On the other hand, H-terminated diamond surface is an ideal start

On the other hand, H-terminated diamond surface is an ideal starting point for covalent attachment of biomolecules [10]. Chemical functionalization can also lead to bio-passivation or bio-active properties[11].This unique combination of the mechanical, chemical, and biocompatible properties [9, 12] with semiconducting properties makes diamond an attractive material for merging solid state and biological systems [13, 14]. For engineered tissue therapies, optimization of implant materials, and cell-based biosensors, characterization of interactions between the cells and surfaces is essential. Cells recognize their surroundings and consequently modify it by a production of appropriate extracellular matrix (ECM) proteins to form the basis for the cell spreading, increased adhesion and expression of differentiated phenotypes [15].

This is a complex and flexible process which is strongly dependent on the cell culture conditions, including the underlying substrate and the pre-adsorbed protein layer. Surface roughness [16] and porosity [17] play significant roles in promoting the cell growth. Hydrophobic and hydrophilic properties of the surfaces influence protein conformations [18, 19] and the cell adsorption and viability [9]. Hence the hydrogen and oxygen-terminated surfaces of diamond are highly relevant for bio-electronics as well as for tissue engineering. So far, the research on the cell-diamond interfaces has been focused mostly on overall homogeneous surface terminations [9, 20, 21].

In this work we show selective adhesion and arrangement of osteoblasts on diamond thin films that are microscopically patterned with H- and O-terminated regions [22, 23]. By controlling the initial cell density and serum concentration in the cell medium we influence cellular colonization of the patterned diamond substrates. Furthermore, we employ atomic force microscopy (AFM) to characterize the structural properties of mediating proteins (fetal bovine serum, a crucial component for the cell growth) adsorbed onto the diamond micro-patterns [19]. The data are used to discuss the selectivity of the cell adhesion on the patterns, i.e. to what degree the cell adhesion and its selectivity is driven by serum adsorption and conformation on H- and O-terminated surfaces or by a direct effect of diamond surface dipoles on the cells. We also provide perspectives for potential bio-electronic applications.

2.?Experimental Carfilzomib SectionDiamond films are grown on (100) oriented silicon substrates (13 mm in diameter, 500 ��m thickness, RMS roughness of < 0.6 nm) by microwave plasma process using total gas pressure 50 mbar, substrate temperature 800��C, 1% CH4 in H2, and total power 2.5 kW. This process results in a growth of continuous, smooth and high quality nanocrystalline diamond (NCD) film [2, 24].

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