-SI-m (r{sup 2} = 0.30–0.41, p < 0.01). Conclusion: SI correction using scale and rescale slopes from DICOM data is the most acceptable algorithm for evaluating delayed-phase Gd-EOB-DTPA hepatic enhancement.

  14. Anti-allergic cromones inhibit histamine and eicosanoid release from activated human and murine mast cells by releasing Annexin A1.

    Directory of Open Access Journals (Sweden)

    Samia Yazid

    Full Text Available BACKGROUND AND PURPOSE: Although the 'cromones' (di-sodium cromoglycate and sodium nedocromil are used to treat allergy and asthma, their 'mast cell stabilising' mechanism of pharmacological action has never been convincingly explained. Here, we investigate the hypothesis that these drugs act by stimulating the release of the anti-inflammatory protein Annexin-A1 (Anx-A1 from mast cells. EXPERIMENTAL APPROACH: We used biochemical and immuno-neutralisation techniques to investigate the mechanism by which cromones suppress histamine and eicosanoid release from cord-derived human mast cells (CDMCs or murine bone marrow-derived mast cells (BMDMCs from wild type and Anx-A1 null mice. KEY RESULTS: CDMCs activated by IgE-FcRε1 crosslinking, released histamine and prostaglandin (PG D2, which were inhibited (30-65% by 5 min pre-treatment with cromoglycate (10 nM or nedocromil (10 nM, as well as dexamethasone (2 nM and human recombinant Anx-A1 (1-10 nM. In CDMCs cromones potentiated (2-5 fold protein kinase C (PKC phosphorylation and Anx-A1 phosphorylation and secretion (3-5 fold. Incubation of CDMCs with a neutralising anti-Anx-A1 monoclonal antibody reversed the cromone inhibitory effect. Nedocromil (10 nM also inhibited (40-60% the release of mediators from murine bone marrow derived-mast cells from wild type mice activated by compound 48/80 and IgE-FcRε1 cross-linking, but were inactive in such cells when these were prepared from Anx-A1 null mice or when the neutralising anti-Anx-A1 antibody was present. CONCLUSIONS AND IMPLICATIONS: We conclude that stimulation of phosphorylation and secretion of Anx-A1 is an important component of inhibitory cromone actions on mast cells, which could explain their acute pharmacological actions in allergy. These findings also highlight a new pathway for reducing mediator release from these cells.

  15. Studies on the release of leukotrienes and histamine by human lung parenchymal and bronchial fragments upon immunologic and nonimmunologic stimulation. Effects of nordihydroguaiaretic acid, aspirin, and sodium cromoglycate

    Science.gov (United States)

    1985-01-01

    Fragments of human lung parenchyma or bronchi were studied by high performance liquid chromatography, gas chromatography-mass spectrometry, and bioassay for the biosynthesis of 5-lipoxygenase metabolites of arachidonic acid, and by radioenzymatic assay for the release of histamine, upon immunologic and nonimmunologic stimulation. Human lung parenchyma were passively sensitized with serum from timothy- positive allergic patients (radioallergosorbent test, 30-40%) and challenged with 0.5 microgram/ml of timothy allergen. Analysis of the incubation media showed the presence of LTB4, LTC4, LTD4, LTE4, and histamine. Maximum release of LTB4 and LTD4 was observed after 15 min of challenge (92.8 +/- 21, and 67.8 +/- 14 pmol/g tissue wet weight, respectively; mean +/- SEM) whereas maximum release of LTC4 was observed after 5 min of challenge (25 +/- 7.1 pmol). In parallel to leukotriene formation, histamine was released rapidly and reached a maximum after approximately 15 min of challenge (2.85 +/- 0.76 nmol/g tissue). When fragments of human lung parenchyma were stimulated with ionophore A23187 (4 microM), we observed a profile of leukotriene and histamine release similar to that seen in response to the allergen. Ionophore A23187 stimulated the release of two- to fivefold greater amounts of leukotrienes and histamine than did the allergen. Release of LTC4 and histamine was maximal after 5 min of stimulation (83 +/- 22.2 and 5.2 +/- 0.95 nmol/g tissue, respectively), whereas LTB4 and LTD4 release reached a maximum after 15 min (438 +/- 66.6 and 205 +/- 68 nmol/g tissue, respectively). In addition, human lung parenchyma metabolized LTB4 into omega-OH-LTB4 and omega-COOH-LTB4. This tissue also released 5-hydroxy-eicosatetraenoic acid (5-Hete), 12-Hete, and 15- Hete. Fragments of human lung bronchi also released a similar profile of leukotrienes (except LTC4) and histamine when challenged with the allergen or ionophore A23187. Maximum release of LTB4 and LTD4 by allergen or ionophore stimulation was observed after approximately 15 min (40 +/- 7.5 and 21 +/- 8 pmol/g tissue, respectively, upon allergen challenge; 100 +/- 13 and 47 +/- 10.6 pmol/g tissue, respectively, upon ionophore stimulation). The maximum release of histamine by bronchi was observed after approximately 15 min of allergen challenge and 5 min of ionophore stimulation (2.25 +/- 0.65 and 3.15 +/- 0.9 nmol/g tissue, respectively). The release of leukotrienes but not of histamine by human lung parenchyma upon both allergen and ionophore challenge was inhibited by nordihydroguaiaretic acid (NDGA) (ID50, 2 X 10(- 6)M).(ABSTRACT TRUNCATED AT 400 WORDS) PMID:2415659

  16. (Liquid + liquid) and (liquid + solid) equilibrium of aqueous two-phase systems containing poly ethylene glycol di-methyl ether 2000 and di-sodium hydrogen phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Zafarani-Moattar, Mohammed Taghi, E-mail: zafarani47@yahoo.co [Physical Chemistry Department, University of Tabriz, Tabriz 51664 (Iran, Islamic Republic of); Nasiri, Saeed [Physical Chemistry Department, University of Tabriz, Tabriz 51664 (Iran, Islamic Republic of)

    2010-09-15

    (Liquid + liquid) equilibrium (LLE) for the {l_brace}poly ethylene glycol di-methyl ether 2000 (PEGDME{sub 2000}) + Na{sub 2}HPO{sub 4} + H{sub 2}O{r_brace} system have been determined experimentally at T = (298.15, 308.15, 313.15, and 318.15) K. The effects of temperature on the binodals and tie-lines for the investigated aqueous two-phase system (ATPS) have been studied. An empirical non-linear expression developed by Merchuk was used for reproducing the experimental binodal data. In this work, the three fitting parameters of the Merchuk equation were obtained with the temperature dependence expressed in the linear form with (T - T{sub 0}) K as a variable. Furthermore, the modified local composition segment-based NRTL and Wilson models and also osmotic virial equation were used to describe the LLE data of the studied system. Also, the effects of the type of salt on LLE are discussed. In addition, the effects of end groups of the polymers PEGDME{sub 2000} and poly ethylene glycol 2000 on phase forming ability were studied. The complete phase diagram for the poly ethylene {l_brace}glycol di-methyl ether 2000 (PEGDME{sub 2000}) + Na{sub 2}HPO{sub 4} + H{sub 2}O{r_brace} system has also been determined at T = 298.15 K.

  17. Methoxyamine, Pemetrexed Disodium, Cisplatin, and Radiation Therapy in Treating Patients With Stage IIIA-IV Non-small Cell Lung Cancer

    Science.gov (United States)

    2016-10-05

    Metastatic Malignant Neoplasm in the Brain; Stage IIIA Large Cell Lung Carcinoma; Stage IIIA Lung Adenocarcinoma; Stage IIIA Non-Small Cell Lung Cancer; Stage IIIB Large Cell Lung Carcinoma; Stage IIIB Lung Adenocarcinoma; Stage IIIB Non-Small Cell Lung Cancer; Stage IV Large Cell Lung Carcinoma; Stage IV Lung Adenocarcinoma; Stage IV Non-Small Cell Lung Cancer

  18. Hepatobiliary transit times of gadoxetate disodium (Primovist) for protocol optimization of comprehensive MR imaging of the biliary system-What is normal?

    Energy Technology Data Exchange (ETDEWEB)

    Ringe, Kristina I., E-mail: ringe.kristina@mh-hannover.de [Duke University Medical Center, Department of Radiology, Box 3808, Durham, NC 27710 (United States); Hannover Medical School, Department of Radiology, Carl-Neuberg Str. 1, 30625 Hannover (Germany); Husarik, Daniela B., E-mail: danielahusarik@yahoo.com [Duke University Medical Center, Department of Radiology, Box 3808, Durham, NC 27710 (United States); Gupta, Rajan T., E-mail: rajan.gupta@duke.edu [Duke University Medical Center, Department of Radiology, Box 3808, Durham, NC 27710 (United States); Boll, Daniel T., E-mail: daniel.boll@duke.edu [Duke University Medical Center, Department of Radiology, Box 3808, Durham, NC 27710 (United States); Merkle, Elmar M., E-mail: elmar.merkle@duke.edu [Duke University Medical Center, Department of Radiology, Box 3808, Durham, NC 27710 (United States)

    2011-08-15

    Objective: The purpose of this study was to determine transit times for excretion of Gd-EOB-DTPA into different segments of the hepatobiliary system in patients with normal liver function. Methods: This retrospective study was IRB approved with a waiver of consent granted. 61 patients (39 female, 22 male, mean age 52.5 years) with normal liver and renal function who underwent contrast enhanced hepatic MRI after injection of 10 mLGd-EOB-DTPA at 1.5 T and 3 T were included. Two readers evaluated all delayed images (3-20 min post contrast) for the presence of contrast agent in the intrahepatic bile ducts (IBD), the common bile duct (CBD), the gallbladder and the duodenum. A two-tailed, unpaired Student's t-test with p < 0.05 deemed significant was used to determine whether transit times were affected by patient gender, age or body mass index. Results: 20 min after contrast initiation, Gd-EOB-DTPA could be detected in the IBD and the CBD in all patients (100%); gallbladder reflux was visible in 53 (86.9%), duodenal excretion in 40 patients (65.5%), respectively. Mean transit times for contrast appearance in the various segments were as follows: IBD 12 min 13 s; CBD 12 min 27 s; gallbladder 13 min 32 s. Transit times were not significantly affected by patient gender, age or BMI. Conclusion: Within 20 min post contrast initiation, Gd-EOB-DTPA can be expected in the IBD and the CBD in patients with normal liver function. However, functional information about the sphincter Oddi complex can be ascertained only in about two thirds of these patients within this timeframe.

  19. Dilithium disodium nickel(II) cyclo-hexa-phosphate dodeca-hydrate, Li(2)Na(2)NiP(6)O(18)·12H(2)O.

    Science.gov (United States)

    Abid, Sonia; Al-Deyab, Salem S; Rzaigui, Mohamed

    2012-08-01

    The crystal structure of Li(2)Na(2)NiP(6)O(18)·12H(2)O is characterized by the presence of six-membered P(6)O(18) (6-) phosphate ring anions (inter-nal symmetry -1) having a chair conformation and three different cations, viz. Li(+), Na(+) and Ni(2+), to counterbalance the anionic charge. All atoms are in general positions except for nickel, which lies on a special position with site symmetry 2. Lithium has a tetra-hedral environment (LiO(4)), and sodium and nickel have octa-hedral environments [NaO(6) and Ni(H(2)O)(6), respectively]. The P(6)O(18) rings are linked via corner sharing by NaO(6) octa-hedra and LiO(4) tetra-hedra to form a three-dimensional framework presenting tunnels running along [010] in which the six-coordinated Ni(2+) cations are located. The structure is stabilized by a network of O-H⋯O hydrogen bonds.

  20. Anti-allergic effect of desloratadine citrate disodium injection%枸地氯雷他定注射液的抗过敏药效研究

    Institute of Scientific and Technical Information of China (English)

    袁馨; 揭琼; 陈美灵; 吴玉林

    2015-01-01

    目的:探讨枸地氯雷他定注射液的抗过敏作用.方法:应用组胺致大鼠皮肤血管通透性增加、4-氨基吡啶(4-AP)致小鼠瘙痒和组胺致豚鼠哮喘模型,评价枸地氯雷他定注射液的抗过敏作用.结果:枸地氯雷他定注射液各组能明显抑制皮内注射25或50 μg组胺后引起的大鼠皮肤血管通透性增高(P<0.01),有效减少了皮肤的蓝染面积.枸地氯雷他定注射液各组对组胺致豚鼠哮喘有明显的拮抗作用,显著延长休克潜伏期(P<0.01).枸地氯雷他定注射液中、高剂量组能显著延长4-AP致小鼠瘙痒的潜伏期及减少瘙痒次数(P<0.01).结论:初步验证了枸地氯雷他定注射液的抗过敏疗效.

  1. Determining the critical micelle concentration of a novel lipid-lowering agent, disodium ascorbyl phytostanyl phosphate (FM-VP4), using a fluorescence depolarization procedure.

    Science.gov (United States)

    Wasan, Kishor M; Choo, Eugene; Sivak, Olena; Wallis, Simon; Letchford, Kevin; Burt, Helen M; Stewart, David J; Lukic, Tatjana

    2004-08-01

    The objective of this study was to determine the critical micelle concentration (CMC) of a novel water-soluble plant sterol derivative (FM-VP4) using a fluorescence depolarization method. The CMC was determined by 1,6-diphenyl-1,3,5-hexatriene (DPH) fluorescence depolarization. Test solutions of various concentrations of sodium dodecylsulphate (SDS) as a positive control or FM-VP4 in water were spiked with 2 microL of 4 mM DPH in tetrahydrofuran (THF) and left overnight to equilibrate in a dark chamber. Fluorescence of each solution was measured at room temperature using a Perseptive Biosystems Cytofluor Series 4000 multi-well plate reader. Fluorescence intensity increases as DPH is incorporated into the hydrophobic core of micelles. Thus, the CMC is the value at which an abrupt increase in intensity is observed. These points were observed at 8 mM and 0.014 mM for SDS and FM-VP4, respectively. Sodium dodecylsulphate was used as a positive control and supports the validity of our results, as the literature values of SDS are reported to be between 8-8.3 mM. The CMC of FM-VP4 is reported to be 0.014 mM.

  2. Drug: D00941 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D00941 Drug Pamidronate disodium hydrate (JAN); Pamidronate disodium (USAN); Pamidronate disodium pentahydr...[ATC:M05BA03] D00941 Pamidronate disodium hydrate (JAN); Pamidronate disodium (USAN) CAS: 109552-15-0 PubChem: 7848004 Dr...[KO:K00787] hsa00900(2224) Terpenoid backbone biosynthesis map07047 Osteoporosis dr...ugs Therapeutic category of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents affe...cting metabolism 399 Miscellaneous 3999 Others D00941 Pamidronate disodium hydrate (JAN); Pamidronate disodi

  3. Determination of Sodium Cromoglycate in Some Cough Preparations of Traditional Chinese Medicine by HPLC%HPLC检测某些止咳中药制剂中色甘酸钠

    Institute of Scientific and Technical Information of China (English)

    李洪亮; 程齐来

    2012-01-01

    建立了检测止咳中药制剂中非法掺人的化学止咳平喘药物色甘酸钠的方法.选用Agilent Eclipse XDB-C18 (4.6mm×150mm,5μm),以甲醇∶ 0.34%磷酸二氢钾=15 ∶ 85(V/V)为流动相.根据所检测到化合物的色谱保留时间,并与对照品比较,鉴别中药制剂中非法掺入的色甘酸钠化学药物.本实验建立的条件能够把中药制剂中添加的化学药物(色甘酸钠)完全分离开来;对20个制剂用建立的分析技术进行了检测,经与相应的标准物质比较,20个样品均未含色甘酸钠.该方法选择性强,灵敏度高,可作为中药制剂中非法加入掺入化学药物成分色甘酸钠的有效检测手段.

  4. HPLC-MS/MS法测定人体色甘酸钠血浆浓度及其药代动力学研究%HPLC-MS/MS method for determination of sodium cromoglycate concentration in human plasma and its pharmacokinetics

    Institute of Scientific and Technical Information of China (English)

    徐晓燕; 张蕊; 袁桂艳; 王本杰; 刘晓燕; 郭瑞臣

    2008-01-01

    采用HPLC-MS/MS法测定人血浆中色甘酸钠浓度,进行其滴鼻液和鼻用喷雾剂的药代动力学研究并评价其生物等效性.采用高效液相分离系统,流动相为乙酸铵-甲醇(含50%乙腈)(15:85),固定相为AGT VenusilXBP C18(250 mm×4.6 mm ID,5μm)色谱柱.采用质谱检测系统,ESI离子源,正离子模式,多级反应监测(MRM)方式,m/z 469→263.1(色甘酸钠),m/z 447.2→327.1(内标,普伐他汀钠).在0.3~20 ng·mL-1色甘酸钠血药浓度呈线性关系,定量限为0.3 ng·mL-1,回收率在94.1%以上,日内日间的RSD均小于14.3%.单剂量给药色甘酸钠鼻用喷雾剂或滴鼻液,其药代动力学参数T1/2分别为(1.82±0.54)和(1.59±0.52)h;Tmax分别为(0.47±0.12)和(0.44±0.15)h;Cmax分别为(9.79±4.66)和(10.88±4.05)ng·mL-1,AUC0-5h分别为(11.52±3.46)和(12.63±4.23)ng·mL-1·h.色甘酸钠鼻用喷雾剂相对生物利用度Fr为(93.6±13.8)%.本法灵敏度高,适用于色甘酸钠治疗药物监测及其药代动力学和生物利用度研究.

  5. 色甘酸钠吸入防治儿童咳嗽变异性哮喘临床观察%Therapeutic effects of sodium cromoglycate inhaler pulmicort on couph variant asthma in children

    Institute of Scientific and Technical Information of China (English)

    刘玉玲

    2003-01-01

    @@ 我们将符合儿童咳嗽变异性哮喘(CVA)诊断[1],应用常规治疗方法效果差的26例患儿,采用色甘酸钠气雾剂吸入治疗,在减轻患儿症状、远期疗效及预防复发等方面取得较好疗效,现报道如下.

  6. Combined sodium cromoglycate and mitomycin C in preventing recurrence of pterygium%色甘酸钠联合丝裂霉素 C防止翼状胬肉复发

    Institute of Scientific and Technical Information of China (English)

    肖斯贤; 徐珊琪

    2001-01-01

    目的 观察色甘酸钠联合0.1 g/L丝裂霉素C对翼状胬肉切除加带蒂结膜瓣移位术后预防胬肉复发的作用。方法 采用随机分组对照法,对 77例(82眼)原发性和复发性翼状胬肉随机分成两组,观察组42例(45眼),对照组35例(37眼),两组均施行胬肉切除加带蒂结膜瓣移位术。观察组术后滴用色甘酸钠滴眼液,4次/d, 共3个月,同时滴用0.1 g/L丝裂霉素 C,2次/d,共6 d ,随访11~20个月,平均13个月。结果 3例(3眼)失访。观察组翼状胬肉复发率2.2%,对照组复发率28%, 两组比较,差异有非常显著性P<0.01。观察组角膜创面愈合延迟,7例有浅层点状角膜炎。结论 翼状胬肉切除加带蒂结膜瓣移位术后滴用色甘酸钠联合0.1 g/L丝裂霉素C能安全、有效地预防翼状胬肉复发。

  7. 高效液相色谱法测定色甘酸钠地塞米松滴鼻液含量%Determination of the Content of Dexamethasone Sodium Phosphate and Sodium Cromoglycate by HPLC

    Institute of Scientific and Technical Information of China (English)

    黄滔敏; 杨鸿; 刘振; 沙云菲; 段更利

    2005-01-01

    目的建立一种HPLC法同时测定地塞米松色甘酸钠滴鼻液中磷酸地塞米松和色甘酸钠含量.方法采用Diamonsil C18(150 mm×4.6 mm,5μm)色谱柱,流动相:A:缓冲液(0.01 mol/L磷酸二氢钾,pH为4.7),B:甲醇,0~5 min:A-B(42:58),6 min后A-B(30:70),流速:1 mL/min,柱温:25℃,检测波长:240 nm.外标法计算含量.结果在该色谱条件下,磷酸地塞米松和色甘酸钠线性良好(r>0.999,n=6),加样回收率为98%~102.55%(n=3),RSD<2.0%(n=3).样品在8 h内稳定.测得样品含量合格,在97%~103%.结论经方法学实验验证,该方法简便,快速,结果准确,可靠,重现性好.

  8. Clinical efficacy of sodium cromoglycate combined with cimetidine in treatment of severe vernal conjunctivitis%色甘酸钠联合西米替丁治疗重症春季结膜炎的临床疗效

    Institute of Scientific and Technical Information of China (English)

    张姝

    2008-01-01

    目的 探讨色甘酸钠联合西米替丁治疗长期反复发作、眼部反应重、部分病例有Trantasdots小点、并发盾状溃疡的重症春季结膜炎的临床疗效.方法 36例随机分为实验组和对照组.实验组21例用色甘酸钠联合西米替丁,西米替丁每次400 mg,3次/d,口服,10~15 d为1个疗程,2%色甘酸钠滴眼液,6次/d滴眼;对照组15例用吲哚美辛口服或阿斯匹林口服,用0.5%可的松滴眼液,3次/d滴眼.结果 实验组治疗后,66.66%患眼病情缓解,28.57%患眼好转,总有效率95.23%;对照组治疗后13.33%患眼病情缓解,46.67%患眼好转,总有效率为60.00%,两组差异极其显著(P<0.01).结论 抗组胺H2受体的免疫调节剂西米替丁全身应用方法简单、经济,无不良反应,是选择应用于重症春季结膜炎的一种新的有效疗法.

  9. Effect of Protoporphyrin Disodium in Vitro on The Anti-HCV Replicon%原卟啉二钠体外对丙型肝炎病毒复制子的抑制作用

    Institute of Scientific and Technical Information of China (English)

    刘群红; 梁勇; 王克霞

    2007-01-01

    目的:探讨原卟啉二钠(PPN)体外对丙型肝炎病毒(HCV)的抑制作用.方法:用不同浓度PPN和利巴韦林处理HCV复制子细胞模型,MTT法检测药物的细胞毒性作用;荧光定量PCR检测HCV RNA.结果:PPN和利巴韦林浓度在1 mg·mL-1以下时,MTT法比色A值比较,实验组与对照组间差异均无显著性,无明显细胞毒性;PPN在1 mg·mL-1时对HCV RNA的抑制率为73.44%,差异有显著性(P<0.05),利巴韦林在1 mg·mL-1时对HCV RNA的抑制率为40.78%,差异无显著性,二者抑制HCV RNA的EC50分别为0.23 mg·mL-1和1.19 mg·mL-1.结论:PPN和利巴韦林浓度在1 mg·mL-1以下时对HCV Replicon细胞生长无毒性作用;PPN具有明显的体外抑制在HCV复制的作用,抑制作用强于利巴韦林.

