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受MIST启发的新型质谱解决方案。

Novel MS solutions inspired by MIST.

作者信息

Ramanathan Ragu, Josephs Jonathan L, Jemal Mohammed, Arnold Mark, Humphreys W Griffith

机构信息

Department of Biotransformation, Pharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Princeton, NJ, 08540, USA.

出版信息

Bioanalysis. 2010 Jul;2(7):1291-313. doi: 10.4155/bio.10.83.

Abstract

To improve patient safety and to help avoid costly late-stage failures, the pharmaceutical industry, along with the US FDA and International Committee on Harmonization (ICH), recommends the identification of differences in drug metabolism between animals used in nonclinical safety assessments and humans as early as possible during the drug-development process. LC-MS is the technique of choice for detection and characterization of metabolites, however, the widely different LC-MS response observed for a new chemical entity (NCE) and its structurally related metabolites limits the direct use of LC-MS responses for quantitative determination of NCEs and metabolites. While no method provides completely accurate universal response, UV, corona charged aerosol detection (CAD), radioactivity, NMR and low-flow (< 20 µl/min) nanospray approaches provide opportunities to quantify metabolites in the absence of reference standards or radiolabeled material with enough precision to meet the needs of early clinical development.

摘要

为提高患者安全性并避免代价高昂的后期失败,制药行业与美国食品药品监督管理局(FDA)及国际协调会议(ICH)建议,在药物研发过程中尽早识别用于非临床安全性评估的动物与人类之间药物代谢的差异。液相色谱-质谱联用(LC-MS)是检测和表征代谢物的首选技术,然而,新化学实体(NCE)与其结构相关代谢物之间观察到的LC-MS响应差异很大,这限制了LC-MS响应在定量测定NCE和代谢物方面的直接应用。虽然没有一种方法能提供完全准确的通用响应,但紫外检测(UV)、电晕带电气溶胶检测(CAD)、放射性检测、核磁共振(NMR)以及低流量(<20 μl/min)纳喷方法,在没有参考标准品或放射性标记物质的情况下,提供了以足够精度定量代谢物的机会,以满足早期临床开发的需求。

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