Electrospun fibers loaded with antimicrobial peptides for treatment of wound infections

被引:7
|
作者
Kielholz, Tobias
Walther, Marcel
Jung, Nathalie
Windbergs, Maike [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Pharmaceut Technol, Max von Laue Str 9, D-60438 Frankfurt, Germany
关键词
Tyrothricin; Antimicrobial peptide; Electrospinning; Drug delivery; Antimicrobial fibers; Wound infection; BACTERICIDAL SUBSTANCES; TYROTHRICIN; NANOFIBERS; TYROCIDINE; GRAMICIDIN;
D O I
10.1016/j.ejpb.2022.09.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The widespread resistance of clinically relevant bacteria against established antibiotics emphasizes the urgent need for novel therapeutics. In this context, wound infections constitute a specific challenge, as most systemically applied antibiotics are insufficiently available at the site of infection. Therefore, the local treatment of infected wounds poses a particular challenge regarding the appropriate release kinetics of actives and their residence time in the wound bed. Consequently, design and development of novel, drug-loaded wound dressings constitute a major research focus for the effective treatment of wound infections. In this study, we employed electrospinning to design drug-loaded wound dressings, incorporating the therapeutically promising antimicrobial peptide tyrothricin. By parallel electrospinning, we combined different ratios of water-soluble polyvinylpyrrolidone and water-insoluble methacrylate copolymer (Eudragit E), in order to take advantage of their specific mechanical stability and dissolution properties. We fabricated fiber mats constituting mechanically stable wound dressings with a controlled drug release profile, combining an initial burst release above the minimal inhibitory concen-tration of known wound pathogens and a subsequent prolonged antimicrobial effect of the active ingredient. Antimicrobial activity against Staphylococcus aureus and Staphylococcus epidermidis was successfully proven, thereby introducing our tyrothricin-loaded fiber mats as a promising prospective therapy against typical wound-associated pathogens.
引用
收藏
页码:246 / 255
页数:10
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