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Osteogenic Activity of Locally Applied Small Molecule Drugs in a Rat Femur Defect Model

The long-term success of arthroplastic joints is dependent on the stabilization of the implant within the skeletal site. Movement of the arthroplastic implant within the bone can stimulate osteolysis, and therefore methods which promote rigid fixation or bone growth are expected to enhance implant s...

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Bibliographic Details
Published in:BioMed research international 2010-01, Vol.2010 (2010), p.1-11
Main Authors: Cottrell, Jessica A., Vales, Francis M., Schachter, Deborah, Wadsworth, Scott, Gundlapalli, Rama, Kapadia, Rasesh, O'Connor, J. Patrick
Format: Article
Language:English
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Summary:The long-term success of arthroplastic joints is dependent on the stabilization of the implant within the skeletal site. Movement of the arthroplastic implant within the bone can stimulate osteolysis, and therefore methods which promote rigid fixation or bone growth are expected to enhance implant stability and the long-term success of joint arthroplasty. In the present study, we used a simple bilateral bone defect model to analyze the osteogenic activity of three small-molecule drug implants via microcomputerized tomography (micro-CT) and histomorphometry. In this study, we show that local delivery of alendronate, but not lovastatin or omeprazole, led to significant new bone formation at the defect site. Since alendronate impedes osteoclast-development, it is theorized that alendronate treatment results in a net increase in bone formation by preventing osteoclast mediated remodeling of the newly formed bone and upregulating osteoblasts.
ISSN:1110-7243
2314-6133
1110-7251
2314-6141
DOI:10.1155/2010/597641