A chitosan derivative-crosslinked hydrogel with controllable release of polydeoxyribonucleotides for wound treatment

被引:39
|
作者
Sun Y. [1 ]
Jing X. [1 ]
Liu Y. [1 ]
Yu B. [1 ,2 ]
Hu H. [1 ]
Cong H. [1 ,2 ,3 ]
Shen Y. [1 ,4 ]
机构
[1] Institute of Biomedical Materials and Engineering, College of Chemistry and Chemical Engineering, College of Materials Science and Engineering, Qingdao University, Qingdao
[2] Laboratory for New Fiber Materials and Modern Textile, Growing Base for State Key Laboratory, Qingdao University, Qingdao
[3] School of Materials Science and Engineering, Shandong University of Technology, Zibo
[4] Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Center for Bionanoengineering, Department of Chemical and Biological Engineering, Zhejiang University, Hangzhou
基金
中国国家自然科学基金;
关键词
Drug delivery; Gene therapy; Nanocomposite hydrogel; PDRN; Wound dressing;
D O I
10.1016/j.carbpol.2022.120298
中图分类号
学科分类号
摘要
Nucleic acid-based agents have advantages in therapeutic efficacy and biological safety. However, due to its facile degradability, it lacks an effective route of administration in wound treatment. Designing smart hydrogels for the spatiotemporally controllable delivery of nucleic acids is of great significance for clinical applications. Here, a near-infrared (NIR)-responsive nanocomposite hydrogel was prepared using methyl methacrylate (GMA)-modified chitosan as the macromolecular cross-linker, N-isopropylacrylamide (NIPAAm) as the backbone, and molybdenum disulfide nanosheets (MoS2 NSs) as the nanocomponents. The polydeoxyribonucleotide (PDRN), a nucleic acid-based agent that promotes tissue regeneration, was loaded and delivered. The photothermal conversion capability of MoS2 NSs enables customized care of PDRNs and antibacterial enhancement. In a full-thickness skin defect model, high-quality wound healing effects were demonstrated under the action of nanocomposite hydrogels. The proposed nanocomposite hydrogel provides a new reference for local delivery of nucleic acid-based agents. © 2022 Elsevier Ltd
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