{"title":"Application of Antimicrobial Peptides in Wound Dressings.","authors":"Aoxun Zhu, Baiqi Chen, Jing Ma, Jiajia Wang, Rongfang Tang, Liangeng Liu, Weixin Sun, Xingzhong Zheng, Guangtao Pan","doi":"10.2147/DDDT.S543233","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":11290,"journal":{"name":"Drug Design, Development and Therapy","volume":"19 ","pages":"8523-8539"},"PeriodicalIF":5.1000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12457083/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Design, Development and Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/DDDT.S543233","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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.
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.