Cited 11 times in
Asiaticoside and polylysine-releasing collagen complex for effectively reducing initial inflammatory response using inflamed induced in vitro model
DC Field | Value | Language |
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dc.contributor.author | 구민아 | - |
dc.contributor.author | 권병주 | - |
dc.contributor.author | 박종철 | - |
dc.contributor.author | 이미희 | - |
dc.date.accessioned | 2021-04-29T16:48:12Z | - |
dc.date.available | 2021-04-29T16:48:12Z | - |
dc.date.issued | 2021-02 | - |
dc.identifier.issn | 0928-4931 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/182027 | - |
dc.description.abstract | Inflammation is a significant clinical problem that can arise from full-thickness wounds or burn injuries or microbial disease. Although topical wound healing substances could promote rapid wound healing by preventing or reducing the consequences of inflammation, there still remains a need for the development of novel substances that can effectively reduce infection and inflammation in initial wound healing phase. In this study, collagen was combined with asiaticoside (AS) and ε-poly-l-lysine (εPLL). This complex was then applied to in vitro models of infection and inflammation. Collagen-AS coatings inhibited the initial inflammatory response to LPS through a sustained release of AS, and a bilayer coating-εPLL showed a notable antimicrobial effect using microbial infection test. In this study, we determined whether asiaticoside and εPLL have anti-inflammatory and antibacterial effects through different mechanisms. Collectively, the collagen-AS/εPLL complex indicated great therapeutic potentials for accelerate wound healing and the complex may be considered as a artificial scaffold substitute product to full-thickness wound healing. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier | - |
dc.relation.isPartOf | MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Asiaticoside and polylysine-releasing collagen complex for effectively reducing initial inflammatory response using inflamed induced in vitro model | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Others | - |
dc.contributor.googleauthor | Gyeung Mi Seon | - |
dc.contributor.googleauthor | Mi Hee Lee | - |
dc.contributor.googleauthor | Min-Ah Koo | - |
dc.contributor.googleauthor | Seung Hee Hong | - |
dc.contributor.googleauthor | Ye Jin Park | - |
dc.contributor.googleauthor | Ha Kyeong Jeong | - |
dc.contributor.googleauthor | Byeong-Ju Kwon | - |
dc.contributor.googleauthor | Dohyun Kim | - |
dc.contributor.googleauthor | Jong-Chul Park | - |
dc.identifier.doi | 10.1016/j.msec.2020.111837 | - |
dc.contributor.localId | A00190 | - |
dc.contributor.localId | A00218 | - |
dc.contributor.localId | A01662 | - |
dc.contributor.localId | A02777 | - |
dc.relation.journalcode | J02186 | - |
dc.identifier.eissn | 0928-4931 | - |
dc.identifier.pmid | 33579475 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0928493120337565 | - |
dc.subject.keyword | Asiaticoside | - |
dc.subject.keyword | Collagen | - |
dc.subject.keyword | Inflammation | - |
dc.subject.keyword | Wound infection | - |
dc.subject.keyword | ε-Poly-l-lysine | - |
dc.contributor.alternativeName | Koo, Min-Ah | - |
dc.contributor.affiliatedAuthor | 구민아 | - |
dc.contributor.affiliatedAuthor | 권병주 | - |
dc.contributor.affiliatedAuthor | 박종철 | - |
dc.contributor.affiliatedAuthor | 이미희 | - |
dc.citation.volume | 121 | - |
dc.citation.startPage | 111837 | - |
dc.identifier.bibliographicCitation | MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, Vol.121 : 111837, 2021-02 | - |
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