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使用Zymark RapidTrace从血液、血清、血浆和尿液样本中自动提取麦角酸二乙酰胺(LSD)和N-去甲基-LSD,并通过液相色谱-串联质谱法进行确认。

Automated extraction of lysergic acid diethylamide (LSD) and N-demethyl-LSD from blood, serum, plasma, and urine samples using the Zymark RapidTrace with LC/MS/MS confirmation.

作者信息

de Kanel J, Vickery W E, Waldner B, Monahan R M, Diamond F X

机构信息

National Medical Services, Inc., Willow Grove, PA, USA.

出版信息

J Forensic Sci. 1998 May;43(3):622-5.

PMID:9608700
Abstract

A forensic procedure for the quantitative confirmation of lysergic acid diethylamide (LSD) and the qualitative confirmation of its metabolite, N-demethyl-LSD, in blood, serum, plasma, and urine samples is presented. The Zymark RapidTrace was used to perform fully automated solid-phase extractions of all specimen types. After extract evaporation, confirmations were performed using liquid chromatography (LC) followed by positive electrospray ionization (ESI+) mass spectrometry/mass spectrometry (MS/MS) without derivatization. Quantitation of LSD was accomplished using LSD-d3 as an internal standard. The limit of quantitation (LOQ) for LSD was 0.05 ng/mL. The limit of detection (LOD) for both LSD and N-demethyl-LSD was 0.025 ng/mL. The recovery of LSD was greater than 95% at levels of 0.1 ng/mL and 2.0 ng/mL. For LSD at 1.0 ng/mL, the within-run and between-run (different day) relative standard deviation (RSD) was 2.2% and 4.4%, respectively.

摘要

本文介绍了一种用于定量确证血液、血清、血浆和尿液样本中麦角酸二乙酰胺(LSD)及其代谢物N-去甲基-LSD的法医程序。使用Zymark RapidTrace对所有样本类型进行全自动固相萃取。提取物蒸发后,采用液相色谱(LC),随后进行正电喷雾电离(ESI+)质谱/质谱(MS/MS),无需衍生化,进行确证。使用LSD-d3作为内标物对LSD进行定量。LSD的定量限(LOQ)为0.05 ng/mL。LSD和N-去甲基-LSD的检测限(LOD)均为0.025 ng/mL。在0.1 ng/mL和2.0 ng/mL水平下,LSD的回收率大于95%。对于1.0 ng/mL的LSD,批内和批间(不同日期)相对标准偏差(RSD)分别为2.2%和4.4%。

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