A review on drug stability

Ashutosh Kumar, Ashutosh Kumar Yadav, Abhishek Yadav, Manish Yadav, Md Akhlak, Shweta Mishra, Jitendra Kumar
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Abstract

Stability is crucial to the process of developing new drugs. Stability studies are regarded as a must for the acceptance and approval of any pharmaceutical product since they guarantee the stability of product quality, safety, and efficacy during the shelf life. This article will reduce the knowledge gap on the most important aspect for researcher or a developer who is developing a formulation by providing a complete information about drug stability, principle of drug degradation, Force degradation studies, Stability studies and their Classification, Factor Affecting Stability of Drug, Mechanism of Drug Degradation, Stability Testing, and Different ways to increase Drug Stability. As the different sources provided in this article which are mentioned above will resolve any problem regarding the stability of drug and by resolving the problem, it will influence a science oriented or research-oriented person to develop any formulation by providing the complete knowledge about this particulate topic.
药物稳定性研究进展
稳定性对开发新药至关重要。稳定性研究被认为是接受和批准任何药品的必要条件,因为它保证了产品在保质期内的质量稳定性、安全性和有效性。本文将通过提供有关药物稳定性、药物降解原理、力降解研究、稳定性研究及其分类、影响药物稳定性的因素、药物降解机制、稳定性测试以及提高药物稳定性的不同方法等方面的完整信息,减少研究人员或正在开发配方的开发人员在最重要方面的知识差距。由于本文中提到的不同来源将解决有关药物稳定性的任何问题,并且通过解决问题,它将影响以科学或研究型为导向的人通过提供有关该颗粒主题的完整知识来开发任何配方。
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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