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采用气相色谱/质谱联用技术对人尿液中的可卡因、苯甲酰爱康宁、爱康宁甲酯进行确证和定量分析。

Confirmation and quantitation of cocaine, benzoylecgonine, ecgonine methyl ester in human urine by GC/MS.

作者信息

Mulé S J, Casella G A

机构信息

New York State DSAS Testing and Research Laboratory, Brooklyn 11217.

出版信息

J Anal Toxicol. 1988 May-Jun;12(3):153-5. doi: 10.1093/jat/12.3.153.

Abstract

A rapid, sensitive, reliable quantitative GC/MS method using 0.2 mL of urine was developed for the confirmation of cocaine use. After a simple organic solvent extraction and derivatization with pentafluoropropionic anhydride, cocaine, benzoylecgonine, and ecgonine methyl ester were identified by GC/MS through the retention time for the total ion current and selected ion monitoring (SIM) for each analyte. Quantitation was achieved by obtaining the calibration curves for the molecular ion ratios of the analyte/ketamine (IS) over a range of 12.5-250 ng/mL (0.1-2 ng total). The extraction efficiency for these analytes ranged from 70 to 82%. The sensitivity limit of detection for each analyte was 12.5 ng/mL (0.1 ng) at p less than 0.01. Intra- and interday precision for these analytes ranged between 14.7 and 29.5% CV. This method is in routine use in our laboratory for the GC/MS confirmation of enzyme immunoassay cocaine-positive urine samples.

摘要

建立了一种快速、灵敏、可靠的定量气相色谱/质谱法,使用0.2 mL尿液来确证可卡因的使用情况。经过简单的有机溶剂萃取并用五氟丙酸酐衍生化后,通过气相色谱/质谱法根据总离子流的保留时间以及对每种分析物的选择离子监测(SIM)来鉴定可卡因、苯甲酰爱康宁和爱康宁甲酯。通过获取分析物/氯胺酮(内标物)分子离子比在12.5 - 250 ng/mL(总量0.1 - 2 ng)范围内的校准曲线来实现定量。这些分析物的萃取效率在70%至82%之间。每种分析物在p小于0.01时的检测灵敏度极限为12.5 ng/mL(0.1 ng)。这些分析物的日内和日间精密度的变异系数(CV)在14.7%至29.5%之间。该方法在我们实验室常规用于气相色谱/质谱法确证酶免疫分析可卡因阳性的尿液样本。

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