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Targeted Drug and Metabolite Imaging: Desorption Electrospray Ionization Combined with Triple Quadrupole Mass Spectrometry
[Image: see text] Mass spectrometry imaging (MSI) has proven to be a valuable tool for drug and metabolite imaging in pharmaceutical toxicology studies and can reveal, for example, accumulation of drug candidates in early drug development. However, the lack of sample cleanup and chromatographic sepa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256344/ https://www.ncbi.nlm.nih.gov/pubmed/30346139 http://dx.doi.org/10.1021/acs.analchem.8b03857 |
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author | Lamont, Lieke Eijkel, Gert B. Jones, Emrys A. Flinders, Bryn Ellis, Shane R. Porta Siegel, Tiffany Heeren, Ron M.A. Vreeken, Rob J. |
author_facet | Lamont, Lieke Eijkel, Gert B. Jones, Emrys A. Flinders, Bryn Ellis, Shane R. Porta Siegel, Tiffany Heeren, Ron M.A. Vreeken, Rob J. |
author_sort | Lamont, Lieke |
collection | PubMed |
description | [Image: see text] Mass spectrometry imaging (MSI) has proven to be a valuable tool for drug and metabolite imaging in pharmaceutical toxicology studies and can reveal, for example, accumulation of drug candidates in early drug development. However, the lack of sample cleanup and chromatographic separation can hamper the analysis due to isobaric interferences. Multiple reaction monitoring (MRM) uses unique precursor ion-product ion transitions to add specificity which leads to higher selectivity. Here, we present a targeted imaging platform where desorption electrospray ionization is combined with a triple quadrupole (QqQ) system to perform MRM imaging. The platform was applied to visualize (i) lipids in mouse brain tissue sections and (ii) a drug candidate and metabolite in canine liver tissue. All QqQ modes were investigated to show the increased detection time provided by MRM as well as the possibility to perform dual polarity imaging. This is very beneficial for lipid imaging because some phospholipid classes ionize in opposite polarity (e.g., phosphatidylcholine/sphingomyelin in positive ion mode and phosphatidylserine/phosphatidylethanolamine in negative ion mode). Drug and metabolite images were obtained to show its strength in drug distribution studies. Multiple MRM transitions were used to confirm the local presence and selective detection of pharmaceutical compounds. |
format | Online Article Text |
id | pubmed-6256344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62563442018-11-29 Targeted Drug and Metabolite Imaging: Desorption Electrospray Ionization Combined with Triple Quadrupole Mass Spectrometry Lamont, Lieke Eijkel, Gert B. Jones, Emrys A. Flinders, Bryn Ellis, Shane R. Porta Siegel, Tiffany Heeren, Ron M.A. Vreeken, Rob J. Anal Chem [Image: see text] Mass spectrometry imaging (MSI) has proven to be a valuable tool for drug and metabolite imaging in pharmaceutical toxicology studies and can reveal, for example, accumulation of drug candidates in early drug development. However, the lack of sample cleanup and chromatographic separation can hamper the analysis due to isobaric interferences. Multiple reaction monitoring (MRM) uses unique precursor ion-product ion transitions to add specificity which leads to higher selectivity. Here, we present a targeted imaging platform where desorption electrospray ionization is combined with a triple quadrupole (QqQ) system to perform MRM imaging. The platform was applied to visualize (i) lipids in mouse brain tissue sections and (ii) a drug candidate and metabolite in canine liver tissue. All QqQ modes were investigated to show the increased detection time provided by MRM as well as the possibility to perform dual polarity imaging. This is very beneficial for lipid imaging because some phospholipid classes ionize in opposite polarity (e.g., phosphatidylcholine/sphingomyelin in positive ion mode and phosphatidylserine/phosphatidylethanolamine in negative ion mode). Drug and metabolite images were obtained to show its strength in drug distribution studies. Multiple MRM transitions were used to confirm the local presence and selective detection of pharmaceutical compounds. American Chemical Society 2018-10-22 2018-11-20 /pmc/articles/PMC6256344/ /pubmed/30346139 http://dx.doi.org/10.1021/acs.analchem.8b03857 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Lamont, Lieke Eijkel, Gert B. Jones, Emrys A. Flinders, Bryn Ellis, Shane R. Porta Siegel, Tiffany Heeren, Ron M.A. Vreeken, Rob J. Targeted Drug and Metabolite Imaging: Desorption Electrospray Ionization Combined with Triple Quadrupole Mass Spectrometry |
title | Targeted Drug and Metabolite Imaging: Desorption Electrospray
Ionization Combined with Triple Quadrupole Mass Spectrometry |
title_full | Targeted Drug and Metabolite Imaging: Desorption Electrospray
Ionization Combined with Triple Quadrupole Mass Spectrometry |
title_fullStr | Targeted Drug and Metabolite Imaging: Desorption Electrospray
Ionization Combined with Triple Quadrupole Mass Spectrometry |
title_full_unstemmed | Targeted Drug and Metabolite Imaging: Desorption Electrospray
Ionization Combined with Triple Quadrupole Mass Spectrometry |
title_short | Targeted Drug and Metabolite Imaging: Desorption Electrospray
Ionization Combined with Triple Quadrupole Mass Spectrometry |
title_sort | targeted drug and metabolite imaging: desorption electrospray
ionization combined with triple quadrupole mass spectrometry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256344/ https://www.ncbi.nlm.nih.gov/pubmed/30346139 http://dx.doi.org/10.1021/acs.analchem.8b03857 |
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