(15e) In Vivo Evaluation of Amorphous Nano Tricalcium Phosphate in Flexible Composites and Injectable Bone Cements

Brunner, T. J. - Presenter, Swiss Federal Institute of Technology (ETH Zurich)
Loher, S. - Presenter, ETH Zurich
Weber, F. E. - Presenter, University Hospital Zurich
von Rechenberg, B. - Presenter, University of Zurich

Bone repair and regeneration of defects with bioresorbable implant materials are in great demand in reconstructive surgery. Many investigated biomaterials consist of calcium phosphates which excel in their biocompatibility, bioactivity and osteoconductivity. However current commercially available products are limited for clinical applications because of their brittleness, incompressibility and difficulty to shape.

The present contribution show two in vivo studies testing flexible bone implants for their advantageous clinical applications. We have prepared an open structured and highly porous network of amorphous calcium phosphate nanoparticles (ATCP) with biodegradable poly(lactide-co-glycolide) (PLGA) fibers [1]. In vitro bioactivity tests in simulated body fluid at 37 °C showed the deposition of a nano-sized hydroxyapatite layer on the fiber surface (Figure) within on single day. In vivo bioactivity tests were performed by creating circular defects in the cranium of rabbits and filled with cotton wool like PLGA/ATCP fibers. Another promising application for ATCP is the application as an injectable bone cement (Figure). A comparison to micron-sized α-TCP [2] showed that our amorphous TCP hardened within 7 ? 15 minutes. Most promising results (resorption rate and new bone formation, histology, etc.) are given in an in vivo study in the femur of sheep.

Figure: Scanning electron microscopy images of cotton wool like appearance of TCP containing poly-(lactide-co-glycolide) fibers having a high in vitro bioactivity (left). Injectable bone cement consisting of amorphous TCP / α-TCP (right).


[1] O.D. Schneider, S. Loher, T.J. Brunner, L. Uebersax, M. Simonet, R.N. Grass, H.P. Merkle and W.J. Stark, J. Biomed Mater Res B, 2007, 84B(2), 350-62.

[2] T.J. Brunner, M. Bohner, C. Dora, C. Gerber, W.J. Stark, J. Biomed. Mater. Res., 2007, 83B(2), 400-7.