Elution Characteristics of Tobramycin from Polycaprolactone in a Rabbit Model
Abstract
This study investigated the elution characteristics of tobramycin from polycaprolactone, a bioabsorbable polymer, in a rabbit model. Sixty rabbits were divided into two groups. Group 1 had polycaprolactone rods impregnated with 6% tobramycin surgically implanted into the proximal femoral intramedullary canal. Group 2 received polymethylmethacrylate rods of like size, shape, and antibiotic concentration. Serum and urine samples were obtained, and tobramycin levels were determined via fluorescent immunosorbent assay. Rabbits were sacrificed as long as 56 days after surgery. Local bone tobramycin concentration was determined using the agar diffusion method. Polycaprolactone delivered a significantly higher peak bone concentration of tobramycin (22.4 ug/mL) than did polymethylmethacrylate (13.59 ug/mL). Polycaprolactone also had a more gradual decrease in local tobramycin concentration than did polymethylmethacrylate. Neither polycaprolactone nor polymethylmethacrylate yielded consistently detectable (> 0.1 ug/mL) serum tobramycin levels. Urine concentrations mirrored those seen in bone, with polycaprolactone achieving significantly higher tobramycin concentrations than did polymethylmethacrylate. Polycaprolactone had superior elution characteristics compared with polymethylmethacrylate in this lapine model, suggesting that polycaprolactone might be a promising local antibiotic delivery vehicle for the treatment of osteomyelitis.
Recommended Citation
K. J. Hendricks et al., "Elution Characteristics of Tobramycin from Polycaprolactone in a Rabbit Model," Clinical Orthopaedics and Related Research, Lippincott Williams & Wilkins, Nov 2001.
Department(s)
Materials Science and Engineering
Sponsor(s)
Orthopaedic Trauma Association
International Standard Serial Number (ISSN)
0009-921X
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2001 Lippincott Williams & Wilkins, All rights reserved.
Publication Date
01 Nov 2001