Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79834
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dc.contributor.authorLee, Wei Lien
dc.contributor.authorShi, Wenxiongen
dc.contributor.authorLow, Zheng Yangen
dc.contributor.authorLi, Shuzhouen
dc.contributor.authorLoo, Say Chye Joachimen
dc.date.accessioned2013-10-31T00:57:38Zen
dc.date.accessioned2019-12-06T13:35:00Z-
dc.date.available2013-10-31T00:57:38Zen
dc.date.available2019-12-06T13:35:00Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationLee, W. L., Shi, W., Low, Z. Y., Li, S., & Loo, S. C. J. (2012). Modeling of drug release from biodegradable triple-layered microparticles. Journal of biomedical materials research part A, 100A(12), 3353-3362.en
dc.identifier.issn1549-3296en
dc.identifier.urihttps://hdl.handle.net/10356/79834-
dc.description.abstractNumerous models that predict drug release from nonerodible reservoir-membrane sphere systems have been presented. Most of these models cater only to a phase of drug release from a constant reservoir. All these models, however, are not applicable to drug release from biodegradable triple-layered microparticle system, in which the drug-loaded core (reservoir) is surrounded by nondrug holding outer layers (membrane). In this article, a mathematical model was developed for ibuprofen release from degradable triple-layered microparticles made of poly(D,L-lactide-co-glycolide, 50:50) (PLGA), poly(L-lactide) (PLLA), and poly(ethylene-co-vinyl acetate, 40 wt % vinyl acetate) (EVA), where ibuprofen was localized within the nonconstant reservoir (EVA core). The model postulated that the drug release through the bulk-degrading PLLA and PLGA layers consisted of two mechanisms: simple diffusional release followed by a degradation-controlled release through a rate-limiting membrane. The proposed model showed very good match with the experimental data of release from microparticles of various layer thicknesses and particle sizes. The underlying drug release mechanisms are dictated by three parameters determined by the model, including constant characteristic of diffusion, end time point of simple diffusion-controlled release and partition coefficient of drug. The presented model is effective for understanding the drug release mechanisms and for the design of this type of dosage form.en
dc.language.isoenen
dc.relation.ispartofseriesJournal of biomedical materials research part Aen
dc.rights© 2012 Wiley Periodicals, Inc. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of biomedical materials research part A, Wiley Periodicals, Inc. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: http://dx.doi.org/10.1002/jbm.a.34292].en
dc.subjectDRNTU::Engineering::Materialsen
dc.titleModeling of drug release from biodegradable triple-layered microparticlesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Materials Science & Engineeringen
dc.identifier.doi10.1002/jbm.a.34292en
dc.description.versionAccepted versionen
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item.grantfulltextopen-
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