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The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers

PURPOSE: Currently, the FDA allows biowaivers for Class I (high solubility and high permeability) and Class III (high solubility and low permeability) compounds of the Biopharmaceutics Classification System (BCS). Scientific evidence should be provided to support biowaivers for BCS Class I and Class...

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Autores principales: Parr, Alan, Hidalgo, Ismael J., Bode, Chris, Brown, William, Yazdanian, Mehran, Gonzalez, Mario A., Sagawa, Kazuko, Miller, Kevin, Jiang, Wenlei, Stippler, Erika S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689772/
https://www.ncbi.nlm.nih.gov/pubmed/26286187
http://dx.doi.org/10.1007/s11095-015-1773-4
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author Parr, Alan
Hidalgo, Ismael J.
Bode, Chris
Brown, William
Yazdanian, Mehran
Gonzalez, Mario A.
Sagawa, Kazuko
Miller, Kevin
Jiang, Wenlei
Stippler, Erika S.
author_facet Parr, Alan
Hidalgo, Ismael J.
Bode, Chris
Brown, William
Yazdanian, Mehran
Gonzalez, Mario A.
Sagawa, Kazuko
Miller, Kevin
Jiang, Wenlei
Stippler, Erika S.
author_sort Parr, Alan
collection PubMed
description PURPOSE: Currently, the FDA allows biowaivers for Class I (high solubility and high permeability) and Class III (high solubility and low permeability) compounds of the Biopharmaceutics Classification System (BCS). Scientific evidence should be provided to support biowaivers for BCS Class I and Class III (high solubility and low permeability) compounds. METHODS: Data on the effects of excipients on drug permeability are needed to demonstrate that commonly used excipients do not affect the permeability of BCS Class III compounds, which would support the application of biowaivers to Class III compounds. This study was designed to generate such data by assessing the permeability of four BCS Class III compounds and one Class I compound in the presence and absence of five commonly used excipients. RESULTS: The permeability of each of the compounds was assessed, at three to five concentrations, with each excipient in two different models: Caco-2 cell monolayers, and in situ rat intestinal perfusion. No substantial increases in the permeability of any of the compounds were observed in the presence of any of the tested excipients in either of the models, with the exception of disruption of Caco-2 cell monolayer integrity by sodium lauryl sulfate at 0.1 mg/ml and higher. CONCLUSION: The results suggest that the absorption of these four BCS Class III compounds would not be greatly affected by the tested excipients. This may have implications in supporting biowaivers for BCS Class III compounds in general.
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spelling pubmed-46897722015-12-31 The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers Parr, Alan Hidalgo, Ismael J. Bode, Chris Brown, William Yazdanian, Mehran Gonzalez, Mario A. Sagawa, Kazuko Miller, Kevin Jiang, Wenlei Stippler, Erika S. Pharm Res Research Paper PURPOSE: Currently, the FDA allows biowaivers for Class I (high solubility and high permeability) and Class III (high solubility and low permeability) compounds of the Biopharmaceutics Classification System (BCS). Scientific evidence should be provided to support biowaivers for BCS Class I and Class III (high solubility and low permeability) compounds. METHODS: Data on the effects of excipients on drug permeability are needed to demonstrate that commonly used excipients do not affect the permeability of BCS Class III compounds, which would support the application of biowaivers to Class III compounds. This study was designed to generate such data by assessing the permeability of four BCS Class III compounds and one Class I compound in the presence and absence of five commonly used excipients. RESULTS: The permeability of each of the compounds was assessed, at three to five concentrations, with each excipient in two different models: Caco-2 cell monolayers, and in situ rat intestinal perfusion. No substantial increases in the permeability of any of the compounds were observed in the presence of any of the tested excipients in either of the models, with the exception of disruption of Caco-2 cell monolayer integrity by sodium lauryl sulfate at 0.1 mg/ml and higher. CONCLUSION: The results suggest that the absorption of these four BCS Class III compounds would not be greatly affected by the tested excipients. This may have implications in supporting biowaivers for BCS Class III compounds in general. Springer US 2015-08-19 2016 /pmc/articles/PMC4689772/ /pubmed/26286187 http://dx.doi.org/10.1007/s11095-015-1773-4 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Paper
Parr, Alan
Hidalgo, Ismael J.
Bode, Chris
Brown, William
Yazdanian, Mehran
Gonzalez, Mario A.
Sagawa, Kazuko
Miller, Kevin
Jiang, Wenlei
Stippler, Erika S.
The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title_full The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title_fullStr The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title_full_unstemmed The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title_short The Effect of Excipients on the Permeability of BCS Class III Compounds and Implications for Biowaivers
title_sort effect of excipients on the permeability of bcs class iii compounds and implications for biowaivers
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689772/
https://www.ncbi.nlm.nih.gov/pubmed/26286187
http://dx.doi.org/10.1007/s11095-015-1773-4
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