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具有抗菌、细胞相容和药物输送性能的仿鲨鱼皮表面。

Biomimetic sharkskin surfaces with antibacterial, cytocompatible, and drug delivery properties.

机构信息

Institute of Biomedical Engineering, Boğaziçi University, 34684 Istanbul, Turkey.

Department of Cardiology, Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital, 34668 Istanbul, Turkey.

出版信息

Biomater Adv. 2022 Mar;134:112565. doi: 10.1016/j.msec.2021.112565. Epub 2021 Nov 27.

Abstract

Fighting with the infection is one of the most challenging and costly burdens of the healthcare system. Several types of antibiotics and antibacterial agents have been designed and used in combating this dilemma. Nevertheless, the overuse of drugs and the difficulties of proper delivery have led to the development of drug-resistance in many species of bacteria which has reduced the efficacy of antibiotics. Furthermore, localized delivery of these drugs can be more effective in eliminating biomaterial surface-associated infection compared to systemic administration. This type of infection occurs mostly by the formation of a bacterial biofilm layer on the surface of the implantable biomaterial which is the interface between the biomaterial and the tissue. Sharkskin topography is known for its antibacterial properties due to its unique pattern. Herein, antibacterial properties and drug release potentials of sharkskin mimicked chitosan membranes are investigated with the aim of studying the impact of this topography in reducing bacterial biofilm formation on drug-loaded polymeric membranes. Ampicillin sodium salt and caffeic acid phenethyl ester (CAPE) loaded chitosan (CH) membranes were fabricated. Gram-positive Staphylococcus aureus bacteria strain is used in antibacterial experiments, and human dermal fibroblast (HDFa) and keratinocyte (HaCaT) cells were used as model cell lines in cytocompatibility tests. Drug release, bacterial biofilm growth, and swelling ratio test results show the superiority of sharkskin topography in controlling the rate of drug release as well as considerably reducing bacterial biofilm formation. Furthermore, it was established that 2.5 mg mL Amp content along with 500 μM CAPE yield in maximum antibacterial effect while not having cytotoxic effects on mammalian cells. Fabricated sharkskin mimicked drug-loaded membrane, which utilizes the combination of antibacterial compounds and antibacterial surface topography, also acts as an effective carrier for high concentrations of drugs.

摘要

与感染作斗争是医疗保健系统最具挑战性和最昂贵的负担之一。已经设计并使用了几种类型的抗生素和抗菌剂来对抗这一困境。然而,药物的过度使用和适当输送的困难导致许多细菌物种产生了耐药性,从而降低了抗生素的疗效。此外,与全身给药相比,这些药物的局部给药在消除生物材料表面相关感染方面更为有效。这种类型的感染主要是由于在可植入生物材料的表面形成细菌生物膜层而发生的,该生物膜层是生物材料与组织之间的界面。鲨鱼皮的拓扑结构因其独特的图案而具有抗菌特性。在此,研究了模仿鲨鱼皮结构的壳聚糖膜的抗菌性能和药物释放潜力,目的是研究这种拓扑结构在减少载药聚合物膜上细菌生物膜形成方面的影响。制备了载有氨苄青霉素钠和咖啡酸苯乙酯(CAPE)的壳聚糖(CH)膜。在抗菌实验中使用革兰氏阳性金黄色葡萄球菌细菌株,并用人真皮成纤维细胞(HDFa)和角质形成细胞(HaCaT)作为细胞相容性测试的模型细胞系。药物释放、细菌生物膜生长和溶胀比测试结果表明,鲨鱼皮拓扑结构在控制药物释放速率以及显著减少细菌生物膜形成方面具有优越性。此外,研究结果表明,2.5mg mL 的氨苄青霉素含量和 500μM 的 CAPE 含量可产生最大的抗菌效果,同时对哺乳动物细胞没有细胞毒性。所制备的模仿鲨鱼皮的载药膜利用了抗菌化合物和抗菌表面拓扑结构的结合,也可作为高浓度药物的有效载体。

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