Gerostamoulos J, Drummer O H
Victorian Institute of Forensic Pathology, Department of Forensic Medicine, Monash University, South Melbourne, Australia.
Forensic Sci Int. 1996 Jan 12;77(1-2):53-63. doi: 10.1016/0379-0738(95)01833-6.
A simple and rapid high-performance liquid chromatographic method is described for the determination of morphine-3-glucuronide, morphine-6-glucuronide, normorphine and morphine in postmortem blood. A solid phase extraction technique employing C18 Sep-Pak cartridges was used to recover morphine and its metabolites from 0.5 ml of blood. Reverse phase ion-pair chromatography was used to achieve separation with a C18 bonded column. The mobile phase consisted of acetonitrile, lauryl sulphate and sodium dihydrogen orthophosphate buffer at low pH. Electrochemical detection (ECD) in series with ultraviolet (UV) spectrophotometric detection (210 nm) was used for quantitation. The lower limit of detection using ECD was 10 ng/ml for all analytes and a linear response was observed to 5000 ng/ml. Coefficients of variation for all analytes ranged between 3-13% for both intra- and inter-assay. This method is reproducible, quick and easy to perform and allows morphine conjugates and morphine to be measured simultaneously in postmortem blood.
描述了一种简单快速的高效液相色谱法,用于测定死后血液中的吗啡 - 3 - 葡萄糖醛酸苷、吗啡 - 6 - 葡萄糖醛酸苷、去甲吗啡和吗啡。采用C18 Sep - Pak柱的固相萃取技术从0.5 ml血液中回收吗啡及其代谢物。使用反相离子对色谱法,通过C18键合柱实现分离。流动相由乙腈、月桂基硫酸盐和低pH值的磷酸二氢钠缓冲液组成。采用电化学检测(ECD)与紫外(UV)分光光度检测(210 nm)串联进行定量。使用ECD时,所有分析物的检测下限为10 ng/ml,在5000 ng/ml范围内观察到线性响应。所有分析物的批内和批间变异系数在3 - 13%之间。该方法具有可重复性,操作快速简便,可同时测定死后血液中的吗啡结合物和吗啡。