Departament de Fisiologia, Facultat de Farmàcia, Universistat de Barcelona, Avda Joan XXIII s/n, 08028 Barcelona, Spain.
J Pharm Biomed Anal. 2011 Dec 15;56(5):976-82. doi: 10.1016/j.jpba.2011.06.018. Epub 2011 Jun 29.
Eicosanoids are oxidized arachidonate-derived lipid products generated by cyclooxygenase, lipoxygenase and cytochrome P-450 pathways. They are involved in diverse processes in health and disease and they are highly bioactive. Gas chromatography and enzyme immunoassays were used to quantify these mediators in the past. However, the recent availability of high-sensitivity liquid chromatography-mass spectrometry has provided a new approach for quantification that minimizes the sample size and the required preparation. This paper describes a rapid and simple technique for the simultaneous quantitative analysis of prostaglandin (PG) E(2) and PGJ(2); leukotrienes (LT) B(4) and D(4); 5-, 12-, 15- and 20-hydroxyeicosatetraenoic acids (HETEs); 13-hydroxyoctadecadienoic acid (13-HODE); 5,6-, 8,9-, 11,12- and 14,15-epoxyeicosatrienoic acids (EETs); and 11,12- and 14,15-dihydroxieicosatrienoic acids (DHETs) in cell culture supernatants and urine. We simultaneously analyzed 14 arachidonic acid metabolites representative from the three pathways, together with 13-HODE, a linoleic-derived product. Solid phase extraction was used for the sample preparation. The recoveries obtained ranged from 25% to 100%, depending on the metabolites. The LC/MS/MS method used the gradient on a C(18) column and electrospray ionization in negative ion detection mode. The method was optimized for sensitivity and for separation within 20 min. The linear ranges of the calibration curves were 0.1-200 ng/ml for PGE(2), PGJ(2), LTB(4), 5-HETE, 12-HETE, 15-HETE, 13-HODE, 11,12-EET, 11,12-DHET and 14,15-DHET, and 1-200ng/ml for LTD(4), 20-HETE, 5,6-EET, 8,9-EET and 14,15-EET. The advantages of this method include minimal sample preparation, high sensitivity and elimination of the problem associated with thermal instability in gas chromatography analysis.
类二十烷酸是由环加氧酶、脂加氧酶和细胞色素 P-450 途径氧化花生四烯酸衍生而来的脂质产物。它们参与健康和疾病中的多种过程,具有高度的生物活性。过去,气相色谱法和酶免疫分析法被用于定量这些介质。然而,最近高灵敏度液相色谱-质谱法的出现为定量分析提供了一种新的方法,这种方法可以最大限度地减少样品量和所需的制备。本文描述了一种快速而简单的技术,用于同时定量分析前列腺素(PG)E2 和 PGJ2;白三烯(LT)B4 和 D4;5-、12-、15-和 20-羟二十碳四烯酸(HETE);13-羟基十八碳二烯酸(13-HODE);5,6-、8,9-、11,12-和 14,15-环氧二十碳三烯酸(EET);以及细胞培养上清液和尿液中的 11,12-和 14,15-二羟二十碳三烯酸(DHET)。我们同时分析了三种途径中具有代表性的 14 种花生四烯酸代谢物,以及来源于亚油酸的产物 13-HODE。固相萃取用于样品制备。回收率取决于代谢物,范围在 25%到 100%之间。LC/MS/MS 方法在 C18 柱上使用梯度,并以负离子检测模式进行电喷雾电离。该方法针对灵敏度和 20 分钟内的分离进行了优化。校准曲线的线性范围为 PGE2、PGJ2、LTB4、5-HETE、12-HETE、15-HETE、13-HODE、11,12-EET、11,12-DHET 和 14,15-DHET 的 0.1-200ng/ml,LTD4、20-HETE、5,6-EET、8,9-EET 和 14,15-EET 的 1-200ng/ml。该方法的优点包括样品制备量少、灵敏度高,以及消除了气相色谱分析中与热不稳定性相关的问题。