Pharmaceutical composition containing an anti-fungus agent and one active substance selected from carveol, eugenol, thymol, borneol, carvacrol, alpha-ionone and beta-ionone
A technology for antifungal agents, ionones, applied to a formulation comprising an antifungal agent and an active substance selected from the group consisting of carveol, eugenol, thymol, borneol, carvacrol, alpha-ionone and beta-ionone In the field of pharmaceutical compositions, it can solve the problems of life expectancy, shortening and affecting the quality of life of immunosuppressed patients who are difficult to treat
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example 1
[0055] Example 1: Treatment of different albicans with carvacrol-enhanced fluconazole (Fluc P) Bead strain
[0056] In vitro experiments: determination of the minimum fungicidal concentration (MFC) against different strains of Candida albicans
[0057] Experiments were performed with several strains of Candida albicans isolated in a hospital environment from the cavity, vagina and alimentary canal and with different sensitivities. The antifungal agent used was fluconazole, an azole derivative which is one of the most effective and widely used antifungal drugs on the market. The antifungal pharmaceutical composition was prepared by mixing different concentrations of fluconazole with sub-inhibitory concentrations of carvacrol in 0.3 g / l solution or vehicle. The pharmaceutical composition according to the invention is named FLUC-P for enhanced fluconazole. In each case, the antifungal activity was determined with fluconazole alone, or with carvacrol alone, or with the compos...
example 2
[0081] Example 2: Treatment of different white Candida chromosus
[0082] Experiments were performed with several strains of Candida albicans with different sensitivities isolated in a hospital setting. The antifungal agent used was voliconazole, which is an azole derivative and is one of the newest antifungal agents on the market. An antifungal pharmaceutical composition according to the present invention is prepared by mixing different concentrations of voriconazole and sub-inhibitory concentrations of carvacrol in 0.3 g / l solution or vehicle. The pharmaceutical composition according to the invention is named Vorico-P for enhanced voriconazole. In each case, antifungal activity was determined with voriconazole alone, or with carvacrol alone, or with the composition of the invention.
[0083] Table 2 shows the results of static experiments used to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) in μg / ml.
[0084] Table 2 ...
example 3
[0089] Example 3: Treatment of different white Candida chromosus
[0090] Experiments were performed with several strains of Candida albicans with different sensitivities isolated in a hospital setting. The antifungal agent used was caspofungin from the echinocandin class, which is the newest antifungal agent on the market. An antifungal pharmaceutical composition according to the present invention is prepared by mixing different concentrations of caspofungin and sub-inhibitory concentrations of carvacrol in 0.3 g / l solution or excipient. The pharmaceutical composition according to the invention is named Caspo-P for enhanced caspofungin. In each case, the antifungal activity was determined with caspofungin alone, or with carvacrol alone, or with the composition of the invention.
[0091] Table 3 shows the results of static experiments used to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) in μg / ml.
[0092] table 3
[00...
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