J. Rivadeneira, Gisela M. Luz, M. Audisio, João F. Mano, Alejandro A. Gorustovich
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引用次数: 9
摘要
摘要为了防止伤口感染的高发,可以在复合材料上添加抗菌药物。本研究首次将抗生素盐酸四环素(tetracycline hydrochloride, TC)掺入通过溶胶-凝胶化学途径获得的纳米SiO2-CaOP2O5生物活性玻璃(n-BG)包被的I型胶原膜中。在37°C下,用共沉淀法将涂有n-BG的胶原膜浸入含有0.25、0.75或1.25 mg mL - 1 TC的模拟体液(SBF)中48小时。抗生素在37°C的蒸馏水中释放72小时。复合材料的抗菌活性在体外通过抑菌带试验和平板计数法进行评价。两种不同的金黄色葡萄球菌菌株,金黄色葡萄球菌ATCC29213和金黄色葡萄球菌ATCC25923暴露于生物材料。结果表明,TC的掺入与SBF中TC的初始浓度有关,而与TC的释放无关。生物材料抑制金黄色葡萄球菌生长,尽管所有浓度的效果相似。结果使我们得出结论,这种新的复合材料在预防伤口感染方面具有潜力。
Novel antibacterial bioactive glass nanocomposite functionalized with tetracycline hydrochloride
Abstract To prevent the high frequency of wound infections, anti-bacterial agents can be loaded onto composites. In the present study, the antibiotic tetracycline hydrochloride (TC)was incorporated, for the first time, in collagen type I membranes coated with nano-sized SiO2-CaOP2O5 bioactive glass (n-BG) obtained by a sol-gel chemical route. Collagen membranes coated with n-BG were immersed in simulated body fluid (SBF) containing 0.25, 0.75 or 1.25 mg mL−1 of TC for 48 h at 37∘C following a coprecipitation method. The antibiotic was released in distilledwater at 37∘C for up to 72 h. The antibacterial activity of the composites was evaluated in vitro by the inhibition zone test and plate count method. Two different Staphylococcus aureus strains, S. aureus ATCC29213 and S. aureus ATCC25923, were exposed to the biomaterials. The results showed that the incorporation but not the release of TC was dependent on the initial concentration of TC in SBF. The biomaterials inhibited S. aureus growth, although the efficacy was similar for all the concentrations. The results allow us to conclude that the new composite could have potential in the prevention of wound infections.
期刊介绍:
Biomedical Glasses is an international Open Access-only journal covering the field of glasses for biomedical applications. The scope of the journal covers the science and technology of glasses and glass-based materials intended for applications in medicine and dentistry. It includes: Chemistry, physics, structure, design and characterization of biomedical glasses Surface science and interactions of biomedical glasses with aqueous and biological media Modeling structure and reactivity of biomedical glasses and their interfaces Biocompatibility of biomedical glasses Processing of biomedical glasses to achieve specific forms and functionality Biomedical glass coatings and composites In vitro and in vivo evaluation of biomedical glasses Glasses and glass-ceramics in engineered regeneration of tissues and organs Glass-based devices for medical and dental applications Application of glasses and glass-ceramics in healthcare.