生物形态碳化硅陶瓷作为抗细菌生物膜药物传递系统的适用性。

ISRN Pharmaceutics Pub Date : 2013-07-07 Print Date: 2013-01-01 DOI:10.1155/2013/104529
P Díaz-Rodríguez, A Pérez-Estévez, R Seoane, P González, J Serra, M Landin
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引用次数: 5

摘要

目前的工作旨在对生物形态碳化硅(bioSiCs)作为骨替代材料有一个新的认识。从各种前体中制备生物制剂,对其进行了表征,并装载了广谱抗生素。已经研究了负载生物硅对预成型金黄色葡萄球菌生物膜的预防和/或处理能力。在陶瓷生产过程中,前驱体特性的差异保持不变。所有的生物材料都允许通过毛细作用加载过程,使加载材料具有取决于其微观结构的药物释放谱。在前6小时内,抗生素在液体介质中的释放量取决于生物碳化硅的孔隙度,但对于所有研究的材料,它可能超过金黄色葡萄球菌的最低抑制浓度,从而阻止细菌的增殖。当使用固体介质进行实验时,生物硅的外表面以及开放的外孔的数量和大小的差异导致了对细菌效果的变化。所有系统的内部结构和表面特性似乎都促进了抗生素对预成型生物膜的治疗活性,与对照相比,减少了生物膜中存在的活菌数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Suitability of Biomorphic Silicon Carbide Ceramics as Drug Delivery Systems against Bacterial Biofilms.

Suitability of Biomorphic Silicon Carbide Ceramics as Drug Delivery Systems against Bacterial Biofilms.

Suitability of Biomorphic Silicon Carbide Ceramics as Drug Delivery Systems against Bacterial Biofilms.

Suitability of Biomorphic Silicon Carbide Ceramics as Drug Delivery Systems against Bacterial Biofilms.

The present work is aimed at getting a new insight into biomorphic silicon carbides (bioSiCs) as bone replacement materials. BioSiCs from a variety of precursors were produced, characterized, and loaded with a broad-spectrum antibiotic. The capacity of loaded bioSiCs for preventing and/or treating preformed S. aureus biofilms has been studied. The differences in precursor characteristics are maintained after the ceramic production process. All bioSiCs allow the loading process by capillarity, giving loaded materials with drug release profiles dependent on their microstructure. The amount of antibiotic released in liquid medium during the first six hours depends on bioSiC porosity, but it could exceed the minimum inhibitory concentration of Staphylococcus aureus, for all the materials studied, thus preventing the proliferation of bacteria. Differences in the external surface and the number and size of open external pores of bioSiCs contribute towards the variations in the effect against bacteria when experiments are carried out using solid media. The internal structure and surface properties of all the systems seem to facilitate the therapeutic activity of the antibiotic on the preformed biofilms, reducing the number of viable bacteria present in the biofilm compared to controls.

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