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There was no distinct difference in the amount of titanium ions released from G4 and G5 particles.

Discussion : Particle release from implantoplasty of dental implants (2)

author: Fadi N Barrak, Siwei Li, Albert M Muntane Julian R Jones | publisher: drg. Andreas Tjandra, Sp. Perio, FISID

There was no distinct difference in the amount of titanium ions released from G4 and G5 particles. Direct exposure to G5 implant particles in culture did result in significantly reduced cell viability at all-time points, from 3 to 10 days of culture, while G4 implant particles demonstrated no adverse effect on cell viability (Fig. 5b). The cytotoxic effects of vanadium are well documented [32, 33], so the further relative reduction in cell viability, compared to control and G4 particles, from 10 days was thought to be due to continued release of V during the culture (there was no distinct difference in the amount of titanium ions released from G4 and G5 particles). The delayed release of the V agrees with corrosion studies on Ti-6Al-4 V alloys, which reported time-dependent corrosion.

There have been suggestions that sufficient irrigation around the implant and suction of metallic debris during surgical procedures, such as implantoplasty, might reduce the deposition of metallic particles and ions into surrounding tissue. However, there is no scientific evidence that such measures can fully remove implantoplasty debris from the surround environment, and these procedures can also disseminate bacteria into the surrounding tissues. Previous studies indicated that the cytotoxicity of vanadium ion is dose dependent, where concentrations of 23–30 μM (1.17–1.53 μg ml−1) significantly reduced cell viability in NIH3T3 fibroblasts. Herein, the V concentration was approximately 0.1 μg ml−1 after 10 days of exposure to DMEM, which does explain the significant reduction in viability of HGFs.

Previous studies suggested the viability of calvarial rat osteoblasts in direct contact with G4 CpTi particles (unspecified grade, particle diameter 3.1 ± 3.6 μm) with a concentration higher than 1.5 mg ml−1 decreased significantly due to rapid phagocytic process. In the present study, the viability of HGFs appeared to be not affected by G4 CpTi implant particles, even at high concentrations (3 mg ml−1). 

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