Multifunctional gelatin nanoparticle stabilized-Pickering emulsion hydrogel based on dextran and amikacin with controlled drug release and enhanced antibacterial capability for promoting infected wound healing

明胶 右旋糖酐 凝聚 伤口愈合 纳米颗粒 壳聚糖 皮克林乳液 乳状液 控制释放 阿米卡星 化学 化学工程 材料科学 纳米技术 色谱法 有机化学 抗生素 医学 生物化学 外科 工程类
作者
Ruiyun Zhang,Xiao Huang,Qiaoli Wu,Shirun Chu,Xue Bai,Yuanyuan Zhou,Jing You,Chen Yang,Huan Tan
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:262: 130172-130172 被引量:2
标识
DOI:10.1016/j.ijbiomac.2024.130172
摘要

Plant essential oils possess broad-spectral antimicrobial property, but the applications are impeded by their insolubility in water, extreme volatility, and strong irritation. Nanoparticle-stabilized emulsion (Pickering emulsion) gels are colloidal systems with ability to accommodate two immiscible phases in one system. The thick adsorption nanoparticle layers and the cross-linked networks in continuous phase could provide protective barriers for antibacterial oil and achieve on-demand controlled release. An emulsion hydrogel templated from gelatin nanoparticle-stabilized emulsion is one-pot constructed by conducting a tunable cross-linking process between oxidized dextran (Odex) and amikacin in the continuous phase and concomitantly trapping tea tree essential oil (TO) droplets in the three-dimensional network. The resulted emulsion hydrogel presents tunable gelation time, adequate mechanical strength, fascinating injectability, and self-healing capability. It is pH-responsiveness and presents controlled release of amikacin and TO, exhibiting a long-term bacteriostasis of 144 h. The emulsion hydrogel facilitates the outstanding wound healing efficiency in 14 days (95.2 ± 0.8 % of wound closure), accompanied with enhanced collagen deposition and angiogenic activities. The incorporation of TO into emulsion hydrogel system reduced its irritation and improved its biosafety, showing potential application in bacteria inhibition even as implants in vivo.
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