Abstract

The objective of this study was to evaluate potential cytotoxicity of TXA on articular cartilage by assessing chondrocyte viability of osteochondral explants after exposure to different concentrations and durations of TXA. Thirty-nine osteochondral plugs (OCPs) were harvested from three adult Yucatan minipigs immediately after their death. OCPs were divided into 13 groups exposed to different concentrations of TXA (1, 2 and 4mg/ml in saline solution) for 1, 3 and 6h. Negative controls were exposed to saline solution for 0, 1, 3 and 6h. Chondrocyte viability was assessed by Live/Dead cell assay and calculated as the ratio of live cells (green fluorescence) to overall cells (green + red cells) for each concentration of TXA and time point in a 50-µm scanned image. No correlation was found between chondrocyte viability, and TXA concentration and time of exposure. Overall, chondrocyte viability ranged from 90 to 99%. There was no statistical difference among control group, 1, 2 and 4mg/ml TXA solutions at each time point [1h (n.s.), 3h (n.s.), 6h (n.s.)]. Similarly, no statistical difference among groups was observed when comparing cell viability at 1, 3 and 6h of TXA exposure, (Fig.2) [1mg/ml (n.s.), 2mg/ml (n.s.), and 4mg/ml (n.s.)]. In conclusion, doses of TXA approximating the current clinical protocols for topical use did not demonstrate any cytotoxic effects on cartilage explants in a Yucatan mini pig model. Thus, supporting the topical application for procedures with intact cartilage, such as partial knee replacement surgery and cartilage repair procedures.

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