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Fabrication of drug-loaded polymer microparticles with arbitrary geometries using a piezoelectric inkjet printing system

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dc.contributor.authorLee, Byung Kook-
dc.contributor.authorYun, Yeon Hee-
dc.contributor.authorChoi, Ji Suk-
dc.contributor.authorChoi, Young Chan-
dc.contributor.authorKim, Jae Dong-
dc.contributor.authorCho, Yong Woo-
dc.date.accessioned2021-06-23T07:39:50Z-
dc.date.available2021-06-23T07:39:50Z-
dc.date.created2021-01-21-
dc.date.issued2012-05-
dc.identifier.issn0378-5173-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/33004-
dc.description.abstractCarrier geometry is a key parameter of drug delivery systems and has significant impact on the drug release rate and interaction with cells and tissues. Here we present a piezoelectric inkjet printing system as a simple and convenient approach for fabrication of drug-loaded polymer microparticles with well-defined and controlled shapes. The physical properties of paclitaxel (PTX)-loaded poly(lactic-co-glycolic acid) (PLGA) inks, such as volatility, viscosity and surface tension, were optimized for piezoelectric inkjet printing, and PTX-loaded PLGA microparticles were fabricated with various geometries, such as circles, grids, honeycombs, and rings. The resulting microparticles with 10% (w/w) PTX exhibited a fairly homogeneous shape and size. The microparticle fabrication by piezoelectric inkjet printing was precise, reproducible, and highly favorable for mass production. The microparticles exhibited a biphasic release profile with an initial burst due to diffusion and a subsequent, slow second phase due to degradation of PLGA. The release rate was dependent on the geometry, mainly the surface area, with a descending rate order of honeycomb > grid, ring > circle. The PTX-loaded microparticles showed a comparable activity in inhibiting the growth of HeLa cells. Our results demonstrate that a piezoelectric inkjet printing system would provide a new approach for large-scale manufacturing of drug carriers with a desired geometry. (C) 2012 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titleFabrication of drug-loaded polymer microparticles with arbitrary geometries using a piezoelectric inkjet printing system-
dc.typeArticle-
dc.contributor.affiliatedAuthorCho, Yong Woo-
dc.identifier.doi10.1016/j.ijpharm.2012.02.011-
dc.identifier.scopusid2-s2.0-84862831272-
dc.identifier.wosid000302364500021-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.427, no.2, pp.305 - 310-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume427-
dc.citation.number2-
dc.citation.startPage305-
dc.citation.endPage310-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusMICROSPHERES-
dc.subject.keywordPlusPARTICLES-
dc.subject.keywordPlusDEVICES-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusSHAPE-
dc.subject.keywordPlusFLOW-
dc.subject.keywordPlusLITHOGRAPHY-
dc.subject.keywordPlusMICROSCALE-
dc.subject.keywordAuthorInkjet printing-
dc.subject.keywordAuthorMicroparticles-
dc.subject.keywordAuthorGeometry-
dc.subject.keywordAuthorDrug release-
dc.subject.keywordAuthorIn vitro cytotoxicity-
dc.identifier.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0378517312001445-
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ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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