确保产品稳定性-选择合适的赋形剂

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
Natalia Veronica , Paul Wan Sia Heng , Celine Valeria Liew
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引用次数: 3

摘要

药品的稳定性是一项重要的产品质量指标。在已知的影响稳定性的因素中,水分通常被认为是通过水解或以水分为介质促进的其他反应导致药物降解的最常见原因。赋形剂是配方中的一个关键实体,可以使药物传递以及有效制造药物剂型。然而,在这方面,对赋形剂在保护水分敏感药物中的作用的应用和理解是有限的。当为含有水分敏感药物的配方选择辅料时,对水分-赋形剂相互作用的更好理解是重要的。本文综述了赋形剂在口服固体剂型中作为保湿剂的作用。它侧重于赋形剂的水分相互作用,以突出某些赋形剂作为水分保护剂的潜力。更具体地说,我们讨论了赋形剂减少药物降解的机制(例如,作为物理屏障,降低水分可用性和流动性)。还提供了评价水分赋形剂相互作用的分析工具的总结。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ensuring Product Stability – Choosing the Right Excipients

The stability of pharmaceuticals is an important product quality attribute. Of the known factors affecting stability, moisture is often perceived as the most common cause of drug degradation by hydrolysis or other reactions facilitated by moisture as a medium. Excipients are a critical entity in formulations to enable drug delivery as well as efficient manufacture of pharmaceutical dosage forms. Yet to this end, there is limited application and understanding of the role of excipients in protecting moisture sensitive drugs. An improved understanding of moisture-excipient interactions is important when selecting excipients for formulations containing moisture sensitive drugs. This review outlines the role of excipients as a moisture protectant in oral solid dosage forms. It focuses on the moisture interactions of excipients in order to highlight the potential of certain excipients as moisture protectants. More specifically, the mechanisms by which excipients can reduce drug degradation (e.g. acting as a physical barrier, reducing moisture availability and mobility) are discussed. A summary of analytical tools to evaluate moisture-excipient interactions is also provided.

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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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