由聚己内酯和明胶组成的药物洗脱纳米纤维伤口敷料可通过减少氧化应激和炎症促进糖尿病伤口愈合:体外和体内研究

IF 2.1 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Shungui Liu, Ziqiu Chen
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引用次数: 0

摘要

糖尿病是一种常见的疾病,经常会导致并发症,其中糖尿病伤口会造成感染、截肢和死亡等严重后果。在目前的研究中,为了改善大鼠模型的伤口愈合,我们在电纺聚己内酯/明胶支架中加入了洛多沙胺。我们使用各种方法对所开发的敷料进行了体外表征,然后将其应用于大鼠切除伤口模型。研究表明,敷料没有毒性,并能促进皮肤成纤维细胞的迁移潜力。伤口愈合研究表明,洛多沙胺敷料的愈合潜力明显高于其他支架,并能促进胶原沉积和上皮化。基因表达研究表明,TNF-α、谷胱甘肽过氧化物酶和超氧化物歧化酶基因在洛多沙胺敷料的作用下明显下调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-eluting nanofibrous wound dressings composed of polycaprolactone and gelatin augment diabetic wounds healing via reducing oxidative stress and inflammation: An in vitro and in vivo study
Diabetes is a prevalent medical condition that often leads to complications, including diabetic wounds that can have serious consequences such as infections, amputations, and death. In the current research, lodoxamide was loaded into electrospun polycaprolacton/gelatin scaffolds In order to improve wound healing in a rat model. Our developed dressings were characterized in vitro using various methods and then applied on a rat model of excisional wound. Study showed that the dressings were not toxic and promoted migration potential of skin-derived fibroblast cells. Wound healing study showed that lodoxamide-loaded dressings had markedly higher healing potential than other scaffolds and augmented collagen deposition and epithelialization. Gene expression studies showed that TNF-α, glutathione peroxidase, and superoxide dismutase genes were significantly downregulated by lodoxamide-loaded scaffolds.
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来源期刊
Journal of Bioactive and Compatible Polymers
Journal of Bioactive and Compatible Polymers 工程技术-材料科学:生物材料
CiteScore
3.50
自引率
0.00%
发文量
27
审稿时长
2 months
期刊介绍: The use and importance of biomedical polymers, especially in pharmacology, is growing rapidly. The Journal of Bioactive and Compatible Polymers is a fully peer-reviewed scholarly journal that provides biomedical polymer scientists and researchers with new information on important advances in this field. Examples of specific areas of interest to the journal include: polymeric drugs and drug design; polymeric functionalization and structures related to biological activity or compatibility; natural polymer modification to achieve specific biological activity or compatibility; enzyme modelling by polymers; membranes for biological use; liposome stabilization and cell modeling. This journal is a member of the Committee on Publication Ethics (COPE).
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