Abstract

All biomaterials initiate a tissue response when implanted in living tissues. Ultimately this reaction causes fibrous encapsulation and hence isolation of the material, leading to failure of the intended therapeutic effect of the implant. There has been extensive bioengineering research aimed at overcoming or delaying the onset of encapsulation. Nanotechnology has the potential to address this problem by virtue of the ability of some nanomaterials to modulate interactions with cells, thereby inducing specific biological responses to implanted foreign materials. To this effect in the present study, we have characterised the growth of fibroblasts on nano-structured sheets constituted by BaTiO3, a material extensively used in biomedical applications. We found that sheets of vertically aligned BaTiO3 nanotubes inhibit cell cycle progression - without impairing cell viability - of NIH-3T3 fibroblast cells. We postulate that the 3D organization of the material surface acts by increasing the availability of adhesion sites, promoting cell attachment and inhibition of cell proliferation. This finding could be of relevance for biomedical applications designed to prevent or minimize fibrous encasement by uncontrolled proliferation of fibroblastic cells with loss of material-tissue interface underpinning long-term function of implants.

Highlights

  • Barium titanate (BaTiO3) belongs to the group of ferroelectric ceramics

  • The presence of vertically aligned nanotubes (VANTs) in the membranes was confirmed by Scanning electron microscopy (SEM), which showed the presence of nanotubular structures filling the nanopores of the template membranes

  • The Xray powder diffraction (XRD) powder diffraction, performed directly on the anodic aluminium oxide (AAO)-NT, demonstrated that VANTs were not constituted by crystalline BaTiO3

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Summary

Introduction

Barium titanate (BaTiO3) belongs to the group of ferroelectric ceramics. It is characterized by high dielectric constant and high Curie temperature [1]. In vitro studies have demonstrated that negatively and positively poled BaTiO3 enhance the formation of bone-like crystals, such as calcium phosphate. The capability of the poled BaTiO3 to enhance the formation of such crystals could explain the results of several in vivo implantation studies with BaTiO3 based grafts [11, 12], in which improved osteogenesis and bone formation around the implant were observed. Charged surfaces could drive preferential absorption of proteins, through electrostatic attraction of protein charged groups [13]. This could explain the bioactivity of poled BaTiO3 and, in particular, its ability to improve cell proliferation in vitro [4]

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