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dc.contributor.author정병문*
dc.date.accessioned2018-12-14T16:30:55Z-
dc.date.available2018-12-14T16:30:55Z-
dc.date.issued2018*
dc.identifier.issn1525-7797*
dc.identifier.otherOAK-22596*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247748-
dc.description.abstractPolycaprolactone (PCL) was reported a long time ago; however, its biomedical applications has not been extensively investigated in comparison with poly(lactide-co-glycolide) (PLGA) due to its too slow degradation profile. Here, we are reporting an oxalate-connected oligocaprolactone multiblock copolymer (PCL-OX) as a fast degradable PCL while maintaining its crystalline properties and low melting point of PCL. The in vivo application of the paclitaxel-loaded PCL-OX microspheres provided a steady plasma drug concentration of 6-9 μg/mL over 28 days, similar to that of the PLGA microspheres. Both PCL and PLGA microspheres were completely cleared two months after in vivo implantation. The PCL-OX microspheres showed a similar tissue compatibility to that of PLGA microspheres in the subcutaneous layer of rats. These findings suggest that PCL-OX is a useful biomaterial that solves the slow degradation problems of PCL and, thus, may find uses in other biomedical applications as an alternative to PLGA. © 2018 American Chemical Society.*
dc.languageEnglish*
dc.publisherAmerican Chemical Society*
dc.titleFast Degradable Polycaprolactone for Drug Delivery*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume19*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage2302*
dc.relation.lastpage2307*
dc.relation.journaltitleBiomacromolecules*
dc.identifier.doi10.1021/acs.biomac.8b00266*
dc.identifier.wosidWOS:000435226200053*
dc.identifier.scopusid2-s2.0-85046937963*
dc.author.googleChang S.H.*
dc.author.googleLee H.J.*
dc.author.googlePark S.*
dc.author.googleKim Y.*
dc.author.googleJeong B.*
dc.contributor.scopusid정병문(7102237959)*
dc.date.modifydate20240118155902*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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