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A Review about Regulatory Status and Recent Patents of Pharmaceutical Co-Crystals

机译:药物共晶体的监管现状和最新专利综述

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摘要

Pharmaceutical Co-crystals are not new, they have gained much attention since the last decade among scientists and pharmaceutical industry. Pharmaceutical co-crystals are multicomponent systems composed of two or more molecules and held together by non-covalent interactions. The development of pharmaceutical co-crystals, a new solid crystalline form, offer superior physico-chemical properties (such as melting point, stability, solubility, permeability, bioavailability, taste masking, etc.) without altering the pharmacological properties. Recently, with the upsurge in the growth of Pharmaceutical co-crystals, the major concern is over the regulatory status of co-crystals. With the new guidelines from United States Food and Drug Administration (USFDA) and European Medicines Agency (EMA), the status has become even more complicated due to significantly different opinions. This review highlights whether co-crystals fulfil the requirements for the grant of a patent or not and how cocrystals are going to affect the present scenario of pharmaceuticals.
机译:药用共晶体并不是什么新鲜事物,自最近十年以来,它们在科学家和制药行业中引起了广泛关注。药物共晶体是由两个或多个分子组成并通过非共价相互作用保持在一起的多组分系统。药物共晶体的开发是一种新的固体晶体形式,可提供优异的物理化学性质(例如熔点,稳定性,溶解性,渗透性,生物利用度,掩味等),而不会改变药理性质。近来,随着药物共晶体的增长高潮,主要关注的是共晶体的调节状态。有了美国食品药品监督管理局(USFDA)和欧洲药品管理局(EMA)的新指南,由于意见截然不同,状态变得更加复杂。这篇综述着重介绍了共晶是否满足授予专利的要求,以及共晶将如何影响药物的现状。

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