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临床样本中N-酰基乙醇胺的同步定量分析。

Simultaneous quantitative analysis of N-acylethanolamides in clinical samples.

作者信息

Ozalp Aliye, Barroso Begona

机构信息

Exploratory Development Department, Astellas Pharma Global Development Europe, AC Leiderdorp, The Netherlands.

出版信息

Anal Biochem. 2009 Dec 1;395(1):68-76. doi: 10.1016/j.ab.2009.08.005. Epub 2009 Aug 8.

DOI:10.1016/j.ab.2009.08.005
PMID:19665986
Abstract

A simple and rapid analytical method is described for the simultaneous quantitative analysis of three different N-acylethanolamides in human biological samples: anandamide (AEA), oleoylethanolamide (OEA), and palmitoylethanolamide (PEA). The method is based on a new hybrid solid phase extraction-precipitation technology followed by ultra-performance liquid chromatography/mass spectrometry (UPLC/MS) analysis using d(4)-AEA as the internal standard. The method is linear up to 100ng/ml with a limit of quantitation of 50pg/ml for AEA and 100pg/ml for OEA and PEA. Good reproducibility, accuracy, and precision were demonstrated during the method validation. Application of this new methodology to the analysis of clinical study samples is presented.

摘要

本文描述了一种简单快速的分析方法,用于同时定量分析人体生物样本中的三种不同的N-酰基乙醇胺:花生四烯酸乙醇胺(AEA)、油酰乙醇胺(OEA)和棕榈酰乙醇胺(PEA)。该方法基于一种新的混合固相萃取-沉淀技术,随后以d(4)-AEA作为内标进行超高效液相色谱/质谱(UPLC/MS)分析。该方法在高达100ng/ml时呈线性,AEA的定量限为50pg/ml,OEA和PEA的定量限为100pg/ml。在方法验证过程中证明了良好的重现性、准确性和精密度。本文还介绍了这种新方法在临床研究样本分析中的应用。

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