Cargando…

In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410

The aim of this study was to investigate the physicochemical and in vitro/ex vivo characteristics of the pyrmidinedione IQP-0410 formulated into transdermal films. IQP-0410 is a potent therapeutic anti-HIV nonnucleoside reverse transcriptase inhibitor that would be subjected to extensive first pass...

Descripción completa

Detalles Bibliográficos
Autores principales: Ham, Anthony S., Lustig, William, Yang, Lu, Boczar, Ashlee, Buckheit, Karen W., Buckheit Jr, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776786/
https://www.ncbi.nlm.nih.gov/pubmed/24058672
http://dx.doi.org/10.1371/journal.pone.0075306
_version_ 1782284883298615296
author Ham, Anthony S.
Lustig, William
Yang, Lu
Boczar, Ashlee
Buckheit, Karen W.
Buckheit Jr, Robert W.
author_facet Ham, Anthony S.
Lustig, William
Yang, Lu
Boczar, Ashlee
Buckheit, Karen W.
Buckheit Jr, Robert W.
author_sort Ham, Anthony S.
collection PubMed
description The aim of this study was to investigate the physicochemical and in vitro/ex vivo characteristics of the pyrmidinedione IQP-0410 formulated into transdermal films. IQP-0410 is a potent therapeutic anti-HIV nonnucleoside reverse transcriptase inhibitor that would be subjected to extensive first pass metabolism, through conventional oral administration. Therefore, IQP-0410 was formulated into ethyl cellulose/HPMC-based transdermal films via solvent casting. In mano evaluations were performed to evaluate gross physical characteristics. In vitro release studies were performed in both Franz cells and USP-4 dissolution vessels. Ex vivo release and permeability assays were performed on human epidermal tissue models, and the permeated IQP-0410 was collected for in vitro HIV-1 efficacy assays in CEM-SS cells and PBMCs. Film formulation D3 resulted in pliable, strong transdermal films that were loaded with 2% (w/w) IQP-0410. Composed of 60% (w/w) ethyl cellulose and 20% (w/w) HPMC, the films contained < 1.2% (w/w) of water and were hygroscopic resulting in significant swelling under humid conditions. The water permeable nature of the film resulted in complete in vitro dissolution and drug release in 26 hours. When applied to ex vivo epidermal tissues, the films were non-toxic to the tissue and also were non-toxic to HIV target cells used in the in vitro efficacy assays. Over a 3 day application, the films delivered IQP-0410 through the skin tissue at a zero-order rate of 0.94 ± 0.06 µg/cm(2)/hr with 134 ± 14.7 µM collected in the basal media. The delivered IQP-0410 resulted in in vitro EC(50) values against HIV-1 of 2.56 ± 0.40 nM (CEM-SS) and 0.58 ± 0.03 nM (PBMC). The film formulation demonstrated no significant deviation from target values when packaged in foil pouches under standard and accelerated environmental conditions. It was concluded that the transdermal film formulation was a potentially viable method of administering IQP-0410 that warrants further development.
format Online
Article
Text
id pubmed-3776786
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37767862013-09-20 In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410 Ham, Anthony S. Lustig, William Yang, Lu Boczar, Ashlee Buckheit, Karen W. Buckheit Jr, Robert W. PLoS One Research Article The aim of this study was to investigate the physicochemical and in vitro/ex vivo characteristics of the pyrmidinedione IQP-0410 formulated into transdermal films. IQP-0410 is a potent therapeutic anti-HIV nonnucleoside reverse transcriptase inhibitor that would be subjected to extensive first pass metabolism, through conventional oral administration. Therefore, IQP-0410 was formulated into ethyl cellulose/HPMC-based transdermal films via solvent casting. In mano evaluations were performed to evaluate gross physical characteristics. In vitro release studies were performed in both Franz cells and USP-4 dissolution vessels. Ex vivo release and permeability assays were performed on human epidermal tissue models, and the permeated IQP-0410 was collected for in vitro HIV-1 efficacy assays in CEM-SS cells and PBMCs. Film formulation D3 resulted in pliable, strong transdermal films that were loaded with 2% (w/w) IQP-0410. Composed of 60% (w/w) ethyl cellulose and 20% (w/w) HPMC, the films contained < 1.2% (w/w) of water and were hygroscopic resulting in significant swelling under humid conditions. The water permeable nature of the film resulted in complete in vitro dissolution and drug release in 26 hours. When applied to ex vivo epidermal tissues, the films were non-toxic to the tissue and also were non-toxic to HIV target cells used in the in vitro efficacy assays. Over a 3 day application, the films delivered IQP-0410 through the skin tissue at a zero-order rate of 0.94 ± 0.06 µg/cm(2)/hr with 134 ± 14.7 µM collected in the basal media. The delivered IQP-0410 resulted in in vitro EC(50) values against HIV-1 of 2.56 ± 0.40 nM (CEM-SS) and 0.58 ± 0.03 nM (PBMC). The film formulation demonstrated no significant deviation from target values when packaged in foil pouches under standard and accelerated environmental conditions. It was concluded that the transdermal film formulation was a potentially viable method of administering IQP-0410 that warrants further development. Public Library of Science 2013-09-18 /pmc/articles/PMC3776786/ /pubmed/24058672 http://dx.doi.org/10.1371/journal.pone.0075306 Text en © 2013 Ham et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Ham, Anthony S.
Lustig, William
Yang, Lu
Boczar, Ashlee
Buckheit, Karen W.
Buckheit Jr, Robert W.
In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title_full In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title_fullStr In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title_full_unstemmed In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title_short In Vitro and Ex Vivo Evaluations on Transdermal Delivery of the HIV Inhibitor IQP-0410
title_sort in vitro and ex vivo evaluations on transdermal delivery of the hiv inhibitor iqp-0410
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776786/
https://www.ncbi.nlm.nih.gov/pubmed/24058672
http://dx.doi.org/10.1371/journal.pone.0075306
work_keys_str_mv AT hamanthonys invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410
AT lustigwilliam invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410
AT yanglu invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410
AT boczarashlee invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410
AT buckheitkarenw invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410
AT buckheitjrrobertw invitroandexvivoevaluationsontransdermaldeliveryofthehivinhibitoriqp0410