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pubmed-article:16052542pubmed:abstractTextAddition of biodegradable polymer shells surrounding polymeric, drug-loaded microparticles offers the opportunity to control drug release rates. A novel fabrication method was used to produce microparticles with precise control of particle diameter and the thickness of the polymer shell. The effect of shell thickness on release of a model drug, piroxicam, has been clearly shown for 2- to 15-microm thick shells of poly(D,L-lactide) (PDLL) surrounding a poly(D,L-lactide-co-glycolide) (PLG) core and compared to pure PLG microspheres loaded with piroxicam. Furthermore, the core-shell microparticles are compared to microspheres containing blended polymers in the same mass ratios to demonstrate the importance of the core-shell morphology. Combining PDLL(PLG) microcapsules of different shell thicknesses allows nearly constant release rates to be attained for a period of 6 weeks.lld:pubmed
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pubmed-article:16052542pubmed:pagination2013-22lld:pubmed
pubmed-article:16052542pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:16052542pubmed:year2005lld:pubmed
pubmed-article:16052542pubmed:articleTitleSmall-molecule release from poly(D,L-lactide)/poly(D,L-lactide-co-glycolide) composite microparticles.lld:pubmed
pubmed-article:16052542pubmed:affiliationDepartment of Chemical and Biomolecular Engineering, University of Illinois, Urbana, Illinois, USA.lld:pubmed
pubmed-article:16052542pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16052542pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:16052542pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:16052542pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed