Adsorption of human plasma fibrinogen (HPF) on 6 differently treated titanium samples (polished, polished and etched, and 4 titanium carbide coatings samples produced by using plasma-enhanced chemical vapour deposition (PECVD) method) is investigated by using diffractive optical element (DOE) sensor. Permittivity (susceptibility) change and fluctuation in optical roughness (R(opt)) of treated titanium surface in the presence of background electrolyte without and with HPF molecules are sensed by using DOE sensor and optical ellipsometry. Correlation between transmitted light and thickness of molecule layer was found. The findings allow to sense temporal organization and severity of adsorption of nano-scale HPF molecules on polished, on polished and etched, and on titanium carbide surface.
The corrosion behavior of the Ti-33.5Nb-5.7Ta alloy (Ti-Nb-Ta) as a biocompatible β-type Ti alloy during long-term immersion in simulated body fluid was investigated. Like pure Ti, pitting corrosion did not occur on Ti-Nb-Ta during anodic polarization. Thus, alloying of Ti with Nb and Ta did not change the chloride-ion sensitivity. Metal ion release of Ti, Nb, and Ta was detected after 7-d immersion in the solution; however, the amounts of ions were much smaller than those from Type316L stainless steel. X-ray photoelectron spectroscopy revealed that the fractions of Nb and Ta in the passive layer increased during the immersion while that of Ti decreased. The corrosion rate of Ti-Nb-Ta determined by electrochemical impedance spectroscopy kept decreasing over a period of 15 d while the thickness of the passive layer did not change after 1 d. Thus, the reconstruction of the passive layer of the alloy was proven to be important for metal ion release during long-term implantation in a living body. Thus, Ti-Nb-Ta has sufficient corrosion resistance as a biocompatible β-type Ti alloy.
Aim This paper deals with the treatment of an atrophied toothless mandible with a fixing bridge carried by two nonstandard implant systems.
Methodology
Adsorption of the elongated human plasma fibrinogen (HPF) and globular human serum albumin molecules on a titanium-based surface is monitored by analyzing permittivity and optical roughness of protein-modified surfaces by using a diffractive optical element (DOE)-based sensor and variable angle spectro-ellipsometry (VASE). Both DOE and VASE confirmed that fibrinogen forms a thicker and more packed surface adlayer compared to a more porous and weakly adsorbed albumin adlayer. A linear relation of the permittivity (ε(')) and dielectric loss (ε('')) was found for some of the dry titanium-doped hydrocarbon (TDHC) surfaces with excellent HPF adsorption ability. We discuss some aspects of TDHC's aging and its possible effects on fibrinogen adsorption.
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