Multifunctional protein-polysaccharide hydrogel with antimicrobial and angiogenic properties to promote infected wound healing

IF 5.5 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Jianfeng Yang , Wenjing Li , Pei Ma , Pan Wang , Tianyu Yao , Yu Mi
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Abstract

Bacterial infections, slow angiogenesis, and wound irregularities continue to present great clinical challenges in infected wound repair. While recent years have seen increasing interest in advanced composite hydrogels with antibacterial, angiogenic, and wound-healing properties, traditional dynamic hydrogels remain limited by inadequate mechanical strength despite their adaptability to irregular wounds. Here, we used double-bonded functionalized recombinant collagen (CFGMA), sulfhydrylated hyaluronic acid (HA-SH), silver ions (Ag+), and VEGF peptide (V-pep), which formed a composite hydrogel that could accommodate irregular wounds as well as have excellent mechanical properties. The CFGMA/HA-SH/Ag+/V-pep hydrogel not only exhibits excellent antibacterial properties, but also has good anti-inflammatory, pro-proliferative and angiogenic effects. In vitro study results indicated that the CFGMA/HA-SH/Ag+/V-pep hydrogel promoted the polarization of macrophages from M1 to M2 type, enhanced the proliferation of L929 and HUVECs, and facilitated the angiogenesis of HUVECs. In vivo experiments indicated that CFGMA/HA-SH/Ag+/V-pep hydrogel effectively killed bacteria, accelerated blood vessel regeneration, and promoted the repair of infected wounds at day 12. Moreover, CFGMA/HA-SH/Ag+/V-pep hydrogel promoted the regeneration of granulation tissue and collagen deposition at the wound site. The prepared hydrogel was antimicrobial, anti-inflammatory, pro-proliferative, promoted vascular regeneration and accelerated wound repair, which could be an effective treatment for infected wounds.

Abstract Image

具有抗菌和血管生成特性的多功能蛋白多糖水凝胶,促进感染伤口愈合
细菌感染、血管生成缓慢和伤口不规则仍然是感染伤口修复的巨大临床挑战。尽管近年来人们对具有抗菌、血管生成和伤口愈合性能的高级复合水凝胶越来越感兴趣,但传统的动态水凝胶仍然受到机械强度不足的限制,尽管它们对不规则伤口具有适应性。本研究采用双键功能化重组胶原蛋白(CFGMA)、巯基透明质酸(HA-SH)、银离子(Ag+)和VEGF肽(V-pep)组成复合水凝胶,既能适应不规则伤口,又具有优异的力学性能。CFGMA/HA-SH/Ag+/V-pep水凝胶不仅具有优异的抗菌性能,而且具有良好的抗炎、促增殖和血管生成作用。体外研究结果表明,CFGMA/HA-SH/Ag+/V-pep水凝胶可促进巨噬细胞从M1型向M2型极化,增强L929和HUVECs的增殖,促进HUVECs血管生成。体内实验表明,CFGMA/HA-SH/Ag+/V-pep水凝胶能有效杀灭细菌,加速血管再生,促进感染创面在第12天的修复。此外,CFGMA/HA-SH/Ag+/V-pep水凝胶促进了肉芽组织的再生和伤口部位胶原的沉积。制备的水凝胶具有抗菌、抗炎、促增殖、促进血管再生、加速创面修复等作用,可作为治疗感染创面的有效药物。
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来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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