Application of Antimicrobial Peptides in Wound Dressings.

IF 5.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-09-19 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S543233
Aoxun Zhu, Baiqi Chen, Jing Ma, Jiajia Wang, Rongfang Tang, Liangeng Liu, Weixin Sun, Xingzhong Zheng, Guangtao Pan
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引用次数: 0

Abstract

Background: Growing antibiotic misuse and the rise of antimicrobial resistance have driven interest in antimicrobial peptides (AMPs) as therapeutic agents for wound dressings and clinical wound management. AMPs are short, cationic peptides with broad‑spectrum activity and diverse mechanisms of action that confer a low propensity for resistance development.

Methods: We performed a focused literature synthesis to review AMP classification, structural features, antimicrobial mechanisms, and strategies for integrating AMPs into wound dressings. We emphasize materials and delivery approaches reported for hydrogels, electrospun fibers, films, scaffolds, and sponges, and we summarize advances in hybrid systems that combine AMPs with functional materials.

Results: AMP‑loaded dressings promote infection control and tissue repair by maintaining a favorable wound microenvironment, enabling controlled peptide release, reducing biofilms, and stimulating cell proliferation and angiogenesis. Hybrid platforms-polysaccharide and stimuli‑responsive hydrogels, metal‑nanoparticle composites, exosome carriers, and cryogels-improve peptide stability and bioavailability while introducing functionalities such as real‑time bacterial sensing, antioxidant activity, and electrical conductivity for electrostimulation. In chronic wounds and burns, AMP‑based dressings show promise for anti‑biofilm activity, immunomodulation, enhanced re‑epithelialization, and reduced risk of resistance compared with conventional antibiotics.

Conclusion: We identify key challenges and propose future directions: rational design of tailored AMPs, smart controlled‑release carriers, nanotechnology‑enabled formulations, and strategies to accelerate clinical translation. Advances in these areas are expected to expedite the clinical adoption of AMP‑based wound therapies, offering safer, more effective, and personalized treatment options.

抗菌肽在伤口敷料中的应用。
背景:越来越多的抗生素滥用和抗菌素耐药性的上升已经引起了人们对抗菌肽(AMPs)作为伤口敷料和临床伤口管理治疗剂的兴趣。amp是短的阳离子肽,具有广谱活性和多种作用机制,具有较低的耐药倾向。方法:我们对AMP的分类、结构特征、抗菌机制以及将AMP整合到伤口敷料中的策略进行了文献综述。我们重点介绍了水凝胶、电纺纤维、薄膜、支架和海绵的材料和递送方法,并总结了将amp与功能材料结合在一起的混合系统的进展。结果:AMP负载敷料通过维持良好的伤口微环境,使肽释放可控,减少生物膜,刺激细胞增殖和血管生成,促进感染控制和组织修复。混合平台-多糖和刺激反应水凝胶,金属纳米颗粒复合材料,外泌体载体和冷冻-提高肽的稳定性和生物利用度,同时引入功能,如实时细菌传感,抗氧化活性和电刺激的导电性。在慢性伤口和烧伤中,与传统抗生素相比,基于AMP的敷料显示出抗生物膜活性、免疫调节、增强再上皮化和降低耐药风险的希望。结论:我们确定了关键挑战并提出了未来的方向:合理设计定制的amp,智能控释载体,纳米技术支持的配方,以及加速临床转化的策略。这些领域的进展有望加快基于AMP的伤口治疗的临床应用,提供更安全、更有效和个性化的治疗选择。
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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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