Exosomes-carried curcumin based on polysaccharide hydrogel promote flap survival

微泡 姜黄素 氧化应激 体内 抗氧化剂 药理学 化学 血管生成 坏死 缺血 生物化学 生物 医学 小RNA 癌症研究 病理 基因 生物技术 心脏病学
作者
Xiangjun Liu,Han Chen,Lanjie Lei,Yang Pu,Yikun Ju,Xingwang Fan,Bairong Fang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:270: 132367-132367 被引量:11
标识
DOI:10.1016/j.ijbiomac.2024.132367
摘要

Flap grafting is a common technique used to repair skin defects in orthopedics and plastic and reconstructive surgeries. However, oxidative stress injury caused by ischemia and ischemia-reperfusion injury at the distal end of the skin flap can cause flap necrosis. Curcumin is a natural compound with anti-inflammatory and antioxidant properties that tackle oxidative stress. However, its applicability is limited by its poor water solubility. Exosomes are membranous vesicles that can be loaded with hydrophobic drugs. They are widely studied in drug delivery applications and can be investigated to augment curcumin efficiency. In this study, a self-healing oxidized pullulan polysaccharide-carboxymethylated chitosan composite hydrogel was used as a curcumin-loaded exosome delivery system to evaluate its impact on the viability of skin flaps. The hydrogel exhibited good self-healing properties that allowed the continuous and stable release of drugs. It had anti-inflammatory and antioxidant properties that could reduce oxidative stress damage due to early ischemia and hypoxia of the skin flap in vitro. Moreover, this composite hydrogel attenuated inflammatory responses, promoted angiogenesis, and reduced the distal necrosis of the flap in vivo. Therefore, our hydrogel provides a novel strategy for skin flap graft protection with reduced necrosis and the potential for broad clinical applications.
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