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Asiaticoside and polylysine-releasing collagen complex for effectively reducing initial inflammatory response using inflamed induced in vitro model
- Source :
- Materials scienceengineering. C, Materials for biological applications. 121
- Publication Year :
- 2020
-
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 e-poly-l-lysine (ePLL). 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-ePLL showed a notable antimicrobial effect using microbial infection test. In this study, we determined whether asiaticoside and ePLL have anti-inflammatory and antibacterial effects through different mechanisms. Collectively, the collagen-AS/ePLL 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.
- Subjects :
- Materials science
Inflammatory response
Bioengineering
Inflammation
02 engineering and technology
Pharmacology
010402 general chemistry
01 natural sciences
In vitro model
Biomaterials
chemistry.chemical_compound
Antimicrobial effect
medicine
Microbial disease
Polylysine
Wound Healing
021001 nanoscience & nanotechnology
In vitro
Triterpenes
0104 chemical sciences
chemistry
Mechanics of Materials
Collagen
medicine.symptom
0210 nano-technology
Wound healing
Subjects
Details
- ISSN :
- 18730191
- Volume :
- 121
- Database :
- OpenAIRE
- Journal :
- Materials scienceengineering. C, Materials for biological applications
- Accession number :
- edsair.doi.dedup.....4bd73bae82aa195722af1be9f3cca6bc