The availability of osteogenic proteins for orthopedic applications has led to great interest in developing delivery systems for these substances. Standard release rate models are applicable in most biological settings, but orthopedic implants usually bear mechanical loads. To determine whether a re
Controlled release of bisphosphonate from a biodegradable implant: Evaluation of release kinetics and anticalcification effect
β Scribed by Dr. Gershon Golomb; Matilda Levi; Joel M. Van Gelder
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1992
- Tongue
- English
- Weight
- 482 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1045-4861
No coin nor oath required. For personal study only.
β¦ Synopsis
The present investigation describes the formulation and the in vivo efficacy of prolonged controlled-release chitosan matrices, containing the novel anticalcification agents adipoyland suberoylbisphosphonate (AdBP and SuBP). Chitosan matrices were prepared by the solvent-cast method and the role of several factors such as polymer molecular weight (MW), crosslinking, and drug load concentration, on the release rate profile have been examined. Crosslinking of chitosan films retarded degradation rate of the polymer but not the release rate of the embedded drug. Chitosan's MW and drug load concentration did not affect drug release rate. The release kinetics of the bisacylphosphonates were characterized by initial burst-effect and pseudo zero-order kinetics in the following release phase. AdBP! chitosan matrices (co-implanted subdermally in rats with the calcifiable bioprosthetic heart valve tissue) significantly inhibited tissue calcification after 15 and 30 days implantation (66.4 and 108.6 pg/mg Ca++ in comparison to 2.7 and 3.6 pg/mg Ca", untreated and treated groups, respectively). No side effects were noted.
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