药物共晶:共晶设计策略

IF 0.2
Preeti Devi, Vikas Budhwar, Saloni Kakkar, Ashwani Kumar
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引用次数: 0

摘要

药用共晶属于一种成分为活性药物成分(API),另一成分为共成体(通常被认为是安全的GRAS)的晶体亚型。在晶格中,这两种组分以固定的化学计量比成氢键。共结晶是一种廉价、简单的提高溶解度的方法,近年来引起了配方师们的极大兴趣。由于共晶可以增强药物的理化性质而不影响其治疗效果,因此药物共晶领域已经达到了一个临界点。除了增加溶解度外,还发现了一些更多的共晶应用,如提高渗透性、生物利用度、稳定性、片剂能力等物理化学性质。文献对共晶进行了广泛的研究,关于共晶的文献也非常多。然而,必须对共晶选择和共晶调节进行详尽的审查。在审查中已作出努力来填补这一空白。本研究除了概述共晶发现的历史背景和里程碑外,重点关注共晶如何增强不同药物的药物特性。本文综述了国内外合成多组分共晶的合理设计和构象选择、氢键、PKa值、Synthonic工程、Cambridge结构数据库、Hansen溶解度参数(HSP)等方法以及知识产权的相关细节。有一个尝试包括报道的共晶体的工作,这有助于理解这个概念。这篇综述文章讨论了美国和欧洲的药品监管机构发布的指导方针,这些指导方针对这些地区的药品注册非常有用。在这里,我们也检查各种市售药品。并简要预测了共结晶的发展前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmaceutical Co-Crystallization: Strategies for Co-Crystal Design
Pharmaceutical co-crystal belongs to a subtype of crystal in which one component is an active pharmaceutical ingredient (API) and the other is coformer (generally regarded as safe GRAS). In the crystal lattice, the two components are hydrogen-bonded in a fixed stoichiometric ratio. Co-crystallization is a cheap and simple alternative to the presently available techniques of solubility enhancement and has gained much interest from the formulators during the recent few years. Because co-crystals can enhance the physiochemical properties of pharmaceuticals without affecting their therapeutic effect, the area of pharmaceutical co-crystals has reached a tipping point. Besides increasing solubility, some more applications of co-crystals have also been identified to enhance physicochemical properties like permeability, bioavailability, stability, tablet ability, etc. Co-crystals have been extensively studied in the literature, and there is a tremendous amount of literature on co-crystals. However, an exhaustive review of coformer selection and co-crystal regulation must be included. An effort has been made in the review to fill this void. The current study focuses on how co-crystallization can enhance the pharmaceutical characteristics of different drugs, besides giving an overview of the historical background and landmarks in discovering co-crystals. In this review paper, we have discussed the rational design of co-crystals and the selection of conformers for the synthesis of multi-component co-crystals, methods like H-bonding, PKa value, Synthonic engineering, Cambridge structural database, Hansen solubility parameter (HSP), etc as well as the IPR related details all across the world. There is an attempt to include reported works on co-crystals, which helps understand the concept. This review paper discusses pharmaceutical regulatory bodies in the US and Europe released guidelines that are highly useful for pharmaceutical product registration in these regions. Here, we also examine various commercially available pharmaceutical drug products. It also briefly predicts the future perspective of co-crystallization.
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525
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