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酮康唑和咪康唑局部用药在人体角质层中的体内药代动力学和药效学

In vivo pharmacokinetics and pharmacodynamics of topical ketoconazole and miconazole in human stratum corneum.

作者信息

Pershing L K, Corlett J, Jorgensen C

机构信息

Department of Medicine, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Antimicrob Agents Chemother. 1994 Jan;38(1):90-5. doi: 10.1128/AAC.38.1.90.

Abstract

A direct study evaluating whether differential drug uptake of topical 2% miconazole and 2% ketoconazole from cream formulations into human stratum corneum correlated with differential pharmacological activity against Candida albicans was investigated in healthy human subjects. A single 24-h topical dose of 2% ketoconazole cream or 2% miconazole cream was applied unoccluded, at the same dose (2.6 mg of formulation per cm2 of surface area), at four skin sites on both ventral forearms of six human subjects. At the end of the treatment, residual drug was removed with a tissue from all sites and the treated site was tape stripped 11 times, either 1, 4, 8, or 24 h later. The first tape disc was discarded. The remaining tape discs, 2 through 11, were combined and extracted for drug quantification by high-performance liquid chromatography and bioactivity against C. albicans growth in vitro. Topical 2% ketoconazole produced 14-, 10-, and 7-fold greater drug concentrations in stratum corneum than 2% miconazole at 1, 4, and 8 h after a single topical dose. Ketoconazole and miconazole concentrations in the stratum corneum were similar 24 h after drug removal. Tape disc extracts from 2% ketoconazole-treated skin sites demonstrated significantly greater bioactivity in the bioassay than 2% miconazole. The increased efficacy of 2% ketoconazole compared with that of 2% miconazole in vitro reflects their differential uptake into the stratum corneum and inherent pharmacological activity. Tape stripping the drug-treated site in conjunction with a bioassay is therefore a useful approach in the determination of bioavailability of topical antifungal agents.

摘要

在健康人体受试者中进行了一项直接研究,以评估乳膏制剂中2%咪康唑和2%酮康唑经皮吸收进入人角质层的差异是否与对白色念珠菌的不同药理活性相关。六名人体受试者双侧前臂腹侧的四个皮肤部位,以相同剂量(每平方厘米表面积2.6毫克制剂),单次非封闭外用2%酮康唑乳膏或2%咪康唑乳膏24小时。治疗结束时,用纸巾从所有部位去除残留药物,并在1、4、8或24小时后对治疗部位进行11次胶带剥离。丢弃第一张胶带盘。将剩余的第2至11张胶带盘合并,通过高效液相色谱法进行药物定量,并检测其对白色念珠菌体外生长的生物活性。单次外用后1、4和8小时,2%酮康唑在角质层中的药物浓度比2%咪康唑高14倍、10倍和7倍。药物去除后24小时,角质层中酮康唑和咪康唑的浓度相似。2%酮康唑治疗皮肤部位的胶带盘提取物在生物测定中显示出比2%咪康唑显著更高的生物活性。2%酮康唑在体外比2%咪康唑疗效更高,这反映了它们在角质层中的吸收差异和内在药理活性。因此,结合生物测定对药物治疗部位进行胶带剥离是测定外用抗真菌剂生物利用度的一种有用方法。

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