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一种用于局部抗菌药物递送的生物粘附纳米粒子-水凝胶混合系统。

A Bioadhesive Nanoparticle-Hydrogel Hybrid System for Localized Antimicrobial Drug Delivery.

机构信息

Department of Polymer Science and Engineering, School of Chemical Engineering and Technology, Tianjin University , Tianjin, 300072, China.

Institute of Functional Nano & Soft Materials (FUNSOM), Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University , Suzhou, Jiangsu 215123, China.

出版信息

ACS Appl Mater Interfaces. 2016 Jul 20;8(28):18367-74. doi: 10.1021/acsami.6b04858. Epub 2016 Jul 11.

Abstract

Effective antibacterial treatment at the infection site associated with high shear forces remains challenging, owing largely to the lack of durably adhesive and safe delivery platforms that can enable localized antibiotic accumulation against bacterial colonization. Inspired by delivery systems mimicking marine mussels for adhesion, herein, we developed a bioadhesive nanoparticle-hydrogel hybrid (NP-gel) to enhance localized antimicrobial drug delivery. Antibiotics were loaded into polymeric nanoparticles and then embedded into a 3D hydrogel network that confers adhesion to biological surfaces. The combination of two distinct delivery platforms, namely, nanoparticles and hydrogel, allows the hydrogel network properties to be independently tailored for adhesion while maintaining controlled and prolonged antibiotic release profile from the nanoparticles. The bioadhesive NP-gel developed here showed superior adhesion and antibiotic retention under high shear stress on a bacterial film, a mammalian cell monolayer, and mouse skin tissue. Under a flow environment, the NP-gel inhibited the formation of an Escherichia coli bacterial film. When applied on mouse skin tissue for 7 consecutive days, the NP-gel did not generate any observable skin reaction or toxicity, implying its potential as a safe and effective local delivery platform against microbial infections.

摘要

由于缺乏能够持久黏附且安全的药物输送平台来实现针对细菌定植的局部抗生素累积,因此,在感染部位实现有效的抗菌治疗并伴有高剪切力仍然具有挑战性。受模仿海洋贻贝用于黏附的输送系统的启发,本文开发了一种生物黏附性纳米颗粒-水凝胶杂化(NP-gel)以增强局部抗菌药物输送。将抗生素载入聚合物纳米颗粒中,然后嵌入 3D 水凝胶网络中,赋予其对生物表面的黏附性。两种不同的输送平台(纳米颗粒和水凝胶)的组合,使得水凝胶网络的性质可以独立地进行黏附性调整,同时保持纳米颗粒中抗生素的控制和延长释放特性。所开发的这种生物黏附性 NP-gel 在细菌膜、哺乳动物细胞单层和小鼠皮肤组织上的高剪切应力下表现出优异的黏附性和抗生素保留性。在流动环境下,NP-gel 抑制了大肠杆菌细菌膜的形成。当连续 7 天应用于小鼠皮肤组织时,NP-gel 未产生任何可观察到的皮肤反应或毒性,这意味着其具有作为针对微生物感染的安全有效的局部输送平台的潜力。

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