Ottria Roberta, Ravelli Alessandro, Gigli Fausto, Ciuffreda Pierangela
Dipartimento di Scienze Biomediche e Cliniche L. Sacco, Università degli Studi di Milano, Via G.B. Grassi, 74-20157 Milano, Italy.
Dipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche, Sezione di Tossicologia Forense, Università degli Studi di Milano, Via Mangiagalli, 37-20133 Milano, Italy.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 May 1;958:83-9. doi: 10.1016/j.jchromb.2014.03.019. Epub 2014 Mar 24.
We describe and validate a sensitive UHPLC-ESI-QTOF-MS method for the simultaneous quantification of seven endocannabinoids and non-endocannabinoids related N-acylethanolamides: N-arachidonoylethanolamide, N-palmitoylethanolamide, N-stearoylethanolamide, N-oleoylethanolamide, N-linoleoylethanolamide, N-α-linolenoylethanolamide and N-eicosapentaenoylethanolamide in several bio-matrices for the purpose of research and clinical application. We examined effects of different liquid-liquid and solid phase extraction on the recovery of endocannabinoids and N-acylethanolamides. Protein precipitation with cooled acetone and extraction with acetonitrile (1% v/v formic acid) using OASIS HLB cartridge gave better results. Separation was performed on a Waters Acquity UPLC HSST3 column using a 9min elution gradient coupled with high resolution mass spectrometry (QTOF/MS). The high sensitivity of the developed method allow its application on sample with low volumes or low levels of endocannabinoids and N-acylethanolamides and make the method suitable for routine measurement in human bio-matrices, such as plasma, serum (500μL), urine (1mL) and tissues (10-30mg). Its application in clinical research could contribute to unravel pathophysiological roles of these family of lipid mediators and disclose novel diagnostic and prognostic markers.
我们描述并验证了一种灵敏的超高效液相色谱-电喷雾电离-四极杆飞行时间质谱法,用于同时定量测定几种生物基质中的七种内源性大麻素以及与非内源性大麻素相关的N-酰基乙醇胺:N-花生四烯酰乙醇胺、N-棕榈酰乙醇胺、N-硬脂酰乙醇胺、N-油酰乙醇胺、N-亚油酰乙醇胺、N-α-亚麻酰乙醇胺和N-二十碳五烯酰乙醇胺,以用于研究和临床应用。我们研究了不同液-液萃取和固相萃取对内源性大麻素和N-酰基乙醇胺回收率的影响。使用冷却的丙酮进行蛋白沉淀,并用含1%(v/v)甲酸的乙腈通过OASIS HLB柱进行萃取,效果更佳。在Waters Acquity UPLC HSST3柱上进行分离,采用9分钟的洗脱梯度,并结合高分辨率质谱(QTOF/MS)。所开发方法的高灵敏度使其能够应用于低体积或内源性大麻素和N-酰基乙醇胺含量低的样品,并使该方法适用于人体生物基质(如血浆、血清(500μL)、尿液(1mL)和组织(10 - 30mg))的常规测量。其在临床研究中的应用有助于阐明这些脂质介质家族的病理生理作用,并揭示新的诊断和预后标志物。