Suppr超能文献

司帕沙星与抗酸剂的相互作用——溶解与吸附研究

Interactions between sparfloxacin and antacids - dissolution and adsorption studies.

作者信息

Hussain Fida, Arayne M Saeed, Sultana Najma

机构信息

Department of Chemistry, University of Karachi, Karachi-75270, Pakistan.

出版信息

Pak J Pharm Sci. 2006 Jan;19(1):16-21.

Abstract

Sparfloxacin is a broad-spectrum oral fluoroquinolone antimicrobial agent with a long elimination half-life, extensively used against both Gram-positive as well as Gram-negative microorganism. Concurrent administration of antacids and sparfloxacin decreases the gastrointestinal absorption of sparfloxacin and therapeutic failure may result. The present study was designed to evaluate the influence of some antacids on the availability of sparfloxacin. The release of sparfloxacin from tablets in the presence of antacids like sodium bicarbonate, calcium hydroxide, calcium carbonate, aluminum hydroxide, magnesium hydroxide, magnesium carbonate, magnesium trisilicate and magaldrate has been studied on BP 2003 dissolution test apparatus. These studies were carried out in simulated gastric and intestinal juices for three hours at 37 degrees C. The results confirmed that the dissolution rate of tablets was markedly retarded in the presence all of antacids studied, whereas magaldrate and calcium carbonate exhibited relatively higher adsorption capacities in simulated gastric juice and magnesium trisilicate and calcium hydroxide in simulated intestinal juice.

摘要

司帕沙星是一种具有较长消除半衰期的广谱口服氟喹诺酮类抗菌剂,广泛用于对抗革兰氏阳性菌和革兰氏阴性菌。抗酸剂与司帕沙星同时服用会降低司帕沙星的胃肠道吸收,可能导致治疗失败。本研究旨在评估某些抗酸剂对司帕沙星有效性的影响。已在BP 2003溶出度试验装置上研究了在碳酸氢钠、氢氧化钙、碳酸钙、氢氧化铝、氢氧化镁、碳酸镁、三硅酸镁和铝镁加等抗酸剂存在下,司帕沙星从片剂中的释放情况。这些研究在模拟胃液和肠液中于37℃进行了3小时。结果证实,在所研究的所有抗酸剂存在下,片剂的溶出速率均明显减慢,而铝镁加和碳酸钙在模拟胃液中表现出相对较高的吸附能力,三硅酸镁和氢氧化钙在模拟肠液中表现出相对较高的吸附能力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验