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Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion

Bibliographic Details
Main Author: Pimenta, A.F.R.
Publication Date: 2016
Other Authors: Ascenso, J., Fernandes, J.C.S., Colaço, R., Serro, A.P., Saramago, B.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.26/20037
Summary: Optimization of drug delivery from drug loaded contact lenses assumes understanding the drug transport mechanisms through hydrogels which relies on the knowledge of drug partition and diffusion coefficients. We chose, as model systems, two materials used in contact lens, a poly-hydroxyethylmethacrylate (pHEMA) based hydrogel and a silicone based hydrogel, and three drugs with different sizes and charges: chlorhexidine, levofloxacin and diclofenac. Equilibrium partition coefficients were determined at different ionic strength and pH, using water (pH 5.6) and PBS (pH 7.4). The measured partition coefficients were related with the polymer volume fraction in the hydrogel, through the introduction of an enhancement factor following the approach developed by the group of C. J. Radke (Kotsmar et al., 2012; Liu et al., 2013). This factor may be decomposed in the product of three other factors EHS, Eel and Ead which account for, respectively, hard-sphere size exclusion, electrostatic interactions, and specific solute adsorption. While EHS and Eel are close to 1, Ead > > 1 in all cases suggesting strong specific interactions between the drugs and the hydrogels. Adsorption was maximal for chlorhexidine on the silicone based hydrogel, in water, due to strong hydrogen bonding. The effective diffusion coefficients, De, were determined from the drug release profiles. Estimations of diffusion coefficients of the non-adsorbed solutes D = De × Ead allowed comparison with theories for solute diffusion in the absence of specific interaction with the polymeric membrane.
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spelling Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusionDrug releaseContact lensHydrogel membranePartition coefficientDiffusion coefficientOptimization of drug delivery from drug loaded contact lenses assumes understanding the drug transport mechanisms through hydrogels which relies on the knowledge of drug partition and diffusion coefficients. We chose, as model systems, two materials used in contact lens, a poly-hydroxyethylmethacrylate (pHEMA) based hydrogel and a silicone based hydrogel, and three drugs with different sizes and charges: chlorhexidine, levofloxacin and diclofenac. Equilibrium partition coefficients were determined at different ionic strength and pH, using water (pH 5.6) and PBS (pH 7.4). The measured partition coefficients were related with the polymer volume fraction in the hydrogel, through the introduction of an enhancement factor following the approach developed by the group of C. J. Radke (Kotsmar et al., 2012; Liu et al., 2013). This factor may be decomposed in the product of three other factors EHS, Eel and Ead which account for, respectively, hard-sphere size exclusion, electrostatic interactions, and specific solute adsorption. While EHS and Eel are close to 1, Ead > > 1 in all cases suggesting strong specific interactions between the drugs and the hydrogels. Adsorption was maximal for chlorhexidine on the silicone based hydrogel, in water, due to strong hydrogen bonding. The effective diffusion coefficients, De, were determined from the drug release profiles. Estimations of diffusion coefficients of the non-adsorbed solutes D = De × Ead allowed comparison with theories for solute diffusion in the absence of specific interaction with the polymeric membrane.ElsevierRepositório ComumPimenta, A.F.R.Ascenso, J.Fernandes, J.C.S.Colaço, R.Serro, A.P.Saramago, B.2018-01-10T12:55:31Z2016-122016-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.26/20037eng0378-517310.1016/j.ijpharm.2016.10.047info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-04-01T17:05:33Zoai:comum.rcaap.pt:10400.26/20037Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T04:48:05.942613Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
title Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
spellingShingle Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
Pimenta, A.F.R.
Drug release
Contact lens
Hydrogel membrane
Partition coefficient
Diffusion coefficient
title_short Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
title_full Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
title_fullStr Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
title_full_unstemmed Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
title_sort Controlled drug release from hydrogels for contact lenses: drug partitioning and diffusion
author Pimenta, A.F.R.
author_facet Pimenta, A.F.R.
Ascenso, J.
Fernandes, J.C.S.
Colaço, R.
Serro, A.P.
Saramago, B.
author_role author
author2 Ascenso, J.
Fernandes, J.C.S.
Colaço, R.
Serro, A.P.
Saramago, B.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Comum
dc.contributor.author.fl_str_mv Pimenta, A.F.R.
Ascenso, J.
Fernandes, J.C.S.
Colaço, R.
Serro, A.P.
Saramago, B.
dc.subject.por.fl_str_mv Drug release
Contact lens
Hydrogel membrane
Partition coefficient
Diffusion coefficient
topic Drug release
Contact lens
Hydrogel membrane
Partition coefficient
Diffusion coefficient
description Optimization of drug delivery from drug loaded contact lenses assumes understanding the drug transport mechanisms through hydrogels which relies on the knowledge of drug partition and diffusion coefficients. We chose, as model systems, two materials used in contact lens, a poly-hydroxyethylmethacrylate (pHEMA) based hydrogel and a silicone based hydrogel, and three drugs with different sizes and charges: chlorhexidine, levofloxacin and diclofenac. Equilibrium partition coefficients were determined at different ionic strength and pH, using water (pH 5.6) and PBS (pH 7.4). The measured partition coefficients were related with the polymer volume fraction in the hydrogel, through the introduction of an enhancement factor following the approach developed by the group of C. J. Radke (Kotsmar et al., 2012; Liu et al., 2013). This factor may be decomposed in the product of three other factors EHS, Eel and Ead which account for, respectively, hard-sphere size exclusion, electrostatic interactions, and specific solute adsorption. While EHS and Eel are close to 1, Ead > > 1 in all cases suggesting strong specific interactions between the drugs and the hydrogels. Adsorption was maximal for chlorhexidine on the silicone based hydrogel, in water, due to strong hydrogen bonding. The effective diffusion coefficients, De, were determined from the drug release profiles. Estimations of diffusion coefficients of the non-adsorbed solutes D = De × Ead allowed comparison with theories for solute diffusion in the absence of specific interaction with the polymeric membrane.
publishDate 2016
dc.date.none.fl_str_mv 2016-12
2016-12-01T00:00:00Z
2018-01-10T12:55:31Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.26/20037
url http://hdl.handle.net/10400.26/20037
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0378-5173
10.1016/j.ijpharm.2016.10.047
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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