Cocrystal: A Review on the Design and Preparation of Pharmaceutical Cocrystals

Tanmay Jit, Dibyendu Shil, Ramesh Kumari Dasgupta, Sanglap Mallick, Saptarshi Mukherjee
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引用次数: 0

Abstract

The majority of the active pharmaceutical components have issues with poor solubility, bioavailability, chemical stability, and moisture absorption. Pharmaceutical crystals are a reliable way to change the aforementioned physicochemical properties of drugs without changing their pharmacological behaviour. However, the success of these approaches depends on the physical and chemical properties of the molecules being developed. The development of drug products with superior physicochemical characteristics, such as melting point, tablet ability, solubility, stability, bioavailability, and permeability, while preserving the pharmacological properties of the active pharmaceutical ingredient is greatly facilitated by co-crystallization of drug substances. All the components of a cocrystal, which is a stoichiometric homogeneous multicomponent system connected by non-covalent interactions, are solid under ambient conditions.
共晶体:药物共晶体的设计与制备综述
大多数活性药物成分都存在溶解度、生物利用度、化学稳定性和吸湿性差的问题。药用晶体是在不改变药物药理特性的前提下改变药物上述理化特性的可靠方法。然而,这些方法的成功与否取决于所开发分子的物理和化学特性。药物物质的共结晶大大促进了在保留活性药物成分药理特性的同时,开发具有熔点、片剂能力、溶解度、稳定性、生物利用度和渗透性等优异理化特性的药物产品。共晶体是一种通过非共价作用连接的化学计量同质多组分系统,其所有成分在环境条件下均为固态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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