Substitution of Brom-Thymol-Blue for Litmus in Routine Laboratory Work.
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An evidence-based systematic review including scientific evidence, expert opinion, folkloric precedent, history, pharmacology, kinetics/dynamics, interactions, adverse effects, toxicology, and dosing.
In order to study the in vitro behavior of the drug used according to our formula cultures of Trichophyton mentagrophytes. Trichophyton rubrum, Trichophyton verrucosum, Trichophyton tonsurans, Microsporum canis, Microsporum gallinae, Microsporum audouinii, Microsporum gypseum and Epidermophyton floccosum were prepared in order to prove its efficacy. It was found no growth in cultures to which the drug was added in different concentrations thus proving its efficacy as a fungistatic element. The inocula obtained were re-cultured in the same medium having no drug and no growth was evidenced; this would suggest its efficacy as a fungicide. This efficacy was proved for the different concentrations, that is, from the minimal coinentration (0.1 ml) up to the 1 ml concentration the drug disclosed fungicide power. The untreated controls which were recultured from the original strains grew according to their common development rhythm.
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The effect of essential oils, eugenol, thymol and menthol, on erythrocytes, hepatocytes, dipalmitoyl phosphatidylcholine (DPPC)-liposomes and surface tension were studied at various concentrations. Maximal inhibition of eugenol, thymol and menthol on the hypotonic hemolysis in rat erythrocytes were observed at a concentration of 2 mM, 1 mM and 1 mM, respectively. Eugenol at 4 mM and thymol at 2 mM caused an acceleration of hypotonic hemolysis. In isolated rat hepatocytes, thymol caused an increase in GOT leakage, but eugenol at 4 mM and menthol at 0.1 and 0.4 mM inhibited the GOT leakage. The leakage of GPT from hepatocytes was inhibited by eugenol at 0.1 mM and 0.4 to 4 mM and menthol at 0.1 to 0.6 mM. The inhibition of eugenol and menthol on the LDH leakage in hepatocytes were observed at a concentration of 0.001 to 4 mM and 0.1, 0.4 and 0.6 mM, respectively. Thymol caused no change in GPT and LDH leakage. Eugenol, thymol and menthol indicated a depression of surface tension at a concentration of 0.1 mM. The rank by order of surface activity was eugenol greater than thymol. Eugenol, thymol and menthol depressed the phase-transition temperature of DPPC-liposomes. The depression of phase-transition temperature by thymol was greater than that by eugenol and menthol. These results suggest the periapical tissue damage produced by essential oils may be related to membrane lysis and surface activity and that their tissue penetration may be related to membrane affinity and lipid solubility.