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Adhesive coacervate as a bioactive coating supplement for wound dressings : 상처 드레싱을 위한 생활성 코팅 보조제로서의 접착성 코아세르베이트
DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | 이강원 | - |
dc.contributor.author | 김영 | - |
dc.date.accessioned | 2023-06-29T02:27:05Z | - |
dc.date.available | 2023-06-29T02:27:05Z | - |
dc.date.issued | 2023 | - |
dc.identifier.other | 000000174286 | - |
dc.identifier.uri | https://hdl.handle.net/10371/194086 | - |
dc.identifier.uri | https://dcollection.snu.ac.kr/common/orgView/000000174286 | ko_KR |
dc.description | 학위논문(석사) -- 서울대학교대학원 : 융합과학기술대학원 응용바이오공학과, 2023. 2. 이강원. | - |
dc.description.abstract | Wound healing using growth factors is a clinically effective treatment method. However, it has a short biological half-life due to protease secreted into the wound area to break down the damaged extracellular matrix (ECM). The study shows a new coating supplement functionalizing adhesiveness using dopamine (DOPA) to the complex coacervate of fucoidan and poly-l-lysine (PLL), showing antioxidant properties that useful in wound healing. The dopamine-complex coacervate (D-Coa) was optimized to form maximum micro-droplets. The D-Coa, dopamine functionalized fucoidan, a marine-derived glycosaminoglycan, and poly-l-lysine (PLL) coacervates have shown promising protein delivery; sustained release profile, superior encapsulation ability, biocompatibility, and protection against harsh in-vivo environment, for tissue engineering applications as our previous fucoidan and poly-l-lysine (PLL) complex coacervate study was shown. Furthermore, the D-Coa was conducted superior adhesive forces and successfully coated onto collagen sponge homogeneously and rapidly. From in vivo performance tests using at skin defect models, our D-Coa coating patch were demonstrated successful wound regeneration. This game changer coating supplements can rescue biological half-life and reduce coating time, preventing limited application of scaffold such as commercially available collagen sponge. | - |
dc.description.tableofcontents | Chapter 1. Introduction 1
Chapter 2. Materials and methods 4 2.1 Material 4 2.2 Synthesis and confimation of DOPA-Fucoidan (D-Fuc) 6 2.3 Surface charge measurements on D-Coa components using Zeta potential 7 2.4 Preparation of D-Fuc/PLL complex coacervate 7 2.5 Adhesive force test 8 2.6 Preparation of D-Coa coated collagen sponge 8 2.7 Protein encapsulation evaluation 9 2.8 Protein releasing profile 11 2.9 Protection test 12 2.10 Biocompatibility test 12 2.11 Proliferation test 13 2.12 Bioacitvity evaluation 13 2.13 In vivo study 15 2.14 Histological evaluation 16 2.15 Qunatitative reverse transcription PCR (qRT-PCR) 16 2.16 Statistical analysis 17 Chapter 3. Results and discussions 18 3.1 Preparation and characterization of DOPA conjugated fucoid (D-Foa) 18 3.2 Preparation and confirmation of adhesive D-Fuc/poly-l-lysine coacervate (D-Coa) 20 3.3 D-Coa as a drug delivery coating system 25 3.4 In vitro biocompatibility and bioactivity of D-Coa coated collagen sponge 30 3.5 In vivo wound healing evaluation of D-Coa coated collagen sponge 34 Chapter 4. Conclusion 51 References 52 국문초록 63 | - |
dc.format.extent | vi ,64 | - |
dc.language.iso | eng | - |
dc.publisher | 서울대학교 대학원 | - |
dc.subject | Coacervate | - |
dc.subject | DOPA | - |
dc.subject | Drug Delivery System(DDS) | - |
dc.subject | sustained release profile | - |
dc.subject.ddc | 660.6 | - |
dc.title | Adhesive coacervate as a bioactive coating supplement for wound dressings | - |
dc.title.alternative | 상처 드레싱을 위한 생활성 코팅 보조제로서의 접착성 코아세르베이트 | - |
dc.type | Thesis | - |
dc.type | Dissertation | - |
dc.contributor.AlternativeAuthor | Young Kim | - |
dc.contributor.department | 융합과학기술대학원 응용바이오공학과 | - |
dc.description.degree | 석사 | - |
dc.date.awarded | 2023-02 | - |
dc.identifier.uci | I804:11032-000000174286 | - |
dc.identifier.holdings | 000000000049▲000000000056▲000000174286▲ | - |
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