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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >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
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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

机译:以中四卟啉为基质的基质辅助激光解吸/电离飞行时间质谱定量分析大鼠血浆中的游离脂肪酸

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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 mu M, 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. (c) 2006 Elsevier Inc. All rights reserved.
机译:游离脂肪酸的定量分析是使用基质辅助的激光解吸/电离飞行时间质谱(MALDI-TOF MS)和中四卟啉卟啉基质进行的。乙酸铯用作阳离子化剂。 MALDI信号是可重现的,并被铯酸铯铯[RCOOCs + Cs](+)所控制。两种Cs离子的加入导致每种脂肪酸的质量偏移为264.8 Da,并且背景峰大大降低。在3.40至150μM的浓度范围内分析的三种代表性脂肪酸的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)。脂肪酸与内标物的相对峰高比允许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。此方法简单,灵敏且快速。因此,它为药物开发和/或开发过程中的游离脂肪酸或其他低分子量化合物的分析提供了一种有吸引力的工具。 (c)2006 Elsevier Inc.保留所有权利。

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