化学
色谱法
亚硝胺
质谱法
串联质谱法
环境化学
有机化学
致癌物
作者
Mousumi Saha,Lingqi Qiu,Stefan Kraft,Daniel Lee,Andreas Kaerner,Christopher J. Welch,Yumin Dai,Hao Li,Scott A. Miller,R. Graham Cooks
标识
DOI:10.1021/acs.analchem.5c03641
摘要
The mutagenic potential of N-nitrosamines has heightened regulatory scrutiny and prompted numerous drug recalls due to their formation as impurities during pharmaceutical manufacturing. However, the simultaneous and rapid analysis of multiple N-nitrosamines remains challenging. In this study, we show a rapid (<1 min) and robust multiple reaction monitoring (MRM) approach for the trace-level quantitation of N-nitrosamines across a wide concentration range (10 ng/mg to 500 μg/mg) in diverse pharmaceutical matrices. Lithium cation (Li+) adduct formation during ionization is utilized to enable diagnostic fragmentation in tandem mass spectrometry (MS/MS), yielding a limit of detection of 5 ng/mg with high quantitative accuracy and precision. This method is also applied to trace analysis of N-nitrosated drug impurities within their parent pharmaceutical matrices. With minimal sample preparation, rapid analysis times, and broad applicability to complex pharmaceutical formulations, this MRM method offers a practical and powerful tool for the identification and quantitation of N-nitrosamines and its potential adoption in pharmaceutical quality control and industrial settings.
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