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负载镁离子的氨甲环酸功能化脱细胞真皮基质海绵:增强止血、血管再生和再上皮化以实现糖尿病伤口的全面愈合

A tranexamic acid-functionalized acellular dermal matrix sponge co-loaded with magnesium ions: Enhancing hemostasis, vascular regeneration, and re-epithelialization for comprehensive diabetic wound healing.

作者信息

Li Tianlong, Wen Qiulan, Zhu Fengyi, Hu Yuting, Gong Jun, Zhang Xibing, Huang Chaoyang, Zhou Hai, Chen Lianglong, Pan Yingsong

机构信息

YunFu People's Hospital, Yunfu 527300, Guangdong, PR China.

Department of Orthopaedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, PR China.

出版信息

Biomater Adv. 2025 Feb;167:214096. doi: 10.1016/j.bioadv.2024.214096. Epub 2024 Oct 31.

DOI:10.1016/j.bioadv.2024.214096
PMID:39500149
Abstract

Excessive inflammation, accumulation of wound exudate, and blood seepage are common in diabetic wounds, hindering cell proliferation and disrupting tissue remodeling, leading to delayed healing. This study presents a multifunctional sponge scaffold (PT@Mg) created by combining an acellular dermal matrix with tranexamic acid and MgO nanoparticles, designed for hemostatic and anti-inflammatory effects. The PT@Mg scaffold effectively absorbs wound fluid while promoting healing. In vivo and in vitro hemostasis experiments demonstrate that the PT@Mg sponge exhibits excellent hydrophilicity, enhancing blood absorption at the wound site, inhibiting fibrinolysis, and expediting hemostasis. Additionally, the sustained release of Mg from the PT@Mg sponge promotes collagen deposition and angiogenesis in diabetic rat wounds, suppressing chronic inflammation and accelerating tissue remodeling and repair.

摘要

过度炎症、伤口渗出物积聚和渗血在糖尿病伤口中很常见,会阻碍细胞增殖并破坏组织重塑,导致愈合延迟。本研究提出了一种多功能海绵支架(PT@Mg),它是通过将无细胞真皮基质与氨甲环酸和氧化镁纳米颗粒结合而成,旨在实现止血和抗炎效果。PT@Mg支架能有效吸收伤口液体,同时促进愈合。体内和体外止血实验表明,PT@Mg海绵具有优异的亲水性,可增强伤口部位的血液吸收,抑制纤维蛋白溶解,并加速止血。此外,PT@Mg海绵中镁的持续释放促进了糖尿病大鼠伤口中的胶原蛋白沉积和血管生成,抑制了慢性炎症,加速了组织重塑和修复。

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