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研究药物经呼气气溶胶排泄 - 基于撞击采样装置和 LC-HRMS/MS 分析的工作流程。

Studying drug excretion into exhaled breath aerosol - A workflow based on an impaction sampling device and LC-HRMS/MS analysis.

机构信息

Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Center for Molecular Signaling (PZMS), Saarland University, Homburg, Germany.

Department of Internal Medicine III, Cardiology, Angiology and Intensive Care Medicine, University Hospital Saarland, Saarland University, Homburg, Germany; Department of Cardiology, Heart Center at University Hospital Basel, Switzerland.

出版信息

Anal Chim Acta. 2024 Sep 22;1323:342991. doi: 10.1016/j.aca.2024.342991. Epub 2024 Aug 8.

Abstract

BACKGROUND

Exhaled breath (EB) aerosol was in principle shown to be a suitable matrix for bioanalysis of volatile but also non-volatile compounds. This attracted particular interest in the field of drug analysis. However, a big gap still exists in the understanding how and which drugs and/or their metabolites are excreted into exhaled breath and could thus actually be detected. The current study aimed to develop an analytical workflow for the qualitative detection of non-volatile drugs in EB aerosol microparticles.

RESULTS

The analyte selection covered different drug classes such as antihypertensives, anticonvulsants or opioid analgesics to investigate and understand the excretion of drugs and their metabolites into EB aerosol. A device for collecting aerosol particles from the lung through impaction was used for the non-invasive sampling procedure. Three expiration cycles per participant and device were collected. The sample preparation consisted of a collector extraction with methanol. Qualitative method development and validation were performed using reversed-phase liquid chromatography (LC) coupled to orbitrap-based high-resolution mass spectrometry (HRMS). Qualitative method validation was done according to published recommendations and international guidelines. Parameters such as selectivity, carry-over, limits of detection and identification, recovery, matrix effects, and long-term stability were evaluated. The limits of detection ranged from 100 pg/collector to 10,000 pg/collector. The procedure was finally used to analyze a total of 31 patient EB samples and demonstrated that e.g., tilidine and its metabolite nortilidine as well as tramadol and its active metabolite O-desmethyltramadol can be detected in EB aerosol.

SIGNIFICANCE AND NOVELTY

The work shows a comprehensive workflow for elucidating drug excretion into exhaled breath aerosol. This bioanalytical strategy and the corresponding novel data from this study are the foundation for further method development and to better understand, which drugs and their metabolites can be addressed by exhaled breath aerosol bioanalysis.

摘要

背景

呼气(EB)气溶胶在原则上被证明是一种适合分析挥发性和非挥发性化合物的基质。这在药物分析领域引起了特别的关注。然而,人们对于哪些药物及其代谢物被排泄到呼气气溶胶中,以及实际上可以检测到哪些药物及其代谢物,仍存在很大的理解差距。本研究旨在开发一种用于定性检测 EB 气溶胶微粒中非挥发性药物的分析工作流程。

结果

分析物的选择涵盖了不同的药物类别,如抗高血压药、抗惊厥药或阿片类镇痛药,以研究和了解药物及其代谢物的排泄情况。使用一种用于通过撞击收集肺部气溶胶颗粒的装置进行非侵入性采样。每位参与者和装置采集三个呼气周期。样品制备包括用甲醇进行收集器提取。采用反相液相色谱(LC)与轨道阱高分辨率质谱(HRMS)相结合的方法进行定性方法开发和验证。定性方法验证按照已发表的建议和国际指南进行。评估了选择性、残留、检测限和鉴定、回收率、基质效应和长期稳定性等参数。检测限范围从 100 pg/收集器到 10,000 pg/收集器。最后,该程序用于分析总共 31 个患者的 EB 样本,结果表明可在 EB 气溶胶中检测到替啶及其代谢物去甲替啶、曲马多及其活性代谢物 O-去甲曲马多等。

意义和新颖性

这项工作展示了一种全面的工作流程,用于阐明药物排泄到呼气气溶胶中。这种生物分析策略以及本研究的相应新数据是进一步方法开发和更好地理解呼气气溶胶生物分析可用于哪些药物及其代谢物的基础。

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