硫酸软骨素
壳聚糖
透明质酸
伤口愈合
化学
体内
抗菌活性
血管生成
糖胺聚糖
炎症
生物物理学
生物化学
细菌
免疫学
医学
生物
解剖
癌症研究
生物技术
遗传学
作者
Swati Sharma,Harishkumar Madhyastha,Shrikant Sitaram Kirwale,Kentaro Sakai,Yash T. Katakia,Syamantak Majumder,Aniruddha Roy
标识
DOI:10.1016/j.carbpol.2022.120126
摘要
None of the currently available wound dressings exhibit combined antibacterial and anti-inflammatory activity. Using polyelectrolyte complexation (PEC) between a cationic polysaccharide chitosan (CH) and an anionic glycosaminoglycan chondroitin sulfate (CS), we have developed a unique in-situ forming scaffold (CH-CS PEC), which develops at the wound site itself to influence the function of the wound bed cells. The current study demonstrated that CH-CS PEC could induce bacterial cell death through membrane pore formation and increased ROS production. Moreover, possibly due to its unique material properties including medium-soft viscoelasticity, porosity, and surface composition, CH-CS PEC could modulate macrophage function, increasing their phagocytic ability with low TNF-α and high IL-10 production. Faster wound closure and decreased CFU count was observed in an in-vivo infected wound model, with reduced NF-κB and increased VE-cadherin expression, indicating reduced inflammation and enhanced angiogenesis. In summary, this study exhibited that CH-CS PEC has substantial antibacterial and immunomodulatory properties.
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