Publication
A poly(ε-caprolactone) device for sustained release of an anti-glaucoma drug
dc.contributor.author | Natu, Mădălina | |
dc.contributor.author | Gaspar, Manuel | |
dc.contributor.author | Ribeiro, Carlos | |
dc.contributor.author | Correia, Ilídio Joaquim Sobreira | |
dc.contributor.author | Silva, Daniela | |
dc.contributor.author | Sousa, Hermínio C. de | |
dc.contributor.author | Gil, Maria | |
dc.date.accessioned | 2018-03-19T10:49:11Z | |
dc.date.available | 2018-03-19T10:49:11Z | |
dc.date.issued | 2011-02-04 | |
dc.description.abstract | Implantable dorzolamide-loaded discs were prepared by blending poly(ε-caprolactone), PCL, with poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide), Lu. By blending, crystallinity, water uptake and mass loss were modified relative to the pure polymers. Burst was diminished by coating the discs with a PCL shell. All samples presented burst release except PCL-coated samples that showed controlled release during 18 days. For PCL-coated samples, barrier control of diffusion coupled with partition control from the core slowed down the release, while for 50/50 Lu/PCL-coated samples, the enhancement in the porosity of the core diminished partition control of drug release. Nonlinear regression analysis suggested that a degradation model fully describes the release curve considering a triphasic release mechanism: the instantaneous diffusion (burst), diffusion and polymer degradation stages. The MTT test indicated that the materials are not cytotoxic for corneal endothelial cells. A good in vitro–in vivo correlation was obtained, with similar amounts of drug released in vitro and in vivo. The discs decreased intraocular pressure (IOP) in normotensive rabbit eyes by 13.0% during 10 days for PCL-coated and by 13.0% during 4 days for 50/50 Lu/PCL-coated samples. The percentages of IOP decrease are similar to those obtained by dorzolamide eyedrop instillation (11.0%). | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Natu, M.V., Gaspar, M.N., Ribeiro, C.A., Correia, I.J., Silva, D., de Sousa, H.C. e Gil, M.H. (2011) “A poly(ε-caprolactone) device for sustained release of an anti-glaucoma drug”, Biomedical Materials, Vol. 6(2): 025003 | pt_PT |
dc.identifier.doi | 10.1088/1748-6041/6/2/025003 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.6/4629 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | IOPSCIENCE | pt_PT |
dc.relation | INTRAOCULAR CONTROLLED RELEASE SYSTEM FOR OPTHALMOLOGIC APPLICATIONS | |
dc.relation | ESTUDOS ESTRUTURAIS, MECANÍSTICOS E FUNCIONAIS DE CANAIS DE CÁLCIO MEMBRANARES | |
dc.relation.publisherversion | http://iopscience.iop.org/article/10.1088/1748-6041/6/2/025003 | pt_PT |
dc.subject | PCL | pt_PT |
dc.subject | Anti-glaucoma | pt_PT |
dc.subject | Sustained release | pt_PT |
dc.title | A poly(ε-caprolactone) device for sustained release of an anti-glaucoma drug | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.awardTitle | INTRAOCULAR CONTROLLED RELEASE SYSTEM FOR OPTHALMOLOGIC APPLICATIONS | |
oaire.awardTitle | ESTUDOS ESTRUTURAIS, MECANÍSTICOS E FUNCIONAIS DE CANAIS DE CÁLCIO MEMBRANARES | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/POSI/SFRH%2FBD%2F30198%2F2006/PT | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT//SFRH%2FBPD%2F19776%2F2004/PT | |
oaire.citation.startPage | 025003 | pt_PT |
oaire.citation.title | Biomedical Materials | pt_PT |
oaire.citation.volume | 6 | pt_PT |
oaire.fundingStream | POSI | |
person.familyName | Fontes Ribeiro | |
person.familyName | Joaquim Sobreira Correia | |
person.familyName | Cipriano de Sousa | |
person.familyName | Gil | |
person.givenName | Carlos | |
person.givenName | Ilídio | |
person.givenName | Hermínio José | |
person.givenName | Maria Helena | |
person.identifier | UMbJ1KMAAAAJ | |
person.identifier | A-8783-2008 | |
person.identifier.ciencia-id | 2917-516B-C827 | |
person.identifier.ciencia-id | F610-7373-DC81 | |
person.identifier.ciencia-id | F61E-906D-549E | |
person.identifier.ciencia-id | 0E10-A6F7-901B | |
person.identifier.orcid | 0000-0002-9707-4895 | |
person.identifier.orcid | 0000-0003-1613-9675 | |
person.identifier.orcid | 0000-0002-2629-7805 | |
person.identifier.orcid | 0000-0003-0657-7751 | |
person.identifier.rid | B-7729-2018 | |
person.identifier.scopus-author-id | 6701724909 | |
person.identifier.scopus-author-id | 7003557499 | |
person.identifier.scopus-author-id | 57201225798 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
rcaap.embargofct | Copyright cedido à editora no momento da publicação | pt_PT |
rcaap.rights | closedAccess | pt_PT |
rcaap.type | article | pt_PT |
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