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Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS via a Modified Microfluidic Open Interface
[Image: see text] We present a modified microfluidic open interface (MOI) for the direct coupling of Bio-SPME to a liquid electron ionization-tandem mass spectrometry (LEI-MS/MS) system as a sensitive technique that can directly analyze biological samples without the need for sample cleanup or chrom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016190/ https://www.ncbi.nlm.nih.gov/pubmed/33213139 http://dx.doi.org/10.1021/jasms.0c00303 |
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author | Rocío-Bautista, Priscilla Famiglini, Giorgio Termopoli, Veronica Palma, Pierangela Nazdrajić, Emir Pawliszyn, Janusz Cappiello, Achille |
author_facet | Rocío-Bautista, Priscilla Famiglini, Giorgio Termopoli, Veronica Palma, Pierangela Nazdrajić, Emir Pawliszyn, Janusz Cappiello, Achille |
author_sort | Rocío-Bautista, Priscilla |
collection | PubMed |
description | [Image: see text] We present a modified microfluidic open interface (MOI) for the direct coupling of Bio-SPME to a liquid electron ionization-tandem mass spectrometry (LEI-MS/MS) system as a sensitive technique that can directly analyze biological samples without the need for sample cleanup or chromatographic separations as well as without measurable matrix effects (ME). We selected fentanyl as test compound. The method uses a C18 Bio-SPME fiber by direct immersion (DI) in urine and plasma and the subsequent quick desorption (1 min) in a flow-isolated volume (2.5 μL) filled with an internal standard–acetonitrile solution. The sample is then transferred to an EI source of a triple-quadrupole mass spectrometer via a LEI interface at a nanoscale flow rate. The desorption and analysis procedure requires less than 10 min. Up to 150 samples can be analyzed without observing a performance decline, with fentanyl quantitation at microgram-per-liter levels. The method workflow is extremely dependable, relatively fast, sustainable, and leads to reproducible results that enable the high-throughput screening of various biological samples. |
format | Online Article Text |
id | pubmed-8016190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80161902021-04-05 Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS via a Modified Microfluidic Open Interface Rocío-Bautista, Priscilla Famiglini, Giorgio Termopoli, Veronica Palma, Pierangela Nazdrajić, Emir Pawliszyn, Janusz Cappiello, Achille J Am Soc Mass Spectrom [Image: see text] We present a modified microfluidic open interface (MOI) for the direct coupling of Bio-SPME to a liquid electron ionization-tandem mass spectrometry (LEI-MS/MS) system as a sensitive technique that can directly analyze biological samples without the need for sample cleanup or chromatographic separations as well as without measurable matrix effects (ME). We selected fentanyl as test compound. The method uses a C18 Bio-SPME fiber by direct immersion (DI) in urine and plasma and the subsequent quick desorption (1 min) in a flow-isolated volume (2.5 μL) filled with an internal standard–acetonitrile solution. The sample is then transferred to an EI source of a triple-quadrupole mass spectrometer via a LEI interface at a nanoscale flow rate. The desorption and analysis procedure requires less than 10 min. Up to 150 samples can be analyzed without observing a performance decline, with fentanyl quantitation at microgram-per-liter levels. The method workflow is extremely dependable, relatively fast, sustainable, and leads to reproducible results that enable the high-throughput screening of various biological samples. American Chemical Society 2020-11-20 2021-01-06 /pmc/articles/PMC8016190/ /pubmed/33213139 http://dx.doi.org/10.1021/jasms.0c00303 Text en © 2020 American Society for Mass Spectrometry. Published by American Chemical Society. All rights reserved. Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Rocío-Bautista, Priscilla Famiglini, Giorgio Termopoli, Veronica Palma, Pierangela Nazdrajić, Emir Pawliszyn, Janusz Cappiello, Achille Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS via a Modified Microfluidic Open Interface |
title | Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS
via a Modified Microfluidic Open Interface |
title_full | Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS
via a Modified Microfluidic Open Interface |
title_fullStr | Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS
via a Modified Microfluidic Open Interface |
title_full_unstemmed | Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS
via a Modified Microfluidic Open Interface |
title_short | Direct Coupling of Bio-SPME to Liquid Electron Ionization-MS/MS
via a Modified Microfluidic Open Interface |
title_sort | direct coupling of bio-spme to liquid electron ionization-ms/ms
via a modified microfluidic open interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016190/ https://www.ncbi.nlm.nih.gov/pubmed/33213139 http://dx.doi.org/10.1021/jasms.0c00303 |
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