Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Shim, Woo Sun | - |
dc.contributor.author | Kim, Jong-Ho | - |
dc.contributor.author | Park, Hungkyu | - |
dc.contributor.author | Kim, Kwangmeyung | - |
dc.contributor.author | Kwon, Ick Chan | - |
dc.contributor.author | Lee, Doo Sung | - |
dc.date.accessioned | 2024-01-21T02:06:42Z | - |
dc.date.available | 2024-01-21T02:06:42Z | - |
dc.date.created | 2021-09-01 | - |
dc.date.issued | 2006-10 | - |
dc.identifier.issn | 0142-9612 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/135087 | - |
dc.description.abstract | A pH- and thermo-sensitive block copolymer was synthesized by adding pH-sensitive sulfamethazine oligomers (SMOs) to either end of a thermo-sensitive poly(epsilon-caprolactone-co-lactide)-poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) (PCLA-PEG-PCLA) block copolymer. The resulting pH- and thermo-sensitive SMO-PCLA-PEG-PCLA-SMO block copolymer solution did not form a gel at high pH (pH 8.0) or at increased temperatures (ca. 70 degrees C), but did form a stable gel under physiological conditions (pH 7.4 and 37 degrees C). The degradation rate of the pH- and thermo-sensitive block copolymer decreased substantially compared with the control block copolymer of PCLA-PEG-PCLA, due to the buffering effect of the SMO-PCLA-PEG PCLA-SMO sulfonamide groups on the acidic monomer-induced rapid degradation of PCLA-PEG-PCLA. This suitable sol-gel transition and sustained biodegradability of the pH- dand thermo-sensitive SMO-PCLA-PEG-PCLA-SMO block copolymers resolves two of the major drawbacks associated with thermo-sensitive block copolymers, namely premature gelation and rapid degradation. interestingly, SMO-PCLA-PEG PCLA-SMO showed no evidence of cytotoxicity in vitro. However, subcutaneous injection of the pH- and thermo-sensitive block copolymer solution (20 wt% in PBS at pH 8.0) into Sprague-Dawley (SD) rats resulted in rapid, stable gel formation, with the injected hydrogel being completely degraded in vivo in just 6 weeks. The injected hydrogel in vivo presented a typical acute inflammation within 2 weeks, although chronic inflammation was not observed during the first 6-week period. As such, the pH- and thermo-sensitive hydrogel of the SMO-PCLA-PEG-PCLA-SMO block copolymer is a suitable candidate for use in drug delivery systems and cell therapy. (c) 2006 Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.subject | IN-VIVO CHARACTERIZATION | - |
dc.subject | DELIVERY | - |
dc.subject | POLYMERS | - |
dc.title | Biodegradability and biocompatibility of a pH- and thermo-sensitive hydrogel formed from a sulfonamide-modified poly(epsilon-caprolactone-co-lactide)-poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) block copolymer | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.biomaterials.2006.05.038 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | BIOMATERIALS, v.27, no.30, pp.5178 - 5185 | - |
dc.citation.title | BIOMATERIALS | - |
dc.citation.volume | 27 | - |
dc.citation.number | 30 | - |
dc.citation.startPage | 5178 | - |
dc.citation.endPage | 5185 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000240506400004 | - |
dc.identifier.scopusid | 2-s2.0-33746079628 | - |
dc.relation.journalWebOfScienceCategory | Engineering, Biomedical | - |
dc.relation.journalWebOfScienceCategory | Materials Science, Biomaterials | - |
dc.relation.journalResearchArea | Engineering | - |
dc.relation.journalResearchArea | Materials Science | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | IN-VIVO CHARACTERIZATION | - |
dc.subject.keywordPlus | DELIVERY | - |
dc.subject.keywordPlus | POLYMERS | - |
dc.subject.keywordAuthor | pH | - |
dc.subject.keywordAuthor | and thermo-sensitive hydrogel | - |
dc.subject.keywordAuthor | sulfonamide-modified block copolymer | - |
dc.subject.keywordAuthor | biodegradability | - |
dc.subject.keywordAuthor | biocompatibility | - |
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