Peer-reviewed veterinary case report
Oxythiamine boosts ketoconazole to fight dog yeast infections
By Siemieniuk, Magdalena et al.·Published in Veterinary dermatology·2018·Department of Cytobiochemistry·View original on PubMed →
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Original publication title: Oxythiamine improves antifungal activity of ketoconazole evaluated in canine Malassezia pachydermatis strains.
- Species:
- dog
Plain-English summary
A study found that a combination of oxythiamine and ketoconazole was more effective against a common skin yeast infection (Malassezia pachydermatis) in dogs than ketoconazole alone. This yeast can cause skin and ear infections, and some strains are becoming resistant to standard treatments. The combination treatment worked well in laboratory tests, showing that lower doses of ketoconazole could still be effective when paired with oxythiamine. This could lead to better topical treatments for dogs suffering from these infections.
People also search for: dog skin infection treatment · Malassezia pachydermatis in dogs · ketoconazole for dog ear infection · oxythiamine for dogs
Abstract
BACKGROUND: Malassezia pachydermatis is an opportunistic yeast involved in skin and ear canal infections of dogs and cats. Reports suggest that strains of M. pachydermatis resistant to commonly used antifungal agents may be emerging. Therefore, new therapeutic strategies should be explored. OBJECTIVES: The synergistic effect of oxythiamine (OT) and ketoconazole (KTC) was analysed using a reference strain and field isolates (n = 66) of M. pachydermatis. Hydrogel formulations containing these components also were evaluated. METHODS AND MATERIALS: The minimum inhibitory concentrations (MICs) and minimum fungicidal concentrations (MFCs) of OT, KTC and their mixtures were determined by a broth macrodilution method. The antifungal effects of hydrogel formulations were determined by a plate diffusion method. RESULTS: The MIC and MFC values of OT were in the range 0.08 × 10to 10 × 10 mg/L. All M. pachydermatis strains showed higher susceptibility to KTC (MICs and MFCs in the range 0.04-0.32 mg/L). Formulations that combined OT and KTC showed a synergistic effect for all tested isolates (n = 66). Hydrogels that contained OT at a concentration of 10 × 10or 20 × 10 mg/L and KTC at the concentration of 0.1 × 10 mg/L showed a stronger effect than a commercially available product with KTC alone (20 × 10 mg/L). CONCLUSIONS AND CLINICAL IMPORTANCE: Synergy of these drugs may allow for successful topical treatment which utilizes lower doses of KTC without changing its therapeutic effectiveness. Hydrogel formulations proved to be attractive drug carriers for potential topical use.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30251451/