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用于分析血液和尿液中麦角酸二乙酰胺(LSD)、异麦角酸二乙酰胺(iso-LSD)、去甲麦角酸二乙酰胺(nor-LSD)和O-羟基麦角酸二乙酰胺(O-H-LSD)的经过验证的超高效液相色谱-串联质谱法。

Validated ultra-performance liquid chromatography-tandem mass spectrometry method for analyzing LSD, iso-LSD, nor-LSD, and O-H-LSD in blood and urine.

作者信息

Chung Angela, Hudson John, McKay Gordon

机构信息

University of Saskatchewan, College of Graduate Studies and Research, Toxicology Graduate Program, Saskatoon, Saskatchewan, Canada.

出版信息

J Anal Toxicol. 2009 Jun;33(5):253-9. doi: 10.1093/jat/33.5.253.

Abstract

The Royal Canadian Mounted Police Forensic Science and Identification Services was looking for a confirmatory method for lysergic acid diethylamide (LSD). As a result, an ultra-performance liquid chromatography-tandem mass spectrometry method was validated for the confirmation and quantitation of LSD, iso-LSD, N-demethyl-LSD (nor-LSD), and 2-oxo-3-hydroxy-LSD (O-H-LSD). Relative retention time and ion ratios were used as identification parameters. Limits of detection (LOD) in blood were 5 pg/mL for LSD and iso-LSD and 10 pg/mL for nor-LSD and O-H-LSD. In urine, the LOD was 10 pg/mL for all analytes. Limits of quantitation (LOQ) in blood and urine were 20 pg/mL for LSD and iso-LSD and 50 pg/mL for nor-LSD and O-H-LSD. The method was linear, accurate, and precise from 10 to 2000 pg/mL in blood and 20 to 2000 pg/mL in urine for LSD and iso-LSD and from 20 to 2000 pg/mL in blood and 50 to 2000 pg/mL in urine for nor-LSD and O-H-LSD with a coefficient of determination (R(2)) > or = 0.99. The method was applied to blinded biological control samples and biological samples taken from a suspected LSD user. This is the first reported detection of O-H-LSD in blood from a suspected LSD user.

摘要

加拿大皇家骑警法医科学与鉴定服务部门正在寻找一种用于麦角酸二乙酰胺(LSD)的确证方法。因此,一种超高效液相色谱-串联质谱法被验证用于LSD、异-LSD、N-去甲基-LSD(去甲-LSD)和2-氧代-3-羟基-LSD(O-H-LSD)的确证和定量。相对保留时间和离子比率被用作鉴定参数。血液中LSD和异-LSD的检测限(LOD)为5 pg/mL,去甲-LSD和O-H-LSD的检测限为10 pg/mL。在尿液中,所有分析物的检测限均为10 pg/mL。血液和尿液中LSD和异-LSD的定量限(LOQ)为20 pg/mL,去甲-LSD和O-H-LSD的定量限为50 pg/mL。该方法在血液中10至2000 pg/mL以及尿液中20至2000 pg/mL范围内对于LSD和异-LSD呈线性、准确且精密,对于去甲-LSD和O-H-LSD在血液中20至2000 pg/mL以及尿液中50至2000 pg/mL范围内呈线性、准确且精密,决定系数(R(2))≥0.99。该方法应用于盲法生物对照样品以及从一名疑似LSD使用者采集的生物样品。这是首次报道在一名疑似LSD使用者的血液中检测到O-H-LSD。

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