A Sustained-Release Nanosystem with MRSA Biofilm-Dispersing and -Eradicating Abilities Accelerates Diabetic Ulcer Healing

茶树油 抗菌剂 生物膜 金黄色葡萄球菌 微生物学 伤口愈合 趋化性 群体感应 化学 药理学 生物 免疫学 细菌 受体 生物化学 精油 食品科学 遗传学
作者
Shan He,Huangding Wen,Nannan Yao,Lu Wang,Junqun Huang,Zhiqing Li
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 18: 3951-3972 被引量:14
标识
DOI:10.2147/ijn.s410996
摘要

Introduction: Drug-resistant bacterial infections and biofilm formation play important roles in the pathogenesis of diabetic refractory wounds. Tea tree oil (TTO) exhibits antimicrobial, antimycotic, and antiviral activities, especially against common clinically resistant strains, such as methicillin-resistant Staphylococcus aureus (MRSA), making it a potential natural antimicrobial for the treatment of acute and chronic wounds. However, TTO is insoluble in water, volatile, light-sensitive, and cytotoxic. While previous macroscopic studies have focused on sterilization with TTO, none have sought to alter its structure or combine it with other materials to achieve sustained release. Methods: Electrospun TTO nanoliposomes (TTO-NLs), arranged linearly via high-pressure homogenization, could stabilize the structure and performance of TTO to achieve slow drug release. Herein, we established a composite nano-sustained release system, TTO-NL/polyvinyl alcohol/chitosan ( [email protected] ), using high-voltage electrospinning. Results: Compared with the control, [email protected] exhibits higher concentrations of the active TTO drug components, terpinen-4-ol and 1,8-cineole. Owing to its increased stability and slow release, early exposure to [email protected] increases the abundance of reactive oxygen species in vitro, ultimately causing the biofilm to disperse and completely killing MRSA without inducing cytotoxic effects to the host. Moreover, in BKS-Lepr em2Cd479 /Gpt mice with a whole-layer skin infection, untargeted metabolomics analysis of wound exudates reveals upregulated PGF2α/FP receptor signaling and interleukin (IL)-1β and IL-6 expression following application of the composite system. The composite also ameliorates the chemotaxis disorder in early treatment and attenuates the wound inflammatory response during the repair stage of diabetic inflammatory wounds, and upregulates VEGF expression in the wound bed. Conclusion: [email protected] demonstrates the remarkable potential for accelerating diabetic and MRSA-infected wound healing. Keywords: electrospinning, MRSA biofilm, antibacterial material, diabetic ulcer, wound healing
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