尿液中合成色胺的填充吸附剂微萃取及离子迁移率光谱测定

IF 5.2 Q1 CHEMISTRY, ANALYTICAL
María Aparici-Lozano, Sergio Armenta, Salvador Garrigues, Francesc A. Esteve-Turrillas
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引用次数: 4

摘要

基于填充吸附剂(MEPS)微萃取和离子迁移率光谱测定,开发了一种测定尿液中N,N-二丙基色胺、5-甲氧基-N,N-二甲基色胺和5-甲氧基-N-甲基-N-异丙胺的方法。填充吸附剂微萃取与离子迁移率光谱法相结合,由于其简单、自动化和便携性,为现场筛选尿液中的新精神活性物质提供了很好的优势。已经评估了样品pH和离子强度以及加载和洗脱步骤的数量的影响。所获得的定量限在21至29µg L−1之间,通过测定在定量限下掺入250和500µg L–1合成色胺的空白尿样来评估准确性和精密度,回收率在76–95%之间,相对标准偏差低于20%。此外,对所提出的提取方法的环境影响和绿色性进行了评估,AGREEprep得分为0.62。因此,所开发的方法可以被认为是一种可靠的、绿色的现场滥用药物消费检测筛查方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Microextraction by packed sorbent of synthetic tryptamines from urine and ion mobility spectrometry determination

Microextraction by packed sorbent of synthetic tryptamines from urine and ion mobility spectrometry determination

A procedure for the determination of N,N-dipropyltryptamine, 5‑methoxy-N,N-dimethyltryptamine, and 5‑methoxy-N-methyl-N-isopropyltryptamine in urine has been developed based on a microextraction by packed sorbent (MEPS) followed by ion mobility spectrometry determination. The combination of microextraction by packed sorbent with ion mobility spectrometry provided promising advantages for in-field screening of new psychoactive substances in urine, due to its simplicity, automation, and portability. The effect of sample pH and ionic strength, and the number of loading and elution steps has been evaluated. The obtained limits of quantification ranged from 21 to 29 µg L−1, and accuracy and precision were evaluated by the determination of blank urine samples spiked at limits of quantification, 250, and 500 µg L−1 synthetic tryptamines, with recovery values in the range of 76–95% and relative standard deviations lower than 20%. Moreover, the environmental impact and greenness of the proposed extraction method has been evaluated, providing an AGREEprep score of 0.62. Thus, the developed methodology can be considered a reliable and green screening methodology for in-field abuse drug consumption detection.

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