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In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin

Aim of this investigation was to study the in vivo and in vitro drug interaction of glimepride with atorvastatin and rosuvastatin. In vitro drug interaction of glimepride with atorvastatin and rosuvastatin was studied using human pooled liver microsomes and evaluated using high performance liquid ch...

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Detalles Bibliográficos
Autores principales: Galani, VJ, Vyas, M
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021697/
https://www.ncbi.nlm.nih.gov/pubmed/21264125
http://dx.doi.org/10.4103/0975-1483.63169
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author Galani, VJ
Vyas, M
author_facet Galani, VJ
Vyas, M
author_sort Galani, VJ
collection PubMed
description Aim of this investigation was to study the in vivo and in vitro drug interaction of glimepride with atorvastatin and rosuvastatin. In vitro drug interaction of glimepride with atorvastatin and rosuvastatin was studied using human pooled liver microsomes and evaluated using high performance liquid chromatography. In vivo pharmacokinetic drug interaction of glimepride (6 mg/kg) in coadministration with atorvastatin (60 mg/kg) and rosuvastatin (60 mg/kg) were studied in rats and analyzed using liquid chromatography tandem mass spectrometry (LC–MS/MS). In in vitro study, atorvastatin decreased its own metabolism as well as the metabolism of glimepiride. Rosuvastatin coadministration with glimepride reduced the metabolism of glimepride and increased the metabolism of its own. In in vivo study, concentration in plasma, C(max), AUC((0–t)) and AUC((0–∞)) (area under the concentration-time curve, AUC) of glimepride was increased significantly in coadministration with atorvastatin whereas there was no significant change was observed in the case of coadministration with rosuvastatin. Half life (T(1/2)) and volume of distribution (V(d)) of glimepride decreased significantly with both atorvastatin and rosuvastatin. Elimination rate constant, K(el) of glimepride increased significantly with both atorvastatin and rosuvastatin. Clearance (Cl) of glimepride decreased significantly but the decrease was more with atorvastatin than with rosuvastatin. It is concluded that glimepride metabolism is little affected by rosuvastatin in vitro, which agreed with the negligible interaction in in vivo study. Thus, from safety point of view rosuvastatin is better to prescribe as a coadministration therapy with glimepiride. On the other hand, atorvastatin could cause an increase in the bioavailability of glimepride per oral and also significantly decrease the metabolism of glimerpride in in vitro study. This may pose a positive implication in clinical practice.
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spelling pubmed-30216972011-01-24 In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin Galani, VJ Vyas, M J Young Pharm Pharmacy Practice Aim of this investigation was to study the in vivo and in vitro drug interaction of glimepride with atorvastatin and rosuvastatin. In vitro drug interaction of glimepride with atorvastatin and rosuvastatin was studied using human pooled liver microsomes and evaluated using high performance liquid chromatography. In vivo pharmacokinetic drug interaction of glimepride (6 mg/kg) in coadministration with atorvastatin (60 mg/kg) and rosuvastatin (60 mg/kg) were studied in rats and analyzed using liquid chromatography tandem mass spectrometry (LC–MS/MS). In in vitro study, atorvastatin decreased its own metabolism as well as the metabolism of glimepiride. Rosuvastatin coadministration with glimepride reduced the metabolism of glimepride and increased the metabolism of its own. In in vivo study, concentration in plasma, C(max), AUC((0–t)) and AUC((0–∞)) (area under the concentration-time curve, AUC) of glimepride was increased significantly in coadministration with atorvastatin whereas there was no significant change was observed in the case of coadministration with rosuvastatin. Half life (T(1/2)) and volume of distribution (V(d)) of glimepride decreased significantly with both atorvastatin and rosuvastatin. Elimination rate constant, K(el) of glimepride increased significantly with both atorvastatin and rosuvastatin. Clearance (Cl) of glimepride decreased significantly but the decrease was more with atorvastatin than with rosuvastatin. It is concluded that glimepride metabolism is little affected by rosuvastatin in vitro, which agreed with the negligible interaction in in vivo study. Thus, from safety point of view rosuvastatin is better to prescribe as a coadministration therapy with glimepiride. On the other hand, atorvastatin could cause an increase in the bioavailability of glimepride per oral and also significantly decrease the metabolism of glimerpride in in vitro study. This may pose a positive implication in clinical practice. Medknow Publications 2010 /pmc/articles/PMC3021697/ /pubmed/21264125 http://dx.doi.org/10.4103/0975-1483.63169 Text en © Journal of Young Pharmacists http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Pharmacy Practice
Galani, VJ
Vyas, M
In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title_full In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title_fullStr In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title_full_unstemmed In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title_short In vivo and In vitro Drug Interactions Study of Glimepride with Atorvastatin and Rosuvastatin
title_sort in vivo and in vitro drug interactions study of glimepride with atorvastatin and rosuvastatin
topic Pharmacy Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021697/
https://www.ncbi.nlm.nih.gov/pubmed/21264125
http://dx.doi.org/10.4103/0975-1483.63169
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