Polyvinyl alcohol nanofiber formulation of the designer antimicrobial peptide APO sterilizes Acinetobacter baumannii-infected skin wounds in mice
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  • 作者:Istvan Sebe ; Eszter Ostorhazi ; Aron Fekete ; Krisztian N. Kovacs
  • 关键词:Antibacterial peptide ; Cutaneous infection ; Nanoformulation ; Topical treatment ; Wound healing
  • 刊名:Amino Acids
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:48
  • 期:1
  • 页码:203-211
  • 全文大小:2,147 KB
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  • 作者单位:Istvan Sebe (1)
    Eszter Ostorhazi (2) (3)
    Aron Fekete (2)
    Krisztian N. Kovacs (4)
    Romana Zelko (1)
    Ilona Kovalszky (5)
    Wenyi Li (6)
    John D. Wade (6)
    Dora Szabo (2)
    Laszlo Otvos Jr. (2) (7)

    1. University Pharmacy Department of Pharmacy Administration, Semmelweis University, Hogyes Endre Street 7-9, Budapest, 1092, Hungary
    2. Institute of Medical Microbiology, Semmelweis University, Nagyvarad ter 4, Budapest, 1089, Hungary
    3. Department of Laboratory Medicine, Semmelweis University, Nagyvarad ter 4, Budapest, 1089, Hungary
    4. Department of Polymer Engineering, Faculty of Mechanical Engineering, Budapest University of Technology and Economics, Muegyetem rkp. 3., Budapest, 1111, Hungary
    5. 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Ulloi ut 26, Budapest, 1085, Hungary
    6. Florey Institute of Neuroscience and Mental Health, University of Melbourne, 3010, Melbourne, VIC, Australia
    7. OLPE, LLC, 801 Mockingbird Lane, Audubon, PA, 19403, USA
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Biochemistry
    Analytical Chemistry
    Biochemical Engineering
    Life Sciences
    Proteomics
    Neurobiology
  • 出版者:Springer Wien
  • ISSN:1438-2199
文摘
Native and designer cationic antimicrobial peptides are increasingly acknowledged as host defense molecules rather than true antimicrobials. Due to their ability to activate the innate immune system, these structures are used to treat uninfected and bacterially-infected wounds, including those harboring Acinetobacter baumannii. Previously we documented that when administered intramuscularly or topically in liquid formulations, the proline-rich host defense peptide dimer A3-APO accelerates uninfected wound re-epithelization and eliminates systemic and local A. baumannii, methicillin-resistant Staphylococcus aureus and other pathogen load from infected lesions better than conventional antibiotics. In the current study we sought to produce and characterize a novel delivery system, suitable for immediate and convenient application in non-hospital environments. The APO monomer was incorporated into polyvinyl alcohol nanofibers and the complex was polymerized into a solid patch dressing. Mice were subjected to skin abrasion where the wounds were either left uninfected or were inoculated with a near lethal dose of multidrug resistant A. baumannii strain. Analyzed after 3 days, APO monomer-containing patches improved wound appearance significantly better than polymer patches without antibiotics. When compared to colistin, the APO patches accelerated wound healing, and statistically significantly reduced wound size and wound bacterial load. The in vivo antimicrobial effect was more extensive than after intramuscular administration of the peptide drug, by using only one tenth of the active pharmaceutical ingredient. These data suggest that the APO monomer-impregnated nanofiber dressing can be developed as an economical first-line treatment option to skin injuries in general and battlefield burn and blast injuries in particular. Keywords Antibacterial peptide Cutaneous infection Nanoformulation Topical treatment Wound healing

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