  10. Emprego do sal di-sódico de edta como padrão no preparo de soluções Use of EDTA disodium salt as standard for preparation of solutions

    Directory of Open Access Journals (Sweden)

    Paulo H. Pereira da Silva

    2007-06-01

    Full Text Available The hydrated sodium salt of EDTA, Na2H2Y·2H2O, cannot be used as a primary standard for titrations due to uncertainties in the water content. An alkalimetric titration of the homogenized solid in the presence of a small excess of BaCl2·2H2O allows one to titrate quantitatively the released two hydrogen cations with end-point indication by phenolphthalein or potentiometry. This leads one to calculate the average molar mass of the reagent and its water content, allowing to use it to prepare EDTA standard solutions. One titrated sample led to the formula Na2H2Y·1.876 H2O, and 370.01 g.mol-1 for the average molar mass.

  11. 抗组胺新药枸地氯雷他定研究综述%A Review of the Research on Desloratadine Citrate Disodium, a New Antihistamine Drug

    Institute of Scientific and Technical Information of China (English)

    刘为中; 何广卫; 崔进

    2014-01-01

    枸地氯雷他定是一种可以口服的抗组胺新药,系列的药理、药效、毒理、药代动力学和临床研究证明了枸地氯雷他定缓解慢性特发性荨麻疹及常年性过敏性鼻炎的全身及局部症状的安全和有效性.

  12. Aqua(μ-cone-26,28-dibutoxy-25,27-bis{N-[5-(dimethylaminonaphthalene-1-sulfonyl]carbamoylmethoxy}-5,11,17,23-tetrakis(1,1-dimethylethylcalix[4]arene(2−disodium acetonitrile tetrasolvate

    Directory of Open Access Journals (Sweden)

    Pogisego Dinake

    2012-04-01

    Full Text Available The structure of the title complex, [Na2(C80H98N4O10S2(H2O]·4CH3CN, obtained after crystallization from acetonitrile, contains two formula units in the asymmetric unit (Z′ = 2 and an estimated four molecules of acetonitrile per calixarene moiety. It is unusual for two Na+ ions to occupy the lower rims of the cone calix[4]arene, as in this case, with one Na+ ion forming two O→ Na+ coordinate bonds with the two butoxy groups and four such bonds with the two N-dansyl carboxamide groups, forming six dative bonds between Na+ and O. On the other hand, the other Na+ ion forms only five O→Na+ coordinate bonds on the far end of the calix[4]arene lower rim, bringing the two dansyl groups in close proximity with each other. There also appears to be an O→Na+ coordination coming from a dangling water molecule. The structure contained both resolved and poorly resolved solvent molecules. The latter were treated using the SQUEEZE routine in PLATON [Spek (2009. Acta Cryst. D65, 148–155].

  13. Metabolism of gold salt in the treatment of rheumatoid arthritis. Tissue distribution of the organic counterpart and their fate in relation to the gold atom after administration of (1,2-dicarboxyethyl thio) gold disodium salt (4-/sup 14/C)

    Energy Technology Data Exchange (ETDEWEB)

    Ishigami, M. (Tokyo Women' s Medical Coll. (Japan))

    1981-11-01

    Radioactive aurothiomalate (4-/sup 14/C) was administrated parenteraly to rats or rabbits, and tissue distribution of radioactivity and their fate were studied. Radioactivity which represented the organic counterpart of the gold salt was relatively quickly taken up into the blood and reduced with half life time of an hour. In the blood, it stayed mainly in the serum while only small portion of it was incorporated into corpuscles. Radioactivities were taken into various organs quickly also, particularly into kidney and bone in high concentrations. High absorption of the radioactivity by skin was observed at the early stage but quickly decreased by time passage. The radioactivity incorporated into organs did not accumulate but disappeared rather quickly, with little differences in the patterns of disappearance from organ to organ. Much radioactivity seemed to move into the digestive tract. Significant amount of radioactivity was recovered in the expired CO/sub 2/. Its discharging speed was nearly parallel to that of the blood radioactivity level. The metabolic pattern of the organic counterpart of the gold was greatly different to that of its gold atom. Soon after the administration, the gold salt was separated into the two portions, gold atom and organic moiety, and then would go through different metabolic courses.

  14. Determination of ethylenediaminetetraacetic acid disodium residues in canned fish by HPLC-MS/MS%HPLC-MS/MS测定鱼罐头中乙二胺四乙酸二钠残留量

    Institute of Scientific and Technical Information of China (English)

    张晓华; 曾繁华; 张锐夫

    2015-01-01

    建立了超高效液相色谱-质谱/质谱测定鱼罐头中乙二胺四乙酸二钠残留量的检测和确证方法.试样中残留的乙二胺四乙酸二钠用水高速匀浆提取,提取液经三氯化铁衍生化、三氯甲烷和MAX阴离子交换柱净化后,用超高效液相色谱-质谱/质谱仪检测和确证,外标法定量.乙二胺四乙酸二钠的浓度在1.0~50.0μg·mL-1范围内时,线性关系良好,乙二胺四乙酸二钠的相关系数(R2)为0.9922.在20~400rmg·kg-1浓度范围内,样品平均加标回收率在80.75%~105.40%之间,相对标准偏差为5.46%~8.95%.乙二胺四乙酸二钠的最低检出限为20mg·kg-1.该方法具有灵敏、准确、稳定等优点,可用于鱼罐头中乙二胺四乙酸二钠残留量测定.

  15. Bola型表面活性剂磺化脱氢松香酸二钠盐的表面化学性质%Surfactivity of the Bolaform Surfactant Disodium Sulfodehydroabietate

    Institute of Scientific and Technical Information of China (English)

    陈立云; 方桂珍; 王献玲; 李珊珊; 李宏振

    2008-01-01

    以脱氢松香酸为原料,经磺化、中和反应合成了一种非对称Bola型表面活性剂磺化脱氢松香酸二钠盐(DSDA),利用FT-IR、1H NMR及MS对目标产物结构进行确证,采用表面张力法确定了DSDA在303.0K、pH值为10.5时的临界胶束浓度(CMC),考察了其在不同NaCl浓度(0~0.50mol/L)下的表面活性.结果表明,DSDA溶液表面张力-浓度曲线出现了一个转折点;一定温度下,随着NaCl浓度的增大,DSDA溶液CMC从25mmol/L降至3.83mmol/L,表面极限吸附量(Г∞)下降,最低表面张力(γCMC)基本不受影响.

  16. Study on the Practicability of Bacterial Endotoxins Test for Adenosine Disodium Triphosphate Raw Material%三磷酸腺苷二钠原料药的细菌内毒素检查法可行性研究

    Institute of Scientific and Technical Information of China (English)

    李薇; 刘肃; 何华红; 吴婷

    2010-01-01

    目的:建立三磷酸腺苷二钠原料药中细菌内毒素的鲎试剂检查方法.方法:复核鲎试剂标示灵敏度,确定样品细菌内毒素限值;通过干扰预试验确定样品稀释倍数,正式干扰试验确定样品的最大无干扰浓度,根据方法对11批样品进行细菌内毒素检查.结果:所用鲎试剂灵敏度均符合规定,样品细菌内毒素限值确定为2.0 EU·mg-1,最大无干扰浓度为0.125 mg·mL-1,11批样品内毒素检查结果均符合规定.结论:采用鲎试剂法检查三磷酸腺苷二钠原料药中细菌内毒素的方法可行,可代替家兔热原检查法.

  17. Research on Anti-Browning of Disodium Stannous Citrate in Canned Agaricus bisporus%柠檬酸亚锡二钠对双孢菇罐头的护色作用

    Institute of Scientific and Technical Information of China (English)

    张婷婷; 夏文水; 姜启兴; 许艳顺

    2013-01-01

    The investigation was conducted to determine the efficacy of DSC as a browning inhibition agent of fresh-cut and canned Agaricus bisporus. DSC and other anti-browning agents as well as the new compound color fixative ware used in pretreatment and canned Agaricus bisporus. Residual activity of PPO and the browning degree (BD) were measured as performance figures. DSC played an important part in enzymatic browning inhibition, compared to other anti-browning agents such as phytic acid,citric acid and VC. The sliced Agaricus bisporuss pretreated with mixed liquor containing 0.2% citric acid,0.03% DSC,0.02% phytic acid,0.03% VC were effectively kept from enzymatic browning and then blanched. In addition,the products with DSC resulted in better performance than those with sodium metabisulphite as well as other anti-browning agents. The best compound color fixative of anti -browning agents in the cans was to be 0.03% DSC, phytic acid 0.02%,citric acid 0.1% and 0.3% CaCi2,which leaded to a similar effect of browning inhibition,as compared with 0.02% of sodium metabisulphite. In general, DSC proves to be able to take the place of sodium metabisulphite and act as a new safe and effective anti-browning agent used in canned Agaric us bisporuss.%研究柠檬酸亚锡二钠(DSC)对双孢菇罐头的护色作用.在双孢菇切片预处理和罐头汤汁中添加DSC与其他常用护色剂及其正交复合护色剂,测定产品的PPO残余酶活和褐变度BD等质量指标.在预处理阶段,较之植酸、柠檬酸、VC,DSC对双孢菇酶促褐变有更佳的抑制作用,预煮前以最佳复合护色剂(质量分数)0.2%柠檬酸,0.03% DSC,0.02%植酸,0.03% VC护色液浸泡预处理可有效防止菇片褐变;DSC用于双孢菇罐头汤汁比其他护色剂有更显著的褐变抑制效果,汤汁复合护色剂的最佳参数组合为(质量分数):0.03% DSC,0.02%植酸,0.3% CaCl2和0.1%柠檬酸,各因素对其影响程度为:DSC>植酸>氯化钙.DSC复合护色剂可有效抑制双孢菇罐头褐变,效果可与焦亚硫酸钠媲美,可作为蘑菇罐头中替代焦亚硫酸钠的新型安全高效护色剂.

  18. The Content Determination of Pamidronate Disodium Injection by Pre-column Derivatization HPLC%柱前衍生化HPLC法测定注射用帕米膦酸二钠含量

    Institute of Scientific and Technical Information of China (English)

    张燕; 戴河双; 胡培; 李开金; 李洁; 罗帅; 陈琴华

    2014-01-01

    目的:建立9-氯甲酸芴甲酯(9-fluorenyl methyl chloroformate,FMOC-Cl)柱前衍生化高效液相色谱法(HPLC)测定注射用帕米膦酸二钠含量的方法.方法:碱性条件下供试品与FMOC衍生化反应,采用Linksil HPLCODS C18色谱柱(4.6 mm×250 mm,5 μm),乙腈-0.4% EDTA(pH=7.2) (25∶ 75)为流动相,流速1 mL ·min-,检测波长为264 nm.结果:帕米膦酸二钠浓度在2~35 μg· mL-1范围内与峰面积呈良好线性关系(r=0.9995),检测限为0.5 μg· mL-1,平均回收率101.2% (n=9).结论:本法简单、准确、灵敏,适用于注射用帕米膦酸二钠的含量测定.

  19. Forty-Five Cases of Chronic Eczema Treated with Jade Screen Capsule in Combination with Desloratadine Citrate Disodium%玉屏风胶囊联合枸地氯雷他定治疗慢性湿疹45例

    Institute of Scientific and Technical Information of China (English)

    戴前梅; 胡春艳; 陈朋; 陈晨; 张明海

    2015-01-01

    目的:观察玉屏风胶囊联合枸地氯雷他定治疗慢性湿疹的临床疗效及对血清IL-10、IgE水平的影响.方法:选择慢性湿疹患者90例,按照随机数字表法分为观察组和对照组,每组45例.对照组给予玉屏风胶囊治疗,观察组给予玉屏风胶囊联合枸地氯雷他定治疗.结果:观察组有效率为93.30%,对照组有效率为82.22%,观察组优于对照组(P<0.05);观察组血清中IL-10、IgE水平优于对照组(P<0.05).结论:玉屏风胶囊联合枸地氯雷他定治疗慢性湿疹疗效显著,并可改善患者血清IL-10、IgE水平.

  20. SAMJ FORUM

    African Journals Online (AJOL)

    2006-09-01

    Sep 1, 2006 ... discoverer of cromoglycate, the first preventative medication used in asthma ... clinical test to determine wheezing in infants and young children ... expiration. In 1971 ... training in allergy to senior paediatric registrars – to date,.

  1. A combined approach to decrease the technological and sensory defects caused by fat and sodium reduction in Bologna-type sausages.

    Science.gov (United States)

    Campagnol, Paulo Cezar Bastianello; Dos Santos, Bibiana Alves; Lorenzo, José Manuel; Cichoski, Alexandre José

    2017-09-01

    The effect of the addition of fructooligosaccharides, transglutaminase, disodium inosinate, and disodium guanylate on some technological and sensory parameters of low-fat and low-salt Bologna-type sausages was evaluated. In the first experiment, sausages with a 25% and 50% fat reduction containing 0, 3%, or 6% fructooligosaccharides were manufactured. Fat reduction adversely affected the emulsion stability, hardness, and sensory properties; however, the addition of 6% fructooligosaccharides reduced the loss of quality associated with a lower fat content. In the second experiment, sausages with a 50% fat reduction containing 6% fructooligosaccharides were produced. Additionally, the salt content was reduced by 50% and transglutaminase, disodium inosinate, and disodium guanylate were added. The combination of transglutaminase (1%), disodium inosinate (0.03%), and disodium guanylate (0.03%) was efficient to supress the technological and sensory defects caused by NaCl reduction in low-fat Bologna-type sausages.

  2. 易激胶囊联合色甘酸钠治疗腹泻型肠易激综合征45例临床观察%Treatment of diarrhea-predominant irritable bowel syndrome by combined therapy of Yiji capsule and sodium cromoglycate

    Institute of Scientific and Technical Information of China (English)

    郑秀丽; 聂淑英; 马圆圆; 高艳红; 符雪松; 尹淑新; 王玉刚

    2013-01-01

    目的 观察易激胶囊联合色甘酸钠治疗腹泻型肠易激综合征(IBS)的临床疗效.方法 将90例腹泻型IBS患者随机分为2组,治疗组45例予易激胶囊联合色甘酸钠治疗,对照组45例仅予色甘酸钠治疗,2组均治疗4周,观察2组治疗前后症状评分变化,评价疗效.结果 2组治疗后症状评分均较本组治疗前降低(P<0.05),且治疗组降低更明显(P<0.05).治疗组总有效率80.0%,对照组总有效率57.8%,2组总有效率比较差异有统计学意义(P<0.05),治疗组疗效优于对照组.结论 易激胶囊联合色甘酸钠治疗腹泻型IBS,较单用易激胶囊治疗可明显提高疗效,不良反应无明显增加.

  3. The preparation of disodium phosphate from waste phosphoric acid liquid and waste al- kali liquid in the process of butachlor%利用丁草胺工艺中的废酸废碱生产磷酸氢二钠

    Institute of Scientific and Technical Information of China (English)

    邹长军; 于林超; 李健秀

    2001-01-01

    以丁草胺生产工艺中的废磷酸和废碱为原料,经反应、浓缩和结晶制备磷酸氢二钠,讨论了不同的工艺条件,得到了纯度和氯含量分别为96.10%、0.04%的产品,达到了一级品标准.

  4. Determination of Disodium thylene Diaminetetraacetate in Samples Based on Ion Chromatography with In Guard H Column%在线预处理对乙二胺四乙酸二钠离子色谱分离的影响及其应用

    Institute of Scientific and Technical Information of China (English)

    张婷婷; 潘广文; 胡忠阳; 叶明立

    2012-01-01

    A method for the determination of EDTA was developed and validated based on ion chromatography with suppressed conductimetric detection and anion exchange column. The pre-concentration of EDTA was obtained on In guard H by using pump and ten ports valve, then the optimization separation condition was performed on a IonPac AS22 (250 mm×4. 0 mm) using 4. 5 mmol/L carbonate and 1. 4 mmol/L bicarbonate buffer solution with 18% acetonitrilc as the mobile phase with Isocratic elution. Good resolution was achieved from commonly coexisting anions and organic acid. The interference of different metal cations (Ca2+ , Mg2+ , Cu2+ , Zn2+ and Fe3 ) and the increase of molar ratio were also examined. The ion chromatographic method was applied for the assay of EDTA in contact lens care solutions,salad and canned foods with simple treatment . The linear range of EDTA was 0. 6 50 mg/kg. The recovery of EDTA was about 91.2%-97.0%.

  5. 液相色谱-串联质谱法测定枸地氯雷他定在大鼠体内的浓度及其药动学%Determination of desloratadine citrate disodium in rat and pharmacokinetic study by LC-MS/MS

    Institute of Scientific and Technical Information of China (English)

    周霞; 许晨昊; 沈晶晶; 范国荣; 杭太俊

    2015-01-01

    目的 建立测定大鼠血浆和尿液中构地氯雷他定的液相色谱-串联质谱(LC-MS/MS)法,并将其应用于枸地氯雷他定在大鼠体内的药动学研究.方法 12只成年健康SD大鼠,随机分成两组,各6只,分别单剂量尾静脉注射枸地氯雷他定0.5 mg· kg-1和灌胃枸地氯雷他定2 mg· kg-1后,于一定时间点采集血浆或尿液,取生物样品50 μL经液液萃取后,以甲醇-0.1%甲酸水溶液(70:30,V/V)为流动相,选用Diamonsil 5u C18色谱柱(4.6 mm × 100 mm,5μm)分离,采用电喷雾离子化进行正离子检测.用于定量分析的离子反应分别为m/z 311→259(构地氯雷他定)和m/z 327→270(氯氮平).使用WinNonlin软件计算药动学参数.结果 单剂量静脉注射枸地氯雷他定0.5 mg· kg-1和单剂量灌胃枸地氯雷他定2 mg·kg-1的主要药动学参数:ρmax分别为(457.00±49.76)和(17.25±4.09) μg· L-1,AUC0-∞分别为(128.80±19.40)和(107.38±10.74) μg·h·L-,tv2分别为(3.47±0.27)和(5.33±0.22)h,MRT分别为(4.19±0.62)和(7.22±0.39)h,绝对生物利用度为20.86%;0~72 h的尿药累积排泄率分别为(1.19±0.21)%和(0.38±0.11)%.结论 建立的液质联用测定构地氯雷他定在血浆和尿液样品的方法,专属灵敏快速,适用于大鼠药动学研究.

  6. Clinical evaluation of Montelukast plus Budesonide nasal spray and Desloratadine citrate disodium in treating moderate and severe persistent allergic rhinitis%孟鲁司特钠联合布地奈德鼻喷雾剂和枸地氯雷他定治疗中-重度持续性变应性鼻炎的临床疗效分析

    Institute of Scientific and Technical Information of China (English)

    王任霞; 张春晖

    2015-01-01

    目的:探讨孟鲁司特钠联合布地奈德鼻喷雾剂和枸地氯雷他定治疗中-重度持续性变应性鼻炎(AR)的临床疗效.方法:随机将70例中-重度持续性AR患者分为实验组(35例)和对照组(35例),实验组给予孟鲁司特钠口服,布地奈德鼻喷雾剂喷鼻,枸地氯雷他定片口服;对照组给予布地奈德鼻喷雾剂喷鼻,枸地氯雷他定片口服.疗程各4周.比较2组患者治疗前、后鼻部症状视觉模拟量表(VAS)评分、鼻-结膜炎相关生活质量(RQLQ)评分及总有效率.结果:①鼻部症状VAS评分:实验组在治疗2周及4周时鼻部症状VAS总评分及各项评分与对照组比较,差异均有统计学意义(P<0.05);②RQLQ评分:4周后2组患者RQLQ评分与治疗前比较均有显著改善,实验组患者鼻部症状评分与对照组比较差异有统计学意义(P<0.05);③总有效率:实验组总有效率(94.29%)与对照组(80.00%)比较,差异有统计学意义(P<0.05).结论:孟鲁司特钠联合布地奈德鼻喷雾剂及枸地氯雷他定在治疗中-重度持续性AR过程中,可以共同发挥作用,迅速缓解临床症状,提高中-重度持续性AR患者的生活质量.

  7. 枸地氯雷他定联合丙酸氟替卡松鼻喷雾剂治疗变应性鼻炎的疗效观察%Clinical efficacy of desloratadine citrate disodium tables in combination with fluticasone propionate nasal spray in the treatment of allergic rhinitis

    Institute of Scientific and Technical Information of China (English)

    李祥东

    2015-01-01

    目的 观察口服枸地氯雷他定联合丙酸氟替卡松鼻喷雾剂(辅舒良)喷鼻治疗变应性鼻炎的临床疗效和安全性.方法 选取我院就诊的220例变应性鼻炎作为研究对象,随机分为A、B、C3组.其中A组予枸地氯雷他定8.8 mg每日1次口服,辅舒良每日1次喷鼻;B组予枸地氯雷他定8.8 mg每日1次口服;C组予辅舒良每日一次喷鼻.均治疗4周,治疗结束后比较3组的疗效及不良反应发生情况,随访0.5 ~1年后比较两组复发率.结果 A组有效率95.89%,明显高于B组81.94%及C组78.67% (P <0.05),B组和C组比较无统计学意义(P>0.05).3组不良反应发生率比较,差异无统计学意义(P>0.05);A组与其它两组复发率比较,差异具有统计学意义(P<0.05).结论 枸地氯雷他定联合辅舒良治疗变应性鼻炎比单一用药的疗效更好,复发率低,安全性好,值得临床推广.

  8. 枸地氯雷他定胶囊联合润燥止痒胶囊治疗慢性荨麻疹的疗效及对血清总IgE的影响%Effect of Runzaozhiyang Capsule combined with desloratadine citrate disodium Tablets in treatment of chronic urticaria and its influence on total serum IgE levels

    Institute of Scientific and Technical Information of China (English)

    冯红霞; 康春义; 郭果香

    2016-01-01

    目的 探讨枸地氯雷他定胶囊联合润燥止痒胶囊治疗慢性荨麻疹的疗效及对血清总IgE水平的影响.方法 采用随机数字表法将2014-2015年120例慢性荨麻疹患者随机分为治疗组和对照组各60例,治疗组给予枸地氯雷他定胶囊联合润燥止瘁胶囊治疗,对照组单纯给予枸地氯雷他定片治疗,4周为1个疗程,分析两组患者治疗的有效率和血清总IgE水平变化.结果 (1)治疗组有效率95%,明显高于对照组的80%,两组比较治疗差异有统计学意义(P<0.05);(2)血清总IgE水平治疗组为(78.34±19.22) IU/ml,较对照组的(112.21±22.33) IU/ml改善明显,两组比较差异有统计学意义(P<0.05).结论 枸地氯雷他定胶囊联合润燥止痒胶囊治疗慢性荨麻疹疗效显著,起效快,血清总IgE水平降低明显.

