Crisante Fernanda, Francolini Iolanda, Bellusci Mariangela, Martinelli Andrea, D'Ilario Lucio, Piozzi Antonella
Department of Chemistry, "Sapienza" University of Rome P.le A. Moro 5, 00185 Rome, Italy.
Eur J Pharm Sci. 2009 Mar 2;36(4-5):555-64. doi: 10.1016/j.ejps.2008.12.006. Epub 2008 Dec 24.
Nano-structured polymers delivering an antibiotic for the prevention of medical device-related infections were developed. Systems consisted of bovine serum albumin or polyallylamine nanoparticles alone or entrapped in a polyurethane and then loaded with cefamandole nafate, chosen as a drug model. Results showed that nanoparticles alone were able to adsorb high antibiotic amounts due to their high surface/volume ratio. However, they released cefamandole in an uncontrolled fashion, leading to a rapid loss of antibacterial activity. Improvements in the release control were obtained when CEF loaded and non-loaded nanoparticles were entrapped in a carboxylated polyurethane. For these systems the drug delivery was at least of 50% with respect to nanoparticles alone with a prolonged antimicrobial activity up to 9 days.
开发了用于预防医疗器械相关感染的纳米结构聚合物,其可递送抗生素。该系统由单独的牛血清白蛋白或聚烯丙胺纳米颗粒组成,或包裹在聚氨酯中,然后负载头孢孟多酯钠作为药物模型。结果表明,由于纳米颗粒具有高的表面/体积比,单独的纳米颗粒能够吸附大量抗生素。然而,它们以不受控制的方式释放头孢孟多,导致抗菌活性迅速丧失。当负载和未负载头孢孟多的纳米颗粒包裹在羧化聚氨酯中时,释放控制得到改善。对于这些系统,相对于单独的纳米颗粒,药物递送至少为50%,抗菌活性可延长至9天。