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Published on: June 5, 2020
Genotoxicity and cytotoxicity in multiple organs induced by titanium miniplates in Wistar rats
Rodrigo Piozzi1, Daniel Araki Ribeiro, Luís Eduardo Marques Padovan
1Department of Oral and Maxillofacial Surgery, University of Sacred Heart, USC, Bauru, SP, Brazil.
Abstract:
Internal fixture materials are currently used as metallic biomaterials in rehabilitation of human body. Nevertheless, metal release due to corrosion phenomena appears to play a crucial role for human health. Thus, the goal of the present study was to evaluate whether liver, kidney, and lung are particularly sensitive organs for DNA damaging and cytotoxicity following implantation of internal fixture materials composed by titanium alloy in vivo. A total of 18 rats underwent surgical titanium miniplates in their tibias, being randomly distributed into three groups: 30 days, 90 days, and 180 days after implantation. A total of six animals served as negative control (animals that not received any implant). After experimental design, the lung, liver, and kidney were removed for histopatological and genotoxic analysis as depicted by H.E. stain and single cell gel (comet) assay, respectively. No significant statistically differences (p > 0.05) for DNA damaging were found to all experimental groups when compared to negative control for all organs evaluated. In addition, no remarkable morphological alterations were detected under histopathological analysis. Taken together, such results suggest that titanium miniplates are neither able to induce DNA damage in multiple organs nor to cause some abnormalities in lung, liver, and kidney.
Insights
Titanium miniplates used in bone repair did not cause DNA damage or organ abnormalities in rat livers, kidneys, or lungs. This study found titanium alloy implants to be safe for these vital organs in vivo.
Area of Science:
- Biomaterials Science
- Toxicology
- Medical Devices
Background:
- Metallic biomaterials, including titanium alloys, are widely used for internal fixtures in human rehabilitation.
- Concerns exist regarding metal ion release from implants due to corrosion, potentially impacting human health.
- The sensitivity of organs like the liver, kidney, and lung to potential genotoxicity and cytotoxicity from implanted materials requires investigation.
Purpose of the Study:
- To evaluate the potential for DNA damage and cytotoxicity in the liver, kidney, and lung following in vivo implantation of titanium alloy miniplates.
- To assess the long-term effects of titanium alloy implants on organ health over 180 days.
Main Methods:
- Titanium alloy miniplates were surgically implanted into the tibias of 18 rats.
- Rats were divided into three groups (30, 90, and 180 days post-implantation) with a negative control group.
- Genotoxicity was assessed using the single cell gel (comet) assay, and histopathological analysis was performed on lung, liver, and kidney tissues.
Main Results:
- No statistically significant differences in DNA damage were observed in the lung, liver, or kidney of rats with titanium implants compared to the control group (p > 0.05).
- Histopathological examination revealed no significant morphological alterations in the evaluated organs across all experimental groups.
- The results indicate a lack of genotoxic or cytotoxic effects from the titanium alloy miniplates in the studied organs.
Conclusions:
- Titanium alloy miniplates used as internal fixture materials do not appear to induce significant DNA damage in the liver, kidney, or lung.
- The implantation of titanium miniplates in vivo did not lead to observable morphological abnormalities in these vital organs.
- These findings suggest that titanium alloy implants are safe concerning genotoxicity and cytotoxicity in the evaluated organs.
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