Published December 1, 2011 | Version v1
Journal article

Zirconium oxide nanotube surface prompts increased osteoblast functionality and mineralization

  • 1. Materials Science and Engineering, University of California at San Diego, La Jolla, CA 92093 (United States)
  • 2. Mechanical and Aerospace Engineering, University of California at San Diego, La Jolla, CA 92093 (United States)

Description

Electrochemical formation of tunable nanoscale oxide layers on biomedical metallic surfaces has recently drawn much attention in biomaterials research. In this study, we report on the cellular response to a unique vertically aligned, laterally spaced nanotube nanostructure made of zirconium oxide (ZrO2) fabricated by anodization. The growth, morphology, and functionality of osteoblasts cultured on ZrO2 nanotubes have been investigated. The initial adhesion and spreading was considerably improved on the nanotube surface as compared to a flat zirconium (Zr) surface without a nanostructure. The morphology of the adhered cells on the nanotube surface elicited a highly organized cytoskeleton with crisscross patterned actin, which was lacking on the flat Zr. Increased alkaline phosphatase activity levels and the formation of calcified extracellular matrix implied improved osteoblast functionality and mineralization on the nanotube substrate. This in vitro study suggests that the ZrO2 nanotubes provided an enhanced osteoblast response and demonstrated their apparent role in providing a platform for bone growth. → Osteoblast cell response was analyzed on zirconium oxide nanotube surface. → We observed improved cell adhesion and spreading. → We detected an increase in osteoblast functionality and mineralization.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.msec.2011.07.016

Additional details

Identifiers

DOI
10.1016/j.msec.2011.07.016;
PII
S0928-4931(11)00198-6;

Publishing Information

Journal Title
Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
Journal Volume
31
Journal Issue
8
Journal Page Range
p. 1716-1722
ISSN
0928-4931

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.