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在抗酸剂存在的情况下格列齐特的体外可用性。

In vitro availability of gliclazide in presence of antacids.

作者信息

Arayne M Saeed, Sultana Najma, Zaman M Kamran

机构信息

Department of Chemistry, University of Karachi.

出版信息

Pak J Pharm Sci. 2003 Jan;16(1):35-49.

Abstract

Gliclazide is the most commonly used sulfonylurea derivative for NIDDM therapy. Due to its prolonged therapy, there is always a likelihood of its use with other drugs. On the other hand antacids are commonly prescribed to encounter gastric acidity etc. Present paper deals with the in vitro availability studies of gliclazide in presence of antacids. These studies were carried out in simulated gastric juice and in buffer of pH 7.4 at body and accelerated temperature. The antacids used in these studies were aluminum hydroxide, aluminum trisilicate, magnesium oxide, magnesium trisilicate, sodium bicarbonate, calcium carbonate, magaldrate and simethicone (2,4-dimethoxypoly-siloxane). It has been found that in case of magnesium oxide, magnesium trisilicate and sodium bicarbonate, availability of gliclazide was enhanced while in rest of the antacids retarded the availability of gliclazide.

摘要

格列齐特是治疗非胰岛素依赖型糖尿病最常用的磺脲类衍生物。由于其治疗周期长,它总是有可能与其他药物联合使用。另一方面,抗酸剂常用于缓解胃酸过多等症状。本文探讨了在抗酸剂存在的情况下格列齐特的体外溶出度研究。这些研究在模拟胃液以及体温和加速温度下pH值为7.4的缓冲液中进行。这些研究中使用的抗酸剂有氢氧化铝、三硅酸铝、氧化镁、三硅酸镁、碳酸氢钠、碳酸钙、铝镁加和西甲硅油(2,4-二甲氧基聚硅氧烷)。已发现,对于氧化镁、三硅酸镁和碳酸氢钠,格列齐特的溶出度提高,而在其他抗酸剂存在时,格列齐特的溶出度受到抑制。

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