  9. Traditional Chinese medicine combine with cold spray and desloratadine citrate disodium tablets treatment of facial glucosteroid-dependence dermatitis%中药配合冷喷枸地氯雷他定治疗激素依赖性皮炎

    Institute of Scientific and Technical Information of China (English)

    刘国栋; 马鑫; 马拴全; 屈煦; 闫小宁

    2015-01-01

    目的 探讨中药生元饮加减方配合冷喷枸地氯雷他定片治疗面部激素依赖性皮炎的临床疗效.方法 选取85例门诊激素依赖性皮炎患者,随机分成治疗组42例和对照组43例.治疗组给予生元饮加减方及枸地氯雷他定片口服,对照组仅口服枸地氯雷他定片,2组均配合外用1‰薄荷溶液冷喷,观察2组治疗前、后皮损减轻情况及疗效.结果 治疗组总有效率90.4%,对照组总有效率72.0%,2组比较,P<0.05.结论 中药生元饮加减方配合冷喷枸地氯雷他定片治疗面部激素依赖性皮炎,能有效改善临床症状,减轻皮损程度.

  10. The effect of Study on patients withchronic urticaria by Huoxue Quzhen decoction combined with Desloratadine Citrate Disodium Tablets%活血祛疹汤联合枸地氯雷他定片治疗慢性荨麻疹57例

    Institute of Scientific and Technical Information of China (English)

    王太山

    2015-01-01

    目的:观察活血祛疹汤联合枸地氯雷他定片治疗慢性荨麻疹的临床疗效.方法:选择2012年2月-2013年1月本院收治的114例慢性荨麻疹患者为研究对象,随机分为对照组和治疗组各57例,对照组采用枸地氯雷他定片治疗,治疗组在对照组基础上采用活血祛疹汤治疗,比较两组患者临床疗效、IgC、IgE及CD4+/CD8+水平,观察患者的不良反应及复发情况.结果:治疗组第1个疗程有效率为75.44%,第2个疗程有效率为91.23%;对照组第1个疗程有效率为63.16%,第2个疗程有效率为80.70%.治疗组有效率均明显高于对照组,差异具有统计学意义(P<0.05).治疗组57例,出现头晕乏力3例,瘙瘁2例,腹泻5例.对照组57例,出现头晕乏力4例,瘙痒5例,嗜睡4例,两组患者均可耐受,3d内症状均自行缓解,未影响继续用药.治疗组的复发率(22.81%)明显低于对照组(68.42%),差异具有统计学意义(P<0.05).两组患者IgG、CD4+/CD8+较治疗前明显升高,IgE明显降低,且组间差异显著,具有统计学意义(P<0.05).结论:活血祛疹汤联合构地氯雷他定片治疗慢性荨麻疹疗效显著,复发率低,可有效降低患者的IgG、IgE及CD4+/CD8+水平.

  11. Drug: D02198 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available and gram-negative bacteria 6133 Oxacephem antibioitics D02198 Latamoxef sodium (JP16); Moxalactam disodium ...llin binding proteins inhibitor Cephems - Oxacephems Latamoxef [ATC:J01DD06] D02198 Latamoxef sodium (JP16);

  12. Drug: D02715 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available osalicylic acid and similar agents A07EC04 Balsalazide D02715 Balsalazide disodium (USAN) USP drug classification [BR:br08302] Inflam...matory Bowel Disease Agents Aminosalicylates Balsalazide D02715 Balsalazide disodiu

  13. C10H18N2Na2O10 inhibition and adsorption mechanism on concrete steel-reinforcement corrosion in corrosive environments

    National Research Council Canada - National Science Library

    Okeniyi, Joshua Olusegun

    2016-01-01

    C10H18N2Na2O10 (ethylenediaminetetra-acetic acid disodium salt) inhibition and adsorption mechanism on the corrosion of steel-reinforcement corrosion in concrete immersed in corrosive environments were investigated in this paper...

  14. Ethylenediaminetetraacetic acid in endodontics

    OpenAIRE

    Mohammadi, Zahed; Shalavi, Sousan; Jafarzadeh, Hamid

    2013-01-01

    Ethylenediaminetetraacetic acid (EDTA) is a chelating agent can bind to metals via four carboxylate and two amine groups. It is a polyamino carboxylic acid and a colorless, water-soluble solid, which is widely used to dissolve lime scale. It is produced as several salts, notably disodium EDTA and calcium disodium EDTA. EDTA reacts with the calcium ions in dentine and forms soluble calcium chelates. A review of the literature and a discussion of the different indications and considerations for...

  15. Application of Novel Nonlinear Optical Materials to Optical Processing

    Science.gov (United States)

    Banerjee, Partha P.

    1999-01-01

    We describe wave mixing and interactions in nonlinear photorefractive polymers and disodium flourescein. Higher diffracted orders yielding forward phase conjugation can be generated in a two-wave mixing geometry in photorefractive polymers, and this higher order can be used for image edge enhancement and correlation. Four-wave mixing and phase conjugation is studied using nonlinear disodium floureschein, and the nature and properties of gratings written in this material are investigated.

  16. Role of sodium cromoglycate in brain protection and its effects on tumor necrosis factor-α and interleukin-1β after global cerebral ischemia-reperfusion injury in gerbils%色甘酸钠对沙土鼠全脑缺血再灌注后脑保护作用及脑组织TNF-α和 IL-1水平的影响

    Institute of Scientific and Technical Information of China (English)

    沈宁; 甘小亮; 庞红宇; 黑子清

    2009-01-01

    目的 观察色甘酸钠对沙土鼠全脑缺血再灌注后脑保护作用及脑组织肿瘤坏死因子(TNF)-α和白细胞介素(IL)-1β水平的影响.方法 24只雄性清洁级蒙古沙土鼠,随机平均分为3组,假手术对照组(对照组):游离双侧颈总动脉但不阻断脑血流;脑缺血再灌注组(模型组):游离双侧颈总动脉并阻断脑血;模型+色甘酸钠组(色甘酸钠组):再灌注后色甘酸钠25 mg/kg间隔1 h分两次经舌静脉注入.实验结束后,处死动物取丘脑,10%甲醛固定,病理切片,HE染色,光镜观察.剩余脑组织左侧制成组织匀浆,测定TNF-α和IL-1β水平,右侧脑组织分别称湿、干重和计算脑含水量. 结果 模型组脑组织含水量最高,色甘酸钠组脑组织含水量低于模型组(P0.05);正常组IL-1β水平低于色甘酸钠组(P<0.05). 结论 色甘酸钠可减轻沙土鼠全脑缺血再灌注脑损伤,可能机制为降低缺血再灌注后脑组织TNF-α和IL-1β水平.

  17. 复方色甘酸钠鼻剂的研制

    Institute of Scientific and Technical Information of China (English)

    孙培红; 王滨; 鲁云兰

    1998-01-01

    @@ 色甘酸钠(Sodium Cromoglycate)与盐酸麻黄素(Ephedrin Hydrochlorid)制成复方制剂,治疗过敏性鼻炎[1],临床观察表明该制剂有收缩血管、减轻鼻粘膜水肿,抗过敏作用,效果满意,未见不良反应.

  18. Insensitivity of volume-sensitive chloride currents to chromones in human airway epithelial cells

    Science.gov (United States)

    Zegarra-Moran, Olga; Lantero, Sabina; Sacco, Oliviero; Rossi, Giovanni A; Galietta, Luis J V

    1998-01-01

    Chromones (sodium cromoglycate and sodium nedocromil) block cell swelling-activated Cl− channels in NIH-3T3 fibroblasts and endothelial cells. This has led to hypothesize that cell volume regulation might be involved in asthma pathogenesis.Using whole-cell patch-clamp experiments, we studied the effect of chromones on volume-sensitive Cl− currents in transformed human tracheal epithelial cells (9HTEo-) and in primary cultures of human bronchial epithelial cells (BE).Cl− currents activated by hypotonic shock were poorly blocked by extracellular nedocromil or cromoglycate. The block was voltage-dependent since it was observed only at positive membrane potentials. At the concentration of 5 mM, the current inhibition by both chromones at +80 mV was about 40% for 9HTEo- and only 20% for BE.Intracellular application of chromones elicited a voltage-independent inhibition in 9HTEo- cells. Under this condition, volume-sensitive Cl− currents were reduced at all membrane potentials (60 and 45% inhibition by 2 mM nedocromil and cromoglycate respectively). In contrast intracellular chromones were ineffective in BE cells.The relative refractoriness to chromones, in contrast with the high sensitivity shown by other Cl− channels, suggests that the epithelial volume-sensitive Cl− channel is not involved in asthma. PMID:9863671

  19. Ethylenediaminetetraacetic acid in endodontics.

    Science.gov (United States)

    Mohammadi, Zahed; Shalavi, Sousan; Jafarzadeh, Hamid

    2013-09-01

    Ethylenediaminetetraacetic acid (EDTA) is a chelating agent can bind to metals via four carboxylate and two amine groups. It is a polyamino carboxylic acid and a colorless, water-soluble solid, which is widely used to dissolve lime scale. It is produced as several salts, notably disodium EDTA and calcium disodium EDTA. EDTA reacts with the calcium ions in dentine and forms soluble calcium chelates. A review of the literature and a discussion of the different indications and considerations for its usage are presented.

  20. 40 CFR 721.9790 - Benzenesulfonic acid, 2,2′-(1,2-ethenediyl)bis[5-[[4-[bis(2-hydroxypropyl) amino]- 6-[(3...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzenesulfonic acid, 2,2â²-(1,2-ethenediyl)bis - 6- -1,3,5-triazin-2-yl]amino]-, disodium salt, compd. with 2,2â²,2â³-nitrilo-tris (1:2); Benzenesulfonic acid, 5- -6- -1,3,5-triazin-2-yl]amino]-2- -6- -1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]-, disodium salt, compd....

  1. Synthesis of isomeric isothiazolo[4',3':4,5]- and isothiazolo[4',5':4,5]thieno[3,2-b]pyrano[2,3-d]pyridines by combination of domino reactions.

    Science.gov (United States)

    Shestopalov, Anatoliy M; Larionova, Natalia A; Fedorov, Alexander E; Rodinovskaya, Lyudmila A; Mortikov, Valery Yu; Zubarev, Andrey A; Bushmarinov, Ivan S

    2013-10-14

    Isothiazolothienopyridines have been prepared by a domino reaction (the SN2 reaction → the Thorpe-Ziegler reaction → the Thorpe-Guareschi reaction type) from disodium 4-cyanoisothiazole-3,5-dithiolate. By changing the order of addition of the alkylation reagents in the reaction with disodium 4-cyanoisothiazole-3,5-dithiolate both possible isomers of the isothiazolothienopyridines are synthesized. These isomers were further used in three-component domino reaction (the Knoevenagel reaction → the Michael reaction → the hetero-Thorpe-Ziegler reaction type) to obtain wide range of isomeric isothiazolothienopyranopyridines.

  2. Enantiomeric pair of copper(II) polypyridyl-alanine complexes: Effect of chirality on their interaction with biomolecules.

    Science.gov (United States)

    Ng, Chew Hee; Chan, Cheang Wei; Lai, Jing Wei; Ooi, Ing Hong; Chong, Kok Vei; Maah, Mohd Jamil; Seng, Hoi Ling

    2016-07-01

    Like chiral organic drugs, the chemical and biological properties of metal complexes can be dependent on chirality. Two pairs of [Cu(phen)(ala)(H2O)]X·xH2O (phen=1.10-phenanthroline: X=NO3(-); ala: l-alanine (l-ala), 1 and d-alanine (d-ala) 2; and (X=Cl(-); ala: l-ala, 3 and d-ala, 4) complex salts (x=number of lattice water molecules) have been synthesized and characterized. The crystal structure of 3 has been determined. The same pair of enantiomeric species, viz. [Cu(phen)(l-ala)(H2O)](+) and [Cu(phen)(d-ala)(H2O)](+), have been identified to be present in the aqueous solutions of both 1 and 3, and in those of both 2 and 4 respectively. Both 3 and 4 bind more strongly to ds(AT)6 than ds(CG)6. There is no or insignificant effect of the chirality of 3 and 4 on the production of hydroxyl radicals, binding to deoxyribonucleic acid from calf thymus (CT-DNA), ds(CG)6, G-quadruplex and 17-base pair duplex, and inhibition of both topoisomerase I and proteasome. Among the three proteasome proteolytic sites, the trypsin-like site is inhibited most strongly by these complexes. However, the chirality of 3 and 4 does affect the number of restriction enzymes inhibited, and their binding constants towards ds(AT)6 and serum albumin.

  3. An efficient route for the synthesis of phosphorus-selenium macro-heterocycles.

    Science.gov (United States)

    Hua, Guoxiong; Slawin, Alexandra M Z; Randall, Rebecca A M; Cordes, David B; Crawford, Luke; Bühl, Michael; Woollins, J Derek

    2013-04-04

    Four-membered ring [PhP(Se)(μ-Se)]2 (Woollins' reagent, WR) reacts with disodium alkenyl-diols followed by in situ ring-closure reaction with appropriate dibromoalkanes affording a series of unusual nine- to fifteen-membered organoselenophosphorus macrocycles bearing the O-P-Se-Cn-Se-P-O or O-P-Se-Cn-O-P-Se linkage.

  4. 76 FR 10587 - Product Cancellation Order for Certain Pesticide Registrations

    Science.gov (United States)

    2011-02-25

    ... Vegetation Prometon Killer. 001448-00093 Busan 1016 Carbamodithioic acid, cyano-, disodium salt Metam- sodium 001448-00361 Busan 1236 Metam-sodium 001663-00035 Grant's Flying & Permethrin Piperonyl Crawling Insect butoxide Killer. Tetramethrin 001677-00219 Sanova Base (25%)... Sodium chlorite 001839-00115 Onyxide 200...

  5. Calcium-binding capacity of organic and inorganic ortho- and polyphosphates

    NARCIS (Netherlands)

    Kort, de E.J.P.; Minor, M.; Snoeren, T.H.M.; Hooijdonk, van A.C.M.; Linden, van der E.

    2009-01-01

    The aim of this research was to determine the calcium-binding capacity of inorganic and organic ortho- and polyphosphates. This calcium-binding capacity can be used to influence the stability of, for example, casein micelles in dairy systems. Four phosphates were selected: disodium uridine

  6. Drug: D09348 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D09348.gif Treatment of rheumatoid arthritis, immune thrombocytopenic purpura, and B-cell lymphoma spleen ty...D09348 Drug Fostamatinib disodium (USAN) C23H24FN6O9P. 6H2O. 2Na 732.1756 732.5148

  7. Oxidative stability of fish oil enriched drinking yoghurt

    DEFF Research Database (Denmark)

    Nielsen, Nina Skall; Debnath, D.; Jacobsen, Charlotte

    2007-01-01

    The oxidative stability of fish oil enriched drinking yoghurt as well as the antioxidative effect of citric acid ester, vitamin K and disodium ethylenediaminetetraacetic acid (EDTA) were investigated by measuring peroxide value and volatile secondary oxidation products and by sensory analysis...

  8. Occurrence of Pospiviroid in potato, tomato and some ornamental ...

    African Journals Online (AJOL)

    USER

    2010-05-03

    May 3, 2010 ... potato samples, 258 tomato leaves and 461 ornamental plants) were tested by reverse ... could be applied to the large-scale and multiple detection of plant ... 0.013 M disodium ethylenediaminetetraacetatet (EDTA) pH 7.0, 4M.

  9. Drug: D00314 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available AL SYSTEM M05 DRUGS FOR TREATMENT OF BONE DISEASES M05B DRUGS AFFECTING BONE STRUCTURE AND MINERALIZATION M0...onate disodium (JP16/USP) Anatomical Therapeutic Chemical (ATC) classification [BR:br08303] M MUSCULO-SKELET

  10. 21 CFR 133.179 - Pasteurized process cheese spread.

    Science.gov (United States)

    2010-04-01

    ... (cellulose gum), car-ra-geenan, oat gum, algin (sodium alginate), pro-pylene glycol alginate, or xanthan gum...: Monosodium phosphate, disodium phosphate, dipotassium phosphate, trisodium phosphate, sodium metaphosphate (sodium hexa-meta-phos-phate), sodium acid pyro-phos-phate, tetra-sodium pyro-phos-phate, sodium aluminum...

  11. Drug: D04039 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D04039 Drug Eprodisate disodium (USAN) C3H6O6S2. 2Na 247.9401 248.1857 D04039.gif T...reatment of secondary (AA) amyloidosis CAS: 36589-58-9 PubChem: 47206004 LigandBox: D04039 NIKKAJI: J534.156

  12. Possible (enzymatic) routes and biological sites for metabolic reduction of BNP7787, a new protector against cisplatin-induced side-effects.

    NARCIS (Netherlands)

    Verschraagen, M.; Boven, E.; Torun, E; Hausheer, FH; Vijgh, van der WJ

    2004-01-01

    Disodium 2,2'-dithio-bis-ethane sulfonate (BNP7787) is under investigation as a potential new chemoprotector against cisplatin-induced nephrotoxicity. The selective protection of BNP7787 appears to arise from the preferential uptake of the drug in the kidneys, where BNP7787 would undergo intracellul

  13. 40 CFR 721.5279 - 2,7-Naphthalenedisulfonic acid, 4-amino-3-[[4′2-amino-4-[(3-butoxy-2-hydroxypropyl)amino]phebyl...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false 2,7-Naphthalenedisulfonic acid, 4-amino-3- phebyl]azo]-3,3â²-dimethyl -4-yl]azo]-5-hydroxy-6-(phenylazo)-, disodium salt. 721.5279 Section 721.5279 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF...

  14. Drug: D03828 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available NTS L01 ANTINEOPLASTIC AGENTS L01B ANTIMETABOLITES L01BA Folic acid analogues L01...7] Pemetrexed [ATC:L01BA04] D03828 Pemetrexed disodium (USAN) Antineoplastics [BR:br08308] Antimetabolites Folic acid analogue

  15. Chelation for Coronary Heart Disease

    Science.gov (United States)

    ... V W X Y Z Chelation for Coronary Heart Disease Share: © AHA Coronary heart disease is a leading cause of death among both ... health approach . The use of disodium EDTA for heart disease has not been approved by the U.S. Food ...

  16. Physical and mechanical properties and fire, decay, and termite resistance of treated oriented strandboard

    Science.gov (United States)

    Nadir Ayrilmis; S Nami Kartal; Theodore L. Laufenberg; Jerrold E. Winandy; Robert H. White

    2005-01-01

    This study evaluated the effects of a number of chemicals on the physical and mechanical properties and fire, decay, and termite resistance of oriented strandboard (OSB) panels. Disodium octaborate tetrahydrate (DOT), boric acid (BA), melamine phosphate (MP), and a BA/DOT mixture were sprayed onto the furnish at varying concentrations. The panels were tested for...

  17. Drug: D03943 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available V VARIOUS V03 ALL OTHER THERAPEUTIC PRODUCTS V03A ALL OTHER THERAPEUTIC PRODUCTS V03AB Antidotes...of drugs in Japan [BR:br08301] 3 Agents affecting metabolism 39 Other agents affecting metabolism 392 Anti...dotes 3921 EDTAs D03943 Calcium disodium edetate hydrate (JAN); Edetate calcium dis

  18. A practical evaluation of detergent and disinfectant solutions on ...

    African Journals Online (AJOL)

    Student01

    2012-01-06

    Jan 6, 2012 ... Key words: Detergents, bacteria, cargo container surfaces, disinfectant. .... chemical test solution using this method was indicated by a > 5 log reduction in the ... AT Special (ATS)1; (<1% disodium metasilicate, 1-5% anionic surfactant .... were tested using one-way analysis of variance (ANOVA) test and.

  19. Electrochemical Detection of Alkaline Phosphatase in BALB/c Mouse Fetal Liver Stromal Cells with Capillary Electrophoresis

    Institute of Scientific and Technical Information of China (English)

    Xue Mei SUN; Dong LI; Zeng Liang BAI; Wen Rui JIN

    2004-01-01

    A method for determination of alkaline phosphatase (ALP) in BALB/c mouse fetal liver stromal cells has been described based on the catalytic reaction. After the cell extract is incubated with the substrate disodium phenyl phosphate, the reaction product phenol generated by ALP is determined by capillary electrophoresis with electrochemical detection.

  20. INFLUENCE OF COMPLEXING AGENT (Na2EDTA) ON CHEMICAL ...

    African Journals Online (AJOL)

    Preferred Customer

    The Cu4SnS4 thin films were deposited onto indium tin oxide glass substrate by ... The synthesis and characterization of metal chalcogenides thin film of different ... as thiourea [18], ammonia [19-20], triethanolamine [21-22], disodium ethylene.

  1. Nonsteroidal Anti-Inflammatory Agents in the Treatment of Asthma in Children

    Directory of Open Access Journals (Sweden)

    Pierre Gaudreault

    1995-01-01

    Full Text Available The increasing scientific information clearly demonstrates the important role of inflammation in asthma. This evidence has led physicians to focus their treatment on the elimination of inflammation instead of working solely against bronchoconstriction. Steroids and nonsteroidal agents are currently used to prevent this inflammatory component. This paper focuses only on nonstcroidal anti-inflammatory agents such as sodium cromoglycate, nedocromil sodium and ketotifen and their use in pediatric asthma. The discussion on each medication addresses its mechanism of action, the evidence concerning its efficacy in pediatrics (ie, clinical pharmacology, acute bronchial challenge, late asthmatic response, bronchial hyperrcactivity, clinical efficacy and the pediatric dose.

  2. Multiple endpoint analysis of BAC-preserved and unpreserved antiallergic eye drops on a 3D-reconstituted corneal epithelial model

    OpenAIRE

    Pauly, A.; Brasnu, E.; Riancho, L.; Brignole-Baudouin, F.; Baudouin, C

    2011-01-01

    Purpose To compare the effects of benzalkonium chloride (BAC)-preserved and unpreserved antiallergic eye drops on the human 3D-reconstituted corneal epithelial model (3D-HCE). Methods 3D-HCE were treated for 24 h followed or not by a 24 h post-incubation recovery period (24 h+24 h) with phosphate-buffered saline (PBS), 0.01% BAC, unpreserved formulations of ketotifen, N Acetyl-Aspartyl Glutamic Acid (NAAGA), cromoglycate, or BAC-preserved commercial formulations of ketotifen, olopatadine, epi...

  3. Specific Oral Tolerance Induction Using IFN-Gamma in 2 Cases of Food-Dependent Exercise-Induced Anaphylaxis

    Directory of Open Access Journals (Sweden)

    Geunwoong Noh

    2013-01-01

    Full Text Available Anaphylaxis induced by exercise after the intake of certain foods is referred to as food-dependent exercise-induced anaphylaxis (FDEIA. Only the preventive medication such as oral sodium cromoglycate and oral combined cetirizine-montelukast was tried in FDEIA. Specific oral tolerance induction (SOTI using IFN-gamma was tried in 2 cases of FDEIA for wheat. Merely, exercise accompanied every treatment just after the intake of allergenic foods during treatment. Patients acquired tolerance for wheat in both cases successfully. After treatment, two patients take wheat in their food living freely. Conclusively, SOTI using IFN-gamma was effective as the causative treatment for allergenic foods in FDEIA.

