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采用负大气压化学电离(APCI)的液相色谱-串联质谱法(LC/MS/MS)快速确证尿液中的11-去甲-9-羧基-Δ⁹-四氢大麻酚(THC-COOH)

Fast confirmation of 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THC-COOH) in urine by LC/MS/MS using negative atmospheric-pressure chemical ionisation (APCI).

作者信息

Weinmann W, Goerner M, Vogt S, Goerke R, Pollak S

机构信息

Institute of Legal Medicine, Klinikum der Albert-Ludwigs-Universität Freiburg i. Br., Albertstrasse 9, D-79104 Freiburg, Germany.

出版信息

Forensic Sci Int. 2001 Sep 15;121(1-2):103-7. doi: 10.1016/s0379-0738(01)00459-5.

Abstract

A fast method using automated solid-phase extraction (SPE) and short-column liquid-chromatography coupled to tandem mass-spectrometry (LC/MS/MS) with negative atmospheric-pressure chemical ionisation (APCI) has been developed for the confirmation of 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THC-COOH) in urine samples. This highly specific method which combines chromatographic separation and MS/MS-analysis can be used for the confirmation of positive immunoassay results with a NIDA cut-off of 15ng/ml. The conjugates of THC-COOH were hydrolysed prior to SPE, and a standard SPE was performed using C18-SPE columns. No derivatisation of the extracts was needed as in GC/MS analysis, and the LC run-time was 6.5min by gradient elution with a retention time of 2.4min. Linearity of calibration was obtained in the range between 0 and 500ng/ml (correlation coefficient R(2)=0.998). Using linear regression (0-50ng/ml) the limit of detection (LOD) was 2.0ng/ml and the limit of quantitation (LOQ) was 5.1ng/ml; day-to-day reproducibility and precision were tested at 15 and 250ng/ml and were 13.4ng/ml+/-3.3% and 255.8ng/ml+/-4.5%, respectively.

摘要

已开发出一种快速方法,该方法采用自动固相萃取(SPE)和短柱液相色谱与串联质谱联用(LC/MS/MS)以及负大气压化学电离(APCI),用于确证尿液样本中的11-去甲-9-羧基-Δ⁹-四氢大麻酚(THC-COOH)。这种将色谱分离与MS/MS分析相结合的高特异性方法,可用于确证免疫分析结果为阳性且NIDA临界值为15ng/ml的情况。THC-COOH的缀合物在SPE之前进行水解,并使用C18-SPE柱进行标准SPE操作。与气相色谱/质谱分析不同,提取物无需衍生化,通过梯度洗脱,液相色谱运行时间为6.5分钟,保留时间为2.4分钟。校准曲线在0至500ng/ml范围内呈线性(相关系数R² = 0.998)。使用线性回归(0至50ng/ml),检测限(LOD)为2.0ng/ml,定量限(LOQ)为5.1ng/ml;在15和250ng/ml水平测试了日间重现性和精密度,分别为13.4ng/ml±3.3%和255.8ng/ml±4.5%。

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