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利用天然同量异位素跃迁扩展定量液相色谱-串联质谱中多重反应监测的线性动态范围。

Expanding the linear dynamic range for multiple reaction monitoring in quantitative liquid chromatography-tandem mass spectrometry utilizing natural isotopologue transitions.

机构信息

Senomyx Inc., 4767 Nexus Centre Drive, San Diego, CA 92121, United States.

出版信息

Talanta. 2011 Dec 15;87:307-10. doi: 10.1016/j.talanta.2011.09.063. Epub 2011 Oct 5.

DOI:10.1016/j.talanta.2011.09.063
PMID:22099684
Abstract

We describe a method for expanding the linear dynamic range for multiple reaction monitoring (MRM) in quantitative liquid chromatography/tandem mass spectrometry (LC-MS/MS) using additional transitions for isotopologues. In addition to the regular transition for the highest possible sensitivity, a transition corresponding to the less abundant isotopologue ions was utilized. This decreases saturation at the ion detector; the sensitivity reduction increases the upper dynamic limit. We demonstrated this for a rat plasma assay for a candidate flavor compound; the linear dynamic range increased by an order of magnitude from 3 to 6,000 ng/mL with the regular MRM alone to 3-60,000 ng/mL using additionally the isotopologue transition.

摘要

我们描述了一种使用同位素加和物的额外转换来扩展定量液相色谱/串联质谱(LC-MS/MS)中多重反应监测(MRM)线性动态范围的方法。除了具有最高灵敏度的常规转换之外,还利用了对应于较少丰度同位素离子的转换。这会降低离子检测器的饱和程度;灵敏度的降低会增加上限动态范围。我们在一种用于候选调味化合物的大鼠血浆分析中证明了这一点;单独使用常规 MRM 的线性动态范围从 3 到 6000ng/mL 增加到 3-60000ng/mL,使用同位素加和物的额外转换。

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