  4. Drug: D04257 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available D04257 Drug Fospropofol disodium (USAN); Aquavan (TN); Lusedra (TN) C13H19O5P. 2Na ...general anesthetics N01AX10 Propofol D04257 Fospropofol disodium (USAN) Target-based classification of drugs [BR:br08310] Ion channels Cys-loop superfamily GABA-A GABAA-receptor [HSA:2554 2555 2556 2557 2558 2559 2560 2561 2562 2563 2564 2565 2566 2567 2568 55879] [KO:K05175 K05176 K05177 K05178 K05179 K05180 K05181 K05182 K05183 K05184 K05185 K05186 K05187 K05188 K05189 K051...92] Propofol [ATC:N01AX10] D04257 Fospropofol

  5. Isotachophoretic determination of ethylenediaminetetraacetate in salad dressing, mayonnaise, and margarine.

    Science.gov (United States)

    Ito, Y; Toyoda, M; Suzuki, H; Iwaida, M

    1980-11-01

    An isotachophoretic method was developed for the determination of EDTA in foods imported by Japan. Skimmed samples of dressings, mayonnaise, or margarine were chromatographed on an anion exchange column, and interfering organic acids were eluted with water and 0.01N HCl. EDTA was eluted with 0.2N HCl and reacted with ferric chloride to form a stable EDTA--Fe complex. Electrophoresis was carried out with dilute HCl containing 0.05% Triton and beta-alanine (pH 3.5) as the leading electrolyte and 0.01M caproic acid as terminating electrolyte. Since uncoupled EDTA showed more than one zone, it was reacted with ferric chloride to form EDTA-Fe complex which showed only a single zone on an isotachopherogram. More than 90% of EDTA spiked at 100 or 1000 ppm level as disodium salt was recovered from the above mentioned three types of food. Detection limit was 10 ppm as disodium EDTA.

  6. Proteolytic activity of beef luncheon fungi as affected by incorporation of some food preservatives.

    Science.gov (United States)

    Saleem, A; El-Said, A H M

    2009-12-01

    Screening of thirty-one fungal isolates (representing 16 genera, 28 species and 3 varieties) collected from beef luncheon meat for their abilities to produce protease enzyme revealed that eleven isolates (35.48%) exhibited high protease production. However, fifteen isolates (48.39%) had moderate ability and 5 isolates (16.13%) were low producers. Aspergillus flavus, Gibberella fujikuroi and Penicillium chrysogenum were the most active producers of protease. The incorporation of five chemical substances used as food preservatives (disodium phosphate, sodium benzoate, citric acid, potassium sorbate and sodium citrate) individually in the culture medium for protease production exhibited depressive effect on protease production as well as on mycelial growth of Aspergillus flavus, Gibberella fujikuroi and Penicillium chrysogenum , except in few cases the mycelial growth of A. flavus and G. fujikuroi was increased by the lowest concentration (100 ppm) of sodium benzoate, citric acid and disodium phosphate.

  7. Modeling Pharmacological Inhibition of Mast Cell Degranulation as a Therapy for Insulinoma

    Directory of Open Access Journals (Sweden)

    Laura Soucek

    2011-11-01

    Full Text Available Myc, a pleiotropic transcription factor that is deregulated and/or overexpressed in most human cancers, instructs multiple extracellular programs that are required to sustain the complex microenvironment needed for tumor maintenance, including remodeling of tumor stroma, angiogenesis, and inflammation. We previously showed in a model of pancreatic β-cell tumorigenesis that acute Myc activation in vivo triggers rapid recruitment of mast cells to the tumor site and that this is absolutely required for angiogenesis and macroscopic tumor expansion. More-over, systemic inhibition of mast cell degranulation with sodium cromoglycate induced death of tumor and endothelial cells in established tumors. Hence, mast cells are required both to establish and to maintain the tumors. Whereas this intimates that selective inhibition of mast cell function could be therapeutically efficacious, cromoglycate is not a practical drug for systemic delivery in humans, and no other systemic inhibitor of mast cell degranulation has hitherto been available. PCI-32765 is a novel inhibitor of Bruton tyrosine kinase (Btk that blocks mast cell degranulation and is currently in clinical trial as a therapy for B-cell non–Hodgkin lymphoma. Here, we show that systemic treatment of insulinoma-bearing mice with PCI-32765 efficiently inhibits Btk, blocks mast cell degranulation, and triggers collapse of tumor vasculature and tumor regression. These data reinforce the notion that mast cell function is required for maintenance of certain tumor types and indicate that the Btk inhibitor PCI-32765 may be useful in treating such diseases.

  8. Treatment of allergic rhinoconjunctivitis: a review of the role of topical levocabastine

    Directory of Open Access Journals (Sweden)

    R. Gerth van Wijk

    1995-01-01

    Full Text Available Lcocabastine is an extremely potent and highly selective H1-receptor antagonist which has been specifically developed as eye drops and nasal spray for the treatment of allergic rhinoconjunctivitis. Clinical experience to date suggests that this topical antihistamine is at least as effective as other current first-line therapeutic approaches for the treatment of this condition, including oral H1-receptor antagonists and sodium cromoglycate. Onset of action is rapid, with clinical effects apparent within minutes of instillation. Moreover, duration of action is sufficiently long to permit a convenient twice-daily dosing regimen. Topical levocabastine is well tolerated with an adverse-effect profile comparable with that of placebo and sodium cromoglycate. As might be expected from the route of drug administration, application site reactions are the most frequent adverse effect associated with levocabastine eye drops and nasal spray with an incidence comparable with that seen in placebotreated controls. The availability of effective and well-tolerated topical antihistamines, such as levocabastine, is an important advance which broadens the range of therapeutic approaches available for the clinical management of allergic rhinoconjunctivitis. Levocabastine appears to be an attractive alternative to oral antihistamines as a first-line therapeutic option for the treatment of this atopic condition.

  9. Local histamine release increases leukocyte rolling in the cerebral microcirculation of the mouse.

    Science.gov (United States)

    Yong, T; Zheng, M Q; Linthicum, D S

    1997-10-01

    Histamine-mediated induction of leukocyte rolling and adhesion in the cerebral microcirculation was examined in two inbred strains of mice (SJL/J and BALB/c). A cranial window was surgically prepared for the visualization of the cerebral microcirculation using intra-vital microscopy. Leukocyte rolling and adhesion to pial venular walls were assessed during off-line video playback analyses. The surgical preparation of the cranial windows was found to trigger 'spontaneous' leukocyte rolling, and this was attributed to disruption of dural mast cells and localized release of vasoactive histamine. This spontaneous leukocyte rolling was observed only in the SJL/J strain of mice, and could be prevented by presurgical treatment with the mast cell stabilizer sodium cromoglycate. BALB/c mice did not show 'spontaneous' leukocyte rolling or adhesion; this strain is known to have low numbers of CNS-associated mast cells. Exogenous histamine, applied topically to the cerebral microcirculation via the cranial window in mice pretreated with sodium cromoglycate, produced significant dose-dependent increases in leukocyte rolling and adhesion to pial venules in SJL/J mice, but not in BALB/c mice. Diphenhydramine (H1 receptor antagonist), but not cimetidine (H2 receptor antagonist), abolished both 'spontaneous' and histamine-induced leukocyte rolling. Anti-P-selectin antibody was found efficiently to block both spontaneous and histamine-induced increases in leukocyte rolling, but not leukocyte adhesion.

  10. The AFM method in studies of muscovite mica and galena surfaces

    Science.gov (United States)

    Leiro, J. A.; Torhola, M.; Laajalehto, K.

    2017-01-01

    Using atomic force microscopy the freshly cleaved muscovite interfaces in dry air and in water have been studied with atomic resolution. Three different surface layers can be observed for this single crystal. This phenomenon has been ascribed to the weak interactions between the atomic planes. Also, the galena surface has been imaged in dry air and in a disodium tetraborate liquid. In this case the differences have not been so striking. The role of rumpling of surface atoms has been considered.

  11. Laser-induced photoelectrochemistry: scavenging of photoemitted electrons in aqueous and non-aqueous solutions by electroactive organic species

    Energy Technology Data Exchange (ETDEWEB)

    Richardson, J.H. (Lawrence Livermore Lab., CA); Kovalenko, L.J.; Deutscher, S.B.; Harrar, J.E.; Perone, S.P.

    1980-01-01

    Photoemission current at a mercury electrode has been characterized electrochemically for aqueous solutions of methyl viologen, the disodium salt of anthraquinone-1,5-disulfonic acid, hydroquinone, p-benzoquinone, and chlorophyllin, and in DMF solutions of N/sub 2/O and anthraquinone. The scavenging species could be determined by comparing photoemission current-voltage curves with polarographic and cyclic voltammetric data. 11 figures.

  12. Use of the Malthus-AT system to assess the efficacy of permeabilizing agents on the activity of antibacterial agents against Pseudomonas aeruginosa.

    Science.gov (United States)

    Ayres, H M; Payne, D N; Furr, J R; Russell, A D

    1998-06-01

    The Malthus-AT system provided a satisfactory method for examining the effects of permeabilizing agents on the activity of sub-inhibitory concentrations of antibacterial agents against Pseudomonas aeruginosa G48. Under this system, disodium edetate potentiated the activity of chlorhexidine diacetate (CHA), cetylpyridinium chloride, para-chlorometaxylenol and triclosan. Nitrilotriacetic acid enhanced the activity of some of the antibacterials tested, whereas sodium polyphosphate markedly reduced the efficacy of CHA.

  13. Research on Colorant Systems Whose Characteristics May be Reversed: Part 2

    Science.gov (United States)

    1976-05-01

    with mixed dyestuffs was as follows: Anthraqu inone-2,6-disulphonic acid (disodium salt) 5.0% Xylene Cyanol FF - 0.1% Titanium dioxide 1.0% Agar 3.0...parts of a 15% diphenylmethane diisocyanate ethylene glycol pentaerythritol terephthalic acid polymer (in m-cresol). This polymer was obtained by...disulfonic acid (Na salt), an adj uvant and differently colored inert pigments. Attempts were made to apply the technique to textile-like materials with

  14. Drug: D02285 [KEGG MEDICUS

    Lifescience Database Archive (English)

    Full Text Available sis treatment and prevention; Paget's disease treatment ATC code: M05BA05 bisphosphonate map07047 Osteoporos...D02285 Drug Tiludronate disodium (USAN); Skelid (TN) C7H7ClO6P2S. 2Na 361.8922 362.5719 D02285.gif Osteoporo...is drugs Anatomical Therapeutic Chemical (ATC) classification [BR:br08303] M MUSCUL

  15. Liver lesions in children post-oncologic therapy: Review of case reports and institutional observation

    Directory of Open Access Journals (Sweden)

    Rebecca Gologorsky

    2015-01-01

    Full Text Available Purpose: Focal nodular hyperplasia (FNH, a benign hepatic tumor with ill-defined etiology, has been increasingly reported in children treated for extra-hepatic malignancies. Serial imaging or biopsy may be needed when survivors present with liver lesions. This study aims to review the literature, compare them with our institution’s cohort and propose a less invasive diagnostic imaging modality for FNH utilizing Magnetic resonance imaging (MRI with gadoxetate disodium. Methods: We reviewed 13 case reports/series published over the last 20 years and compared them to our retrospective review of 16 childhood cancer survivors (CCS found to have liver lesions on various imaging studies. Several patients underwent biopsy for diagnosis. Results: No specific generalizations could be made in terms of which specific chemotherapeutic agents cause FNH. Seven out of 11 patients underwent radiotherapy and/or hematopoietic stem cell transplant. Additionally, 36% (4/11 had been treated for neuroblastoma. From the literature review, the use of MRI with gadoxetate disodium was difficult to evaluate. Imaging was mainly accomplished using ultrasound, computerized tomography and MRI with gadolinium. The results were often indeterminate and resulted in biopsy in 6 cases in our institution. In contrast, 5 patients underwent initial MRI with gadoxetate disodium, which confirmed the diagnosis of FNH. Conclusion: CCS have an increased risk of developing liver lesions. Consistent with previously published literature, patients exposed to radiotherapy or cytoreductive agents used for hematopoietic stem cell transplants appeared to be at higher risk. A significant proportion (36%, 4/11 of our patients with FNH was previously treated for neuroblastoma. With the introduction of MRI with gadoxetate disodium, imaging may be a viable alternative to biopsy. 

  16. Tissue Distribution of Exogenously Administered Human Serum Butyrylcholinesterase-Soman Conjugate(HuBuChE-GD) in Guinea Pigs to Predict its Toxicity

    Science.gov (United States)

    2010-02-01

    Groningen, The Netherlands). Disodium hydrogen phosphate and potassium dihydrogen phosphate were obtained from Merck (Darmstadt, Germany... phosphate buffer , pH 8.0 at 25 °C. The enzyme was divided over two 10 kD cut off filters and the enzyme was washed with phosphate buffered saline...was dissolved in scintillation fluid without any pre- preparation. Additionally 25% homogenates of the tissues in phosphate buffered saline were

  17. Structural determination of unknown subsidiary colors in food yellow no. 5 (Sunset yellow FCF).

    Science.gov (United States)

    Yamada, M; Nakamura, M; Yamada, T; Maitani, T; Goda, Y

    1996-08-01

    Major unknown subsidiary colors A (Sub A) and B (Sub B) in commercial Sunset Yellow FCF (Food Yellow No. 5 in Japan) have been isolated by preparative HPLC. Spectroscopic analyses of Sub A and Sub B revealed that their structures are trisodium salt of 6-hydroxy-7-(4-sulfophenyl)-5-(4-sulfophenylazo)-2-naphthale nesulfonic acid, and disodium salt of 3-hydroxy-4-(4-sulfophenylazo)-2-naphthalenesulfonic acid, respectively.

  18. Rapid complexometric analysis of brass with CTDA.

    Science.gov (United States)

    Goetz, C A; Loomis, T C

    1966-07-01

    A method for the analysis of brass is presented. The lead, iron, nickel and zinc components are determined titrimetrically with the complexing agent CDTA (disodium dihydrogen 1,2-diaminocyclohexane N,N,N',N'-tetraacetate [also known as HexaVer]). The copper and the tin are weighed as metallic copper and as stannic oxide. The method is more rapid and convenient, especially for routine analysis, than the all-gravimetric procedure and it provides at least equal accuracy and precision.

  19. Synthesis of Hydrophobic, Crosslinkable Resins.

    Science.gov (United States)

    1985-12-01

    bisphenol and aqueous sodium hydroxide, and the water was removed by azeotropic distillation using toluene . 0L 4.5. REACTION OF 4,4" THiODIPHENOL WITH DCpX...disodium salt of the bisphenol was prepared in DMSO using aqueous NaOH, then azeotropic distillation of the water with toluene . DCpX was then added, but...HPI.C, with THF/ water mixtures as the, mobile phase has .- - ..- "*.* -- .-. . ......................................................... CH3 HO-OT-C

  20. Final Environmental Assessment Test Operations at Arnold Engineering Development Center. Volumes 1 & 2

    Science.gov (United States)

    2008-06-01

    dioxide injection; flash mix of potassium permanganate, alum , and lime; mixing in flocculation cham- Facility Facility Served Limitations Limiting...ETHYLENEDIAMINE TETRAACETIC ACID, DISODIUM SALT , DIHYDRATE S311-500 180672 1 500 ML EXTERIOR ACRYLIC PAINT, WHITE 520/ACRI-SHIELD EXTERIOR ACRYLIC 181902 1 1...182343 1 16 OZF MACHINE CLEANER INTERNATIONAL MACHINE CLEANER 550-LF 180337 3 55 GL MAGIC BOND EPOXY STICK-GREEN, WHITE, ALUM , COPPER, BLUE 11600 180310

  1. Anti-inflammatory gallic Acid and wedelolactone are G protein-coupled receptor-35 agonists.

    Science.gov (United States)

    Deng, Huayun; Fang, Ye

    2012-01-01

    G protein-coupled receptor-35 (GPR35) has been shown to be a target of the asthma drugs cromolyn disodium and nedocromil sodium. Gallic acid and caffeic acids are reported to modulate allergic reactions via unknown mode(s) of action. Here we attempt to elucidate whether both phenolic acids share a common mode of action with the two asthma drugs. Label-free dynamic mass redistribution (DMR) assays showed that both phenolic acids triggered robust DMR signals in HT-29 cells, whose characteristics were similar to that of cromolyn disodium. Both phenolic acids resulted in detectable β-arrestin translocation signals in an engineered U2OS cell line stably expressing a C-terminal-modified GPR35, but with lower efficacy than cromolyn disodium. Antiallergic wedelolactone was found to be a potent β-arrestin-biased GPR35 agonist. These results suggest that certain anti-inflammatory phytochemicals including gallic acid and wedelolactone may modulate inflammatory allergic action via their agonism at GPR35. GPR35 may represent a target for the treatment of allergic disorders including asthma.

  2. Liver perfusion in dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI): comparison of enhancement in Gd-BT-DO3A and Gd-EOB-DTPA in normal liver parenchyma

    Energy Technology Data Exchange (ETDEWEB)

    Schalkx, Hanke J.; Bosch, Maurice A.A.J. van den; Veldhuis, Wouter B.; Leeuwen, Maarten S. van [University Medical Center Utrecht, Department of Radiology, PO Box 58800, Utrecht (Netherlands); Stralen, Marijn van; Pluim, Josien P.W. [University Medical Center Utrecht, Image Sciences Institute, Utrecht (Netherlands); Coenegrachts, Kenneth [Department of Radiology, Bruges (Belgium); Kessel, Charlotte S. van; Hillegersberg, Richard van [University Medical Center Utrecht, Department of Surgery, Utrecht (Netherlands); Erpecum, Karel J. van [University Medical Center Utrecht, Department of Gastroenterology, Utrecht (Netherlands); Verkooijen, Helena M. [University Medical Center Utrecht, Clinical epidemiologist, Department of Radiology, Utrecht (Netherlands)

    2014-09-15

    Within-patient comparison of the enhancement patterns of normal liver parenchyma after gadobutrol and gadoxetate disodium, with emphasis on the start of hepatocytic uptake of gadoxetate disodium. Twenty-one patients (12 female, 9 male) without chronic liver disease underwent 1.5-T contrast-enhanced MRI twice, once with an extracellular contrast agent (gadobutrol) and once with a hepatospecific agent (gadoxetate disodium), using a T1-weighted keyhole sequence. Fifteen whole-liver datasets were acquired up to 5 min for both contrast agents and two additional datasets, up to 20 min, for gadoxetate. Signal intensities (SI) of the parenchyma, aorta and portal vein were measured and analysed relative to pre-contrast parenchymal SI. After gadoxetate, in 29 % of the patients the parenchymal SI decreased by ≥5 % after the initial vascular-phase-induced peak, while in the other 71 % the parenchymal SI remained stable or gradually increased until up to 20 min after the initial peak. The hepatocytic gadoxetate uptake started at a mean of 37.8 s (SD 14.7 s) and not later than 76 s after left ventricle enhancement. Parenchymal enhancement due to hepatocytic uptake of gadoxetate can start as early as in the late arterial phase. This may confound the assessment of lesion appearance as compared to extracellular contrast such as gadobutrol. (orig.)

  3. Synthesis, Structural Characterization, and Antitumor Activity of a Ca(II Coordination Polymer Based on 1,6-Naphthalenedisulfonate and 4,4′-Bipyridyl

    Directory of Open Access Journals (Sweden)

    Xishi Tai

    2013-08-01

    Full Text Available A novel Ca(II coordination polymer, [CaL(4,4′-bipyridyl(H2O4]n (L = 1,6-naphthalenedisulfonate, was synthesized by reaction of calcium perchlorate with 1,6-naphthalenedisulfonic acid disodium salt and 4,4′-bipyridyl in CH3CH2OH/H2O. It was characterized by elemental analysis, IR, molar conductivity and thermogravimetric analysis. X-ray crystallography reveals that the Ca(II coordination polymer belongs to the orthorhombic system, with space group P212121. The geometry of the Ca(II ion is a distorted CaNO6 pengonal bipyramid, arising from its coordination by four water molecules, one nitrogen atom of 4,4′-bipyridyl molecule, and two oxygen atoms from two L ligands. The complex molecules form a helical chain by self-assembly. The antitumor activity of 1,6-naphthalenedisulfonic acid disodium salt and the Ca(II coordination polymer against human hepatoma smmc-7721 cell line and human lung adenocarcinoma A549 cell line reveals that the Ca(II coordination polymer inhibits cell growth of human lung adenocarcinoma A549 cell line with IC50 value of 27 μg/mL, and is more resistive to human lung adenocarcinoma A549 cell line as compared to 1,6-naphthalenedisulfonic acid disodium salt.

  4. RECOVERY OF DAMAGES IN THE SKIN OF ARSENIC EXPOSED CLARIAS BATRACHUS (LINN. FOLLOWING WITHDRAWAL OF THE STRESS

    Directory of Open Access Journals (Sweden)

    A. K. Singh ، T. K. Banerjee

    2008-10-01

    Full Text Available The bottom dwelling air-breathing catfish, Clarias batrachus (Linn. also respires via its skin (an accessory water-breathing organ. Prolonged (90 days exposure to disodium arsenate heptahydrate has caused massive damage (e.g. wear and tear of various cellular components including club cells, hypertrophy and hyperplasia of the goblet mucous cells, altered staining and the slimy secretion to the epidermis of its skin. The present study investigated the recovery in architecture of the damaged epidermis following return of the 90 days disodium arsenate heptahydrate exposed fish to clean water. The significant regeneration of its different cellular components (epithelial cells, Club cells, Mucous cells took place after 24 h of withdrawal when sloughing; wear and tear and other damages of the epidermis of the skin got substantially reduced. The histopathological alterations which still continued included squeezing out of contents of the Club cells that formed a thin layer on the body surface. Regeneration of the Club cells continued throughout the epidermis even though the newly formed Club cells still showed massive sign of degeneration. Altered staining behaviour and hyperactivity of the Mucous cells continues even after prolonged withdrawal of the stress of the arsenic salt. Similarly the glycoproteins of the slime secreted by the mucous cells retained their sulphate moieties. This indicates that disodium arsenate heptahydrate induces certain permanent non-reversible damages including altered mucogenic activity in the epidermis of the skin of C. batrachus.

