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Simple Fabrication Method for a Porous Poly(vinyl alcohol) Matrix by Multisolvent Mixtures for an Air-Exposed Model of the Lung Epithelial System

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dc.contributor.authorChae, Su-Kyoung-
dc.contributor.authorMun, Cho Hay-
dc.contributor.authorNoh, Da-Yoon-
dc.contributor.authorKong, Edward-
dc.contributor.authorLee, Sang-Hoon-
dc.date.accessioned2021-09-05T03:57:51Z-
dc.date.available2021-09-05T03:57:51Z-
dc.date.created2021-06-15-
dc.date.issued2014-10-21-
dc.identifier.issn0743-7463-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/97073-
dc.description.abstractWe introduce a simple and easy method for fabricating a thin and porous matrix that can be used as an extracellular matrix (ECM). A porous poly(vinyl alcohol) (PVA) matrix was created through recrystallization by multiple solvents under distilled water (DW), isopropyl alcohol (IPA), and a combination of DW and IPA. The crysatllization was driven by precipitating and dissolving a solute in a solution of a solvent and a nonsolvent, which induced the formation of microspheres in the IPA. The crystal structure depended on the ratio of the solvent/nonsolvent and the concentration of the PVA aqueous solution; these properties were used to tune the thickness, size, and porosity of the matrices. The resulting PVA matrix was chemically stabilized through a reaction with glutaraldehyde in the IPA solution. We demonstrated that a very thin and porous PVA matrix provided an effective functional model of the lung epithelial system. Lung epithelial cells (A549) displayed a high affinity for this matrix, which was permeable to the culture medium. These properties facilitated culturing under the air environment.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectOSTEOGENIC DIFFERENTIATION-
dc.subjectSTEM-CELLS-
dc.subjectIN-VITRO-
dc.subjectSCAFFOLDS-
dc.subjectPOROSITY-
dc.subjectPROLIFERATION-
dc.subjectHYDROGELS-
dc.subjectMEMBRANE-
dc.subjectFIBERS-
dc.subjectSCALE-
dc.titleSimple Fabrication Method for a Porous Poly(vinyl alcohol) Matrix by Multisolvent Mixtures for an Air-Exposed Model of the Lung Epithelial System-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Sang-Hoon-
dc.identifier.doi10.1021/la501453h-
dc.identifier.scopusid2-s2.0-84908072322-
dc.identifier.wosid000343638800001-
dc.identifier.bibliographicCitationLANGMUIR, v.30, no.41, pp.12107 - 12113-
dc.relation.isPartOfLANGMUIR-
dc.citation.titleLANGMUIR-
dc.citation.volume30-
dc.citation.number41-
dc.citation.startPage12107-
dc.citation.endPage12113-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusOSTEOGENIC DIFFERENTIATION-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordPlusPOROSITY-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusHYDROGELS-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusFIBERS-
dc.subject.keywordPlusSCALE-
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