Synergetic dual antibiotics-loaded chitosan/poly (vinyl alcohol) nanofibers with sustained antibacterial delivery for treatment of XDR bacteria-infected wounds

乙烯醇 抗菌活性 抗生素 粘菌素 鲍曼不动杆菌 微生物学 化学 壳聚糖 细菌 生物 铜绿假单胞菌 有机化学 聚合物 遗传学
作者
Sanaz Alizadeh,Paniz Farshi,Navid Farahmandian,Zahra Aliakbar Ahovan,Ali Hashemi,Mohammad Majidi,Abdolnaser Azadbakht,Mahsa Darestanifarahani,Koushan Sineh Sepehr,Subhas C. Kundu,Mazaher Gholipourmalekabadi
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:229: 22-34 被引量:22
标识
DOI:10.1016/j.ijbiomac.2022.11.288
摘要

Resistance of bacterial pathogens to conventional antibiotics has remained a significant challenge in managing post-wound infections, especially in developing countries. Here, a nanofibrous chitosan/poly (vinyl alcohol) (CS/PVA) mat was designed for controlled delivery of three different concentrations of two antibiotics (colistin/meropenem ratio of 32/64 μg/ml (AB1), 64/128 μg/ml (AB2), and 128/256 (AB3) μg/ml) with synergistic antibacterial activity against ATCC and extensively drug-resistant (XDR) Acinetobacter baumannii clinical isolates. The scaffolds showed a uniform fibrous structure with no bead formation with a sustained release of the antibiotics for one week. The elongation at break, wettability, porosity, and average fiber diameter decreased with increased antibiotics concentrations. Young's modulus and tensile strength showed a significant increase after adding antibiotics. All the constructs showed excellent in vitro cytocompatibility for fibroblasts and biocompatibility in an animal model. The antibacterial assays confirmed the dose-dependent antibacterial activity of the CS/PVA. The scaffolds loaded with AB2 and AB3 showed biocidal properties against ATCC, while only CS/PVA/AB3 had antibacterial activity against XDR clinical isolates. This study suggests the CS/PVA/AB3 nanofibrous scaffold contained 128/256 μg/ml colistin/meropenem as an excellent antibacterial wound dressing for protection of skin wounds from XDR clinical isolates and now promises to proceed with pre-clinical investigations.
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