Volume 57, Issue 4 pp. 588-596

Preparation and analysis of macroporous TiO2 films on Ti surfaces for bone–tissue implants

F. Ahu Akin

F. Ahu Akin

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607-7061

Search for more papers by this author
Hala Zreiqat

Hala Zreiqat

School of Pathology, University of New South Wales, Sydney, NSW 2052, Australia

Search for more papers by this author
Sandra Jordan

Sandra Jordan

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607-7061

Search for more papers by this author
Muthu B.J. Wijesundara

Muthu B.J. Wijesundara

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607-7061

Search for more papers by this author
Luke Hanley

Corresponding Author

Luke Hanley

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607-7061

Department of Chemistry, University of Illinois at Chicago, Chicago, Illinois 60607-7061Search for more papers by this author

Abstract

This article describes the preparation and analysis of macroporous TiO2 films on Ti surfaces, for application in bone tissue–Ti implant interfaces. These TiO2 bioceramic films have a macroporous structure consisting of monodisperse, three-dimensional, spherical, interconnected pores adjustable in the micron size range. Micron-sized polystyrene (PS) bead templates are used to precisely define the pore size, creating macroporous TiO2 films with 0.50, 16, and 50 μm diameter pores, as shown by scanning electron microscopy. X-ray photoelectron spectroscopy shows the films to be predominantly composed of TiO2, with ∼10% carbon. X-ray diffraction reveal rutile as the main phase when fired to the optimal temperature of 950°C. Preliminary experiments find that the in vitro proliferation of human bone-derived cells (HBDC) is similar on all three pore sizes. However, higher [3H]thymidine incorporation by the HBDC is observed when they are grown on 0.50- and 16-μm pores compared to the 50-μm pores, suggesting an enhanced cell proliferation for the smaller pores. © 2001 John Wiley & Sons, Inc. J Biomed Mater Res 57: 588–596, 2001

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.