头孢金刚醇
聚氨酯
纳米颗粒
牛血清白蛋白
药物输送
化学
吸附
抗菌剂
抗生素
头孢呋辛
药品
聚合物
核化学
材料科学
纳米技术
色谱法
医学
头孢菌素
有机化学
药理学
生物化学
作者
Fernanda Crisante,Iolanda Francolini,Mariangela Bellusci,Andrea Martinelli,L. D’Ilario,Antonella Piozzi
标识
DOI:10.1016/j.ejps.2008.12.006
摘要
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.
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