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以中四(对磺酸基苯基)卟啉为基质,采用基质辅助激光解吸/电离飞行时间质谱法对大鼠血浆中的游离脂肪酸进行定量分析。

Quantitative analysis of free fatty acids in rat plasma using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry with meso-tetrakis porphyrin as matrix.

作者信息

Yu Haiqiang, Lopez Edwin, Young Stephen W, Luo Jian, Tian Hui, Cao Ping

机构信息

Department of Chemistry, University of the Pacific, Stockton, CA 95211, USA.

出版信息

Anal Biochem. 2006 Jul 15;354(2):182-91. doi: 10.1016/j.ab.2006.04.050.

DOI:10.1016/j.ab.2006.04.050
PMID:16769030
Abstract

Quantitative analysis of free fatty acids was achieved using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) with a meso-tetrakis porphyrin matrix. Cesium acetate was employed as a cationizing agent. The MALDI signal was reproducible and dominated by cesiated cesium carboxylates [RCOOCs + Cs]+. The addition of two Cs ions resulted in a mass shift of 264.8 Da for each fatty acid and greatly reduced background peaks. A linear relationship between fatty acid concentration and corresponding fatty acid to internal standard peak intensity ratio was observed for three representative fatty acids analyzed across a concentration range from 4.40 to 150 microM, with correlation coefficients between 0.986 and 0.987. The application of this method was demonstrated with the analysis of free fatty acids in nonfasted and fasted rat plasmas. A total of eight free fatty acids (14:0, 16:0, 16:1, 17:0, 18:0, 18:1, 18:2, and 20:4) were detected. The relative peak height ratios of the fatty acids to the internal standard allow quantitative measurements of the free fatty acids. It was shown that the levels of free fatty acids were higher in fasted rats than in rats in a nonfasted state. This method is simple, sensitive, and fast. Thus, it provides an appealing tool for the analysis of free fatty acids or other low-molecular weight compounds during drug discovery and/or development.

摘要

使用带有中四(对磺酸苯基)卟啉基质的基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)对游离脂肪酸进行定量分析。乙酸铯用作阳离子化剂。MALDI信号具有可重复性,且以铯化羧酸铯[RCOOCs + Cs]+为主。添加两个Cs离子会使每种脂肪酸的质量位移264.8 Da,并大大减少背景峰。在所分析的浓度范围为4.40至150 microM的三种代表性脂肪酸中,观察到脂肪酸浓度与相应脂肪酸与内标峰强度比之间存在线性关系,相关系数在0.986至0.987之间。通过分析非禁食和禁食大鼠血浆中的游离脂肪酸证明了该方法的应用。总共检测到八种游离脂肪酸(14:0、16:0、16:1、17:0、18:0、18:1、18:2和20:4)。脂肪酸与内标的相对峰高比可对游离脂肪酸进行定量测量。结果表明,禁食大鼠的游离脂肪酸水平高于非禁食状态的大鼠。该方法简单、灵敏且快速。因此,它为药物发现和/或开发过程中游离脂肪酸或其他低分子量化合物的分析提供了一个有吸引力的工具。

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