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Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration
The gingiva is the target site for some topical drugs, but the permeability of human gingiva has not been systematically evaluated. Pigs are a common animal model for in vitro membrane transport studies. The objectives of this study were to: (a) determine the permeability coefficients of freshly exc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222406/ https://www.ncbi.nlm.nih.gov/pubmed/37242734 http://dx.doi.org/10.3390/pharmaceutics15051492 |
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author | Wanasathop, Apipa Choi, Hyojin Alex Nimmansophon, Patcharawan Murawsky, Michael Krishnan, Deepak G. Li, S. Kevin |
author_facet | Wanasathop, Apipa Choi, Hyojin Alex Nimmansophon, Patcharawan Murawsky, Michael Krishnan, Deepak G. Li, S. Kevin |
author_sort | Wanasathop, Apipa |
collection | PubMed |
description | The gingiva is the target site for some topical drugs, but the permeability of human gingiva has not been systematically evaluated. Pigs are a common animal model for in vitro membrane transport studies. The objectives of this study were to: (a) determine the permeability coefficients of freshly excised human gingiva using model permeants, (b) compare the permeability coefficients of fresh human gingiva with those of fresh porcine gingiva, (c) evaluate the effect of freezing duration on the permeability of porcine gingiva, and (d) compare the permeability coefficients of fresh and cadaver (frozen) human gingiva. A goal was to examine the feasibility of using porcine gingiva as a surrogate for human gingiva. The potential of using frozen tissues in permeability studies of gingiva was also examined. Fresh and frozen porcine gingiva, fresh human gingiva, and frozen cadaver human gingiva were compared in the transport study with model polar and lipophilic permeants. The fresh porcine and human tissues showed similarities in the “permeability coefficient vs. octanol–water distribution coefficient” relationship. The porcine gingiva had a lower permeability than that of the human, with a moderate correlation between the permeability of the fresh porcine and fresh human tissues. The permeability of the porcine tissues for the model polar permeants increased significantly after the tissues were frozen in storage. Moreover, the frozen human cadaver tissue could not be utilized due to the high and indiscriminating permeability of the tissue for the permeants and large tissue sample-to-sample variabilities. |
format | Online Article Text |
id | pubmed-10222406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102224062023-05-28 Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration Wanasathop, Apipa Choi, Hyojin Alex Nimmansophon, Patcharawan Murawsky, Michael Krishnan, Deepak G. Li, S. Kevin Pharmaceutics Article The gingiva is the target site for some topical drugs, but the permeability of human gingiva has not been systematically evaluated. Pigs are a common animal model for in vitro membrane transport studies. The objectives of this study were to: (a) determine the permeability coefficients of freshly excised human gingiva using model permeants, (b) compare the permeability coefficients of fresh human gingiva with those of fresh porcine gingiva, (c) evaluate the effect of freezing duration on the permeability of porcine gingiva, and (d) compare the permeability coefficients of fresh and cadaver (frozen) human gingiva. A goal was to examine the feasibility of using porcine gingiva as a surrogate for human gingiva. The potential of using frozen tissues in permeability studies of gingiva was also examined. Fresh and frozen porcine gingiva, fresh human gingiva, and frozen cadaver human gingiva were compared in the transport study with model polar and lipophilic permeants. The fresh porcine and human tissues showed similarities in the “permeability coefficient vs. octanol–water distribution coefficient” relationship. The porcine gingiva had a lower permeability than that of the human, with a moderate correlation between the permeability of the fresh porcine and fresh human tissues. The permeability of the porcine tissues for the model polar permeants increased significantly after the tissues were frozen in storage. Moreover, the frozen human cadaver tissue could not be utilized due to the high and indiscriminating permeability of the tissue for the permeants and large tissue sample-to-sample variabilities. MDPI 2023-05-13 /pmc/articles/PMC10222406/ /pubmed/37242734 http://dx.doi.org/10.3390/pharmaceutics15051492 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wanasathop, Apipa Choi, Hyojin Alex Nimmansophon, Patcharawan Murawsky, Michael Krishnan, Deepak G. Li, S. Kevin Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title | Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title_full | Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title_fullStr | Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title_full_unstemmed | Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title_short | Permeability of Fresh and Frozen Porcine and Human Gingiva and the Effect of Storage Duration |
title_sort | permeability of fresh and frozen porcine and human gingiva and the effect of storage duration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222406/ https://www.ncbi.nlm.nih.gov/pubmed/37242734 http://dx.doi.org/10.3390/pharmaceutics15051492 |
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