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Cited 10 time in webofscience Cited 24 time in scopus
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dc.contributor.authorJin Chul Kim-
dc.contributor.authorJungwoon Jung-
dc.contributor.authorYecheol Rho-
dc.contributor.authorMihee Kim-
dc.contributor.authorWonsang Kwon-
dc.contributor.authorHeesoo Kim-
dc.contributor.authorIk Jung Kim-
dc.contributor.authorJung Ran Kim-
dc.contributor.authorRee, M-
dc.date.accessioned2016-03-31T09:31:15Z-
dc.date.available2016-03-31T09:31:15Z-
dc.date.created2011-08-12-
dc.date.issued2011-07-
dc.identifier.issn1525-7797-
dc.identifier.other2011-OAK-0000023878-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/17293-
dc.description.abstractTwo new DNA-mimicking brush polymers were synthesized: poly[oxy(11-(3-(9-adeninyl)propionato)-undecanyl-1-thiomethyl)ethylene] (PECH-AS) and poly[oxy(11-(5-(9-adenylethyloxy)-4-oxopentanoato)undecanyl-1-thiomethyl)ethylene] (PECH-AS). These polymers were found to be thermally stable up to 220 degrees C and could be applied easily by conventional coating processes to produce good quality films. Interestingly, both brush polymers formed molecular multibilayer structures to provide an adenine-rich surface. Despite the structural similarities, PECH-AS surprisingly exhibited higher hydrophilicity and better water sorption properties than PECH-AP. These differences were attributed to the chemical structures in the bristles of the polymers. The adenine-rich surfaces of the polymer films demonstrated selective protein adsorption, suppressed bacterial adherence, facilitated HEp-2 cell adhesion, and exhibited good biocompatibility in mice. However, the high hydrophilicity and good water sorption characteristics of the PECH-AS film suggest that this brush polymer is better suited to applications requiring good biocompatibility and reduced chance of bacterial infection compared with the PECH-AP film.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfBIOMACROMOLECULES-
dc.titleWell-Defined DNA-Mimic Brush Polymers Bearing Adenine Moieties: Synthesis, Layer-by-Layer Self-Assembly, and Biocompatibility-
dc.typeArticle-
dc.contributor.college첨단재료과학부-
dc.identifier.doi10.1021/BM200572T-
dc.author.googleKim, JC-
dc.author.googleJung, J-
dc.author.googleRho, Y-
dc.author.googleKim, M-
dc.author.googleKwon, W-
dc.author.googleKim, H-
dc.author.googleKim, IJ-
dc.author.googleKim, JR-
dc.author.googleRee, M-
dc.relation.volume12-
dc.relation.issue7-
dc.relation.startpage2822-
dc.relation.lastpage2833-
dc.contributor.id10115761-
dc.relation.journalBIOMACROMOLECULES-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOMACROMOLECULES, v.12, no.7, pp.2822 - 2833-
dc.identifier.wosid000292617700047-
dc.date.tcdate2019-01-01-
dc.citation.endPage2833-
dc.citation.number7-
dc.citation.startPage2822-
dc.citation.titleBIOMACROMOLECULES-
dc.citation.volume12-
dc.contributor.affiliatedAuthorRee, M-
dc.identifier.scopusid2-s2.0-79960209588-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc8-
dc.description.scptc20*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusX-RAY-SCATTERING-
dc.subject.keywordPlusTRANSFER RADICAL POLYMERIZATION-
dc.subject.keywordPlusLIQUID-CRYSTALLINE POLYMERS-
dc.subject.keywordPlusSURFACE-PLASMON RESONANCE-
dc.subject.keywordPlusOPENING METATHESIS POLYMERIZATION-
dc.subject.keywordPlusORGANOSILICATE DIELECTRIC FILMS-
dc.subject.keywordPlusSHORT SIDE-GROUPS-
dc.subject.keywordPlusTHIN-FILMS-
dc.subject.keywordPlusPROTEIN ADSORPTION-
dc.subject.keywordPlusDIBLOCK COPOLYMER-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-

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