Please use this identifier to cite or link to this item:
doi:10.22028/D291-42784
Title: | Studying drug excretion into exhaled breath aerosol - A workflow based on an impaction sampling device and LC-HRMS/MS analysis |
Author(s): | Maalouli Schaar, Juel Kunz, Michael Wagmann, Lea Beck, Olof Mahfoud, Felix Meyer, Markus R. |
Language: | English |
Title: | Analytica Chimica Acta |
Volume: | 1323 |
Publisher/Platform: | Elsevier |
Year of Publication: | 2024 |
Free key words: | Exhaled breath Method development Qualitative method validation Drug excretion Application testing LC-HRMS |
DDC notations: | 610 Medicine and health |
Publikation type: | Journal Article |
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. |
DOI of the first publication: | 10.1016/j.aca.2024.342991 |
URL of the first publication: | https://doi.org/10.1016/j.aca.2024.342991 |
Link to this record: | urn:nbn:de:bsz:291--ds-427846 hdl:20.500.11880/38371 http://dx.doi.org/10.22028/D291-42784 |
ISSN: | 0003-2670 |
Date of registration: | 6-Sep-2024 |
Description of the related object: | Supplementary data |
Related object: | https://ars.els-cdn.com/content/image/1-s2.0-S000326702400792X-mmc1.pdf |
Faculty: | M - Medizinische Fakultät |
Department: | M - Experimentelle und Klinische Pharmakologie und Toxikologie M - Innere Medizin |
Professorship: | M - Prof. Dr. Michael Böhm M - Prof. Dr. Markus Meyer |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
Files for this record:
File | Description | Size | Format | |
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1-s2.0-S000326702400792X-main.pdf | 1,6 MB | Adobe PDF | View/Open |
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