  5. Negative effect of dissolved organic compounds on settling behavior of synthetic monominerals in red mud

    Institute of Scientific and Technical Information of China (English)

    王梦; 胡慧萍; 刘锦伟; 陈启元

    2016-01-01

    Hydration grossular and hematite monominerals were synthesized. The effects of dissolved organic compounds (including sodium formate, sodium acetate, sodium oxalate, sodium salicylate or disodium phthalate) on the settling performance of hydration grossular or hematite slurries were studied. The settling of the slurries was also investigated with the addition of sodium polyacrylate (PAAS) or hydroxamated polyacrylamide flocculant (HCPAM). The adsorption mechanism of organic compounds on monominerals surfaces was studied by FT-IR and XPS, respectively. A deterioration in settling is observed in order of disodium phthalate>sodium salicylate>sodium oxalate>sodium formate (or sodium acetate). Moreover, PAAS can efficiently eliminate the negative effects of organic compounds on the settling performance of the hydration grossular slurry. HCPAM can efficiently eliminate the negative effects of sodium formate, sodium acetate and sodium oxalate on the settling performance of the hematite slurry, but it only partially improves the settling performance of hematite slurry containing sodium salicylate or disodium phthalate. FT-IR and XPS results show that organic compounds are physically adsorbed on hydration grossular surface, and chemisorptions of organic compounds occur on hematite surface with a bidentate chelating complex.

  6. Effects of phosphate addition on methane fermentation in the batch and upflow anaerobic sludge blanket (UASB) reactors.

    Science.gov (United States)

    Suzuki, Sho; Shintani, Masaki; Sanchez, Zoe Kuizon; Kimura, Kohei; Numata, Mitsuru; Yamazoe, Atsushi; Kimbara, Kazuhide

    2015-12-01

    Ammonia inhibition of methane fermentation is one of the leading causes of failure of anaerobic digestion reactors. In a batch anaerobic digestion reactor with 429 mM NH3-N/L of ammonia, the addition of 25 mM phosphate resulted in an increase in methane production rate. Similar results were obtained with the addition of disodium phosphate in continuous anaerobic digestion using an upflow anaerobic sludge blanket (UASB) reactor. While methane content and production rate decreased in the presence of more than 143 mM NH3-N/L of ammonium chloride in UASB, the addition of 5 mM disodium phosphate suppressed ammonia inhibition at 214 mM NH3-N/L of ammonium chloride. The addition prevented acetate/propionate accumulation, which might be one of the effects of the phosphate on the ammonia inhibition. The effects on the microbial community in the UASB reactor was also assessed, which was composed of Bacteria involved in hydrolysis, acidogenesis, acetogenesis, and dehydrogenation, as well as Archaea carrying out methanogenesis. The change in the microbial community was observed by ammonia inhibition and the addition of phosphate. The change indicates that the suppression of ammonia inhibition by disodium phosphate addition could stimulate the activity of methanogens, reduce shift in bacterial community, and enhance hydrogen-producing bacteria. The addition of phosphate will be an important treatment for future studies of methane fermentation.

  7. Safety and Efficacy of Gadoxetate Disodium–Enhanced Liver MRI in Pediatric Patients Aged >2 Months to <18 Years—Results of a Retrospective, Multicenter Study

    Science.gov (United States)

    Geller, James; Kasahara, Mureo; Martinez, Mercedes; Soresina, Annarosa; Kashanian, Fran; Endrikat, Jan

    2016-01-01

    PURPOSE To assess the safety and efficacy of gadoxetate disodium–enhanced liver MR imaging in pediatric patients. MATERIAL AND METHODS Retrospective, multicenter study including pediatric patients aged >2 months to <18 years who underwent contrast-enhanced liver MRI due to focal liver lesions. A single intravenous bolus injection of 0.025 to 0.05 mmol/kg body weight of gadoxetate disodium was administered. Adverse events (AEs) up to 24 hours after injection were recorded and a one-year follow-up was conducted for all serious and unexpected AEs. Efficacy was defined based on the additional diagnostic information obtained from the combined (pre- and postcontrast) image sets as compared with the precontrast image sets by blinded reading. RESULTS A total of 52 patients for safety and 51 patients for efficacy analyses were evaluated. Twenty-two patients (42.3%) reported a total of 51 serious AEs (SAEs) and one AE after one year. No SAE or AE was related to gadoxetate disodium injection. Gadoxetate disodium–related effects on vital signs were not seen. Additional diagnostic information was obtained for 86.3% of patients. The three most improved efficacy variables were lesion-to-background contrast, lesion characterization, and improved border delineation in 78.4%, 76.5%, and 70.6% of patients, respectively. CONCLUSION Gadoxetate disodium in pediatric patients did not raise any clinically significant safety concern. Contrast enhancement provided additional clinically relevant information. PMID:27478381

  8. IR spectroscopic investigation of the inhibition of the glycation process by acetylsalicylic acid

    Science.gov (United States)

    Otero de Joshi, Virginia; Gil, Herminia; Contreras, Silvia; Velasquez, William; Joshi, Narahari V.

    2000-05-01

    An IR spectroscopic study was carried out at room temperature for Human Serum albumin (HSA) glycated with fructose and glucose and inhibited with acetylsalicylic acid. The glycation process was carried out in our laboratory by a conventional method to confirm earlier reported observation of the effect of glycation on the intensity variation of the IR spectra, particularly, in the range 1500 cm-1 to 1700 cm-1 and around 3300 cm-1. IR spectra reveal that the effects of glycation of HSA by fructose are more intense than with glucose, which is the expected. Bovine serum albumin was also glycated using Glucose-6-phosphate disodium salt, and gamma-globulin was glycate with glucose, As expected, the glycation process was more intense with glucose-t-phosphate disodium salt. Acetyl salicylic acid was also used and its inhibitor effects could be observed in both cases, with glucose and with glucose-6-phosphate disodium salt even though, to a smaller extent with the latter. This is consistent with the earlier data and is explained on the basis of the attachment of macromolecules to (epsilon) -NH2 groups of lysines. The experimental results confirm that acetylsalicylic acid, indeed, acts as an inhibitor by acetylation of the (epsilon) -NG2 group where the sugars are supposed to be attached.

  9. Influence of chemical agents on the surface area and porosity of active carbon hollow fibers

    Directory of Open Access Journals (Sweden)

    LJILJANA M. KLJAJEVIĆ

    2011-09-01

    Full Text Available Active carbon hollow fibers were prepared from regenerated polysulfone hollow fibers by chemical activation using: disodium hydrogen phosphate 2-hydrate, disodium tetraborate 10-hydrate, hydrogen peroxide, and diammonium hydrogen phosphate. After chemical activation fibers were carbonized in an inert atmosphere. The specific surface area and porosity of obtained carbons were studied by nitrogen adsorption–desorption isotherms at 77 K, while the structures were examined with scanning electron microscopy and X-ray diffraction. The activation process increases these adsorption properties of fibers being more pronounced for active carbon fibers obtained with disodium tetraborate 10-hydrate and hydrogen peroxide as activator. The obtained active hollow carbons are microporous with different pore size distribution. Chemical activation with phosphates produces active carbon material with small surface area but with both mesopores and micropores. X-ray diffraction shows that besides turbostratic structure typical for carbon materials, there are some peaks which indicate some intermediate reaction products when sodium salts were used as activating agent. Based on data from the electrochemical measurements the activity and porosity of the active fibers depend strongly on the oxidizing agent applied.

  10. Investigation of the Role of Mast Cells in Acupuncture Effects and Their Sensitivity to Physical Stimuli During TCM Treatment

    Institute of Scientific and Technical Information of China (English)

    张迪; 丁光宏; 顾全保; Wolfgang Schwarz

    2008-01-01

    Objective: To better understand the function of mast cells in acupuncture points (acupoints) inacupuncture-induced analgesia. The author tested their sensitivity to mechanical, thermo and light stimulation.Methods: The tail flick model was applied to measure analgesia in rats, and the author determined the density of mast cells in tissue slices and their degranulation ratio before/after acupuncture. The author also applied the patch-clamp technique to investigate activation of human mast cells (HMC 1 cell line) by mechanical stress or noxious heat, and the author optically observed degranulation phenomena of mast cell in response to red laser light.Results: Manual stimulation by acupuncture at Zusanli (ST 36) of the rat resulted in analgesia and the effect was more pronounced than after stimulation of a sham point nearby the acupuncture point. A higher density of mast cells was found at Zusanli (ST 36) than at the sham point, and acupuncture caused a remarkable increase in degranulation. Pretreatment with disodinm chromoglycate (DSCG, a mast cell stabilizer) injected into Zusanli (ST 36) impaired the analgesic effect of acupuncture. In whole-cell patch-clamp, increasing hydrostatic pressure induced a current that could be inhibited by 10 ~tM of ruthenium red (RuR), an inhibitor of TRPV2. Temperatures above 50~C, which are reached during moxibustion, induced a similar RuR-sensitive current. Laser light of 640 nm (48 mW) applied to acupoints had been shown previously to be highly effective in analgesia. 20 min of light application induced pronounced degranulation in HMC 1 that could be blocked by 0.02 g/mL DSCG as well as by RuR. Conclusion: The author found that mechanical stimulation of acupoints is associated with mast cell degranulation and mast-cell degranulation can be correlated with acupuncture-induced analgesia. The author suggest that TRPV2 plays a key role in mast-ceU degranulation in response to mechanical, thermal (moxibustion) as well as laser

  11. Impact of inhalation therapy on oral health

    Directory of Open Access Journals (Sweden)

    Navneet Godara

    2011-01-01

    Full Text Available Inhalation therapy has been employed as the mainstay of the treatment in chronic respiratory diseases such as asthma and chronic obstructive pulmonary disease (COPD. Beta-2 agonists, anticholinergic bronchodilators, inhaled corticosteroids, and sodium cromoglycate are often used alone or in combination in an inhaled form. Studies have shown that inhaled drugs used in the treatment have some adverse effects on the oral health based on their dosage, frequency, and duration of use. Several oral conditions such as xerostomia, dental caries, candidiasis, ulceration, gingivitis, periodontitis, and taste changes have been associated with inhalation therapy. Since the prevalence of chronic respiratory diseases is rising, it is important to provide optimal oral care to the individuals receiving inhalation therapy. This article will review the influence of inhaled drugs on the oral health of individuals and adequate management and prevention of the same.

  12. Immediate response to cigarette smoke

    Energy Technology Data Exchange (ETDEWEB)

    Rees, P.J.; Chowienczyk, P.J.; Clark, T.J.

    1982-06-01

    Using an automated method of calculating airways resistance in the body plethysmograph, we have investigated changes occurring immediately after inhalation of cigarette smoke. Decreases in specific conductance occurred by the time of the first measurement seven or eight seconds after exposure to single inhalations of cigarette smoke in 12 smokers and 12 non-smokers. Less than half of the initial change was present 40 seconds after the inhalation. Initial responses were greater in the non-smokers. Responses recurred with repeated inhalations in smokers and non-smokers. Prior administration of salbutamol and ipratropium bromide significantly inhibited the response and this inhibition appeared to be greater in non-smokers. Sodium cromoglycate inhaled as a dry powder had no effect on the response.

  13. "THE ROLE OF PROSTAGLANDINS AND MAST CELLS IN THE MODULATION OF ACUTE ACID-INDUCED TRACHEAL CONTRACTION IN RAT"

    Directory of Open Access Journals (Sweden)

    M. H. Pipelzadeh

    2004-05-01

    Full Text Available The exact role of the epithelial lining of the trachea in modulating the bronchial tone is controversial. The present study was an attempt to verify the role of both prostaglandins and mast cells in the acute phase of acid inspiration in rat. Four groups (n = 6 of N. Mari rats were employed. The first group was used as placebo control, and normal saline was injected. To the second group hydrochloric acid (25 µl with pH of 1.3 was injected into the trachea through the criothyroid membrane. The third and fourth groups were pretreated for three consecutive days either with indomethacin (10 mg/Kg or nebulized sodium cromoglycate (20 mg/Kg, 1 hour prior to installation of the acid. Three minutes after instillation of acid, the trachea was removed. The tracheal spirals were prepared and immediately suspended in an organ bath containing Tyrode’s solution. Dose response curves to acetylcholine (10-9 to 10-3M were constructed. The results showed that the responses to acetylcholine in the acid treated trachea were significantly (P<0.01 reduced compared with the control saline treated trachea due to acute acid-induced tracheal contraction. Incubation with atropine, induced reduction of baseline tension and reversed the responses to acetylcholine. Both indomethacin and sodium cromoglycate, reversed the responses to acetylcholine and were in similar range as the control trachea. In conclusion, it seems that both prostaglandins and mast cells are important mediators in the acute phase of airway smooth muscle contraction following instillation of acid.

  14. Functionalization of carbon nanotubes with a pH-responsive molecule to produce a pH sensor

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Liping; Nakayama, Tomonobu; Tomimoto, Hiroyuki; Shingaya, Yoshitaka [Nano Functionality Integration Group, National Institute for Materials Science, Tsukuba 305-0044 (Japan); Huang Qing, E-mail: zhao.liping@nims.go.j, E-mail: NAKAYAMA.Tomonobu@nims.go.j [Nanoscale Materials Center, National Institute for Materials Science, Tsukuba 305-0044 (Japan)

    2009-08-12

    Carbon nanotubes were functionalized with the ratiometric pH-responsive dye molecule 6,8-dihydroxy-1,3-pyrenedisulfonic acid disodium salt, which enabled them to indicate pH values over the range of pH 5.6-8.3. The nanotubes were coated with a layer of electron-donating ZnPc, which strengthened the CNT-dye interaction. The range of pH response is relevant for biological systems, which makes the nanotubes suitable for a wide range of applications within nanobiotechnology.

  15. Bis(4-cyano-1-methylpyridinium bis(1,2-dicyanoethene-1,2-dithiolato-κ2S,S′cuprate(II

    Directory of Open Access Journals (Sweden)

    Na Wang

    2012-02-01

    Full Text Available The title ion-pair compound, (C7H7N22[Cu(C4N2S22], was obtained by the direct reaction of CuCl2·2H2O, disodium maleonitriledithiolate (Na2mnt and 4-cyano-1-methylpyridinium iodide. The anion and one pyridinium cation lie entirely on a mirror plane, whereas for the other cation, a crystallographic mirror plane runs through the N and para-C atoms of the pyridine ring, the methyl C atom, and the cyano group. In the crystal, ions are linked into a three-dimensional network by C—H...N hydrogen bonds.

  16. In vitro inhibition of hyaluronidase by sodium copper chlorophyllin complex and chlorophyllin analogs

    Directory of Open Access Journals (Sweden)

    McCook JP

    2015-08-01

    Full Text Available John P McCook,1 Peter L Dorogi,2 David B Vasily,3 Dustin R Cefalo4 1Discovery Partners, LLC, Frisco, TX, 2CHL Industries, LLC, Easton, PA, 3Aesthetica Cosmetic and Laser Surgery Center, Bethlehem, PA, 4Frontier Scientific, Inc., Logan, UT, USA Background: Inhibitors of hyaluronidase are potent agents that maintain hyaluronic acid homeostasis and may serve as anti-aging, anti-inflammatory, and anti-microbial agents. Sodium copper chlorophyllin complex is being used therapeutically as a component in anti-aging cosmeceuticals, and has been shown to have anti-hyaluronidase activity. In this study we evaluated various commercial lots of sodium copper chlorophyllin complex to identify the primary small molecule constituents, and to test various sodium copper chlorophyllin complexes and their small molecule analog compounds for hyaluronidase inhibitory activity in vitro. Ascorbate analogs were tested in combination with copper chlorophyllin complexes for potential additive or synergistic activity. Materials and methods: For hyaluronidase activity assays, dilutions of test materials were evaluated for hydrolytic activity of hyaluronidase by precipitation of non-digested hyaluronate by measuring related turbidity at 595 nm. High-performance liquid chromatography and mass spectroscopy was used to analyze and identify the primary small molecule constituents in various old and new commercial lots of sodium copper chlorophyllin complex. Results: The most active small molecule component of sodium copper chlorophyllin complex was disodium copper isochlorin e4, followed by oxidized disodium copper isochlorin e4. Sodium copper chlorophyllin complex and copper isochlorin e4 disodium salt had hyaluronidase inhibitory activity down to 10 µg/mL. The oxidized form of copper isochlorin e4 disodium salt had substantial hyaluronidase inhibitory activity at 100 µg/mL but not at 10 µg/mL. Ascorbate derivatives did not enhance the hyaluronidase inhibitory activity of

  17. Synthesis and Characterization of Ion-exchange Sulfonated Poly (ether sulfone)

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    N,N'-Bis(3-hydroxyphenyl)-1,8,4,5-naphthalenetetracarboxylic bisimide was prepared from the reaction of 1,8,4,5-naphthalenetetrcarboxylic acid dianhydride and 2-aminophenol in N,N-dimethylformamide. Polymerization of this bisimide with 4,4'-difluorodiphenylsulfone and disodium 3,3'-disulfonate4,4'-difluorodiphenylsulfone gave ion-exchange sulfonated poly(ether sulfone). The structure of the title compound was characterized with 1H-NMR and its polymer was characterized with FT-IR.

  18. Crystal structure of Na2HfSi2O7 by Rietveld refinement

    Directory of Open Access Journals (Sweden)

    Nicolas Massoni

    2016-10-01

    Full Text Available The structure of triclinic disodium hafnium disilicate, Na2HfSi2O7, has been determined by laboratory powder X-ray diffraction and refined by the Rietveld refinement. The structure is a framework made of alternate layers of HfO6 octahedra and SiO4 tetrahedra linked by common O atoms. Sodium atoms are located in the voids of the framework, aligned into tunnels along the [010] direction. Na2HfSi2O7 is isostructural with the parakeldyshite Na2ZrSi2O7 phase.

  19. 7-{[2-(4-Hydroxyphenylmethylidene]amino}-1,3-thiazol-4-yl-2-(methoxyiminoacetyl]amino}-3-{[(2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-ylsulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid

    Directory of Open Access Journals (Sweden)

    Ghulam Fareed

    2012-05-01

    Full Text Available Novel 7-{[2-(4-hydroxyphenylmethylidene]amino}-1,3-thiazol-4-yl-2-(methoxyiminoacetyl]amino}-3-{[(2-methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-ylsulfanyl]methyl}-8-oxo-5-thia-1azabicyclo [4.2.0]oct-2-ene-2-carboxylic acid was prepared by condensation of ceftriaxone disodium (1 with 4-hydroxybenzaldehyde (2 in ethanol under reflux conditions for 3–4 h. The structure of synthesized compound was elucidated using LCMS, 1H-NMR, and CHN techniques.

  20. Determination and validation of zonisamide and its four related substances by HPLC and UV-spectrophotometry

    Directory of Open Access Journals (Sweden)

    Hosseini Maryam

    2010-01-01

    Full Text Available A selective and sensitive liquid chromatographic method has been developed for simultaneous determination of zonisamide and its four related substances in pharmaceutical dosage forms. The assay involved an isocratic elution in perfectsil Target C18 column using a mobile phase composition of disodium hydrogen phosphate buffer, acetonitrile and methanol (650:150:200 v/v, pH adjusted to 3±0.05 with flow rate 1.2 ml/min and analyte monitored at 240 nm. Also a simple and precise spectrophotometric method was developed for dissolution studies. These proposed methods are sensitive, accurate, reproducible and useful for the routine determination of zonisamide in pharmacy.

  1. A strong steric hindrance effect on ground state, excited state, and charge separated state properties of a CuI-diimine complex captured by X-ray transient absorption spectroscopy

    DEFF Research Database (Denmark)

    Huang, J.; Mara, M.W.; Stickrath, A.B.

    2014-01-01

    Photophysical and structural properties of a CuI diimine complex with very strong steric hindrance, [CuI(dppS)2]+ (dppS = 2,9-diphenyl-1,10-phenanthroline disulfonic acid disodium salt), are investigated by optical and X-ray transient absorption (OTA and XTA) spectroscopy. The bulky phenylsulfonic...... of metal complex/semiconductor NP hybrids but also provide guidance for designing efficient CuI diimine complexes with optimized structures for application in solar-to-electricity conversion. This journal is...

  2. Eco-friendly coloration of linen to ameliorate its practical approach

    Directory of Open Access Journals (Sweden)

    Pervez Md. Nahid

    2017-01-01

    Full Text Available Reactive dyes are the perfect choice for dyeing of cellulosic fibers due to produce a wide gamut of bright colors with excellent color fastness, however environmental pollution is increasing in recent days seeing that of making use of inorganic salt and alkali. This paper offers a new avenue for eco-friendly dyeing of linen fiber by incorporating biodegradable alkaline organic salts in presence of three commercial reactive dyes and amongst them organic salt i.e. disodium maleate showed superior result in terms of color strength (K/S, dye exhaustion (%, color fastness, tensile strength and crease recovery angle parameters that were evaluated by traditional technique.

  3. Fluorinated aromatic diamine

    Science.gov (United States)

    Jones, Robert J. (Inventor); O'Rell, Michael K. (Inventor); Hom, Jim M. (Inventor)

    1980-01-01

    This invention relates to a novel aromatic diamine and more particularly to the use of said diamine for the preparation of thermally stable high-molecular weight polymers including, for example, polyamides, polyamideimides, polyimides, and the like. This diamine is obtained by reacting a stoichometric amount of a disodium salt of 2,2-bis(4-hydroxyphenyl) hexafluoropropane with 4-chloronitrobenzene to obtain an intermediate, 2,2-bis[4-(4-nitrophenoxy)phenyl] hexafluoropropane, which is reduced to the corresponding 2,2-bis[4-(4-aminophenoxy)phenyl] hexafluoropropane.

  4. Isolation and structures of some selenium and tellurium derivatives of 1, 4, 5, 8, 9, 12-hexabromododecahydrotriphenylene as co-crystals of triphenylene

    Indian Academy of Sciences (India)

    Poonam Rajesh Prasad; Harkesh B Singh; Ray J Butcher

    2014-09-01

    The synthesis and characterization of low-valent organoselenium and tellurium derivatives of hexabromododecahydrotriphenylene has been attempted. The reaction of hexabromododecahydrotriphenylene with in situ generated disodium dichalcogenides (Na2E2; E = Se, Te) afforded insoluble chalcododecahydrotriphenylene derivatives, 20, 21 respectively. Attempted aromatization of 20 and 21 using DDQ (2, 3-dichloro-5, 6-dicyano-1,4-benzoquinone) as an oxidizing agent afforded the co-crystals. The hexaselenophenyl derivative, 22 and the hexaselenocyanate derivative 23 were synthesized by the reaction of in situ generated sodium arylselenolate/potassium selenocyanate with hexabromododecahydrotriphenylene, respectively. The compounds were characterized by common spectroscopic tools and a few by single crystal x-ray crystallographic studies.

  5. Gadolinium contrast agent selection and optimal use for body MR imaging.

    Science.gov (United States)

    Guglielmo, Flavius F; Mitchell, Donald G; Gupta, Shiva

    2014-07-01

    Proper selection of a gadolinium-based contrast agent (GBCA) for body magnetic resonance imaging (MRI) cases requires understanding the indication for the MRI exam, the key features of the different GBCAs, and the effect that the GBCA has on the selected imaging protocol. The different categories of GBCAs require timing optimization on postcontrast sequences and adjusting imaging parameters to obtain the highest T1 contrast. Gadoxetate disodium has many advantages when evaluating liver lesions, although there are caveats and limitations that need to be understood. Gadobenate dimeglumine, a high-relaxivity GBCA, can be used for indications when stronger T1 relaxivity is needed.

