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Structure-Property Relationships of 3D-Printable Chain-Extended Block Copolymers with Tunable Elasticity and Biodegradability

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dc.contributor.authorKim, Ryung Il-
dc.contributor.authorLee, Geonchang-
dc.contributor.authorLee, Jung-Hyun-
dc.contributor.authorPark, Ji Jong-
dc.contributor.authorLee, Albert S.-
dc.contributor.authorHwang, Seung Sang-
dc.date.accessioned2022-02-21T10:42:45Z-
dc.date.available2022-02-21T10:42:45Z-
dc.date.created2022-02-08-
dc.date.issued2021-09-09-
dc.identifier.issn2637-6105-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/136373-
dc.description.abstractElastomeric bioscaffolds with tunable elasticity and biodegradability were synthesized via ring opening polymerization of polycaprolactone (PCL) and polylactide (PLA) with a bifunctional polyethylene glycol macroinitiator, followed by chain extension with diisocyanate to form urethane linkages. Through fine tuning of the macroinitiator and PCL/PLA weight fraction and molecular weight, a data set of elastomeric bioscaffolds gives structure-property insights into their thermal, mechanical, and biodegradability properties as they relate to triblock copolymer composition and mechanical weight. These materials were targeted to be 3D-printed by commercial devices, and their unique rheological properties enable impeccable multiscale microstructure formation. Simplicity in synthesis and fabrication as well as tunable biodegradability (1 day to 2 months) and elasticity (modulus 32-94 MPa) suggest the vast wide-ranging utility and prospective application in bioscaffolds for future therapeutic treatments.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCRYSTALLIZATION BEHAVIOR-
dc.subjectPOLYCAPROLACTONE-
dc.subjectPOLYMERS-
dc.subjectDEGRADATION-
dc.subjectBLENDS-
dc.subjectPCL-
dc.subjectCOMPOSITE-
dc.subjectSCAFFOLDS-
dc.subjectBIOINK-
dc.subjectPLA-
dc.titleStructure-Property Relationships of 3D-Printable Chain-Extended Block Copolymers with Tunable Elasticity and Biodegradability-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Jung-Hyun-
dc.identifier.doi10.1021/acsapm.1c00860-
dc.identifier.scopusid2-s2.0-85114347324-
dc.identifier.wosid000696179100039-
dc.identifier.bibliographicCitationACS APPLIED POLYMER MATERIALS, v.3, no.9, pp.4708 - 4716-
dc.relation.isPartOfACS APPLIED POLYMER MATERIALS-
dc.citation.titleACS APPLIED POLYMER MATERIALS-
dc.citation.volume3-
dc.citation.number9-
dc.citation.startPage4708-
dc.citation.endPage4716-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusBIOINK-
dc.subject.keywordPlusBLENDS-
dc.subject.keywordPlusCOMPOSITE-
dc.subject.keywordPlusCRYSTALLIZATION BEHAVIOR-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusPCL-
dc.subject.keywordPlusPLA-
dc.subject.keywordPlusPOLYCAPROLACTONE-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusSCAFFOLDS-
dc.subject.keywordAuthor3D printing-
dc.subject.keywordAuthorbiodegradable polymers-
dc.subject.keywordAuthorbioelastomer-
dc.subject.keywordAuthorblock copolymer-
dc.subject.keywordAuthorpolyurethane-
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