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在多种体外试验条件下对联苯苄唑对光滑假丝酵母和白色念珠菌的抗真菌作用进行评估。

An evaluation of the antifungal effect of bifonazole on Torulopsis glabrata and Candida albicans under various in vitro test conditions.

作者信息

Barug D, Bastiaanse H B

出版信息

Arzneimittelforschung. 1983;33(4):524-8.

PMID:6409128
Abstract

1-[(4-Biphenylyl)-phenylmethyl]-1H-imidazole (bifonazole, Bay h 4502, Mycospor) showed in vitro significant inhibitory activity against Torulopsis glabrata, Candida albicans, Pityrosporum ovale, Corynebacterium acnes and Staphylococcus epidermidis. The antifungal activity of bifonazole against T. glabrata and C. albicans varied with the in vitro test conditions. There was a tendency for minimal inhibitory concentrations to increase as fungal inoculum size was increased and as incubation time was prolonged. For T. glabrata, but not for C. albicans, minimal inhibitory concentrations were lower in liquid than on solid culture media. The antifungal activity was less pronounced at low pH values. Because of these variations laboratory tests for the in vitro determination of antifungal sensitivities should be carried out under standardized test conditions such as small inocula, a limited incubation period and appropriate culture media. The solubility of bifonazole in aqueous solution is very low. In addition, more bifonazole dissolves at low than at high pH values.

摘要

1-[(4-联苯基)-苯基甲基]-1H-咪唑(联苯苄唑,拜耳h 4502,霉克舒)在体外对光滑球拟酵母菌、白色念珠菌、卵形糠秕孢子菌、痤疮丙酸杆菌和表皮葡萄球菌显示出显著的抑制活性。联苯苄唑对光滑球拟酵母菌和白色念珠菌的抗真菌活性随体外试验条件而变化。随着真菌接种量的增加和培养时间的延长,最低抑菌浓度有升高的趋势。对于光滑球拟酵母菌,而非白色念珠菌,液体培养基中的最低抑菌浓度低于固体培养基。在低pH值时抗真菌活性不太明显。由于这些变化,体外抗真菌敏感性测定的实验室试验应在标准化试验条件下进行,如小接种量、有限的培养期和合适的培养基。联苯苄唑在水溶液中的溶解度非常低。此外,在低pH值下比在高pH值下溶解的联苯苄唑更多。

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