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Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections

Desorption/ionization (DI)-mass spectrometric (MS) methods offer considerable advantages of rapidity and low-sample input for the analysis of solid biological matrices such as tissue sections. The concept of desorption electrospray ionization (DESI) offers the possibility to ionize compounds from so...

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Autores principales: Fresnais, Margaux, Liang, Siwen, Breitkopf, Marius, Lindner, Joshua Raoul, Claude, Emmanuelle, Pringle, Steven, Levkin, Pavel A., Demir, Konstantin, Benzel, Julia, Sundheimer, Julia, Statz, Britta, Pajtler, Kristian W., Pfister, Stefan M., Haefeli, Walter E., Burhenne, Jürgen, Longuespée, Rémi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228120/
https://www.ncbi.nlm.nih.gov/pubmed/35745613
http://dx.doi.org/10.3390/ph15060694
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author Fresnais, Margaux
Liang, Siwen
Breitkopf, Marius
Lindner, Joshua Raoul
Claude, Emmanuelle
Pringle, Steven
Levkin, Pavel A.
Demir, Konstantin
Benzel, Julia
Sundheimer, Julia
Statz, Britta
Pajtler, Kristian W.
Pfister, Stefan M.
Haefeli, Walter E.
Burhenne, Jürgen
Longuespée, Rémi
author_facet Fresnais, Margaux
Liang, Siwen
Breitkopf, Marius
Lindner, Joshua Raoul
Claude, Emmanuelle
Pringle, Steven
Levkin, Pavel A.
Demir, Konstantin
Benzel, Julia
Sundheimer, Julia
Statz, Britta
Pajtler, Kristian W.
Pfister, Stefan M.
Haefeli, Walter E.
Burhenne, Jürgen
Longuespée, Rémi
author_sort Fresnais, Margaux
collection PubMed
description Desorption/ionization (DI)-mass spectrometric (MS) methods offer considerable advantages of rapidity and low-sample input for the analysis of solid biological matrices such as tissue sections. The concept of desorption electrospray ionization (DESI) offers the possibility to ionize compounds from solid surfaces at atmospheric pressure, without the addition of organic compounds to initiate desorption. However, severe drawbacks from former DESI hardware stability made the development of assays for drug quantification difficult. In the present study, the potential of new prototype source setups (High Performance DESI Sprayer and Heated Transfer Line) for the development of drug quantification assays in tissue sections was evaluated. It was demonstrated that following dedicated optimization, new DESI XS enhancements present promising options regarding targeted quantitative analyses. As a model compound for these developments, ulixertinib, an inhibitor of extracellular signal-regulated kinase (ERK) 1 and 2 was used.
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spelling pubmed-92281202022-06-25 Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections Fresnais, Margaux Liang, Siwen Breitkopf, Marius Lindner, Joshua Raoul Claude, Emmanuelle Pringle, Steven Levkin, Pavel A. Demir, Konstantin Benzel, Julia Sundheimer, Julia Statz, Britta Pajtler, Kristian W. Pfister, Stefan M. Haefeli, Walter E. Burhenne, Jürgen Longuespée, Rémi Pharmaceuticals (Basel) Article Desorption/ionization (DI)-mass spectrometric (MS) methods offer considerable advantages of rapidity and low-sample input for the analysis of solid biological matrices such as tissue sections. The concept of desorption electrospray ionization (DESI) offers the possibility to ionize compounds from solid surfaces at atmospheric pressure, without the addition of organic compounds to initiate desorption. However, severe drawbacks from former DESI hardware stability made the development of assays for drug quantification difficult. In the present study, the potential of new prototype source setups (High Performance DESI Sprayer and Heated Transfer Line) for the development of drug quantification assays in tissue sections was evaluated. It was demonstrated that following dedicated optimization, new DESI XS enhancements present promising options regarding targeted quantitative analyses. As a model compound for these developments, ulixertinib, an inhibitor of extracellular signal-regulated kinase (ERK) 1 and 2 was used. MDPI 2022-06-01 /pmc/articles/PMC9228120/ /pubmed/35745613 http://dx.doi.org/10.3390/ph15060694 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fresnais, Margaux
Liang, Siwen
Breitkopf, Marius
Lindner, Joshua Raoul
Claude, Emmanuelle
Pringle, Steven
Levkin, Pavel A.
Demir, Konstantin
Benzel, Julia
Sundheimer, Julia
Statz, Britta
Pajtler, Kristian W.
Pfister, Stefan M.
Haefeli, Walter E.
Burhenne, Jürgen
Longuespée, Rémi
Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title_full Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title_fullStr Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title_full_unstemmed Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title_short Analytical Performance Evaluation of New DESI Enhancements for Targeted Drug Quantification in Tissue Sections
title_sort analytical performance evaluation of new desi enhancements for targeted drug quantification in tissue sections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228120/
https://www.ncbi.nlm.nih.gov/pubmed/35745613
http://dx.doi.org/10.3390/ph15060694
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