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“砖”式微型质谱仪上的并行伪-MRM 用于高通量多靶筛选。

Parallel Pseudo-MRM on the "brick" miniature mass spectrometer for high throughput multi-target screening.

机构信息

School of Life Science, Beijing Institute of Technology, Beijing, 100081, China.

School of Life Science, Beijing Institute of Technology, Beijing, 100081, China; Kunshan Nier Precision Instrumentation Inc. Kunshan, Suzhou, 215316, China.

出版信息

Talanta. 2023 Jan 15;252:123866. doi: 10.1016/j.talanta.2022.123866. Epub 2022 Aug 24.

DOI:10.1016/j.talanta.2022.123866
PMID:36041316
Abstract

With increasingly improved analytical performances, miniature mass spectrometers are expandingly applied in more application scenarios. The capability of high throughput analysis of multi-targets is a crucial function of a miniature mass spectrometer, especially for in-situ applications. As a powerful method for target screening, multiple reaction monitoring (MRM) was conventionally realized on triple quadrupole (QQQ) mass spectrometers. Previously, pseudo-multiple reaction monitoring (pseudo-MRM) operation mode has been realized on a "brick" mass spectrometer equipped with a single ion trap. However, pseudo-MRM on an ion trap was realized through the tandem-in-time fashion, and the throughput of pseudo-MRM was still limited. As a continuous effort to boost performances of the "brick" miniature mass spectrometer, parallel pseudo-MRM mode was developed, and the throughput could be raised up to 10 times for multi-target screening. To achieve better isolation and collision induced dissociation (CID) efficiencies, the mass range of interest was divided into several segments based on optimized Mathieu q value. The fast screening of 10 different drugs was used as an illustrative example. Furthermore, parallel quantitative analysis was also demonstrated and verified using the internal standard calibration method.

摘要

随着分析性能的不断提高,微型质谱仪在更多的应用场景中得到了广泛的应用。高通量分析多目标的能力是微型质谱仪的一个关键功能,特别是对于原位应用。作为一种强大的目标筛选方法,多反应监测 (MRM) 传统上是在三重四极杆 (QQQ) 质谱仪上实现的。以前,在配备单个离子阱的“砖式”质谱仪上已经实现了伪多反应监测 (pseudo-MRM) 操作模式。然而,离子阱上的 pseudo-MRM 是通过串联时间方式实现的,pseudo-MRM 的通量仍然有限。作为提高“砖式”微型质谱仪性能的持续努力,开发了并行伪-MRM 模式,可将多目标筛选的通量提高 10 倍。为了实现更好的隔离和碰撞诱导解离 (CID) 效率,根据优化的 Mathieu q 值将感兴趣的质量范围分成几个部分。以快速筛选 10 种不同药物为例进行了说明。此外,还使用内部标准校准方法进行了并行定量分析的演示和验证。

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