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通过超高效液相色谱-高分辨质谱法对毛发中的合成卡西酮及其代谢物进行靶向筛查和定量分析。

Targeted screening and quantification of synthetic cathinones and metabolites in hair by UHPLC-HRMS.

作者信息

La Maida N, Mannocchi G, Pichini S, Basile G, Di Giorgi A, Busardò F P, Marchei E

机构信息

Department of Excellence of Biomedical Science and Public Health, University "Politecnica delle Marche" of Ancona, Ancona, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2022 Jul;26(14):5033-5042. doi: 10.26355/eurrev_202207_29289.

Abstract

OBJECTIVE

Synthetic cathinones (SCs) are new psychoactive substances with sympathomimetic effects, which emerged into the illegal drug market to replace controlled stimulants. Since every year more powerful and toxic substances enter the illicit market, there is the need for analytical methodologies able to detect these new compounds in conventional and non-conventional biological matrices. We sought to develop and validate a targeted screening and quantification method for thirty-two parent SCs and two metabolites in hair samples by ultra-high-performance liquid chromatography coupled to high resolution mass spectrometry (UHPLC-HRMS).

MATERIALS AND METHODS

20 mg hair samples were soaked in 250 µL of 2 mM ammonium formate, methanol and acetonitrile mixture (50/25/25, v/v/v) and incubated overnight at 40°C. After incubation, the samples were evaporated to dryness under nitrogen stream and reconstituted with 100 µL of mobile phase mix (A:B, 80:20) and 10 µL were injected into UHPLC-HRMS. A Q ExactiveTM Focus Orbitrap Mass spectrometer with full scan and targeted data-dependent MS/MS scan acquisition was used for the screening and quantitation analysis.

RESULTS

The assay was linear from 5 to 500 pg/mg hair for all the analytes under investigation. Intra-day and inter-day precision were always < 15% and matrix effect and analytical recovery were always within acceptable criteria (±25% and >50%, respectively). The developed method was applied to authentic hair samples from SCs consumers. The most prevalent found SCs were 3,4-Methylenedioxy-α-Pyrrolidinohexanophenone with a concentration range of 6.0-1,000.0 pg/mg along with α-Pyrrolidinohexiophenone (54.0 and 554.0 pg/mg, respectively), 3-Methylmetcathinone (556.0 and 5,000.0 pg/mg) and 4-Methylethcathinone (11.5 and 448.0 pg/mg) CONCLUSIONS: The developed method showed good selectivity, specificity, an easy and low-cost sample preparation and an analysis time compatible with a high throughput laboratory.

摘要

目的

合成卡西酮(SCs)是一类具有拟交感神经作用的新型精神活性物质,已进入非法毒品市场以取代受管制的兴奋剂。由于每年都有更强效和有毒的物质进入非法市场,因此需要能够在常规和非常规生物基质中检测这些新化合物的分析方法。我们试图开发并验证一种通过超高效液相色谱-高分辨率质谱联用(UHPLC-HRMS)对毛发样本中的32种母体SCs和2种代谢物进行靶向筛查和定量的方法。

材料与方法

将20mg毛发样本浸泡在250μL 2mM甲酸铵、甲醇和乙腈的混合物(50/25/25,v/v/v)中,在40°C下孵育过夜。孵育后,样品在氮气流下蒸发至干,并用100μL流动相混合物(A:B,80:20)复溶,取10μL注入UHPLC-HRMS。使用具有全扫描和靶向数据依赖型MS/MS扫描采集功能的Q ExactiveTM Focus Orbitrap质谱仪进行筛查和定量分析。

结果

所有研究分析物在5至500pg/mg毛发范围内呈线性。日内和日间精密度始终<15%,基质效应和分析回收率始终在可接受标准范围内(分别为±25%和>50%)。所开发的方法应用于SCs使用者的真实毛发样本。最常见的SCs是3,4-亚甲基二氧基-α-吡咯烷基己酮,浓度范围为6.0 - 1000.0pg/mg,以及α-吡咯烷基己酮(分别为54.0和554.0pg/mg)、3-甲基甲卡西酮(556.0和5000.0pg/mg)和4-甲基乙卡西酮(11.5和448.0pg/mg)。结论:所开发的方法具有良好的选择性、特异性、简便且低成本的样品制备方法,以及与高通量实验室相兼容的分析时间。

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