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Local Application of BMP-2 Specific Plasmids in Fibrin Glue does not Promote Implant Fixation

DOI: 10.1186/1471-2474-12-163

Keywords: BMP-2, gene transfer, non viral gene vector, COPROG, implant healing, fibrin glue

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Abstract:

Sixty rabbits were divided into 4 groups. All of them received nailing of both tibiae. The verum group had the nails inserted with the COPROG vector and BMP-2 plasmids using fibrin glue as a carrier. Controls were a group with fibrin glue only and a blank group. After 28 and 56 days, these three groups were sacrificed and one tibia was randomly chosen for biomechanical testing, while the other tibia underwent histomorphometrical examination. In a fourth group, a reporter-gene was incorporated in the fibrin glue instead of the BMP-2 formula to prove that transfection was successful.Implant fixation strength was significantly lower after 28 and 56 days in the verum group. Histomorphometry supported the findings after 28 days, showing less bone-implant contact.In the fourth group, successful transfection could be confirmed by detection of the reporter-gene in 20 of 22 tibiae. But, also systemic reporter-gene expression was found in heterotopic locations, showing an undesired spreading of the locally applied gene formula.Our results underline the transfecting capability of this vector and support the idea that BMP-2 might diminish osseointegration. Further studies are necessary to specify the exact mechanisms and the systemic effects.Total hip and total knee arthroplasties (THA, TKA) in the industrialized countries are increasing and demographic data suggest that this progress is going to continue [1-3]. According to the Swedish National Total Hip Arthroplasty Register with more than 270,000 registered THA from 1979-2006, the leading cause for component failure in THA is aseptic implant loosening [4]. Besides osteolysis due to wear debris (especially of polyethylene components) it is assumed that a lack of initial bony incorporation of the implant favors aseptic loosening. Bone ingrowth does not occur properly if micromotion exceeds 150 μm [5]. Therefore, many attempts have been made to improve the incorporation of the implant. The design of the prosthesis has a large i

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