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Inhibition of bacterial adhesion on biocompatible zwitterionic SBA-15 mesoporous materials

In this manuscript in vitro bacterial adhesion assays using Escherichia coli on different SBA-15 nanostructured ceramics have been performed. For this purpose pure silica, NH 2 or COOH monofunctionalized, and NH 2/ COOH bifunctionalized SBA-15 mesoporous materials have been used. Material characteri...

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Bibliographic Details
Published in:Acta biomaterialia 2011-07, Vol.7 (7), p.2977-2985
Main Authors: Izquierdo-Barba, Isabel, Sánchez-Salcedo, Sandra, Colilla, Montserrat, Feito, María José, Ramírez-Santillán, Cecilia, Portolés, María Teresa, Vallet-Regí, María
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Language:English
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Summary:In this manuscript in vitro bacterial adhesion assays using Escherichia coli on different SBA-15 nanostructured ceramics have been performed. For this purpose pure silica, NH 2 or COOH monofunctionalized, and NH 2/ COOH bifunctionalized SBA-15 mesoporous materials have been used. Material characterization reveals that both NH 2/ COOH and NH 2 functionalized SBA-15 materials exhibit a zwitterionic character due to the presence of - NH 3 + / COO − or - NH 3 + / SiO − moieties, respectively. In vitro adhesion assays have been carried out at the pH at which the zwitterionic nature of both of these samples is preserved, i.e. pH 5.5. The results show that the presence of both positive and negative moieties with an overall neutral charge leads to reduced E. coli adhesiveness. In vitro tests with cultured human Saos-2 osteoblasts have been carried out to evaluate the biocompatibility of the different materials at the physiological pH of 7.4. The results demonstrate that all materials exhibit good biocompatibility, with Saos-2 osteoblasts adhering, proliferating and maintaining their morphological and functional characteristics. This novel family of zwitterionic mesoporous materials opens up promising expectations in diverse biomedical applications, such as preventing some side-effects associated with bone implant infections.
ISSN:1742-7061
1878-7568
DOI:10.1016/j.actbio.2011.03.005