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J Biomed Mater Res ; 57(2): 313-20, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11484196

ABSTRACT

Room temperature processed silica sol-gel (xerogel) was investigated as a novel controlled release carrier of antibiotics (vancomycin). Xerogel characteristics, in vitro release properties, and bactericidal efficacy of the released antibiotic were determined. The xerogel/vancomycin composite showed a long-term sustained release (up to 6 weeks). In addition, bactericidal efficacy of released vancomycin was retained. The kinetics of release and the amount released were dose dependent. The initial, first-order release was followed by a near-zero-order release. The time to transition from the first- to zero-order release increased with vancomycin load (from 2 to 3 weeks with load increase from 2.2 to 11.1 mg/g). Regardless of the load, about 70% of the original vancomycin content was released by the transitional point, and the cumulative release after 6 weeks of immersion was about 90%. This study, combined with other reports documenting biocompatibility and controlled resorbability of the xerogel/drug composite in vivo, suggests that silica xerogel is a promising controlled release material for the treatment of bone infections.


Subject(s)
Delayed-Action Preparations , Drug Carriers , Silicon Dioxide , Vancomycin/pharmacokinetics , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacokinetics , Anti-Bacterial Agents/pharmacology , Gels/chemistry , Microbial Sensitivity Tests , Silica Gel , Silicon Dioxide/chemical synthesis , Silicon Dioxide/chemistry , Spectroscopy, Fourier Transform Infrared , Temperature , Vancomycin/chemistry , Vancomycin/pharmacology
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