Suppr超能文献

气相色谱-质谱法测定指甲中的苯丙胺类兴奋剂、氯胺酮及其代谢物。

Determination of amphetamine-type stimulants, ketamine and metabolites in fingernails by gas chromatography-mass spectrometry.

机构信息

Drug Analysis Laboratory, Forensic Science Division, Supreme Prosecutors' Office, Seoul, Republic of Korea.

出版信息

Forensic Sci Int. 2010 Jan 30;194(1-3):108-14. doi: 10.1016/j.forsciint.2009.10.023. Epub 2009 Nov 18.

Abstract

A gas chromatography-mass spectrometry (GC-MS) method was developed and validated for the simultaneous qualification and quantification of methamphetamine (MA), amphetamine (AP), 3,4-methylenedioxy-N-methylamphetamine (MDMA), 3,4-methylenedioxy-N-amphetamine (MDA), ketamine (KET) and norketamine (NKT) in fingernails. Fingernail samples (20mg) were washed with distilled water and methanol, digested with 1.0M sodium hydroxide at 95 degrees C for 30 min, and then extracted with ethyl acetate. Extract solutions were evaporated to dryness, derivatized using heptafluorobutyric anhydride (HFBA) at 60 degrees C for 30 min, and analyzed by GC-MS. The linear ranges were 0.1-20.0 ng/mg for AP, MDMA and NKT, 0.2-20.0 ng/mg for MA and MDA, and 0.4-20.0 ng/mg for KET, with the coefficients of determination (r(2)>or=0.9989). The intra- and inter-day precisions were within 7.1% and 10.6%, respectively. The intra- and inter-day accuracies were -10.9% to 0.8% and -4.3% to 4.5%, respectively. The limits of detections (LODs) and the limits of quantifications (LOQs) for each analyte were lower than 0.094 ng/mg and 0.314 ng/mg, respectively. The recoveries were in the range of 72.3-94.9%. The average fingernail growth rates of two subjects for three years and six subjects for two months were 3.12 mm/month and 3.16 mm/month, respectively. The method proved to be suitable also for the simultaneous detection and quantification of MA, MDMA, KET and their metabolites in fingernails.

摘要

建立并验证了一种气相色谱-质谱联用(GC-MS)方法,用于同时定性和定量检测指甲中的甲基苯丙胺(MA)、苯丙胺(AP)、3,4-亚甲二氧基-N-甲基苯丙胺(MDMA)、3,4-亚甲二氧基-N-苯丙胺(MDA)、氯胺酮(KET)和去甲氯胺酮(NKT)。指甲样品(20mg)用蒸馏水和甲醇洗涤,在 95°C 下用 1.0M 氢氧化钠消化 30 分钟,然后用乙酸乙酯提取。提取液在 60°C 下用七氟丁酰酐(HFBA)衍生 30 分钟,然后用 GC-MS 分析。AP、MDMA 和 NKT 的线性范围为 0.1-20.0ng/mg,MA 和 MDA 的线性范围为 0.2-20.0ng/mg,KET 的线性范围为 0.4-20.0ng/mg,相关系数(r(2)>or=0.9989)。日内和日间精密度分别在 7.1%和 10.6%以内。日内和日间准确度分别为-10.9%至 0.8%和-4.3%至 4.5%。每个分析物的检测限(LOD)和定量限(LOQ)均低于 0.094ng/mg 和 0.314ng/mg。回收率在 72.3-94.9%之间。两名受试者三年内和六名受试者两个月内的平均指甲生长速度分别为 3.12mm/月和 3.16mm/月。该方法还证明适用于同时检测和定量指甲中的 MA、MDMA、KET 及其代谢物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验