Medical Mycology · 1980 · 19 citations · 5 references
Life SciencesDermatologyPharmacologyAllergyMycologyStructure-activity RelationshipsAntifungal AgentsAntifungal PharmacologyAntifungal TherapyFungal PathogenesisFungal Secondary MetabolitesFungal Bioactive CompoundsFungal RemediesNatural Antifungal CompoundsNew Antifungal AgentsSkin Sensitivity ReactionsTopical Antifungal AgentsTopical AntifungalsTrichophyton Infections
The antimycotic activity of ethane-1,2-diol, propane-1,2-diol, butane-1,3-diol, pentane-1,5-diol, and hexane-2,5-diol in vitro against Pityrosporum orbiculare, Candida albicans, Trichophyton rubrum, T. mentagrophytes var. interdigitale and Epidermophyton floccosum was studied. Ethane-1,2-diol had the lowest activity (MIC of 40–100 g 1-1), and hexane-2,5-diol the highest activity (MIC of 10–40g 1-1). Among the higher diols there can be both effective antifungal agents and substances with a lower risk of allergic and irritative skin reactions than propane-1,2-diol. L'activité antimycotique de ethane-1,2-diol, propane-1,2-diol, butane-1,3-diol, pentane-1,5-diol et hexane-2,5-diol in vitro contre Pityrosporum orbiculare, Candida albicans, Trichophyton rubrum, T. mentagrophytes var.interdigitale et Epidermophyton floccosum a été etudiée. Ethane-1,2-diol a fait preuve de l'activité la plus basse et hexane-2,5-diol l'activité la plus haute. Parmi les dioles d'un pois moleculaire plus elevé il peut y avoir non seulement agents antimycotique effective mais aussi des substances d'un, risque réduit de produire des effects allergiques et irriatifes sur la peau que propane-1,2-diol.
5
Toxicity and metabolism of industrial solvents
Food and Cosmetics Toxicology · 1966 · 473 citations
Recent Advances in Dermatopharmacology
Thomas H. Rea · Archives of Dermatology · 1978 · 48 citations
Medicine, Dermatology, Pharmacology +13