具有增强止血和抗菌性能的可生物降解聚合物微球,用于伤口愈合。

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xuelian Hu, Sai Li, Yuji Pu, Bin He
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引用次数: 0

摘要

止血是伤口愈合的第一步,但经常会出现大量出血和感染等重大挑战。在这项研究中,我们开发了两亲性可生物降解的聚酯基分段聚氨酯(SPU)微球,用表没食子儿茶素没食子酸酯(EGCG)-Ag纳米颗粒和海藻酸钙交联壳修饰,将血液吸收与Ca2+的促凝特性和EGCG的负电荷结合起来,在凝血级联的各个阶段发挥协同止血作用。与SPU微球(685.0 s)相比,SPU@EAg@CaAlg微球的体外凝血时间(328.7 s)缩短了一半。SPU@EAg@CaAlg在三种大鼠止血模型中的止血时间和出血量均有所减少。此外,EGCG-Ag纳米颗粒在体外和体内都具有很强的抗菌和抗炎特性。体内感染创面模型表明SPU@EAg@CaAlg能有效清除细菌,降低促炎因子水平,促进创面愈合。因此,改性SPU微球是一种有前途的有效止血应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biodegradable Polymeric Microspheres with Enhanced Hemostatic and Antibacterial Properties for Wound Healing.

Hemostasis is the initial step in wound healing, yet significant challenges, such as massive bleeding and infection, often arise. In this study, we developed amphiphilic biodegradable polyester-based segmented polyurethane (SPU) microspheres modified with epigallocatechin gallate (EGCG)-Ag nanoparticles and calcium-alginate cross-linking shell, combining blood absorption with the pro-coagulation properties of Ca2+ and the negative charge of EGCG for synergistic hemostatic effects across various stages of the coagulation cascade. The in vitro blood clotting time of the SPU@EAg@CaAlg microsphere (328.7 s) was reduced by half compared to the SPU microsphere (685.0 s). SPU@EAg@CaAlg exhibited a reduced hemostatic time and blood loss in three rat hemostatic models. Additionally, EGCG-Ag nanoparticles imparted strong antibacterial and anti-inflammatory properties both in vitro and in vivo. In vivo infected wound model demonstrated that SPU@EAg@CaAlg effectively eliminated bacteria and reduced the levels of pro-inflammatory factors, thereby promoting wound healing. Thus, the modified SPU microspheres present a promising candidate for effective hemostatic applications.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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