Eliminating pharmaceutical impurities: Recent advances in detection techniques.

David Q Liu, Mingjiang Sun, Lianming Wu
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引用次数: 0

Abstract

The elimination of organic impurities to produce highly pure drug substances is an important goal of process chemistry. For the detection of general impurities, hyphenated techniques (eg, liquid chromatography-mass spectrometry [LC-MS]) play a critical role in rapid structural identification (qualitative detection) and in understanding the mechanisms of formation of the impurities, enabling informed decisions to control and eliminate the impurities resulting from the chemical process where possible. Concern regarding genotoxic impurities (GTIs), which must typically be controlled at low parts-per-million limits, continues to increase, and significant advances have been achieved in recent years for the selective and sensitive quantitation (quantitative detection) of such impurities. Conventional detection techniques, such as ultraviolet (UV) detection, are often inadequate for the detection of potentially minute quantities of GTIs; therefore, various advanced MS-based detection strategies, either stand-alone or in conjunction with chemical approaches, are playing an increasing role in this field. The primary aim of this review is to highlight recent advances in qualitative and quantitative detection of impurities at trace levels, with a particular focus on GTIs.

消除药物杂质:检测技术的最新进展。
消除有机杂质以生产高纯度原料药是过程化学的一个重要目标。对于一般杂质的检测,联用技术(例如,液相色谱-质谱[LC-MS])在快速结构鉴定(定性检测)和理解杂质形成机制方面发挥着关键作用,使明智的决定能够控制和消除化学过程中产生的杂质。对基因毒性杂质(GTIs)的关注持续增加,这种杂质通常必须控制在百万分之低的限度内,近年来在这种杂质的选择性和敏感定量(定量检测)方面取得了重大进展。常规检测技术,如紫外线检测,往往不足以检测潜在微量的gti;因此,各种先进的基于质谱的检测策略,无论是单独的还是与化学方法相结合,都在这一领域发挥着越来越大的作用。本综述的主要目的是强调在痕量杂质的定性和定量检测方面的最新进展,特别关注gti。
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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