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固体口服剂型中药物盐的稳定性。

Stability of pharmaceutical salts in solid oral dosage forms.

作者信息

Nie Haichen, Byrn Stephen R, Zhou Qi Tony

机构信息

a Formulation Sciences, Teva Pharmaceuticals , West Chester , PA , USA.

b Department of Industrial and Physical Pharmacy , Purdue University , West Lafayette , IN , USA.

出版信息

Drug Dev Ind Pharm. 2017 Aug;43(8):1215-1228. doi: 10.1080/03639045.2017.1304960. Epub 2017 Apr 18.

Abstract

Using pharmaceutical salts in solid dosage forms can raise stability concerns, especially salt dissociation which can adversely affect the product performance. Therefore, a thorough understanding of the salt instability encountered in solid-state formulations is imperative to ensure the product quality. The present article uses the fundamental theory of acid base, ionic equilibrium, relationship of pH and solubility as a starting point to illustrate and interpret the salt formation and salt disproportionation in pharmaceutical systems. The criteria of selecting the optimal salt form and the underlying theory of salt formation and disproportionation are reviewed in detail. Factors influencing salt stability in solid dosage forms are scrutinized and discussed with the case studies. In addition, both commonly used and innovative strategies for preventing salt dissociations in formulation, on storage and during manufacturing will be suggested herein. This article will provide formulation scientists and manufacturing engineers an insight into the mechanisms of salt disproportionation and salt formation, which can help them to avoid and solve the instability issues of pharmaceutical salts in the product design.

摘要

在固体剂型中使用药用盐可能会引发稳定性问题,尤其是盐解离,这可能会对产品性能产生不利影响。因此,深入了解固态制剂中遇到的盐不稳定性对于确保产品质量至关重要。本文以酸碱、离子平衡、pH与溶解度关系的基本理论为出发点,阐述并解释药物系统中的盐形成和盐歧化现象。详细综述了选择最佳盐形式的标准以及盐形成和歧化的基础理论。通过案例研究对影响固体剂型中盐稳定性的因素进行了仔细审查和讨论。此外,本文还将提出在制剂、储存和制造过程中防止盐解离的常用策略和创新策略。本文将为制剂科学家和制造工程师提供对盐歧化和盐形成机制的深入了解,这有助于他们在产品设计中避免和解决药用盐的不稳定性问题。

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