Pipette tip-electrospray mass spectrometry for determining opioids in urine, from on-site micro-handling to high-throughput centrifugal microextraction

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2024-05-31 DOI:10.1016/j.sampre.2024.100118
Jaime Millán-Santiago, Rafael Lucena, Soledad Cárdenas
{"title":"Pipette tip-electrospray mass spectrometry for determining opioids in urine, from on-site micro-handling to high-throughput centrifugal microextraction","authors":"Jaime Millán-Santiago,&nbsp;Rafael Lucena,&nbsp;Soledad Cárdenas","doi":"10.1016/j.sampre.2024.100118","DOIUrl":null,"url":null,"abstract":"<div><p>Pipette tip-electrospray is a useful technique that synergically combines sample preparation and ambient ionization mass spectrometry for the rapid analysis of samples. In this work, the development of pipette tip extraction (PTE) is evaluated under two workflows that can be adapted to different analytical scenarios. Micro-handling PTE (MH-PTE) is an inherently portable technique that can be on-site applied. Centrifugal PTE (C-PTE), firstly presented here, allows a high sample throughput just requiring a benchtop centrifuge. The combination of both MH-PTE and C-PTE with pipette tip-electrospray is evaluated in this work for determining codeine and morphine, two metabolically related drugs, in urine and applied to the analysis of real samples. In the case of MH-PTE, intended to be on-site applied, the chemical stability of the analytes once extracted in the tips plays a crucial role. This stability has been studied in detail, simulating several transport/storage conditions compatible with regular postal services. The analytical features of both combinations are similar, although C-PTE provides a better sensitivity in terms of limit of detection (0.3 µg L<sup>−1</sup> for codeine and 0.6 µg L<sup>−1</sup> for morphine) compared to MH-PTE (0.6 µg L<sup>−1</sup> for codeine and 1.5 µg L<sup>−1</sup> for morphine). Moreover, the sample throughput provided by C-PTE is higher (up to 72 samples <em>h</em><sup>−1</sup>) than that provided by MH-PTE (up to 12 samples <em>h</em><sup>−1</sup>).</p></div>","PeriodicalId":100052,"journal":{"name":"Advances in Sample Preparation","volume":"11 ","pages":"Article 100118"},"PeriodicalIF":5.2000,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772582024000172/pdfft?md5=19a369205bf3f3bdae5be0d44b901171&pid=1-s2.0-S2772582024000172-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Sample Preparation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772582024000172","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Pipette tip-electrospray is a useful technique that synergically combines sample preparation and ambient ionization mass spectrometry for the rapid analysis of samples. In this work, the development of pipette tip extraction (PTE) is evaluated under two workflows that can be adapted to different analytical scenarios. Micro-handling PTE (MH-PTE) is an inherently portable technique that can be on-site applied. Centrifugal PTE (C-PTE), firstly presented here, allows a high sample throughput just requiring a benchtop centrifuge. The combination of both MH-PTE and C-PTE with pipette tip-electrospray is evaluated in this work for determining codeine and morphine, two metabolically related drugs, in urine and applied to the analysis of real samples. In the case of MH-PTE, intended to be on-site applied, the chemical stability of the analytes once extracted in the tips plays a crucial role. This stability has been studied in detail, simulating several transport/storage conditions compatible with regular postal services. The analytical features of both combinations are similar, although C-PTE provides a better sensitivity in terms of limit of detection (0.3 µg L−1 for codeine and 0.6 µg L−1 for morphine) compared to MH-PTE (0.6 µg L−1 for codeine and 1.5 µg L−1 for morphine). Moreover, the sample throughput provided by C-PTE is higher (up to 72 samples h−1) than that provided by MH-PTE (up to 12 samples h−1).

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
从现场微处理到高通量离心微萃取,用于测定尿液中阿片类物质的移液器吸头-电喷雾质谱法
移液器吸头电喷雾技术是一种有用的技术,它将样品制备和环境电离质谱技术协同结合起来,实现了样品的快速分析。在这项工作中,根据两种工作流程对移液器吸头萃取(PTE)的发展进行了评估,这两种工作流程可适用于不同的分析场景。微处理 PTE(MH-PTE)是一种可现场应用的便携式技术。本文首次介绍的离心 PTE(C-PTE)只需一台台式离心机即可实现高样品通量。本研究评估了 MH-PTE 和 C-PTE 与吸头电喷雾技术的结合,用于测定尿液中的可待因和吗啡这两种代谢相关的药物,并将其应用于实际样品的分析。MH-PTE 用于现场应用,分析物在吸头中提取后的化学稳定性起着至关重要的作用。我们对这种稳定性进行了详细研究,模拟了与常规邮政服务相适应的几种运输/储存条件。两种组合的分析特性相似,但就检测限而言,C-PTE 的灵敏度(可待因为 0.3 µg L-1 ,吗啡为 0.6 µg L-1)高于 MH-PTE(可待因为 0.6 µg L-1 ,吗啡为 1.5 µg L-1)。此外,C-PTE 提供的样本吞吐量(最多 72 个样本/小时-1)比 MH-PTE 提供的样本吞吐量(最多 12 个样本/小时-1)高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
3.50
自引率
0.00%
发文量
0
期刊最新文献
Determination of steroid hormones in sea urchins by microwave-assisted extraction and ultrahigh-performance liquid chromatography tandem mass spectrometry Extraction of synthetic cathinones from biological samples: A systematic review Microextraction by packed sorbent: Introducing a novel hybrid silica-based chitosan-graphene oxide biosorbent for the evaluation of pesticides and antibiotics in food matrices One step derivatization and switchable hydrophilicity solvent-based microextraction for the determination of adamantane analogues in human urine by HPLC-FLD Recent advances in the application of MOFs and COFs composites for sample preparation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1