An antibacterial nanoclay- and chitosan-based quad composite with controlled drug release for infected skin wound healing

PLGA公司 壳聚糖 伤口愈合 生物相容性 生物医学工程 组织粘连 化学 复合数 材料科学 粘附 药理学 体外 外科 医学 复合材料 生物化学 有机化学
作者
Wenlong Wei,Mayue Wang,Ziru Liu,Wen Jiang Zheng,Pier‐Luc Tremblay,Tian Zhang
出处
期刊:Carbohydrate Polymers [Elsevier BV]
卷期号:324: 121507-121507 被引量:20
标识
DOI:10.1016/j.carbpol.2023.121507
摘要

Microbial infections of surgical sites and other wounds represent a major impediment for patients. Multifunctional low-cost dressings promoting tissue reparation while preventing infections are of great interest to medical professionals. Here, clay-based laponite nanodiscs (LAP) were loaded with the antibacterial drug kanamycin (KANA) before being embedded into a poly(lactic-co-glycolic acid) (PLGA) membrane and coated with the biopolymer chitosan (CS). Results indicated that these biocompatible materials combined the excellent capacity of LAP for controlled drug release with the mechanical robustness of PLGA and the antibacterial properties of CS as well as its hydrophilicity to form a composite highly suitable as an infection-preventing wound dressing. In vitro, PLGA/LAP/KANA/CS released drugs in a sustainable manner over 30 d, completely inhibited the growth of infectious bacteria, prompted the adhesion fibroblasts, and accelerated their proliferation 1.3 times. In vivo, the composite enabled the fast healing of infected full-thickness skin wounds with a 96.19 % contraction after 14 d. During the healing process, PLGA/LAP/KANA/CS stimulated re-epithelization, reduced inflammation, and promoted both angiogenesis and the formation of dense collagen fibers with an excellent final collagen volume ratio of 89.27 %. Thus, multifunctional PLGA/LAP/KANA/CS made of low-cost components demonstrated its potential for the treatment of infected skin wounds.
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