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Pepsin-inspired polyurethanes containing a tyrosine-fumaric acid-tyrosine segment

dc.citation.epage503en_US
dc.citation.issue2en_US
dc.citation.spage498en_US
dc.citation.volume3en_US
dc.citation.woscount5
dc.contributor.authorLu, Haoxiangen_US
dc.contributor.authorWang, Weien_US
dc.contributor.authorZheng, Zhenen_US
dc.contributor.authorSun, Peiyuen_US
dc.contributor.authorWang, Xinlingen_US
dc.contributor.authorChang, Feng-Chihen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:21:33Z
dc.date.available2014-12-08T15:21:33Z
dc.date.issued2012en_US
dc.description.abstractTwo kinds of novel peptide mimetic pepsin-inspired degradable polyurethanes were synthesized and characterized. A synthetic pseudo tripeptide acted as chain extender and provided active sites for pepsin biodegradation. In vitro degradation behavior was investigated in simulated gastric fluid containing pepsin, and assessed by H-1 NMR, mass loss and SEM. The results indicated that the pseudo peptide bonds in polyurethanes were effectively digested by the action of pepsin. Furthermore, the rate and degree of pepsin-inspired polyurethanes in simulated gastric fluid containing pepsin could be controlled by alteration of the soft segments and activity of pepsin. The influence of the polymers on human umbilical vein endothelial cells was evaluated by WST-1 assay. The results indicated that the polymers sustained much higher cell viability than the controls.en_US
dc.identifier.doi10.1039/c2py00481jen_US
dc.identifier.issn1759-9954en_US
dc.identifier.journalPOLYMER CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c2py00481jen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/15311
dc.identifier.wosnumberWOS:000298991200034
dc.language.isoen_USen_US
dc.titlePepsin-inspired polyurethanes containing a tyrosine-fumaric acid-tyrosine segmenten_US
dc.typeArticleen_US

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