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一种用于评估基于多糖的结肠特异性给药系统的新型溶出方法:动物牺牲的合适替代方法。

A novel dissolution method for evaluation of polysaccharide based colon specific delivery systems: A suitable alternative to animal sacrifice.

作者信息

Singh Sachin Kumar, Yadav Ankit Kumar, Prudhviraj G, Gulati Monica, Kaur Puneet, Vaidya Yogyata

机构信息

School of Pharmaceutical Sciences, Lovely Professional University, Phagwara 144411, Punjab, India.

School of Pharmaceutical Sciences, Lovely Professional University, Phagwara 144411, Punjab, India.

出版信息

Eur J Pharm Sci. 2015 Jun 20;73:72-80. doi: 10.1016/j.ejps.2015.03.012. Epub 2015 Mar 28.

DOI:10.1016/j.ejps.2015.03.012
PMID:25829049
Abstract

The most extensively used test for predicting in-vivo release kinetics of a drug from its orally administered dosage forms is dissolution testing. For polysaccharide based, colon targeted oral delivery systems, the entire path of the gut traversed by the dosage form needs to be simulated for assessing its in-vivo dissolution pattern. This includes the dissolution testing sequentially in simulated gastric fluid (SGF), simulated intestinal fluid (SIF) and simulated colonic fluid (SCF). For SGF and SIF, simple and standardized composition is well-known. However, preparation of SCF requires addition of either the colonic contents of rodents or human faecal slurry. A method is proposed, wherein a mixture of five probiotics cultured in the presence of a prebiotic under anaerobic conditions is able to surrogate the colonic fluid. Release profiles of drug from colon targeted delivery systems in this medium were studied and compared to those generated in the conventionally used media containing rodent caecal contents and human faecal slurry. The results from the three studies were found to be quite similar. These findings suggest that the proposed medium may prove to be useful not only as a biorelevant and discriminatory method but may also help in achieving the 3Rs objective regarding the ethical use of animals.

摘要

用于预测药物口服剂型体内释放动力学的最广泛使用的测试是溶出度测试。对于基于多糖的结肠靶向口服给药系统,需要模拟剂型在肠道中走过的整个路径,以评估其体内溶出模式。这包括依次在模拟胃液(SGF)、模拟肠液(SIF)和模拟结肠液(SCF)中进行溶出度测试。对于SGF和SIF,其简单且标准化的成分是众所周知的。然而,制备SCF需要添加啮齿动物的结肠内容物或人粪便悬液。本文提出了一种方法,即在益生元存在下于厌氧条件下培养的五种益生菌的混合物能够替代结肠液。研究了药物在该介质中从结肠靶向给药系统的释放曲线,并与在含有啮齿动物盲肠内容物和人粪便悬液的传统使用介质中产生的释放曲线进行了比较。发现这三项研究的结果非常相似。这些发现表明,所提出的介质不仅可能被证明是一种生物相关且具有区分性的方法,而且还可能有助于实现关于动物伦理使用的3R目标。

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