  6. Transient washout of hepatic hemangiomas: Potential pitfall mimicking malignancy

    Directory of Open Access Journals (Sweden)

    David J.S. Becker-Weidman, MD

    2016-06-01

    Full Text Available Hemangiomas are the most common tumor of the liver and distinguishing them from malignancy is important. This is a report of 3 hemangiomas in 2 patients that exhibit transient washout of gadoxetate disodium (Eovist, relative to blood pool and liver parenchyma, a characteristic that is used to diagnose hepatocellular carcinoma in at-risk patients. It is important to recognize that high-flow hemangiomas can exhibit transient washout when using a small volume of injected contrast agent. This finding is unlikely to be present on CT examinations because of the larger volume of contrast administered.

  7. The dehydrated copper silicate Na2[Cu2Si4O11]: a three-dimensional microporous framework with a linear Si—O—Si linkage

    OpenAIRE

    2008-01-01

    The structure of the title dehydrated copper silicate, disodium dicopper undecaoxide tetrasilicate, Na2(Cu2O11Si4), was determined by single-crystal X-ray diffraction from a non-merohedral twin. It exhibits an effective three-dimensional microporous framework with the major channels, in which the Na+ cations are placed, running along the a-axis direction and smaller channels observed along the b-axis direction. The structure is unusual in that it contains a symmetry-constrained Si—OR...

  8. Ultrafast dynamics of two copper bis-phenanthroline complexes measured by x-ray transient absorption spectroscopy

    DEFF Research Database (Denmark)

    Kelley, Matthew S.; Shelby, Megan L.; Mara, Michael W.

    2017-01-01

    have the general formula [Cu(I)(R)2]+, where R = 2,9-dimethyl-1,10-phenanthroline (dmp) and 2,9-diphenyl-1,10-phenanthroline disulfonic acid disodium salt (dpps). [Cu(I)(dmp)2]+ has methyl groups at the 2,9 positions of phenanthroline (phen) and adopts a pseudo-tetrahedral geometry. In contrast, [Cu......(I)(dpps)2]+ possesses two bulky phenyl-sulfonate groups attached to each phen ligand that force the molecule to adopt a flattened tetrahedral geometry in the ground state. Previously, optical transient absorption (OTA) and synchrotron based XTA experiments with 100 ps time resolution have been employed...

  9. Spontaneous, Metal-Catalyzed, and Enzyme-Catalyzed Decarboxylation of Oxalosuccinic Acid.

    Science.gov (United States)

    1980-01-01

    M sodium phosphate buffer , pH = 7.5. It was stored in the refrigerator. The concentration of the enzyme was 10 mg/ml. Each 35 milligram of enzyme had...at 250C; 2. Potassium dihydrogen phosphate /disodium hydrogen phosphate , 0.0250 molal, pH = 6.863 at 250C; and 3. Sodium tetraborate decahydrate (Borax...C -C + NAD(P) I + NAD(P)H (2) /I H \\HO C OH 0 OH III distinct enzymes, one specific for nicotinamide adenine dinucleotide phosphate (NADP +), and one

  10. Combustion Product Evaluation of Various Charge Sizes and Propellant Formulations. Task 1 Report: Sampling and Analytical Procedures Proposed for Use in Gun Propellant Combustion Product Characterization

    Science.gov (United States)

    1988-01-01

    12. Buffer : dissolve 96 g hydrated disodium hydrogen phosphate and 10 g {IIsodium dihydrogen phosphate in 5 1 deionized water (pH1 7.5). 13. Sodium...g N~aA;z, in distilled water and dilute to 1 liter. I 23. Silica Gel. 24. Sodium phosphate buffer (11% w/v): dissolve 11 g trisodium phosphate , 2m...flask. If less than 50 ml is taken, dilute IIV-132 I I I ; ,to 50 ml with 0.25 N sodium hydroxide solution (Subsection F.4.). Add 15.0 ml sodium phosphate

  11. Pseudothrombocytopenia with multiple anticoagulant sample collection tubes

    Science.gov (United States)

    Kovacs, Ferenc; Varga, Marina; Pataki, Zsolt; Rigo, Erzsebet

    2016-01-01

    The knowledge of pseudothrombocytopenia (PTCP) is important for the accuracy of a clinical assessment and for avoiding unnecessary treatment. An elderly patient was hospitalized with left lung pneumonia. Severe thrombocytopenia [platelet (PLT) number: 18 × 109/L] without any clinical bleeding was found in ethylenediaminetetraacetic acid blood collection tube. PLT measurement was repeated in various anticoagulant [sodium citrate, lithium heparin, disodium oxalate, hirudin, and magnesium sulfate (Mg-sulfate)] sample collection tubes and all of them showed thrombocytopenia except with Mg-sulfate. To the best of our knowledge, PTCP with five anticoagulant sample collection tubes has not been reported earlier.

  12. Dehydration studies using a novel multichamber microscale fluid bed dryer with in-line near-infrared measurement

    DEFF Research Database (Denmark)

    Räsänen, Eetu; Rantanen, Jukka; Mannermaa, Jukka-Pekka

    2003-01-01

    of solid materials. The temperature and the moisture content of the process air were demonstrated to be significant factors for the solid-state stability of theophylline. The presented setup is a material and cost-saving approach for studying the influence of different process parameters on dehydration....... The materials studied were disodium hydrogen phosphates with three different levels of hydrate water and wet theophylline granules. Measured process parameters of fluid bed drying were logged, including in-line NIR signals. Off-line analyses consisted of X-ray powder diffraction patterns, Fourier transform NIR...

  13. Microwave-Assisted Hydrothermal Synthesis of Cellulose/Hydroxyapatite Nanocomposites

    Directory of Open Access Journals (Sweden)

    Lian-Hua Fu

    2016-09-01

    Full Text Available In this paper, we report a facile, rapid, and green strategy for the synthesis of cellulose/hydroxyapatite (HA nanocomposites using an inorganic phosphorus source (sodium dihydrogen phosphate dihydrate (NaH2PO4·2H2O, or organic phosphorus sources (adenosine 5′-triphosphate disodium salt (ATP, creatine phosphate disodium salt tetrahydrate (CP, or D-fructose 1,6-bisphosphate trisodium salt octahydrate (FBP through the microwave-assisted hydrothermal method. The effects of the phosphorus sources, heating time, and heating temperature on the phase, size, and morphology of the products were systematically investigated. The experimental results revealed that the phosphate sources played a critical role on the phase, size, and morphology of the minerals in the nanocomposites. For example, the pure HA was obtained by using NaH2PO4·2H2O as phosphorus source, while all the ATP, CP, and FBP led to the byproduct, calcite. The HA nanostructures with various morphologies (including nanorods, pseudo-cubic, pseudo-spherical, and nano-spherical particles were obtained by varying the phosphorus sources or adjusting the reaction parameters. In addition, this strategy is surfactant-free, avoiding the post-treatment procedure and cost for the surfactant removal from the product. We believe that this work can be a guidance for the green synthesis of cellulose/HA nanocomposites in the future.

  14. Detection of contact hypersensitivity to corticosteroids in allergic contact dermatitis patients who do not respond to topical corticosteroids.

    Science.gov (United States)

    Gönül, Müzeyyen; Gül, Ulker

    2005-08-01

    The delayed hypersensitivity development against topical corticosteroids which are used in allergic contact dermatitis (ACD) treatment is an important clinical problem. In our study, 41 ACD patients who did not show any response to topical corticosteroid treatment were patch tested with corticosteroid series and the commercial preparations of corticosteroids and their vehicles. In corticosteroid series, there were budesonide, bethametasone-17-valerate, triamcinolone acetonide, tixocortol pivalate, alclomethasone-17-21-dipropionate, clobetasole-17-propionate, dexamethasone-21-phosphate disodium and hydrocortisone-17-butyrate. We detected positive reaction to corticosteroids in 9 of our cases (22%) (5 single and 4 multiple). The sensitivity was mostly produced by tixocortol pivalate (6 patients). This was followed by triamcinolone acetonide (2 patients) budesonide (2 patients), alclomethasone dipropionate (2 patients), dexamethasone 21 phosphate disodium (2 patients) and betamethasone-17-valerate (1 patient). As a result, it should not be forgotten that the corticosteroids used to treat ACD patients may cause ACD themselves. In ACD patients who did not respond to corticosteroid treatment, routinely applying patch test with corticosteroids should be helpful in directing the treatment.

  15. Endocrine and pharmacological suppressors of bone turnover protect against osteopenia in ovariectomized rats.

    Science.gov (United States)

    Wronski, T J; Dann, L M; Scott, K S; Crooke, L R

    1989-08-01

    This study was designed to test the hypothesis that endocrine and pharmacological suppressors of bone turnover prevent the development of osteopenia during estrogen deficiency. Sham-operated control and ovariectomized (OVX) rats were treated intermittently with vehicle alone, estrogen, or the diphosphonate compounds etidronate disodium (EHDP) and NE-58095 [2-(3-pyridinyl)2-hydroxyethylidene-1,1-bisphosphonate disodium] for 35 or 70 days after surgery. Their proximal tibiae were processed undecalcified for quantitative bone histomorphometry. Vehicle-treated OVX rats were characterized by decreased cancellous bone volume and 3- to 4-fold increases in osteoblast surface, osteoclast surface, bone formation rate, and bone resorption rate. Treatment of OVX rats with estrogen and NE-58095 provided complete protection against bone loss and significantly depressed all of the above indices of bone turnover. OVX rats treated with EHDP exhibited at least partial protection against bone loss and decreased bone turnover. EHDP induced a mild mineralization defect, as indicated by a prolonged mineralization lag time at the tibial endocortical surface. The new diphosphonate compound NE-58095 did not impair bone mineralization. Our results indicate that endocrine and pharmacological suppressors of bone turnover prevent the development of osteopenia during the early stages of estrogen deficiency. If confirmed by clinical trials in humans, diphosphonate compounds may prove to be an alternative to estrogen for the prevention of postmenopausal bone loss.

  16. Solvothermal synthesis of Pt-Pd alloys with selective shapes and their enhanced electrocatalytic activities

    Science.gov (United States)

    Zhang, Zhi-Cheng; Hui, Jun-Feng; Guo, Zhen-Guo; Yu, Qi-Yu; Xu, Biao; Zhang, Xin; Liu, Zhi-Chang; Xu, Chun-Ming; Gao, Jin-Sen; Wang, Xun

    2012-03-01

    Pt-Pd bimetallic alloy nanostructures with highly selective morphologies such as cube, bar, flower, concave cube, and dendrite have been achieved through a facile one-pot solvothermal synthesis. The effects of shape-controllers (sodium dodecyl sulfate (SDS), ethylenediamine-tetraacetic acid disodium salt (EDTA-2Na), NaI) and solvents (water/DMF) on the morphologies were systematically investigated. The electrocatalytic activities of these Pt-Pd alloy nanostructures toward formic acid oxidation were tested. The results indicated that these alloy nanocrystals exhibited enhanced and shape-dependent electrocatalytic activity toward formic acid oxidation compared to commercial Pt black and Pt/C catalysts.Pt-Pd bimetallic alloy nanostructures with highly selective morphologies such as cube, bar, flower, concave cube, and dendrite have been achieved through a facile one-pot solvothermal synthesis. The effects of shape-controllers (sodium dodecyl sulfate (SDS), ethylenediamine-tetraacetic acid disodium salt (EDTA-2Na), NaI) and solvents (water/DMF) on the morphologies were systematically investigated. The electrocatalytic activities of these Pt-Pd alloy nanostructures toward formic acid oxidation were tested. The results indicated that these alloy nanocrystals exhibited enhanced and shape-dependent electrocatalytic activity toward formic acid oxidation compared to commercial Pt black and Pt/C catalysts. Electronic supplementary information (ESI) available: See DOI: 10.1039/c2nr12135b

  17. Effect of glycine on pH changes and protein stability during freeze-thawing in phosphate buffer systems.

    Science.gov (United States)

    Pikal-Cleland, Katherine A; Cleland, Jeffrey L; Anchordoquy, Thomas J; Carpenter, John F

    2002-09-01

    Previous studies have established that the selective precipitation of a less soluble buffer component during freezing can induce a significant pH shift in the freeze concentrate. During freezing of sodium phosphate solutions, crystallization of the disodium salt can produce a pH decrease as great as 3 pH units which can dramatically affect protein stability. The objective of our study was to determine how the presence of glycine (0-500 mM), a commonly used bulking agent in pharmaceutical protein formulations, affects the pH changes normally observed during freezing in sodium phosphate buffer solutions and to determine whether these pH changes contribute to instability of model proteins in glycine/phosphate formulations. During freezing in sodium phosphate buffers, the presence of glycine significantly influenced the pH. Glycine at the lower concentrations (phosphate buffer, possibly by reducing the nucleation rate of salt and thereby decreasing the extent of buffer salt crystallization. The presence of glycine at higher concentration (> 100 mM) in the sodium phosphate buffer resulted in a more complete crystallization of the disodium salt as indicated by the frozen pH values closer to the equilibrium value (pH 3.6). Although high concentrations of glycine can facilitate more buffer salt crystallization and these pH shifts may prove to be potentially damaging to the protein, glycine, in its amorphous state, can also act to stabilize a protein via the preferential exclusion mechanism.

  18. Removal of Mg2+, K+, SO4-2 Ions from Seawater by Precipitation Method

    Directory of Open Access Journals (Sweden)

    Pujiastuti Caecilia

    2016-01-01

    Full Text Available Removal of Mg2+, K+, and SO4-2 ions in seawater has been successfully done by precipitation in a mixing tank method. This study aims to remove the content of magnesium ions (Mg+, potassium (K+ and sulfate (SO4-2 in sea water with the addition of chemicals disodium phosphate (1.2 % volume, calcium chloride (2 % volume and sodium hydroxide (2% volume. Stirring is performed at 100 rpm and the pH solution is adjusted to 9. Disodium phosphate serves to bind magnesium ions and potassium, CaCl2 serves to bind the sulfate ion, while sodium hydroxide is used to adjust the pH of the solution mixture and also reacted with magnesium ions. In total, the removal efficiencies of Mg2+, K+ and SO4-2 ions in seawater were 97%, 96%, and 92%, respectively. The precipitated solids contains component of PO4- (14.5%, Mg2+(13.8%, SO4-2 (28.2%, Ca2+ (24.1% and K+ (1.9% ions.

  19. Determination of 5,7-dichloroquinolin-8-ol and 5-chloroquinolin-8-ol in bulk drug powder and pharmaceutical preparation by TLC

    Directory of Open Access Journals (Sweden)

    B H Pavithra

    2011-01-01

    Full Text Available Aim: The study aims to develop a simple, rapid and economical normal phase thin layer chromatography (TLC method for identification and quantification of 5,7-dichloroquinolin-8-ol and 5-chloroquinolin-8-ol, two active ingredients of halquinol, an antimicrobial agent. Materials and Methods: The analysis was performed on silica gel 60 TLC plates pre-washed with disodium ethylenedinitrilotetraacetic acid disodium salt (Na 2 EDTA solution with methanol-ethyl acetate-iso-propyl alcohol-ammonia solution [8:20:1:0.6 (v/v] as the mobile phase. Detection and quantification was performed densitometrically at 247 nm. Results: Responses of both 5,7-dichloroquinolin-8-ol and 5-chloroquinolin-8-ol were linear functions of concentration in the range of 300-800 ng. The intraday precision and intermediate precision of the method for 5,7-dichloroquinolin-8-ol and 5-chloroquinolin-8-ol was determined and it was found to be precise. Conclusion: The TLC method developed for simultaneous quantitative determination of 5,7-dichloroquinolin-8-ol and 5-chloroquinolin-8-ol was found to be simple and economical. Therefore, it can be used in routine quality control analysis of halquinol in bulk drug powder and halquinol bolus.

  20. TLC--densitometric method for qualitative analysis of betamethasone and its related compounds in pharmacautical preparations.

    Science.gov (United States)

    Dolowy, Małgorzata; Pyka, Alina

    2014-01-01

    A new simple and rapid TLC-densitometric procedure for the separation and identification of betamethasone and its related substances, betamethasone-17,21-dipropionate, betamethasone-17-valerate, betamethasone-21-valerate and also betamethasone disodium phosphate was developed. One of the chromatographic systems proposed in this study, which has been satisfactory applied in separation of four pairs of examined compounds was silica gel 60F254 (E. Merck, Art. 1.05554) and a mixture containing chloroform-methanol-acetic acid (99.5%) in volume composition 28:5:0.5. Densitometric measurements were done using densitometer TLC Scanner 3 at 246 nm. The proposed method was checked in terms of its specificity for the determination of betamethasone-17,21-dipropionate and betamethasone disodium phosphate in commercially available products containing both compounds, separately, as active ingredients. The results showed that the method is suitable for qualitative analysis of betamethasone derivatives in simple and combined pharmaceuticals in various dosage forms e.g., lotion and injection solution. It also can be applied in quality control of pharmaceutical formulations of betamethasone and its related compounds in form of salts and esters.

  1. Cardiovascular follow-up at school age after perinatal glucocorticoid exposure in prematurely born children: perinatal glucocorticoid therapy and cardiovascular follow-up.

    Science.gov (United States)

    de Vries, Willem B; Karemaker, Rosa; Mooy, Nicole F; Strengers, Jan L M; Kemperman, Hans; Baerts, Wim; Veen, Sylvia; Visser, Gerard H A; Heijnen, Cobi J; van Bel, Frank

    2008-08-01

    To study whether antenatal or neonatal glucocorticoid therapy to reduce the incidence and severity of chronic lung disease in preterm infants is associated with long-term adverse cardiac effects and hypertension. Retrospective matched-cohort study. Outpatient clinic of a tertiary care hospital. One hundred ninety-three children aged 7 to 10 years who had been born prematurely between December 2, 1993, and September 15, 1997. Main Exposure Neonatal treatment with dexamethasone disodium phosphate(n = 48) or the clinically equally effective glucocorticoid hydrocortisone (n = 51), or only antenatal treatment with betamethasone disodium phosphate and betamethasone acetate (n = 51). These 3 groups were compared with a reference group of prematurely born children who had not been exposed to perinatal glucocorticoid therapy (n = 43). General hemodynamic data (heart rate and blood pressure), cardiovascular function as assessed at echocardiography, intima-media thickness of the carotid arteries, and cardiac biochemical features as early markers of expansion and volume overload of the cardiac left ventricle (B-type natriuretic peptide and N-terminal pro-B-type natriuretic peptide). No significant group differences were found for heart rate, blood pressure, biochemical features, intima-media thickness, or systolic or diastolic left ventricular function. Although no differences were found in blood pressure and cardiovascular function at school age in children antenatally or neonatally treated with glucocorticoids, further cardiovascular follow-up may be advisable because cardiovascular dysfunction may become apparent only later in life.

  2. Complexometric determination, Part II: Complexometric determination of Cu2+-ions

    Directory of Open Access Journals (Sweden)

    Rajković Miloš B.

    2002-01-01

    Full Text Available A copper-selective electrode of the coated wire type based on sulphidized copper wire was applied successfully for determining Cu(II ions by complexometric titration with the disodium salt of EDTA (complexon III. By the formation of internal complex compounds with the Cu(II ion, the copper concentration in the solution decreases, and all this is followed by a change of potential of the indicator system Cu-DWISE (or Cu-EDWISE/SCE. At the terminal point of titration, when all the Cu(II ions are already utilized for the formation of the complex with EDTA, there occurs a steep rise of potential, thus enabling us, through the first or second derivative to note the quantity of copper that is present in the solution. Copper-selective electrode showed a responsivity towards titration with EDTA as a complexing agent, with the absence of "fatigue" due to a great number of repeated measurings. Errors occurring during quantitative measurements were more a characteristic of the overall procedure which involve, because of the impossibility of the complete absence of subjectivity, a constant error, and the reproducibility of the results confirmed this fact. The disodium salt of EDTA appeared as a very efficient titrant in all titrations and with various concentrations ot Cu(II ions in the solution, with somewhat weaker response at lower concentrations in the solution.

  3. Tungsten oxide thin films obtained by anodisation in low electrolyte concentration

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Nadja B.D. da [Centro de Ciências Químicas, Farmacêuticas e de Alimentos, Universidade Federal de Pelotas, Campus Capão do Leão, s/n, Pelotas, RS (Brazil); Pazinato, Julia C.O. [Instituto de Química, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500 Porto Alegre, RS (Brazil); Sombrio, Guilherme; Pereira, Marcelo B.; Boudinov, Henri [Instituto de Física, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500 Porto Alegre, RS (Brazil); Gündel, André; Moreira, Eduardo C. [Universidade Federal do Pampa, Travessa 45, 1650 Bagé, RS (Brazil); Garcia, Irene T.S., E-mail: irene.garcia@ufrgs.br [Instituto de Química, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500 Porto Alegre, RS (Brazil)

    2015-03-02

    Tungsten oxide nanostructured films were grown on tungsten substrates by anodisation under a fixed voltage and with sodium fluoride as electrolyte. The effect of the anion chloride and the influence of the modifying agent disodium hydrogen phosphate in the tungsten oxide films were also investigated. The structural characterisation of the films was performed by scanning electron microscopy, atomic force microscopy and Raman spectroscopy. The band gap was determined through diffuse reflectance spectroscopy. The thin films were photoluminescent and emitted in the range of 300 to 630 nm when irradiated at 266 nm. The synthesised films efficiently degraded of methyl orange dye in the presence of hydrogen peroxide and 250 nm radiation. The modifying agent was responsible for the improvement of the photocatalytic activity. Films with similar photocatalytic performance were obtained when the system sodium fluoride and disodium hydrogen phosphate were replaced by sodium chloride. The porous structure and low band gap values were responsible for the photocatalytic behaviour. - Highlights: • Tungsten oxide thin films were obtained by anodisation of tungsten in aqueous media. • The performance of the NaCl, NaF and NaF/Na{sub 2}HPO{sub 4} as electrolytes was investigated. • The relation between structure and optical behaviour has been discussed. • Films obtained with NaCl and NaF/Na{sub 2}HPO{sub 4} present similar photocatalytic activity.

