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人血清、痰液和支气管肺泡灌洗液中类二十烷酸及其相关代谢物的同步液相色谱-串联质谱分析

Simultaneous LC-MS/MS analysis of eicosanoids and related metabolites in human serum, sputum and BALF.

作者信息

Thakare Rhishikesh, Chhonker Yashpal S, Gautam Nagsen, Nelson Amy, Casaburi Richard, Criner Gerard, Dransfield Mark T, Make Barry, Schmid Kendra K, Rennard Stephen I, Alnouti Yazen

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE, USA.

Pulmonary and Critical Care Medicine Section, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Biomed Chromatogr. 2018 Mar;32(3). doi: 10.1002/bmc.4102. Epub 2017 Oct 17.

Abstract

The differences among individual eicosanoids in eliciting different physiological and pathological responses are largely unknown because of the lack of valid and simple analytical methods for the quantification of individual eicosanoids and their metabolites in serum, sputum and bronchial alveolar lavage fluid (BALF). Therefore, a simple and sensitive LC-MS/MS method for the simultaneous quantification of 34 eicosanoids in human serum, sputum and BALF was developed and validated. This method is valid and sensitive with a limit of quantification ranging from 0.2 to 3 ng/mL for the various analytes, and has a large dynamic range (500 ng/mL) and a short run time (25 min). The intra- and inter-day accuracy and precision values met the acceptance criteria according to US Food and Drug Administration guidelines. Using this method, detailed eicosanoid profiles were quantified in serum, sputum and BALF from a pilot human study. In summary, a reliable and simple LC-MS/MS method to quantify major eicosanoids and their metabolites was developed and applied to quantify eicosanoids in human various fluids, demonstrating its suitability to assess eicosanoid biomarkers in human clinical trials.

摘要

由于缺乏有效且简便的分析方法来定量血清、痰液和支气管肺泡灌洗液(BALF)中单个类二十烷酸及其代谢产物,不同的类二十烷酸引发不同生理和病理反应的差异在很大程度上尚不明确。因此,开发并验证了一种用于同时定量人血清、痰液和BALF中34种类二十烷酸的简单且灵敏的液相色谱 - 串联质谱(LC-MS/MS)方法。该方法有效且灵敏,各种分析物的定量限在0.2至3 ng/mL之间,具有较大的动态范围(500 ng/mL)和较短的运行时间(25分钟)。日内和日间的准确度和精密度值符合美国食品药品监督管理局指南的验收标准。使用该方法,在一项小型人体研究中对血清、痰液和BALF中的详细类二十烷酸谱进行了定量。总之,开发了一种可靠且简单的LC-MS/MS方法来定量主要类二十烷酸及其代谢产物,并将其应用于定量人体各种体液中的类二十烷酸,证明了其在人体临床试验中评估类二十烷酸生物标志物的适用性。

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