完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Lu, Haoxiang | en_US |
dc.contributor.author | Wang, Wei | en_US |
dc.contributor.author | Zheng, Zhen | en_US |
dc.contributor.author | Sun, Peiyu | en_US |
dc.contributor.author | Wang, Xinling | en_US |
dc.contributor.author | Chang, Feng-Chih | en_US |
dc.date.accessioned | 2014-12-08T15:21:33Z | - |
dc.date.available | 2014-12-08T15:21:33Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.issn | 1759-9954 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/15311 | - |
dc.identifier.uri | http://dx.doi.org/10.1039/c2py00481j | en_US |
dc.description.abstract | Two 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.language.iso | en_US | en_US |
dc.title | Pepsin-inspired polyurethanes containing a tyrosine-fumaric acid-tyrosine segment | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1039/c2py00481j | en_US |
dc.identifier.journal | POLYMER CHEMISTRY | en_US |
dc.citation.volume | 3 | en_US |
dc.citation.issue | 2 | en_US |
dc.citation.spage | 498 | en_US |
dc.citation.epage | 503 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000298991200034 | - |
dc.citation.woscount | 5 | - |
顯示於類別: | 期刊論文 |