首页> 美国卫生研究院文献>Acta Pharmaceutica Sinica. B >Separation and simultaneous quantitation of PGF2α and its epimer 8-iso-PGF2α using modifier-assisted differential mobility spectrometry tandem mass spectrometry
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Separation and simultaneous quantitation of PGF2α and its epimer 8-iso-PGF2α using modifier-assisted differential mobility spectrometry tandem mass spectrometry

机译:修饰辅助差动淌度串联质谱法同时分离和定量测定PGF2α及其差向异构体8-iso-PGF2α

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摘要

Because many therapeutic agents are contaminated by epimeric impurities or form epimers as a result of metabolism, analytical tools capable of determining epimers are increasingly in demand. This article is a proof-of-principle report of a novel DMS–MS/MS method to separate and simultaneously quantify epimers, taking PGF2α and its 8-epimer, 8-iso-PGF2α, as an example. Good accuracy and precision were achieved in the range of 10–500 ng/mL with a run time of only 1.5 min. Isopropanol as organic modifier facilitated a good combination of sensitivity and separation. The method is the first example of the quantitation of epimers without chromatographic separation.
机译:由于许多新陈代谢的结果,许多治疗剂被表观异构体杂质污染或形成差向异构体,因此越来越需要能够确定差向异构体的分析工具。本文是一种新颖的DMS-MS / MS方法的原理验证报告,该方法可以分离并同时定量差向异构体,以PGF2α及其8-epimer,8-iso-PGF2α为例。在10–500μng / mL的范围内,仅1.5μmin的运行时间即可获得良好的准确性和精密度。异丙醇作为有机改性剂促进了灵敏度和分离的良好结合。该方法是无需色谱分离即可定量差向异构体的第一个实例。

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