Enhanced wound repair ability of arginine-chitosan nanocomposite membrane through the antimicrobial peptides-loaded polydopamine-modified graphene oxide

被引:33
|
作者
Fu, Chuan [1 ]
Qi, Zhiping [1 ]
Zhao, Chengliang [2 ]
Kong, Weijian [1 ]
Li, Hongru [1 ]
Guo, Wenlai [2 ]
Yang, Xiaoyu [1 ]
机构
[1] Second Hosp Jilin Univ, Dept Orthopaed Surg, Changchun 130021, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Spinal Surg, Qingdao 266000, Peoples R China
关键词
Chitosan; Graphene oxide; Antimicrobial peptides; Arginine; Wound dressing; SILVER NANOPARTICLES; DELIVERY; DIFFERENTIATION; BIOSYNTHESIS; DERIVATIVES; SCAFFOLDS; NANOFIBER; HYDROGELS; ALGINATE; GROWTH;
D O I
10.1186/s13036-021-00268-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Skin wound healing is a complicated and lengthy process, which is influenced by multiple factors and need a suitable cellular micro-environment. For skin wound, wound dressings remain a cornerstone of dermatologic therapy at present. The dressing material can create an effective protective environment for the wound, and the interactions between the dressing and the wound has a great impact on the wound healing efficiency. An ideal wound dressing materials should have good biocompatibility, moisturizing property, antibacterial property and mechanical strength, and can effectively prevent wound infection and promote wound healing. In this study, in order to design wound dressing materials endowed with excellent antibacterial and tissue repair properties, we attempted to load antimicrobial peptides onto dopmine-modified graphene oxide (PDA@GO) using lysozyme (ly) as a model drug. Then, functionalized GO was used to the surface modification of arginine-modified chitosan (CS-Arg) membrane. To evaluate the potential of the prepared nanocomposite membrane in wound dressing application, the surface morphology, hydrophilic, mechanical properties, antimicrobial activity, and cytocompatibility of the resulting nanocomposite membrane were analyzed. The results revealed that prepared nanocomposite membrane exhibited excellent hydrophilic, mechanical strength and antimicrobial activity, which can effectively promote cell growth and adhesion. In particular, using PDA@GO as drug carrier can effectively maintain the activity of antimicrobial peptides, and can maximize the antibacterial properties of the nanocomposite membrane. Finally, we used rat full-thickness wound models to observe wound healing, and the surface interactions between the prepared nanocomposite membrane and the wound. The results indicated that nanocomposite membrane can obviously accelerated wound closure, and the wounds showed reduced inflammation, improved angiogenesis and accelerated re-epithelialization. Therefore, incorporation of antimicrobial peptides-functionalize graphene oxide (ly-PDA@GO) into CS-Arg membrane was a viable strategy for fabricating excellent wound dressing. Together, this study not only prepared a wound dressing with excellent tissue repair ability, but also provided a novel idea for the development of graphene oxide-based antibacterial dressing.
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页数:16
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  • [1] Enhanced wound repair ability of arginine-chitosan nanocomposite membrane through the antimicrobial peptides-loaded polydopamine-modified graphene oxide
    Chuan Fu
    Zhiping Qi
    Chengliang Zhao
    Weijian Kong
    Hongru Li
    Wenlai Guo
    Xiaoyu Yang
    Journal of Biological Engineering, 15
  • [2] Polydopamine-modified graphene oxide nanocomposite membrane for proton exchange membrane fuel cell under anhydrous conditions
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    JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (25) : 9548 - 9558