Our novel selenium-based topical small-molecule medication is not toxic and safe in studies run to date.
Stable and non-toxic compound in tests run to date.
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No loss of cell viability.
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No loss of metabolic function.
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Enhanced migration of fibroblast cells, which contributes to skin-tissue repair.
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No significant upregulation of (Se-dependent) thioredoxin reductase, or glutathione peroxidase at either protein or activity levels.
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Protects human coronary artery endothelial cells against oxidative damage.
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No sign of inflammation or adverse effects when applied topically on mouse skin wounds in wild-type and diabetic mice. Improves wound healing.
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Oral dosing of mice over a 12-week period:
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does not alter consumption of drinking water;
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no change to body weight;
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no weight gain over time;
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no overt signs of distress or discomfort;
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no noticeable behavioural changes.
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The therapeutic agent remains intact following treatment, with no obvious metabolites observed in plasma or tissue.
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No obvious signs of overt toxicity to liver or kidneys.
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No inflammatory-marker changes in mouse plasma.
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Human and veterinary applications.