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Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds

PURPOSE: To examine the utility of human plasma as an assay medium in Caco-2 permeability studies to overcome poor mass balance and inadequate sink conditions frequently encountered with lipophilic compounds. METHODS: Caco-2 permeability was assessed for reference compounds with known transport mech...

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Autores principales: Katneni, Kasiram, Pham, Thao, Saunders, Jessica, Chen, Gong, Patil, Rahul, White, Karen L., Abla, Nada, Chiu, Francis C. K., Shackleford, David M., Charman, Susan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156755/
https://www.ncbi.nlm.nih.gov/pubmed/30225649
http://dx.doi.org/10.1007/s11095-018-2493-3
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author Katneni, Kasiram
Pham, Thao
Saunders, Jessica
Chen, Gong
Patil, Rahul
White, Karen L.
Abla, Nada
Chiu, Francis C. K.
Shackleford, David M.
Charman, Susan A.
author_facet Katneni, Kasiram
Pham, Thao
Saunders, Jessica
Chen, Gong
Patil, Rahul
White, Karen L.
Abla, Nada
Chiu, Francis C. K.
Shackleford, David M.
Charman, Susan A.
author_sort Katneni, Kasiram
collection PubMed
description PURPOSE: To examine the utility of human plasma as an assay medium in Caco-2 permeability studies to overcome poor mass balance and inadequate sink conditions frequently encountered with lipophilic compounds. METHODS: Caco-2 permeability was assessed for reference compounds with known transport mechanisms using either pH 7.4 buffer or human plasma as the assay medium in both the apical and basolateral chambers. When using plasma, P(app) values were corrected for the unbound fraction in the donor chamber. The utility of the approach was assessed by measuring the permeability of selected antimalarial compounds using the two assay media. RESULTS: Caco-2 cell monolayer integrity and P-gp transporter function were unaffected by the presence of human plasma in the donor and acceptor chambers. For many of the reference compounds having good mass balance with buffer as the medium, higher P(app) values were observed with plasma, likely due to improved acceptor sink conditions. The lipophilic antimalarial compounds exhibited low mass balance with buffer, however the use of plasma markedly improved mass balance allowing the determination of more reliable P(app) values. CONCLUSIONS: The results support the utility of human plasma as an alternate Caco-2 assay medium to improve mass balance and permeability measurements for lipophilic compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11095-018-2493-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-61567552018-10-10 Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds Katneni, Kasiram Pham, Thao Saunders, Jessica Chen, Gong Patil, Rahul White, Karen L. Abla, Nada Chiu, Francis C. K. Shackleford, David M. Charman, Susan A. Pharm Res Research Paper PURPOSE: To examine the utility of human plasma as an assay medium in Caco-2 permeability studies to overcome poor mass balance and inadequate sink conditions frequently encountered with lipophilic compounds. METHODS: Caco-2 permeability was assessed for reference compounds with known transport mechanisms using either pH 7.4 buffer or human plasma as the assay medium in both the apical and basolateral chambers. When using plasma, P(app) values were corrected for the unbound fraction in the donor chamber. The utility of the approach was assessed by measuring the permeability of selected antimalarial compounds using the two assay media. RESULTS: Caco-2 cell monolayer integrity and P-gp transporter function were unaffected by the presence of human plasma in the donor and acceptor chambers. For many of the reference compounds having good mass balance with buffer as the medium, higher P(app) values were observed with plasma, likely due to improved acceptor sink conditions. The lipophilic antimalarial compounds exhibited low mass balance with buffer, however the use of plasma markedly improved mass balance allowing the determination of more reliable P(app) values. CONCLUSIONS: The results support the utility of human plasma as an alternate Caco-2 assay medium to improve mass balance and permeability measurements for lipophilic compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11095-018-2493-3) contains supplementary material, which is available to authorized users. Springer US 2018-09-17 2018 /pmc/articles/PMC6156755/ /pubmed/30225649 http://dx.doi.org/10.1007/s11095-018-2493-3 Text en © The Author(s) 2018 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
Katneni, Kasiram
Pham, Thao
Saunders, Jessica
Chen, Gong
Patil, Rahul
White, Karen L.
Abla, Nada
Chiu, Francis C. K.
Shackleford, David M.
Charman, Susan A.
Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title_full Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title_fullStr Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title_full_unstemmed Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title_short Using Human Plasma as an Assay Medium in Caco-2 Studies Improves Mass Balance for Lipophilic Compounds
title_sort using human plasma as an assay medium in caco-2 studies improves mass balance for lipophilic compounds
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156755/
https://www.ncbi.nlm.nih.gov/pubmed/30225649
http://dx.doi.org/10.1007/s11095-018-2493-3
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