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Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion

The intestinal transport of lamivudine, a nucleotide reverse transcriptase inhibitor, was investigated using the single pass intestinal perfusion technique in male Wistar rats. Single pass intestinal perfusion was performed in small intestine at a flow rate of 0.20 ml/min. Lamivudine exhibits a high...

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Detalles Bibliográficos
Autores principales: Patel, J. R., Barve, Kalyani H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660879/
https://www.ncbi.nlm.nih.gov/pubmed/23716881
http://dx.doi.org/10.4103/0250-474X.108441
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author Patel, J. R.
Barve, Kalyani H.
author_facet Patel, J. R.
Barve, Kalyani H.
author_sort Patel, J. R.
collection PubMed
description The intestinal transport of lamivudine, a nucleotide reverse transcriptase inhibitor, was investigated using the single pass intestinal perfusion technique in male Wistar rats. Single pass intestinal perfusion was performed in small intestine at a flow rate of 0.20 ml/min. Lamivudine exhibits a high intestinal permeability over the length of the small intestine indicative of compounds that are well absorbed. The P(eff) of lamivudine is in the range of drugs with high intestinal permeability and high fraction of dose absorbed indicating that lamivudine readily crosses the intestine. This also suggests that lamivudine belongs to biopharmaceutics classification system class I and is a good candidate for biopharmaceutics classification system based biowaiver. The permeability values obtained from this study may be useful in models of exposure assessment.
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spelling pubmed-36608792013-05-28 Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion Patel, J. R. Barve, Kalyani H. Indian J Pharm Sci Short Communication The intestinal transport of lamivudine, a nucleotide reverse transcriptase inhibitor, was investigated using the single pass intestinal perfusion technique in male Wistar rats. Single pass intestinal perfusion was performed in small intestine at a flow rate of 0.20 ml/min. Lamivudine exhibits a high intestinal permeability over the length of the small intestine indicative of compounds that are well absorbed. The P(eff) of lamivudine is in the range of drugs with high intestinal permeability and high fraction of dose absorbed indicating that lamivudine readily crosses the intestine. This also suggests that lamivudine belongs to biopharmaceutics classification system class I and is a good candidate for biopharmaceutics classification system based biowaiver. The permeability values obtained from this study may be useful in models of exposure assessment. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3660879/ /pubmed/23716881 http://dx.doi.org/10.4103/0250-474X.108441 Text en Copyright: © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Patel, J. R.
Barve, Kalyani H.
Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title_full Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title_fullStr Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title_full_unstemmed Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title_short Intestinal Permeability of Lamivudine Using Single Pass Intestinal Perfusion
title_sort intestinal permeability of lamivudine using single pass intestinal perfusion
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660879/
https://www.ncbi.nlm.nih.gov/pubmed/23716881
http://dx.doi.org/10.4103/0250-474X.108441
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