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利用载有细菌响应型微球的可溶解微针进行选择性递送来改善生物膜皮肤感染的治疗

Selective delivery of silver nanoparticles for improved treatment of biofilm skin infection using bacteria-responsive microparticles loaded into dissolving microneedles.

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, Hasanuddin University, Makassar 90245, Indonesia.

School of Pharmacy, Queen's University Belfast, Belfast BT9 7BL, UK.

出版信息

Mater Sci Eng C Mater Biol Appl. 2021 Jan;120:111786. doi: 10.1016/j.msec.2020.111786. Epub 2020 Dec 10.

DOI:10.1016/j.msec.2020.111786
PMID:33545912
Abstract

The treatment of infected chronic wounds has been hampered by development of bacterial biofilms and the low penetration of antibacterial compounds delivered by conventional dosage forms. Numerous bacterial biofilm formers have shown resistance to synthetic antibacterial agents. In this study, we explore the potential of silver nanoparticles (NPs) synthesized using green tea extract as antibiofilm agents against Staphylococcus aureus (SA) and Pseudomonas aeruginosa (PA) biofilms. Due to the toxicity of silver NPs, for the first time, silver NPs were incorporated into bacteria-responsive microparticles (MPs) prepared from poly (Ɛ-caprolactone) decorated with chitosan. The in vitro release of silver NPs from MPs increased up to 9-times in the presence of SA and PA, showing the selectivity of this approach. Incorporation of the MPs into dissolving microneedles (DMNs) could enhance the dermatokinetic profiles of silver NPs compared to DMNs containing silver NPs without MP formulations and conventional cream formulations. Furthermore, 100% of bacterial bioburdens were eradicated on ex vivo biofilm model in rat skin following 60 h of the administration of this system. The findings revealed here confirmed the feasibility of the loading of silver NPs into responsive MPs for improved antibiofilm activities when delivered using DMNs. Following on from these promising results, toxicity and in vivo pharmacodynamic studies should now be carried out in an appropriate model.

摘要

受限于细菌生物膜的形成以及传统剂型传递的抗菌化合物的低渗透性,感染性慢性创面的治疗一直受到阻碍。许多细菌生物膜形成者对合成抗菌剂表现出耐药性。在这项研究中,我们探索了使用绿茶提取物合成的银纳米粒子(NPs)作为抗生物膜剂对抗金黄色葡萄球菌(SA)和铜绿假单胞菌(PA)生物膜的潜力。由于银 NPs 的毒性,我们首次将银 NPs 掺入由壳聚糖修饰的聚(Ɛ-己内酯)制备的细菌响应型微球(MPs)中。在存在 SA 和 PA 的情况下,从 MPs 中释放的银 NPs 的体外释放增加了 9 倍,显示了这种方法的选择性。与不含 MPs 配方和常规乳膏配方的载有银 NPs 的 DMNs 相比,将 MPs 掺入可溶解微针(DMN)中可以增强银 NPs 的皮肤动力学特性。此外,在大鼠皮肤的体外生物膜模型中,在给予该系统 60 小时后,100%的细菌生物负荷被消除。这里揭示的研究结果证实了将银 NPs 负载到响应性 MPs 中以提高使用 DMN 递送时的抗生物膜活性的可行性。在这些有希望的结果之后,现在应该在适当的模型中进行毒性和体内药效学研究。

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