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Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma
In this work a hydrophilic interaction liquid chromatography/positive ion electrospray mass spectrometric assay (HILIC/ESI-MS) has been developed and fully validated for the quantitation of metformin and rosuvastatin in human plasma. Sample preparation involved the use of 100 μL of human plasma, fol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100608/ https://www.ncbi.nlm.nih.gov/pubmed/29954074 http://dx.doi.org/10.3390/molecules23071548 |
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author | Antonopoulos, Nikolaos Machairas, Giorgos Migias, George Vonaparti, Ariadni Brakoulia, Vasiliki Pistos, Constantinos Gennimata, Dimitra Panderi, Irene |
author_facet | Antonopoulos, Nikolaos Machairas, Giorgos Migias, George Vonaparti, Ariadni Brakoulia, Vasiliki Pistos, Constantinos Gennimata, Dimitra Panderi, Irene |
author_sort | Antonopoulos, Nikolaos |
collection | PubMed |
description | In this work a hydrophilic interaction liquid chromatography/positive ion electrospray mass spectrometric assay (HILIC/ESI-MS) has been developed and fully validated for the quantitation of metformin and rosuvastatin in human plasma. Sample preparation involved the use of 100 μL of human plasma, following protein precipitation and filtration. Metformin, rosuvastatin and 4-[2-(propylamino) ethyl] indoline 2 one hydrochloride (internal standard) were separated by using an X-Bridge-HILIC BEH analytical column (150.0 × 2.1 mm i.d., particle size 3.5 μm) with isocratic elution. A mobile phase consisting of 12% (v/v) 15 mM ammonium formate water solution in acetonitrile was used for the separation and pumped at a flow rate of 0.25 mL min(−1). The linear range of the assay was 100 to 5000 ng mL(−1) and 2 to 100 ng mL(−1) for metformin and rosuvastatin, respectively. The current HILIC-ESI/MS method allows for the accurate and precise quantitation of metformin and rosuvastatin in human plasma with a simple sample preparation and a short a chromatographic run time (less than 15 min). Plasma samples from eight patients were further analysed proving the capability of the proposed method to support a wide range of clinical studies. |
format | Online Article Text |
id | pubmed-6100608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61006082018-11-13 Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma Antonopoulos, Nikolaos Machairas, Giorgos Migias, George Vonaparti, Ariadni Brakoulia, Vasiliki Pistos, Constantinos Gennimata, Dimitra Panderi, Irene Molecules Article In this work a hydrophilic interaction liquid chromatography/positive ion electrospray mass spectrometric assay (HILIC/ESI-MS) has been developed and fully validated for the quantitation of metformin and rosuvastatin in human plasma. Sample preparation involved the use of 100 μL of human plasma, following protein precipitation and filtration. Metformin, rosuvastatin and 4-[2-(propylamino) ethyl] indoline 2 one hydrochloride (internal standard) were separated by using an X-Bridge-HILIC BEH analytical column (150.0 × 2.1 mm i.d., particle size 3.5 μm) with isocratic elution. A mobile phase consisting of 12% (v/v) 15 mM ammonium formate water solution in acetonitrile was used for the separation and pumped at a flow rate of 0.25 mL min(−1). The linear range of the assay was 100 to 5000 ng mL(−1) and 2 to 100 ng mL(−1) for metformin and rosuvastatin, respectively. The current HILIC-ESI/MS method allows for the accurate and precise quantitation of metformin and rosuvastatin in human plasma with a simple sample preparation and a short a chromatographic run time (less than 15 min). Plasma samples from eight patients were further analysed proving the capability of the proposed method to support a wide range of clinical studies. MDPI 2018-06-27 /pmc/articles/PMC6100608/ /pubmed/29954074 http://dx.doi.org/10.3390/molecules23071548 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Antonopoulos, Nikolaos Machairas, Giorgos Migias, George Vonaparti, Ariadni Brakoulia, Vasiliki Pistos, Constantinos Gennimata, Dimitra Panderi, Irene Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title | Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title_full | Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title_fullStr | Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title_full_unstemmed | Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title_short | Hydrophilic Interaction Liquid Chromatography-Electrospray Ionization Mass Spectrometry for Therapeutic Drug Monitoring of Metformin and Rosuvastatin in Human Plasma |
title_sort | hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry for therapeutic drug monitoring of metformin and rosuvastatin in human plasma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100608/ https://www.ncbi.nlm.nih.gov/pubmed/29954074 http://dx.doi.org/10.3390/molecules23071548 |
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