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基于生物药剂学分类系统的难溶性药物制剂设计:基本方法与实际应用。

Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.

机构信息

Department of Pharmacokinetics and Pharmacodynamics and Global Center of Excellence (COE) Program, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.

出版信息

Int J Pharm. 2011 Nov 25;420(1):1-10. doi: 10.1016/j.ijpharm.2011.08.032. Epub 2011 Aug 30.

Abstract

The poor oral bioavailability arising from poor aqueous solubility should make drug research and development more difficult. Various approaches have been developed with a focus on enhancement of the solubility, dissolution rate, and oral bioavailability of poorly water-soluble drugs. To complete development works within a limited amount of time, the establishment of a suitable formulation strategy should be a key consideration for the pharmaceutical development of poorly water-soluble drugs. In this article, viable formulation options are reviewed on the basis of the biopharmaceutics classification system of drug substances. The article describes the basic approaches for poorly water-soluble drugs, such as crystal modification, micronization, amorphization, self-emulsification, cyclodextrin complexation, and pH modification. Literature-based examples of the formulation options for poorly water-soluble compounds and their practical application to marketed products are also provided. Classification of drug candidates based on their biopharmaceutical properties can provide an indication of the difficulty of drug development works. A better understanding of the physicochemical and biopharmaceutical properties of drug substances and the limitations of each delivery option should lead to efficient formulation development for poorly water-soluble drugs.

摘要

由于水溶解度差而导致的口服生物利用度低,这使得药物研发更加困难。目前已经开发出了各种方法,重点是提高水溶性差的药物的溶解度、溶解速率和口服生物利用度。为了在有限的时间内完成开发工作,对于水溶性差的药物的药物开发,建立合适的制剂策略应该是关键考虑因素。本文基于药物物质的生物药剂学分类系统,综述了可行的制剂选择。本文描述了改善水溶性差药物的基本方法,如晶体修饰、微粉化、无定形化、自乳化、环糊精包合和 pH 值改变。还提供了基于文献的水溶性差化合物的制剂选择实例及其在市售产品中的实际应用。基于候选药物的生物药剂学性质进行分类,可以提示药物研发工作的难度。更好地了解药物物质的物理化学和生物药剂学特性,以及每种传递方式的局限性,将有助于水溶性差药物的高效制剂开发。

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