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一种 UPLC-MS/MS 方法,用于分析头发中的 75 种苯乙胺及其衍生物。

A UPLC-MS/MS methodological approach for the analysis of 75 phenethylamines and their derivatives in hair.

机构信息

Department of Forensic Toxicology, Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Science Platform, Academy of Forensic Science, Shanghai, China; College of Medicine and Forensics, Xi'an Jiaotong University Health Science Center, Xi'an, China.

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

出版信息

J Pharm Biomed Anal. 2023 May 30;229:115367. doi: 10.1016/j.jpba.2023.115367. Epub 2023 Mar 25.

Abstract

A rapid ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for the targeted analysis of 75 phenethylamines and their derivatives from the hair matrix. The monitored classes of phenethylamines included the 2C series, D series, N-benzyl derivatives, mescaline-derived compounds, MDMA analogs, and benzodifurans. Approximately 20 mg of hair was weighed and pulverized with 0.1% formic acid in methanol by cryogenic grinding. After ultrasonication, centrifugation, and filtration, the supernatant was analyzed by LC-MS/MS operating in the scheduled multiple reaction monitoring mode. Phenethylamines and their derivatives were separated in 13 min on a biphenyl column (2.6 µm, 100 Å, 100 × 3.0 mm) using a gradient eluting mobile phase composed of 0.1% formic acid in water and acetonitrile. The developed and validated method showed good selectivity, sensitivity (LOD: 0.5-10 pg/mg and LOQ: 1-20 pg/mg), linearity (R > 0.997), accuracy and precision (< 20%), and stability. The method also showed good recovery and acceptable matrix effects for most of the targeted compounds. This analytical approach was successfully applied for the identification and quantification of phenethylamines in hair from authentic forensic cases.

摘要

建立并验证了一种快速超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于靶向分析头发基质中 75 种苯乙胺及其衍生物。监测的苯乙胺类别包括 2C 系列、D 系列、N-苄基衍生物、三甲氧基苯乙胺类化合物、MDMA 类似物和苯并二呋喃。称取约 20mg 头发,用甲醇中的 0.1%甲酸在低温下研磨粉碎。超声处理、离心和过滤后,上清液通过 LC-MS/MS 以预定多重反应监测模式进行分析。苯乙胺及其衍生物在 13 分钟内在双苯柱(2.6μm,100Å,100×3.0mm)上分离,采用由水中 0.1%甲酸和乙腈组成的梯度洗脱流动相。所建立和验证的方法具有良好的选择性、灵敏度(LOD:0.5-10pg/mg 和 LOQ:1-20pg/mg)、线性(R>0.997)、准确性和精密度(<20%)以及稳定性。该方法还显示出大多数靶向化合物良好的回收率和可接受的基质效应。该分析方法成功应用于真实法医案例中头发中苯乙胺的鉴定和定量。

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