  4. CLINICAL PICTURE AND THERAPEUTIC MANAGEMENT OF LEAD TOXICOSIS IN SHEEP

    Directory of Open Access Journals (Sweden)

    H. Zaneb, K. Pervez, M. S. Sarwar, S. Sindhu.

    2003-12-01

    Full Text Available The project was aimed at evaluation of comparative therapeutic efficacy of two treatment regimes for the treatment of lead poisoning in sheep. For this purpose 20, two-months-old, lambs of Buchi breed were used as experimental animals. Five animals were kept as healthy control, whereas the remaining 15 animals were given oral aqueous solution of lead acetate daily. The dose was started from 5 mg/kg bodyweight and was increased gradually till it reached 100 mg/kg body weight by the end of 2nd month when clinical toxicosis was observed. Clinical findings included diarrhea, hindquarter weakness and reduction of feed intake, accompanied by anemia and elevated blood lead levels up to 2.72 ppm. The 15 toxicated animals were divided into three groups A, B and C comprising of 5 animals each. Disodium calcium edetate, which was used to treat animals of group A, resulted in 52.7% fall in blood lead level in 5 days. A combination of disodium calcium edetate and thiamine hydrochloride was used to treat animals of group B, which showed 73.8% fall in blood lead levels. Group C served as untreated control. Thus, combination therapy appears to be more effective for treatment of lead toxicosis.

  5. The effect of selected supercritical CO2 plant extract addition on user properties of shower gels

    Directory of Open Access Journals (Sweden)

    Vogt Otmar

    2014-12-01

    Full Text Available The formulations of washing cosmetics i.e. shower gels, containing extracts obtained during supercritical CO2 extraction process as active ingredient, were developed. The subject of the study was the analysis of the physicochemical and user properties of the obtained products. In the work supercritical CO2 extracts of black currant seeds, strawberry seeds, hop cones and mint leafs were used. The formulation contains a mixture of surfactants (disodium cocoamphodiacetate, disodium laureth sulfosuccinate, cocoamide DEA, cocoamidepropyl betaine, Sodium Laureth Sulfate. Various thickener agents were applied to the obtained desired rheological properties of the cosmetics. Among others, sorbitol acetal derivatives, methylhydroxypropylcellulose and C10-30 alkyl acrylate crosspolymer were used. For stable products, the effect of extracts addition (black currants seeds, strawberries seeds, mint and hops, obtained from supercritical CO2 extraction process on the cosmetics properties, such as pH, viscosity, detergency and foam ability, were determined. The obtained results showed that the extracts could be used as components of shower gels.

  6. Use of potassium chloride and flavor enhancers in low sodium Cheddar cheese.

    Science.gov (United States)

    Grummer, J; Bobowski, N; Karalus, M; Vickers, Z; Schoenfuss, T

    2013-03-01

    We investigated use of potassium chloride (KCl) to maintain both the salty flavor and to replace the preservative effects of salt when reducing the sodium content in natural cheese. Because salt replacers can affect flavor because of inherent off-flavors, such as bitter and metallic, we examined the use of flavor enhancers for their ability to modulate some of these undesirable sensory effects. Stirred-curd Cheddar-style cheese was manufactured using 2 cheese-making procedures (different curd knife sizes and target salting titratable acidities), in duplicate. Curd was salted with sodium chloride (NaCl) or 60% reduced sodium blends of NaCl and KCl (2 different sources). Curd was also salted at a 60% reduced sodium rate with NaCl and KCl with added flavor enhancers. A hydrolyzed vegetable protein/yeast extract blend, a natural "potassium-blocking type" flavor, disodium inosinate, or disodium guanylate were each blended with the reduced sodium salt blend and added to curd at the salting step. The resulting blocks of cheese were aged for 5 mo and evaluated monthly for chemical, microbial, and sensory differences. At 5 mo of aging, we measured liking for the cheeses using a consumer panel. Overall, cheeses were well liked by the consumer panel, and the scores of reduced sodium cheese with 2 different KCl sources were not different from those of the full-sodium control. The addition of flavor enhancers to Cheddar curd had mixed results, with one improving the consumer flavor liking only slightly over KCl, and one (disodium inosinate) significantly reducing consumer flavor liking scores, presumably due to the amount of umami flavor it contributed. Potassium chloride replacement salts sourced from different manufacturers affected the chemical and flavor properties of cheese, and changes to pH and temperature targets may be necessary to yield cheese with the moisture and pH targets desired. The cheese-making procedure used also influenced flavors observed, which resulted in

  7. Mineral concentrations of plasma and liver after injection with a trace mineral complex differ among Angus and Simmental cattle.

    Science.gov (United States)

    Pogge, D J; Richter, E L; Drewnoski, M E; Hansen, S L

    2012-08-01

    To examine the effects of cattle breed on the clearance rate of an injectable mineral product, 10 Angus and 10 Simmental steers were blocked by breed and initial BW (332 ± 33 kg) and injected with either Multimin 90 (MM) or sterilized saline (CON) at a dose of 1 mL/45 kg BW. Multimin 90 contains 15 mg Cu/mL (as Cu disodium EDTA), 60 mg Zn/mL (as Zn disodium EDTA), 10 mg Mn/mL (as Mn disodium EDTA), and 5 mg Se/mL (as sodium selenite). Steers received a corn-silage-based diet, and inorganic sources of Cu, Zn, Mn, and Se were supplemented at NRC recommended amounts. Jugular blood was collected immediately before injection and at 8 and 10 h post-injection and on days 1, 8, and 15 post-injection. Liver biopsies were collected 3 d before injection and on days 1, 8, and 15 post-injection. Liver and plasma mineral concentration and glutathione peroxidase (GSH-Px) activity data were analyzed as repeated measures. Plasma concentrations of Zn, Mn, and Se were greater (P = 0.01) and Cu tended to be greater (P = 0.12) post-injection in MM steers compared with the CON steers. Regardless of treatment, Simmental cattle had lower plasma concentrations of Cu, Zn, and Se (P ≤ 0.05) when compared with Angus cattle. Erythrocyte GSH-Px activity was greater (P = 0.01) in MM steers compared with CON steers. Liver concentrations of Cu, Zn, and Se were greater (P = 0.05) in MM steers compared with CON steers post-injection. Liver Mn concentrations tended to be greater (P = 0.06) in MM steers compared with CON steers in the days post-injection. Interestingly, Simmental cattle exhibited greater (P = 0.01) liver Mn concentrations in the days after injection compared with Angus cattle (7.0 and 6.0 mg Mn/kg for Simmental and Angus cattle, respectively), regardless of treatment. It is unclear if this breed difference is biologically relevant; however, these data may suggest that differences in liver excretion of Mn exist between the two breeds. Overall, use of an injectable trace mineral

  8. New bone-seeking agent. Animal study of Tc-99m-incadronate

    Energy Technology Data Exchange (ETDEWEB)

    Shigematsu, Makoto; Shiomi, Susumu; Iwao, Hiroshi; Ochi, Hironobu [Osaka City Univ. (Japan). Graduate School of Medicine

    2002-02-01

    Disodium cycloheptylaminomethylenediphosphonate monohydrate (incadronate disodium) is a third-generation bisphosphonate compound which potently inhibits bone resorption, and a highly effective drug in the treatment of metastatic bone disease. We first labeled incadronate disodium with {sup 99m}Tc, and examined its biodistribution and bone uptake after intravenous injection in rats to assess its potential for clinical use as a bone-seeking agent for judgment of the therapeutic effect of incadronate on bone metastases. Bone scan with {sup 99m}Tc-labeled incadronate ({sup 99m}Tc-incadronate) may yield important information prior to the use of incadronate for treatment of bone metastases. Synthesis of {sup 99m}Tc-incadronate was carried out by reduction of {sup 99m}Tc-pertechnetate in the presence of SnCl{sub 2} and N{sub 2} gas. Normal rats were injected with 18.5 MBq (0.5 mCi) {sup 99m}Tc-incadronate in a volume of 0.1 ml intravenously and then sacrificed at 15 min, 30 min, 1 h or 2 h (six rats at each time point) after injection. Samples of muscle, stomach, small intestine, kidney, liver and bone (femur) were taken and weighed. In addition, a 1-ml sample of blood was drawn from the heart, and urine was taken from the urinary bladder immediately after sacrifice. Samples were measured for radioactivity and expressed as percent uptake of injected dose per gram or per milliliter (% ID/g or ml). Bone-to-blood and bone-to-muscle uptake ratios were determined from the % ID/g or ml values for these organs. The greatest accumulation of {sup 99m}Tc-incadronate was found in bone. Radioactivity in bone was as high as 3.22{+-}0.68% ID/g at 2 hours after injection. Scintigraphic images of {sup 99m}Tc-incadronate in normal rats revealed highly selective skeletal uptake. {sup 99m}Tc-incadronate exhibited high uptake in bone, and relatively low uptake in soft tissue, suggesting that it may be useful as a bone-seeking agent for judgment of the therapeutic effect of incadronate on

  9. Conception, preparation and properties of functional carrier particles for pulmonary drug delivery.

    Science.gov (United States)

    Odziomek, Marcin; Sosnowski, Tomasz R; Gradoń, Leon

    2012-08-20

    The effectiveness of aerosol therapy is significantly reduced by the mucus layer covering the airways of the tracheobronchial tree. According to the present concept, drug particles are delivered to the lung together with the functional carrier particle that facilitates both the drug transport into the lungs and the penetration of deposited particles through the mucus. The approach of manufacturing multi-component powders with mucoactive compounds and anti-asthmatic medicines (DSCG) bound together in a single particle is additionally considered. Powders were produced with the spray-drying technique from aqueous precursor solutions containing pure low molecular weight dextran, pure mannitol and dextran/mannitol-N-acetyl cysteine (NAC) mixtures (4:1 and 1:1). NAC has been selected for this purpose as a compound, which is known to be mucolytic. Dextran and mannitol are potentially applicable in the field of inhalation drug delivery. They have been used as stabilizers of functional carrier particles. Powders were characterized for their yield and physicochemical properties including: morphology (SEM), moisture content and thermal properties (DSC). Aerosol performance was determined with NGI impactor after standardized aerosolization of the produced powders in a commercial DPI. Particle size distributions of dextran-NAC powders were characterized by high fine particle fraction (45-62%), which assures good particle deposition in the lower airways. The thermodynamic properties of the powders based on the temperature of the glass transition T(g) (50-63 °C) suggest the required stability during storage at moderate humidity. Preliminary examination of the required properties of these particles confirms their potential as functional carriers for pulmonary drug delivery. Copyright © 2012 Elsevier B.V. All rights reserved.

  10. Cyanide formation by the cyanide distillation of nitrate. Zen shian joryuji ni okeru shosan ion ga kanyosuru shian kagobutsu ion no seisei

    Energy Technology Data Exchange (ETDEWEB)

    Ogura, H. (The Chiba Prefectural Lab. of Water Pollution, Chiba (Japan))

    1994-06-10

    Cyanide ion is formed by reacting disodium ethylenediamine-tetra-acetate (EDTA) with a sample containing nitrous ion. Further, it is known that cyanide ions are also generated from the reaction between EDTA and the product of the reaction of oxide and the substance like hydroxyl ammonium chloride which is added to reduce the oxide contained in the sample. In the present researches, the possibility of the formation of cyanide ions from the nitric acid used popularly in the manufactory of plating and surface-treatment is examined. It is expected that if nitric ion takes a part in the formation of cyanide ion, the reaction reducing the nitric ion into nitrous ion would happen as the former step thereof. Therefore, the cyanide distillation of nitric ions co-existing with the reducing agent is carried out, and it is confirmed that cyanide ion is formed with the participation of EDTA. 14 refs., 1 fig., 7 tabs.

  11. IN SITU PREPARED TiO2 NANOPARTICLES CROSS-LINKED SULFONATED PVA MEMBRANES WITH HIGH PROTON CONDUCTIVITY FOR DMFC

    Directory of Open Access Journals (Sweden)

    Jignasa N. Solanki

    2016-07-01

    Full Text Available Organic/inorganic membranes based on sulfonated poly(vinyl alcohol (SPVA and in situ prepared TiO2 nanoparticles nanocomposite membranes with various compositions were prepared to use as proton exchange membranes in direct membrane fuel cells. Poly(vinyl alcohol (PVA was sulfonated and cross-linked separately by 4-formylbenzene-1,3-disulfonic acid disodium salt hydrate and glutaraldehyde. The ion exchange capacity and proton conductivity of the membranes increased with increasing amount of TiO2 nanoparticles. The composite membranes with 15 wt% TiO2 exhibited excellent proton conductivity of 0.0822 S cm-1, as well as remarkably low methanol permeability of 1.11×10-9 cm2 s-1. The thermal stability and durability were also superior and performance in methanol fuel cell was also reasonably good

  12. Influence of complexing agents on the preparation of bimetallic platinum-ruthenium catalysts supported on O-functionalized graphite cloths

    Energy Technology Data Exchange (ETDEWEB)

    Sieben, J.M., E-mail: jmsieben@uns.edu.a [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Universidad Nacional del Sur., Av. Alem 1253, (B8000CPB) Bahia Blanca (Argentina); Duarte, M.M.E.; Mayer, C.E. [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Universidad Nacional del Sur., Av. Alem 1253, (B8000CPB) Bahia Blanca (Argentina)

    2010-02-18

    Electrodeposition of bimetallic Pt-Ru catalysts on O-functionalized graphite cloths from H{sub 2}PtCl{sub 6} and RuCl{sub 3} solutions containing trisodium citrate (Cit) and disodium dihydrogen ethylenediaminetetraacetate (Na{sub 2}H{sub 2}EDTA) was investigated. SEM analysis of the electrode prepared without complexant showed a relatively compact and rough deposit displaying a 'tree cortex' structure, whereas uniform size and globular shape particles regularly distributed over the support surface were obtained using citrate and Na{sub 2}H{sub 2}EDTA as complexants. In addition, XRD diffraction and EDX analysis revealed that the catalysts prepared using the complexants showed smaller size particles and lower Ru content. Electrocatalytic activity measurements indicated that the most active electrode for methanol oxidation was obtained with Na{sub 2}H{sub 2}EDTA as additive.

  13. 复合抑菌法在涮肉调料中的应用%Influence of composite bacteriostatic methods on meat condiment

    Institute of Scientific and Technical Information of China (English)

    高璇璇; 汪建明

    2012-01-01

    对4℃保存的涮肉调料检测初始菌数,本批次样品菌落总数为930000cfu/g,对样品进行复合抑菌剂实验.选择甘氨酸、脱氢醋酸钠、双乙酸钠、EDTA二钠、尼泊金酯钠进行单因素实验,剂量分别为各自国标上限的25%、50%、75%、100%,实验结果认为EDTA二钠与尼泊金酯钠的抑菌效果最好,最佳添加量均为国标上限50%.研究抑菌剂种类对贮藏时间影响的实验,影响效果依次为:EDTA二钠>尼泊金酯钠>甘氨酸>脱氢醋酸钠>双乙酸钠.对复合抑菌剂进行正交实验,最佳方案为尼泊金酯钠添加0.0063g,ED-TA二钠添加0.0028g,甘氨酸添加0.0500g,脱氢醋酸钠添加0.0125g.实验结果菌落总数为15000cfu/g.%The meat condiment which had been stored under 4t was detected, the total number of bacterial colony of the batch of samples was 930000cfu/g, We used the batch of samples to detect the experiment of composite preservatives. The single factor experiment was investigated by choosing glycine, dehydrogenation sodium acetate, double acetic acid sodium, EDTA disodium salt, and 4 - hydroxy - benzoic acid ester sodium. The dose of these preservatives added 25% , 50% , 75% , and 100% of their national standard. The results showed EDTA disodium salt and 4 - hydroxy - benzoic acid ester sodium had the optimum conditions, their most optimal adding quantities were both 50% of their national standard. The result suggested influence of these preservatives on storage time which was as follows: EDTA disodium salt > 4 - hydroxy - benzoic acid ester sodium > glycine > dehydrogenation sodium acetate > double acetic acid sodium. The Orthogonal experimental design was conducted for composite preservatives, the optimum conditions was the specific data were 4 - hydroxy - benzoic acid ester sodium added 0. 0063g, EDTA disodium salt added 0. 0028g, glycine added 0. 0500 g, dehydrogenation sodium acetate added 0. 0125g. The total number of bacterial colony of

  14. Preparation and properties of a cerium-containing hydroxyapatite coating on commercially pure titanium by micro-arc oxidation

    Institute of Scientific and Technical Information of China (English)

    HUANG Yong; WANG Yingjun; NING Chengyun; NAN Kaihui; HAN Yong

    2008-01-01

    A porous cerium-containing hydroxyapatite coating on commercially pure titanium was prepared by micro-arc oxidation (MAO) in an electrolytic solution containing calcium acetate, β-glycerol phosphate disodium salt pentahydrate (β-GP), and cerium nitrate. The thickness, phase, composition morphology, and biocompatibility of the oxide coating were characterized by X-ray diffraction (XRD), electron probe microanalysis (EPMA), scanning electron microscopy (SEM) with energy dispersive X-ray spectrometer (EDS), and cell culture. The thickness of the MAO film is about 15-25μm, and the coating is porous and uneven, without any apparent interface to the titanium substrates. The results of XRD and EDS show that the porous coating is made up of hydroxyapatite (HA) film containing Ce. The favorable osteoblast cell affinity makes the Ce-HA film have a good biocompatibility. The Ce-HA film is expected to have significant medical applications as dental implants and artificial bone joints.

  15. Interference of Lithium in Measuring Magnesium by Complexometry: Discussions of the Mechanism

    Directory of Open Access Journals (Sweden)

    Jie Gao

    2013-01-01

    Full Text Available There is usually a large concentration of magnesium in the brine of salt lakes and as a consequence it is difficult to measure Mg2+ accurately with the complexometric titration by ethylenediaminetetraacetic acid disodium salt (EDTA because of the large levels of Li+ also coexisting in brine samples. In this study, a relationship between the relative error related to the number of drops of the indicator and the NMR spectra of anhydrous ethanol and n-butanol, with or without LiCl, was analyzed and compared. It was then possible to suggest a mechanism to explain the interference of Li+ when measuring Mg2+ and to control the interference in the alcohol mixture because Li+ can then complex with the alcohols and mainly form a complex with n-butanol.

  16. A spot test for detection of cobalt release – early experience and findings

    DEFF Research Database (Denmark)

    Thyssen, Jacob P.; Menné, Torkil; Johansen, Jeanne D.

    2010-01-01

    Background: It is often difficult to establish clinical relevance of metal exposure in cobalt-allergic patients. Dermatologists and patients may incorrectly assume that many metallic items release cobalt at levels that may cause cobalt dermatitis. Cobalt-allergic patients may be unaware...... that they are exposed to cobalt from handling work items, causing hand dermatitis. Objectives: To present early findings with a newly developed cobalt spot test. Methods and Results: A cobalt spot test based on disodium-1-nitroso-2-naphthol-3,6-disulfonate was able to identify cobalt release at 8.3 ppm. The test may...... also be used as a gel test if combined with an agar preparation. We found no false-positive reactions when testing metals and alloys known not to contain cobalt. However, one cobalt-containing alloy, which elicited cobalt dermatitis in cobalt-allergic patients, was negative upon cobalt gel testing...

  17. Study of the Agglomeration of 5 to 25nm Gold Nanoparticles as a Function of Viscosity and Ionic Concentration

    Science.gov (United States)

    Stefankiewicz, Adam; Dobbins, Tabbetha

    2013-03-01

    Gold nanoparticles (AuNPs) attached to carcinoma cells and treated with light irradiation are able to convert the light into heat energy, thus killing those cells. In order to get the particles to the affected area, they may be entered into the circulatory system where the environment is highly viscous and comprised of high salt concentrations. This study examines the aggregation behavior of gold nanoparticles under those conditions. Surface charge creates coulombic repulsion between particles. Likewise, highly viscous solutions will prevent aggregation by limiting the rate of transport of gold through the solution. This study examines the aggregation behavior of gold nanopartilces as a function of viscosity (varied using polyethylene glycol). The study also examines the role of excess ions in the solution (varied using 5-Bromo-4-chloro-3-indolyl phosphate disodium salt). The aggregation phenomena was explored using dynamic light scattering for particle size analysis. Early results are presented here.

  18. An epifluorescence microscopy method for direct detection and enumeration of the fungilike marine protists, the thraustochytrids

    Digital Repository Service at National Institute of Oceanography (India)

    Raghukumar, S.; Schaumann, K.

    (Gaertner 19 6 8) and a liquid medium of the following composition at pH 6.5-7.3: glucose, 1.0 g; peptone, 1.0 g; yeast extract, 2.0 g; disodium hydrogen phosphate, Notes 183 0.125 g; ferric chloride, 0.002 g; seawater, 1,000 ml. Cells were harvested....4 x 10” 0.1 x 106 1.7x 108 0.6x lo5 5.0~ lo9 0.9 x 106 1.8 x lOlo Acriflavine (3,6-diamino- 1 O-methyl acri- dinium chloride mixed with 3,6-acridine di- amine) is a cationic acridine dye (Windholz 1983) and has been used as a fluorescent stain...

  19. Polymer Electrolyte Membrane Fuel Cell Performance of a Sulfonated Poly(Arylene Ether Benzimidazole Copolymer Membrane

    Directory of Open Access Journals (Sweden)

    Hasan Ferdi Gerçel

    2016-01-01

    Full Text Available Disodium-3,3′-disulfonate-4,4′-dichlorodiphenylsulfone (SDCDPS and 5,5′-bis[2-(4-hydroxyphenylbenzimidazole] (HPBI monomers were synthesized. Binding these monomers via nucleophilic aromatic polycondensation reaction, a sulfonated poly(arylene ether benzimidazole copolymer was synthesized. Structures of monomers and copolymer were confirmed by proton nuclear magnetic resonance spectroscopy (1H NMR and Fourier transform infrared (FTIR spectroscopy analyses. Proton exchange membrane was prepared by dissolving copolymer in dimethylacetamide (DMAc and casting onto a glass plate. Copolymer membrane was doped with sulfuric acid to ensure proton exchange character. Single cell performance of the copolymer membrane was tested in a polymer electrolyte membrane fuel cell test station. The highest power density of the membrane was measured as 23.7 mW cm−2 at 80°C. Thermogravimetric analysis (TGA showed that as the degree of disulfonation is increased thermal stability of the copolymer is increased.

  20. [(n-C4H9)3SnO2C(CH2)2CO2Sn(C4H9-n)3]:A Novel Three-dimensional Framework Structure of Organotin Complex

    Institute of Scientific and Technical Information of China (English)

    尹汉东; 王传华; 马春林; 王勇; 房海霞

    2003-01-01

    The bis(tributyltin) ester of succinic acid was synthesized by the reaction of disodium salt of succinic acid with tributyltin chloride in a molar ratio of 1:2. The crystal structure was determined by X-ray single-crystal diffraction. It belongs to orthorhombic with space group Pccn, a = 20.949(3), b = 17.470(3), c = 20.345(3)(A。), V = 7446(2) (A。)3, Z = 8, Dc = 1.242 g/cm3, β = 1.365 mm-1, F(000) = 2864, R = 0.0544 and wR = 0.1417. The tin atom is of five-coordination in a trigonal bipyramidal structure by bridging two carboxylate groups in different directions and the resulting structure which contains straight twist large ring channels along the axes of a, b and c is a three-dimensional framework polymer containing two different tin atoms.

