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In vitro and in vivo testing of bioabsorbable antibiotic containing bone filler for osteomyelitis treatment

2006; Wiley; Volume: 78A; Issue: 3 Linguagem: Inglês

10.1002/jbm.a.30766

1552-4965

Jyri K Koort, Esa Suokas, Minna Veiranto, Tatu J. Mäkinen, Jari Jalava, Pertti Törmälä, Hannu T. Aro,

Surgical site infection prevention

Abstract The use of local antibiotics from a biodegradable implant is appealing concept for treatment of chronic osteomyelitis. Our aim was to develop a new drug delivery system based on controlled ciprofloxacin release from poly( D / L ‐lactide). Cylindrical composite pellets (1.0 × 0.9 mm) were manufactured from bioabsorbable poly( D / L ‐lactide) matrix and ciprofloxacin (7.4 wt %). In vitro studies were carried out to delineate the release profile of the antibiotic and to verify its antimicrobial activity by means of MIC testing. A long‐term study in rabbits was performed to validate the release of ciprofloxacin from the composite in vivo . Therapeutic level of ciprofloxacin (>2 μg/mL) was maintained between 60 and 300 days and the concentration remained below the potentially detrimental level of 20 μg/mL in vitro . The released ciprofloxacin had retained its antimicrobial properties against common pathogens. In an exploratory long‐term in vivo study with three rabbits, ciprofloxacin could not be detected from the serum after moderate filling (160 mg) of the tibia (follow‐up 168 days), whereas after high dosing (a total dose of 1000 mg in both tibias) ciprofloxacin was found temporarily at low serum concentrations (14–34 ng/mL) during the follow‐up of 300 days. The bone concentrations of ciprofloxacin could be measured in all samples at 168 and 300 days. The tested copolylactide matrix seems to be a promising option in selection of resorbable carriers for sustained release of antibiotics, but the composite needs modifications to promote ciprofloxacin release during the first 60 days of implantation. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006