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酮康唑,一种口服抗真菌药:咪唑类药物的实验室及临床评估

Ketoconazole, an oral antifungal: laboratory and clinical assessment of imidazole drugs.

作者信息

Borelli D, Bran J L, Fuentes J, Legendre R, Leiderman E, Levine H B, Restrepo A, Stevens D A

出版信息

Postgrad Med J. 1979 Sep;55(647):657-61. doi: 10.1136/pgmj.55.647.657.

Abstract

Miconazole, a parenterally administered imidazole antifungal agent has been shown to produce responses in systemic fungal infections in man. Ketoconazole, an analogue, can be given by mouth. It is inhibitory in vitro at low concentrations to most fungi. Blood levels after oral administration to animals and man greatly exceed these inhibitory concentrations for several hours. The efficacy of this drug has been demonstrated in animal models. Initial clinical evaluation has produced responses to therapy with 200-400 mg/day in 13 of 16 evaluable patients with systemic and superficial fungal infections, involving 10 fungal pathogens. No toxicity has been noted to date in these human studies. Ketoconazole is a promising agent needing further extensive evaluation.

摘要

咪康唑是一种经肠胃外给药的咪唑类抗真菌药,已证明它对人类的全身性真菌感染有疗效。酮康唑是其类似物,可以口服。它在体外对大多数真菌在低浓度时即有抑制作用。给动物和人类口服后,血药浓度在数小时内大大超过这些抑制浓度。该药的疗效已在动物模型中得到证实。初步临床评估显示,16例可评估的全身性和浅表性真菌感染患者(涉及10种真菌病原体)中,有13例对每天200 - 400毫克的治疗有反应。在这些人体研究中,迄今为止尚未发现毒性。酮康唑是一种有前景的药物,需要进一步广泛评估。

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