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UHPLC-MS/MS 法同时检测人发中 16 种色胺及其代谢物及其在实际法医案例中的应用。

UHPLC-MS/MS method for simultaneously detecting 16 tryptamines and their metabolites in human hair and applications to real forensics cases.

机构信息

Department of Forensic Toxicology, Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Science Platform, Academy of Forensic Science, Shanghai 200063, China.

Department of Forensic Toxicology, Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Science Platform, Academy of Forensic Science, Shanghai 200063, China; School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenhe District, Shenyang 110016, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Nov 30;1159:122392. doi: 10.1016/j.jchromb.2020.122392. Epub 2020 Oct 16.

Abstract

Tryptamines are hallucinogenic substances many of which have appeared recently as novel psychoactive substances (NPS). Herein, we describe the establishment of a rapid UHPLC-MS/MS quantitative method for the targeted screening of 16 tryptamines of abuse in hair. Twenty milligram pieces of hair were pulverized below 4 °C in 0.5 mL of deionized water containing 0.1% formic acid and an internal standard (2 ng/mL psilocin-d and psilocybin-d). After subsequent centrifugation, 5 μL of the supernatant was injected into a LC-MS/MS system fitted with a Waters Acquity UPLC HSS T column (100 mm × 2.1 mm, 1.8 μm). The column was gradient eluted at 0.3 mL/min with mobile phases composed of 20 mmol/L ammonium acetate, 5% acetonitrile, and 0.1% formic acid in water (solvent A) and acetonitrile (solvent B). Limits of detection ranged between 0.1 and 20 pg/mg, with limits of quantitation ranging from 3 to 50 pg/mg. The calibration curves for all analytes were linear (r > 0.992). Accuracies varied between 91% and 114%, with intraday precision RSDs < 14% and interday precision RSDs of between 1.3% and 14%. The recoveries of all tryptamines were in the 85-115% range, with the matrix effect ranging from 95% to 112%. The validated method was successfully used to analyse 191 hair samples from suspected tryptamine users, 77 of which were 5-MeO-DiPT-positive, while the 16 tryptamines and their metabolites were not detected in the remaining 114 hair samples. 5-MeO-DiPT and its 5-MeO-NiPT, 5-OH-DiPT, and 4-OH-DiPT metabolites were concurrently detected in 34 hair samples. 5-MeO-DiPT, as the parent drug, was the parent substance found in the hair samples.

摘要

色胺类物质是许多具有致幻作用的物质,其中许多最近已作为新型精神活性物质(NPS)出现。在此,我们描述了一种快速 UHPLC-MS/MS 定量方法的建立,用于在头发中靶向筛选 16 种滥用色胺。将 20 毫克的头发在低于 4°C 的条件下在 0.5 毫升去离子水中粉碎,其中含有 0.1%甲酸和内标物(2ng/mL 裸头草碱-d 和赛洛西宾-d)。随后进行离心,取 5μL 上清液注入配备 Waters Acquity UPLC HSS T 柱(100mm×2.1mm,1.8μm)的 LC-MS/MS 系统。采用 20mmol/L 乙酸铵、5%乙腈和 0.1%甲酸的水溶液(溶剂 A)和乙腈(溶剂 B)在 0.3mL/min 的流速下进行梯度洗脱。检测限范围在 0.1 到 20pg/mg 之间,定量限范围在 3 到 50pg/mg 之间。所有分析物的校准曲线均呈线性(r>0.992)。准确度在 91%到 114%之间变化,日内精密度 RSDs<14%,日间精密度 RSDs 在 1.3%到 14%之间。所有色胺的回收率在 85-115%之间,基质效应在 95%-112%之间。验证后的方法成功地用于分析了 191 份疑似色胺使用者的头发样本,其中 77 份 5-MeO-DiPT 呈阳性,而其余 114 份头发样本中未检测到 16 种色胺及其代谢物。在 34 份头发样本中同时检测到 5-MeO-DiPT 及其 5-MeO-NiPT、5-OH-DiPT 和 4-OH-DiPT 代谢物。5-MeO-DiPT 作为母体药物,是在头发样本中发现的母体物质。

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