Applied Science and Technology Department - DISAT, Politecnico di Torino, Turin, Italy.
J Biomater Appl. 2013 Aug;28(2):308-19. doi: 10.1177/0885328212447665. Epub 2012 Jun 7.
A bioactive glass and its corresponding glass-ceramic have been used to investigate the possibility to load a common antibiotic (carbenicillin) on their surface during the reactivity processes which occur by dipping these materials in a simulated body fluid. The materials bioactivity in the early stage of simulated body fluid treatment has been investigated by means of scanning electron microscopy (SEM-EDS) and X-ray diffraction. The uptake of carbenicillin has been performed by dipping the samples in simulated body fluid solution with a drug concentration of 500 mg/l for 6, 12 and 24 h. Some glass samples underwent a pre-treatment in simulated body fluid, for different time frames, in order to form a silica gel layer before the surface exposition to antibiotic. The carbenicillin release has been measured in water up to 36 h. The amount of incorporated and released antibiotic has been estimated by UV visible spectrophotometer. All samples were able to incorporate a significant amount of antibiotic and it was possible to tailor the drug release by modifying the simulated body fluid pre-treatment.
一种生物活性玻璃及其相应的玻璃陶瓷已被用于研究在将这些材料浸入模拟体液中发生的反应过程中,是否有可能将一种常见抗生素(羧苄青霉素)负载到其表面上。通过扫描电子显微镜(SEM-EDS)和 X 射线衍射研究了材料在模拟体液处理的早期阶段的生物活性。通过将样品浸入药物浓度为 500mg/L 的模拟体液溶液中 6、12 和 24 小时来进行羧苄青霉素的摄取。一些玻璃样品在模拟体液中进行了不同时间的预处理,以便在表面暴露于抗生素之前形成硅胶层。在 36 小时内,在水中测量了羧苄青霉素的释放。通过紫外可见分光光度计估算了掺入和释放的抗生素的量。所有样品都能够掺入大量的抗生素,并且可以通过修改模拟体液预处理来控制药物释放。