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采用选择离子监测的气相色谱-质谱法测定生物体液中的二氢埃托啡。

Determination of dihydroetorphine in biological fluids by gas chromatography-mass spectrometry using selected-ion monitoring.

作者信息

Liu F, Luo Y, Feng J, Hu X

机构信息

Institute of Pharmacology and Toxicology, Beijing, China.

出版信息

J Chromatogr B Biomed Appl. 1996 Apr 26;679(1-2):113-8. doi: 10.1016/0378-4347(96)00044-8.

Abstract

A method for the determination of dihydroetorphine hydrochloride, a powerful anaesthetic and analgesic drug, in biological fluids by GC-MS with selected-ion monitoring using etorphine as internal standard was established. Dihydroetorphine was extracted from human blood and urine with dichloromethane and then derivatized with N-heptafluorobutyrylimidazole after concentration to dryness. A dihydroetorphine monoheptafluorobutyl derivative was formed which showed good behavior on GC-MS with electronic-impact ionization. The main fragment, m/z 522, which is the base peak, was selected as the ion for quantitation and the corresponding ion, m/z 520, was selected for monitoring the internal standard, etorphine. The recoveries and coefficients of variation of the whole procedure were determined with five controlled dihydroetorphine-free urine and plasma samples spiked with different concentrations of dihydroetorphine. The concentration of dihydroetorphine for quantitation was in the range 1-20 ng/ml for urine and 2.5-250 ng/ml for plasma. The correlation coefficients of the standard curves are sufficient to determine the dihydroetorphine. The accuracy for quantitation of dihydroetorphine in urine and plasma is less than 10.6%.

摘要

建立了一种采用气相色谱-质谱联用仪(GC-MS)选择离子监测模式,以埃托啡为内标物测定生物样品中强效麻醉镇痛药盐酸二氢埃托啡的方法。二氢埃托啡用二氯甲烷从人血和尿中萃取,浓缩至干后用N-七氟丁酰咪唑衍生化。形成了二氢埃托啡单七氟丁基衍生物,其在GC-MS电子轰击电离模式下表现良好。选择基峰m/z 522作为定量离子,选择相应离子m/z 520监测内标物埃托啡。用5份添加不同浓度二氢埃托啡的无二氢埃托啡对照尿样和血浆样品测定了整个过程的回收率和变异系数。尿中二氢埃托啡的定量浓度范围为1 - 20 ng/ml,血浆中为2.5 - 250 ng/ml。标准曲线的相关系数足以测定二氢埃托啡。尿样和血浆中二氢埃托啡定量的准确度小于10.6%。

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