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Mammalian Cell Interactions with Nanophase Materials

Published online by Cambridge University Press:  01 February 2011

Rena Bizios
Rena Bizios*
Affiliation:
Department of Biomedical Engineering and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, NY, 12180-3590, USA
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Abstract

Adhesion of differentiated mammalian cells from various hard and soft tissues, including adult mesenchymal stem cells is different on nanophase than on microphase/conventional ceramics (such as alumina, titania and hydroxylapatite) as well as on composites of these ceramics with either poly(L-lactic) acid or poly(methyl) methacrylate. Most importantly, nanophase materials promote selective interactions, for example, of osteoblasts but not of fibroblasts. The type, amount and conformation of adsorbed proteins (such as fibronectin, collagen and vitronectin) are key aspects of the underlying mechanism(s) of subsequent cell interactions with nanophase materials. These cellular/molecular results provide evidence that nanophase biomaterials have the potential for improving the efficacy of implants and for promoting neotissue formation pertinent to tissue engineering, regenerative medicine and other clinical applications.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 845: Symposium AA – Nanoscale Materials Science in Biology and Medicine , 2004 , AA1.5
Copyright
Copyright © Materials Research Society 2005

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References

REFERENCES

[1] Webster, T.J., Siegel, R.W. and Bizios, R., Biomaterials 20, 1221 (1999).Google Scholar
[2] Webster, T.J., Ergun, C., Doremus, R.H., Siegel, R.W. and Bizios, R., Biomaterials 21, 1803 (2000).Google Scholar
[3] Webster, T.J., Ergun, C., Doremus, R.H., Siegel, R.W. and Bizios, R., J. Biomed. Mat. Res. 51, (2000).Google Scholar
[4] McManus, A.J, Doremus, R.H., Siegel, R.W. and Bizios, R., J. Biomed. Mat. Res. 72, 98 (2005).Google Scholar
[5] Dee, K.C, Andersen, T.T. and Bizios, R., Tissue Eng. 1, 135 (1995).Google Scholar
[6] Dee, K.C, Andersen, T.T. and Bizios, R., J. Biomed. Mat. Res. 40, 371 (1998).Google Scholar
[7] Hasenbein, M.E., Andersen, T.T. and Bizios, R., Biomaterials 23, 3937 (2002).Google Scholar
[8] Dulgar-Tulloch, A. J., Doctoral Thesis, Rensselaer Polytechnic Institute, Troy, NY (2005).Google Scholar
[9] Webster, T.J., Doctoral Thesis, Rensselaer Polytechnic Institute, Troy, NY (2000).Google Scholar
[10] Webster, T.J., Schadler, L.S., Siegel, R.W. and Bizios, R., Tissue Eng. 7, 291 (2001).Google Scholar
[11] Puleo, D.A. and Bizios, R., Bone 12, 271 (1991).Google Scholar
[12] Puleo, D.A. and Bizios, R., Bone and Mineral 18, 215 (1992).Google Scholar