작용기가 도입된 양친매성 폴리에틸렌 글리콜-폴리에스터 블록 공중합체의 합성과 특성 분석
DC Field | Value | Language |
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dc.contributor.author | Kim, Jae Il | - |
dc.date.accessioned | 2018-11-08T08:02:59Z | - |
dc.date.available | 2018-11-08T08:02:59Z | - |
dc.date.issued | 2012-02 | - |
dc.identifier.other | 12466 | - |
dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/9832 | - |
dc.description | 학위논문(석사)아주대학교 일반대학원 :분자과학기술학과,2012. 2 | - |
dc.description.tableofcontents | Chapter Ⅰ. General Introduction 1.1. Functional polyesters 1.2. Applications Chapter Ⅱ. Examination of phase transition behavior of ion group functionalized MPEG-b-PCL diblock copolymers Ⅱ.1. Introduction Ⅱ.2. Experimental section Ⅱ.3. Results and Discussion Ⅱ.4. Conclusion Ⅱ.5. Reference Chapter Ⅲ. An injectable biodegradable temperature-responsive gel with an adjustable persistence window Ⅲ.1. Introduction Ⅲ.2. Experimental section Ⅲ.3. Results and Discussion Ⅲ.4. Conclusion Ⅲ.5. Reference Abstract (in Korean) | - |
dc.language.iso | eng | - |
dc.publisher | The Graduate School, Ajou University | - |
dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
dc.title | 작용기가 도입된 양친매성 폴리에틸렌 글리콜-폴리에스터 블록 공중합체의 합성과 특성 분석 | - |
dc.title.alternative | Jae Il Kim | - |
dc.type | Thesis | - |
dc.contributor.affiliation | 아주대학교 일반대학원 | - |
dc.contributor.alternativeName | Jae Il Kim | - |
dc.contributor.department | 일반대학원 분자과학기술학과 | - |
dc.date.awarded | 2012. 2 | - |
dc.description.degree | Master | - |
dc.identifier.localId | 570287 | - |
dc.identifier.url | http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012466 | - |
dc.subject.keyword | 양친매성 공중합체 | - |
dc.subject.keyword | 폴리에스터 | - |
dc.subject.keyword | 하이드로젤 | - |
dc.description.alternativeAbstract | Several thermogelling block copolymers have been developed for biomedical applications, such as drug or cell delivery carriers. The amphiphilic block copolymers containing hydrophilic and hydrophobic segment exhibit thermal phase transition mediated by hydrophobic interactions among hydrophobic segments. The formation of a crystalline domain via hydrophobic interactions is sensitive to the identity of the hydrophobic segment. Thus, the functional groups on amphiphilic block copolymers can engage in intra- and intermolecular interactions to effect hydrophobic interactions. The aim of this thesis is to prepare an unique amphiphilic diblock copolymer with thermogelling property. In this thesis, MPEG-b-PCL diblock copolymers are selected in an attempt to prepare thermogelling polymer system via controllable intra- and intermolecular interactions. In the chapter 2, MPEG-b-PCL diblock copolymers with anionic and cationic groups into the hydrophobic PCL chain end positions are prepared and examined at the thermogelling transitions as a function of temperature. MPEG-b-PCL diblock copolymers with anionic and cationic groups exhibited the formation and destruction of a structured gel network of MPEG-b-PCL diblock copolymers, depended on the crystallinity and hydrophobicity of the PCL domains in aqueous media. In the chapter 3, MPEG-b-(PCL-ran-PLLA) diblock copolymers with various groups into the hydrophobic PLLA chain pendant positions are prepared and examined at the thermogelling transitions as a function of temperature. Intra- and inter-molecular interactions among hydrophobic PCL and PLA domains can stabilize or destabilize aggregation among the hydrophobic segments, which is a prerequisite for achieving thermogelling polymer system. In conclusion, these results show that novel amphiphilic diblock copolymers prepared in this work may serve as a thermogelling polymer system with an adjustable temperature-responsive window. | - |
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