Determination of amphetamines in hair samples using microextraction by packed sorbent and gas chromatography-mass spectrometry.

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Drug Testing and Analysis Pub Date : 2024-07-31 DOI:10.1002/dta.3779
Bruno Pires, Ana Y Simão, Tiago Rosado, Mário Barroso, Eugenia Gallardo
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Abstract

Several protocols for the analysis of amphetamine-type stimulants (ATS) in hair have been developed over the years, with microextraction by packed sorbent (MEPS) being used for drugs like opiates, cocaine and ketamine. However, concerning ATS determination in hair samples, this approach has only been applied so far to amphetamine (AMP) and methamphetamine (MAMP). This study aimed at developing and validating a MEPS-based procedure for the determination in hair of not only AMP and MAMP but also of 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethamphetamine (MDMA), 1-(1,3-benzodioxol-5-yl)propan-2-yl (ethyl)amine (MDE) and N-methyl-1-(1,3-benzodioxol-5-yl)-2-aminobutane (MBDB) as well. Hair, 50 mg, was incubated with 1 M sodium hydroxide (NaOH) at 45°C overnight, neutralization with 10 M hydrochloric acid (HCl) and centrifugation followed. The design of experiments approach was used for MEPS optimization, with the final optimized conditions including conditioning (250 μL methanol and deionized water), loading (18 × 100 μL) and elution (7 × 100 μL 2% NH4OH in acetonitrile). The eluted extract was evaporated to dryness and underwent microwave-assisted derivatization with N-methyl-bis(trifluoroacetamide) (MBTFA), and it was afterwards injected onto the gas chromatography-mass spectrometer (GC-MS). The obtained recoveries ranged between 8% and 14% for AMP, 14% and 20% for MAMP, 10% and 15% for MDA, 18% and 28% for MDMA, 25% and 43% for MDE and 34% and 52% for MBDB, and the method was linear from 0.2 to 5.0 ng/mg. Precision and accuracy were in accordance with international method validation guidelines. This novel method involving MEPS coupled to GC-MS offers a swift, eco-friendly and cost-effective alternative to traditional procedures for detecting these AMPs in hair samples.

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利用填料吸附剂微萃取和气相色谱-质谱法测定毛发样本中的苯丙胺。
多年来,已开发出几种分析毛发中苯丙胺类兴奋剂(ATS)的方案,其中填料吸附剂微萃取(MEPS)被用于阿片剂、可卡因和氯胺酮等药物。然而,关于毛发样本中苯丙胺类兴奋剂的测定,迄今为止这种方法只应用于苯丙胺(AMP)和甲基苯丙胺(MAMP)。本研究旨在开发和验证一种基于 MEPS 的程序,该程序不仅可用于检测毛发中的苯丙胺类兴奋剂和甲基苯丙胺,还可用于检测 3,4-亚甲二氧基苯丙胺(MDA)、3,4-亚甲二氧基甲基苯丙胺(MDMA)、1-(1,3-苯并二氧戊环-5-基)丙-2-基(乙基)胺(MDE)和 N-甲基-1-(1,3-苯并二氧戊环-5-基)-2-氨基丁烷(MBDB)。将 50 毫克毛发与 1 M 氢氧化钠(NaOH)在 45°C 下培养过夜,然后用 10 M 盐酸(HCl)中和并离心。采用实验设计法对 MEPS 进行优化,最终优化的条件包括调节(250 μL 甲醇和去离子水)、加载(18 × 100 μL)和洗脱(7 × 100 μL 2% NH4OH 在乙腈中的溶液)。洗脱后的提取物蒸发至干,用 N-甲基-双(三氟乙酰胺)(MBTFA)进行微波衍生,然后注入气相色谱-质谱仪(GC-MS)。结果表明,AMP 的回收率为 8%-14%,MAMP 的回收率为 14%-20%,MDA 的回收率为 10%-15%,MDMA 的回收率为 18%-28%,MDE 的回收率为 25%-43%,MBDB 的回收率为 34%-52%。精密度和准确度符合国际方法验证准则。与传统方法相比,这种将 MEPS 与 GC-MS 相结合的新方法为检测头发样本中的这些 AMPs 提供了一种快速、环保和经济的替代方法。
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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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