  1. Familial calcific band-shaped keratopathy: report of two new cases with early recurrence.

    Science.gov (United States)

    Arora, Ritu; Shroff, Daraius; Kapoor, Seema; Nigam, Sonu; Narula, Ritesh; Chauhan, Deepender; Jain, Priyanka

    2007-01-01

    We report two siblings with the rare entity of familial calcific band-shaped keratopathy (BSK). Detailed ophthalmic and systemic investigations failed to reveal any underlying causative pathology. Topical disodium ethylenediamine-tetraacetate (EDTA) was applied for 30 min to all four eyes. In addition the right eye of the younger sibling required a superficial keratectomy. An improvement in corneal clarity was seen in the immediate postoperative period in both siblings. Histopathology of the keratectomy specimen revealed linear extracellular sub-epithelial granular calcium deposits. However, an early recurrence was noted in all four eyes at four weeks postoperatively. We report the second instance in the English literature of this entity. Band-shaped keratopathy presenting without an obvious etiology merits a complete systemic and ophthalmic workup. Patients with familial idiopathic BSK could be cases with poor prognosis for treatment with EDTA due to an early recurrence of the disease.

  2. Familial calcific band-shaped keratopathy: Report of two new cases with early recurrence

    Directory of Open Access Journals (Sweden)

    Arora Ritu

    2007-01-01

    Full Text Available We report two siblings with the rare entity of familial calcific band-shaped keratopathy (BSK. Detailed ophthalmic and systemic investigations failed to reveal any underlying causative pathology. Topical disodium ethylenediamine-tetraacetate (EDTA was applied for 30 min to all four eyes. In addition the right eye of the younger sibling required a superficial keratectomy. An improvement in corneal clarity was seen in the immediate postoperative period in both siblings. Histopathology of the keratectomy specimen revealed linear extracellular sub-epithelial granular calcium deposits. However, an early recurrence was noted in all four eyes at four weeks postoperatively. We report the second instance in the English literature of this entity. Band-shaped keratopathy presenting without an obvious etiology merits a complete systemic and ophthalmic workup. Patients with familial idiopathic BSK could be cases with poor prognosis for treatment with EDTA due to an early recurrence of the disease.

  3. Acute effects of vascular modifying agents in solid tumors assessed by noninvasive laser Doppler flowmetry and near infrared spectroscopy

    DEFF Research Database (Denmark)

    Kragh, Michael; Quistorff, Bjørn; Horsman, Michael R;

    2002-01-01

    The potential of noninvasive laser Doppler flowmetry (LDF) and near infrared spectroscopy (NIRS) to detect acute effects of different vascular-modifying agents on perfusion and blood volume in tumors was evaluated. C3H mouse mammary carcinomas (approximately 200 mm(3)) in the rear foot of CDF1 mice...... were treated with flavone acetic acid (FAA, 150 mg/kg), 5,6-dimethylxanthenone-4-acetic acid (DMXAA, 20 mg/kg), combretastatin A-4 disodium phosphate (CA4DP, 250 mg/kg), hydralazine (HDZ, 5 mg/kg), or nicotinamide (NTA, 500 mg/kg). Tumor perfusion before and after treatment was evaluated by noninvasive...... LDF, using a 41 degrees C heated custom-built LDF probe with four integrated laser/receiver units, and tumor blood volume was estimated by NIRS, using light guide coupled reflectance measurements at 800+/-10 nm. FAA, DMXAA, CA4DP, and HDZ significantly decreased tumor perfusion by 50%, 47%, 73...

  4. Simple automated preparation of O-[{sup 11}C]methyl-L-tyrosine for routine clinical use

    Energy Technology Data Exchange (ETDEWEB)

    Ishikawa, Yoichi [CYRIC Tohoku University, Aramaki, Aoba-ku, Sendai 980-8578 (Japan); Iwata, Ren [CYRIC Tohoku University, Aramaki, Aoba-ku, Sendai 980-8578 (Japan)]. E-mail: rencyric@cyric.tohoku.ac.jp; Furumoto, Shozo [TUBERO, Tohoku University, Sendai 980-8575 (Japan); Pascali, Claudio [National Cancer Institute, 20133 Milan (Italy); Bogni, Anna [National Cancer Institute, 20133 Milan (Italy); Kubota, Kazuo [International Medical Center, Tokyo 162-8655 (Japan); Ishiwata, Kiichi [Tokyo Metropolitan Institute of Gerontology, Tokyo 173-0022 (Japan)

    2005-07-01

    The previously reported preparation of O-[{sup 11}C]methyl-L-tyrosine ([{sup 11}C]MT), a promising tumor imaging agent, has been now considerably simplified and automated. Main changes were the use of [{sup 11}C]methyl iodide ([{sup 11}C]MeI) in the reaction with L-tyrosine disodium and the use of solid phase extraction on commercially available cartridges instead of HPLC for the final purification. An injectable saline solution of [{sup 11}C]MT was obtained within 30 min after EOB with radiochemical yield of ca. 60% (decay-corrected, based on [{sup 11}C]MeI). Radiochemical purity was over 97%. The automated preparation was carried out using a miniature module employing manifold valves.

  5. Effects of different fixatives on the TrkB-immunoreactivity in rat brain

    Institute of Scientific and Technical Information of China (English)

    张富兴; 黎振航; 李金莲; 岑国欣; 陈应城

    2003-01-01

    Objective: To find out an effective fixative in immunohistochemistry for high-affinity neurotrophin receptor-tyrosine kinase (Trk) B. Methods: Comparing the results from four groups of adult rats which were fixed by different fixatives before the brain sections were processed for TrkB immunohistochemistry. Results: In the four groups, TrkB immunoreactive cells were observed throughout the whole brain, but the intensity of immunoreactive cells and the background staining exhibited a marked difference among the groups. Conclusion: Using 0.3%-0.5% paraformaldehyde in 75% saturated picric acid 0.1 mol/L di-sodium hydrogen phosphate buffer as the fixative may yield the best quality of TrkB immunoreactivity.

  6. Validated Reverse Phase HPLC Method for the Determination of Impurities in Etoricoxib

    Directory of Open Access Journals (Sweden)

    S. Venugopal

    2011-01-01

    Full Text Available This paper describes the development of reverse phase HPLC method for etoricoxib in the presence of impurities and degradation products generated from the forced degradation studies. The drug substance was subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. The degradation of etoricoxib was observed under base and oxidation environment. The drug was found stable in other stress conditions studied. Successful separation of the drug from the process related impurities and degradation products were achieved on zorbax SB CN (250 x 4.6 mm 5 μm particle size column using reverse phase HPLC method. The isocratic method employed with a mixture of buffer and acetonitrile in a ratio of 60:40 respectively. Disodium hydrogen orthophosphate (0.02 M is used as buffer and pH adjusted to 7.20 with 1 N sodium hydroxide solution. The HPLC method was developed and validated with respect to linearity, accuracy, precision, specificity and ruggedness.

  7. Effect of Sodium Carboxymethyl Celluloses on Water-catalyzed Self-degradation of 200-degree C-heated Alkali-Activated Cement

    Energy Technology Data Exchange (ETDEWEB)

    Sugama T.; Pyatina, T.

    2012-05-01

    We investigated the usefulness of sodium carboxymethyl celluloses (CMC) in promoting self-degradation of 200°C-heated sodium silicate-activated slag/Class C fly ash cementitious material after contact with water. CMC emitted two major volatile compounds, CO2 and acetic acid, creating a porous structure in cement. CMC also reacted with NaOH from sodium silicate to form three water-insensitive solid reaction products, disodium glycolate salt, sodium glucosidic salt, and sodium bicarbonate. Other water-sensitive solid reaction products, such as sodium polysilicate and sodium carbonate, were derived from hydrolysates of sodium silicate. Dissolution of these products upon contact with water generated heat that promoted cement’s self-degradation. Thus, CMC of high molecular weight rendered two important features to the water-catalyzed self-degradation of heated cement: One was the high heat energy generated in exothermic reactions in cement; the other was the introduction of extensive porosity into cement.

  8. NEAR INFRARED ELECTROCHROMIC VARIABLE OPTICAL ATTENUATOR FABRICATED BY LAYER-BY-LAYER ASSEMBLY*

    Institute of Scientific and Technical Information of China (English)

    Jia Zheng; Yi-jun Zheng; Xin-hua Wan

    2011-01-01

    An electrochromic variable optical attenuator (ECVOA) was fabricated by layer-by-layer (LBL) assembly of disodium N,N-bis(p-sulfonatophenyl)naphthalenedicarboximide (Naph-SO3Na) and common cationic polymer poly(diallyldimethylammonium) chloride (PDDA). The UV-Vis absorption spectra of the multilayer films revealed that approximately an equal amount of Naph-SO3Na was assembled in each deposition cycle. Upon one-electron reduction, multilayer films exhibited intense absorption around 452 nm and also a broad absorption band from 1200 nm to 1900 nm. Owing to the improved ionic conductivity, the optical attenuation at 1550 nm of the films showed rapid response time and reached 1.3 dB/μm within 5 s. These results indicate that layer-by-layer assembly could be an effective method for the preparation of ECVOA operating in near infrared region.

  9. Genotoxic potency of mercuric chloride in gill cells of marine gastropod Planaxis sulcatus using comet assay

    Digital Repository Service at National Institute of Oceanography (India)

    Bhagat, J.; Ingole, B.S.

    as controls. Cell harvesting The shells of the snails were gently broken and the gills were excised out carefully. Gills were chopped into small pieces in 1 ml of cold extrusion buffer (71.2 mM NaCl, 5 mM EGTA, 50.4 mM guaiacol glycerol ether, pH 7... (2.5 M NaCl, 0.1 M di-sodium EDTA, 0.01 M Tris Buffer, 0.2 M NaOH, pH 10.0) at 4ºC in dark for 1 h. Alkaline DNA unwinding was carried out in a gel electrophoresis chamber containing a freshly prepared ice-cold electrophoretic buffer (300 mM NaOH, 1...

  10. Photodynamic inactivation of prions by disulfonated hydroxyaluminium phthalocyanine.

    Science.gov (United States)

    Janouskova, Olga; Rakusan, Jan; Karaskova, Marie; Holada, Karel

    2012-11-01

    Sulfonated phthalocyanines (Pcs) are cyclic tetrapyrroles that constitute a group of photosensitizers. In the presence of visible light and diatomic oxygen, Pcs produce singlet oxygen and other reactive oxygen species that have known degradation effects on lipids, proteins and/or nucleic acids. Pcs have been used successfully in the treatment of bacterial, yeast and fungal infections, but their use in the photodynamic inactivation of prions has never been reported. Here, we evaluated the photodynamic activity of the disodium salt of disulfonated hydroxyaluminium phthalocyanine (PcDS) against mouse-adapted scrapie RML prions in vitro. PcDS treatment of RML brain homogenate resulted in a time- and dose-dependent inactivation of prions. The photodynamic potential of Pcs offers a new way to inactivate prions using biodegradable compounds at room temperature and normal pressure, which could be useful for treating thermolabile materials and liquids.

  11. Oxidative flavour deterioration of fish oil enriched milk

    DEFF Research Database (Denmark)

    Bruni Let, Mette; Jacobsen, Charlotte; Frankel, E.N.

    2003-01-01

    The oxidative deterioration of milk emulsions supplemented with 1.5 wt-% fish oil was investigated by sensory evaluation and by determining the peroxide value and volatile oxidation products after cold storage. Two types of milk emulsions were produced, one with a highly unsaturated tuna oil (38 wt......-% of n-3 fatty acids) and one with cod liver oil (26 wt-% of n-3 fatty acids). The effect of added calcium disodium ethylenediaminetetraacetate (EDTA) on oxidation was also investigated. Emulsions based on cod liver oil with a slightly elevated peroxide value (1.5 meq/kg) oxidised significantly faster...... than the tuna oil emulsions, having a lower initial peroxide value (0.1 meq/kg). In the tuna oil emulsions the fishy off-flavour could not be detected throughout the storage period. Addition of 5-50 ppm EDTA significantly reduced the development of volatile oxidation products in the cod liver oil...

  12. Optical principle of pH measurement for detection of auxin flow through cellular membrane

    Science.gov (United States)

    Podrazky, Ondrej; Mrazek, Jan; Seidl, Miroslav; Kasik, Ivan; Tobiska, Petr; Matejec, Vlastimil; Martan, Tomas; Aubrecht, Jan

    2007-05-01

    The paper shows an approach to the determination of pH changes of solutions with a fine spatial resolution by means of fiber-optic tapers and fluorescence detection. This approach can be adopted for the determination of auxin flow through celluar membranes. Spectral absorption and fluorescence of pH transducers, namely of fluorescein, carboxyfluorescein, 6,8-dihydroxy-1,3-pyrenedisulfonic acid disodium salt and 2',7'-bis(2-carbonylethyl)-5(6)-carboxyfluorescein, were tested. The approach, based on the determination of a shift of the maxima of their fluorescence peaks, was employed for processing the measured fluorescence data in bulk solutions. Suitable tapered fiber probes were prepared and in vitro demonstrated for pH monitoring in a pH range from 6 to 7.

  13. Reduction to benzidine is not necessary for the covalent binding of a benzidine azodye to rat liver DNA.

    Science.gov (United States)

    Kennelly, J C; Shaw, A; Martin, C N

    1984-09-28

    The DNA binding of 2 benzidine azodyes, Congo Red and Direct Blue 6, was compared in rat liver. Both dyes showed binding consequent upon metabolism to benzidine, and in each case hydrolysis of the liver DNA yielded N-(deoxyguanosin-8-yl)-N'-acetylbenzidine. The majority of Direct Blue 6-derived radioactivity bound to DNA was present as at least one other novel species. Our preliminary work on the major Direct Blue 6 DNA adduct suggests its structure may be disodium 8-amino-2-[4-(N-deoxyguanosin-8-yl)-aminobiphenyl-4'-yl] azo-1-hydroxynaphthalene-3,6-disulphonate. This adduct may form as a result of the susceptibility of the dye to hepatic azoreductase and its apparent existence may explain the observed potent carcinogenicity of dyes such as Direct Blue 6.

  14. Stability and Determination of Metamizole Sodium by Capillary Electrophoresis Analysis Combined with Infra-red Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    XIANG Qian; NIU Gang; WU Xian-hua; CHEN Gang

    2007-01-01

    Metamizole sodium was chosen as a representative of unstable analytes for investigation by discusing the effects of oxygen and solvent on its degradation reaction using the capillary electrophoresis technique. A possible degradation mechanism was deduced from the observed behavior and was confirmed by infra-red spectroscopic study. The degradation reaction could be inhibited obviously by methanol instead of water as the solvent of analyte. Under the optimized conditions: separation voltage of 20 kV, and 5 mmol/L disodium hydrogen phosphate and 5 mmol/L borax with 10% methanol(pH 9. 12) as the running buffer, the standard curve of metamizole sodium was linear in a range of 3.77-74.07 mg/L. A satisfactory result was achieved when the technique was used to detect metamizole sodium in tablet.

  15. Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia

    Science.gov (United States)

    Tuschl, Karin; Meyer, Esther; Valdivia, Leonardo E.; Zhao, Ningning; Dadswell, Chris; Abdul-Sada, Alaa; Hung, Christina Y.; Simpson, Michael A.; Chong, W. K.; Jacques, Thomas S.; Woltjer, Randy L.; Eaton, Simon; Gregory, Allison; Sanford, Lynn; Kara, Eleanna; Houlden, Henry; Cuno, Stephan M.; Prokisch, Holger; Valletta, Lorella; Tiranti, Valeria; Younis, Rasha; Maher, Eamonn R.; Spencer, John; Straatman-Iwanowska, Ania; Gissen, Paul; Selim, Laila A. M.; Pintos-Morell, Guillem; Coroleu-Lletget, Wifredo; Mohammad, Shekeeb S.; Yoganathan, Sangeetha; Dale, Russell C.; Thomas, Maya; Rihel, Jason; Bodamer, Olaf A.; Enns, Caroline A.; Hayflick, Susan J.; Clayton, Peter T.; Mills, Philippa B.; Kurian, Manju A.; Wilson, Stephen W.

    2016-01-01

    Although manganese is an essential trace metal, little is known about its transport and homeostatic regulation. Here we have identified a cohort of patients with a novel autosomal recessive manganese transporter defect caused by mutations in SLC39A14. Excessive accumulation of manganese in these patients results in rapidly progressive childhood-onset parkinsonism–dystonia with distinctive brain magnetic resonance imaging appearances and neurodegenerative features on post-mortem examination. We show that mutations in SLC39A14 impair manganese transport in vitro and lead to manganese dyshomeostasis and altered locomotor activity in zebrafish with CRISPR-induced slc39a14 null mutations. Chelation with disodium calcium edetate lowers blood manganese levels in patients and can lead to striking clinical improvement. Our results demonstrate that SLC39A14 functions as a pivotal manganese transporter in vertebrates. PMID:27231142

  16. Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.

    Science.gov (United States)

    Tuschl, Karin; Meyer, Esther; Valdivia, Leonardo E; Zhao, Ningning; Dadswell, Chris; Abdul-Sada, Alaa; Hung, Christina Y; Simpson, Michael A; Chong, W K; Jacques, Thomas S; Woltjer, Randy L; Eaton, Simon; Gregory, Allison; Sanford, Lynn; Kara, Eleanna; Houlden, Henry; Cuno, Stephan M; Prokisch, Holger; Valletta, Lorella; Tiranti, Valeria; Younis, Rasha; Maher, Eamonn R; Spencer, John; Straatman-Iwanowska, Ania; Gissen, Paul; Selim, Laila A M; Pintos-Morell, Guillem; Coroleu-Lletget, Wifredo; Mohammad, Shekeeb S; Yoganathan, Sangeetha; Dale, Russell C; Thomas, Maya; Rihel, Jason; Bodamer, Olaf A; Enns, Caroline A; Hayflick, Susan J; Clayton, Peter T; Mills, Philippa B; Kurian, Manju A; Wilson, Stephen W

    2016-05-27

    Although manganese is an essential trace metal, little is known about its transport and homeostatic regulation. Here we have identified a cohort of patients with a novel autosomal recessive manganese transporter defect caused by mutations in SLC39A14. Excessive accumulation of manganese in these patients results in rapidly progressive childhood-onset parkinsonism-dystonia with distinctive brain magnetic resonance imaging appearances and neurodegenerative features on post-mortem examination. We show that mutations in SLC39A14 impair manganese transport in vitro and lead to manganese dyshomeostasis and altered locomotor activity in zebrafish with CRISPR-induced slc39a14 null mutations. Chelation with disodium calcium edetate lowers blood manganese levels in patients and can lead to striking clinical improvement. Our results demonstrate that SLC39A14 functions as a pivotal manganese transporter in vertebrates.

  17. Studies on the adsorption of sulfo-group-containing aromatics by chitosan-β-cyclodextrin.

    Science.gov (United States)

    Shi, Wenjian; Chen, Shuwei; Chang, Fei; Han, Yue; Zhang, Yuanzhang

    2012-01-01

    Chitosan-β-cyclodextrin (CTS-CD) prepared through a crosslinking reaction between chitosan and β-cyclodextrin was employed to adsorb the three following sulfo-group-containing aromatics: disodium 2-naphthol-3,6-disulfonate (R salt), 2-naphthalene sulfonic acid (NSA), and sodium dodecylbenzene sulfonate (SDBS). At 318 K, the saturated adsorption capacity of CTS-CD for R salt, NSA, and SDBS was 431, 416, and 376 mg/g, respectively. The experimental data fitted the second-order model well and the rate constant of the adsorption increased with the temperature increment. The values of apparent activation energy for R salt, NSA, and SDBS were calculated as 33.2, 34.2, and 16.8 kJ/mol respectively. The isothermal adsorption was found following the Langmuir adsorption equation. The negative values of ΔG and the positive values of ΔH indicated that the adsorption process was spontaneous and exothermic.

  18. Stability of O/W Emulsion with Synthetic Perfumes Oxidized by Singlet Oxygen

    Directory of Open Access Journals (Sweden)

    Naoki Watabe

    2013-01-01

    Full Text Available We prepared O/W emulsion composed of a synthetic perfume, n-dodecane, protoporphyrin IX disodium salt (PpIX-2Na, sodium dodecyl sulfate, and water and investigated oxidative decomposition of the synthetic perfume in the emulsion and change in the stability of the emulsion by singlet oxygen (1O2 generated by photosensitization of PpIX-2Na. We used eugenol, linalool, benzyl acetate, α-ionone, α-hexylcinnamaldehyde, and d-limonene as a synthetic perfume. The stability of the O/W emulation including eugenol and linalool significantly decreased with increasing light irradiation time. The decrease in the emulsion stability may be attributable to oxidative decomposition of eugenol and linalool by 1O2 and enlargement of the oil droplet size.

  19. Mechanistic insight into benzenethiol catalyzed amide bond formations from thioesters and primary amines

    DEFF Research Database (Denmark)

    Stuhr-Hansen, Nicolai; Bork, Nicolai; Strømgaard, Kristian

    2014-01-01

    The influence of arylthiols on cysteine-free ligation, i.e. the reaction between an alkyl thioester and a primary amine forming an amide bond, was studied in a polar aprotic solvent. We reacted the ethylthioester of hippuric acid with cyclohexylamine in the absence or presence of various quantities...... of thiophenol (PhSH) in a slurry of disodium hydrogen phosphate in dry DMF. Quantitative conversions into the resulting amide were observed within a few hours in the presence of equimolar amounts of thiophenol. Ab initio calculations showed that the reaction mechanism in DMF is similar to the well-known aqueous...... in the aromatic thioester amidation reaction. Under similar conditions, cysteine-free ligation was achieved by coupling a fully side-chain protected 15 amino acid phosphopeptide thioester to the free N-terminal of a side-chain protected 9 amino acid peptide producing the corresponding 24 amino acid phosphopeptide....

  20. The dehydrated copper silicate Na2[Cu2Si4O11]: a three-dimensional microporous framework with a linear Si—O—Si linkage

    Directory of Open Access Journals (Sweden)

    Filipe A. Almeida Paz

    2008-02-01

    Full Text Available The structure of the title dehydrated copper silicate, disodium dicopper undecaoxide tetrasilicate, Na2(Cu2O11Si4, was determined by single-crystal X-ray diffraction from a non-merohedral twin. It exhibits an effective three-dimensional microporous framework with the major channels, in which the Na+ cations are placed, running along the a-axis direction and smaller channels observed along the b-axis direction. The structure is unusual in that it contains a symmetry-constrained Si—O—Si angle of 180°. The Cu centre is coordinated to five O atoms, exhibiting a slightly distorted square-pyramidal coordination geometry. The Na cation is interacting with five neighbouring O atoms, exhibiting an uncharacteristic coordination environment.