Zhaoyuan Guo, Xiaoli Jiang, Yagang Zhang and Yabin Zhu
{"title":"A fine-tuned thermosensitive hydrogel for wound reparation via phase transition offering excellent antibacterial activity†","authors":"Zhaoyuan Guo, Xiaoli Jiang, Yagang Zhang and Yabin Zhu","doi":"10.1039/D4NJ05316H","DOIUrl":null,"url":null,"abstract":"<p >It is crucial to provide a physical shield and moist environment for accelerated wound healing. Herein, we developed a fine-tuned thermosensitive polymer hydrogel system (poly(<em>ε</em>-caprolactone-glycolide)–poly(ethylene glycol)–poly(<em>ε</em>-caprolactone-glycolide), PCGA–PEG–PCGA) to serve as a shield for wound repair. By modulating the hydrophobic block length, a more stable gel phase was achieved owing to the increased exposure to hydrophobic regions, which facilitated the formation of stronger hydrophobic channels. This system remained in a liquid state at room temperature, allowing for easy application, and transformed into a gel at physiological temperature, conforming to the wound site. The hydrogel demonstrated an excellent physical shielding effect, as evidenced by the inhibition of bacterial growth in transwell experiments. Additionally, broad-spectrum antimicrobial silver nanoparticles (AgNPs) were incorporated following a non-antibiotic-dependent strategy to reduce the risk of infection. The addition of AgNPs did not affect the gelation of the copolymers. The antibacterial dressing (AgNPs/Gel) exhibited a potent antibacterial effect <em>in vitro</em>. <em>In vivo</em> experiments using full-thickness skin defect models revealed that AgNPs/Gel exhibited significant healing, as indicated by fewer inflammatory cells, increased collagen fiber deposition, and enhanced angiogenesis. The thermosensitive hydrogel containing silver nanoparticles is a promising antibacterial dressing for accelerating wound healing.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 25","pages":" 10587-10596"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj05316h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
It is crucial to provide a physical shield and moist environment for accelerated wound healing. Herein, we developed a fine-tuned thermosensitive polymer hydrogel system (poly(ε-caprolactone-glycolide)–poly(ethylene glycol)–poly(ε-caprolactone-glycolide), PCGA–PEG–PCGA) to serve as a shield for wound repair. By modulating the hydrophobic block length, a more stable gel phase was achieved owing to the increased exposure to hydrophobic regions, which facilitated the formation of stronger hydrophobic channels. This system remained in a liquid state at room temperature, allowing for easy application, and transformed into a gel at physiological temperature, conforming to the wound site. The hydrogel demonstrated an excellent physical shielding effect, as evidenced by the inhibition of bacterial growth in transwell experiments. Additionally, broad-spectrum antimicrobial silver nanoparticles (AgNPs) were incorporated following a non-antibiotic-dependent strategy to reduce the risk of infection. The addition of AgNPs did not affect the gelation of the copolymers. The antibacterial dressing (AgNPs/Gel) exhibited a potent antibacterial effect in vitro. In vivo experiments using full-thickness skin defect models revealed that AgNPs/Gel exhibited significant healing, as indicated by fewer inflammatory cells, increased collagen fiber deposition, and enhanced angiogenesis. The thermosensitive hydrogel containing silver nanoparticles is a promising antibacterial dressing for accelerating wound healing.