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使用混合三重四极杆-线性离子阱质谱仪评估多反应监测立方技术用于分析大鼠脊髓中速激肽相关肽段。

Evaluation of multiple reaction monitoring cubed for the analysis of tachykinin related peptides in rat spinal cord using a hybrid triple quadrupole-linear ion trap mass spectrometer.

作者信息

Pailleux Floriane, Beaudry Francis

机构信息

Groupe de Recherche en Pharmacologie Animal du Québec (GREPAQ), Département de Biomédecine Vétérinaire, Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada.

Groupe de Recherche en Pharmacologie Animal du Québec (GREPAQ), Département de Biomédecine Vétérinaire, Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 1;947-948:164-7. doi: 10.1016/j.jchromb.2013.12.025. Epub 2013 Dec 30.

Abstract

Targeted peptide methods generally use HPLC-MS/MRM approaches. Although dependent on the instrumental resolution, interferences may occur while performing analysis of complex biological matrices. HPLC-MS/MRM(3) is a technique, which provides a significantly better selectivity, compared with HPLC-MS/MRM assay. HPLC-MS/MRM(3) allows the detection and quantitation by enriching standard MRM with secondary product ions that are generated within the linear ion trap. Substance P (SP) and neurokinin A (NKA) are tachykinin peptides playing a central role in pain transmission. The objective of this study was to verify whether HPLC-MS/MRM(3) could provide significant advantages over a more traditional HPLC-MS/MRM assay for the quantification of SP and NKA in rat spinal cord. The results suggest that reconstructed MRM(3) chromatograms display significant improvements with the nearly complete elimination of interfering peaks but the sensitivity (i.e. signal-to-noise ratio) was severely reduced. The precision (%CV) observed was between 3.5% and 24.1% using HPLC-MS/MRM and in the range of 4.3-13.1% with HPLC-MS/MRM(3), for SP and NKA. The observed accuracy was within 10% of the theoretical concentrations tested. HPLC-MS/MRM(3) may improve the assay sensitivity to detect difference between samples by reducing significantly the potential of interferences and therefore reduce instrumental errors.

摘要

靶向肽方法通常采用高效液相色谱-质谱/多反应监测(HPLC-MS/MRM)方法。尽管依赖于仪器分辨率,但在对复杂生物基质进行分析时可能会出现干扰。HPLC-MS/MRM(3)是一种技术,与HPLC-MS/MRM分析相比,它具有显著更好的选择性。HPLC-MS/MRM(3)通过用线性离子阱中产生的二级产物离子富集标准MRM来实现检测和定量。P物质(SP)和神经激肽A(NKA)是速激肽肽,在疼痛传递中起核心作用。本研究的目的是验证HPLC-MS/MRM(3)在定量大鼠脊髓中的SP和NKA方面是否比更传统的HPLC-MS/MRM分析具有显著优势。结果表明,重建的MRM(3)色谱图显示出显著改善,几乎完全消除了干扰峰,但灵敏度(即信噪比)严重降低。使用HPLC-MS/MRM时观察到的精密度(%CV)在3.5%至24.1%之间,使用HPLC-MS/MRM(3)时对于SP和NKA在4.3 - 13.1%范围内。观察到的准确度在测试的理论浓度的10%以内。HPLC-MS/MRM(3)可能通过显著降低干扰的可能性来提高检测样品间差异的分析灵敏度,从而减少仪器误差。

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