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氟康唑三种每周一次剂量(150毫克、300毫克或450毫克)治疗手指甲远端甲下甲真菌病的药代动力学。

Pharmacokinetics of three once-weekly dosages of fluconazole (150, 300, or 450 mg) in distal subungual onychomycosis of the fingernail.

作者信息

Savin R C, Drake L, Babel D, Stewart D M, Rich P, Ling M R, Breneman D, Scher R K, Martin A G, Pariser D M, Pariser R J, Ellis C N, Kang S, Friedman D, Katz H I, McDonald C J, Muglia J, Webster G, Elewski B E, Leyden J J, Bucko A D, Tschen E H, Hanifin J M, Morman M R, Hilbert J

机构信息

Savin Dermatology Center, New Haven, Connecticut 06511, USA.

出版信息

J Am Acad Dermatol. 1998 Jun;38(6 Pt 2):S110-6. doi: 10.1016/s0190-9622(98)70494-3.

Abstract

BACKGROUND

Fluconazole has proven to be safe and effective for a variety of superficial and systemic fungal infections. Preliminary analysis of extensive Phase III studies suggests that it is very effective for the treatment of onychomycosis. Its pharmacokinetic properties, including low molecular weight and high water-solubility, suggest a unique ability to penetrate the nail. This feature is likely to account in part for fluconazole's effectiveness in the treatment of onychomycosis.

OBJECTIVE

Determinations of plasma and fingernail concentrations of fluconazole were performed as part of a larger study comparing the safety and efficacy of once-weekly fluconazole (150, 300, and 450 mg) to placebo in the treatment of distal subungual onychomycosis of the fingernails caused by dermatophytes. The relationship between fluconazole concentrations and efficacy was also examined.

METHODS

Pharmacokinetic studies were performed by means of plasma and fingernail samples from 133 patients, a subset of 349 patients participating in a double-blind, placebo-controlled clinical trial of fluconazole administered in once-weekly doses of 150, 300, or 450 mg until cure of onychomycosis or for a maximum of 9 months. Blood and fingernail samples for pharmacokinetic analysis were taken at baseline, at week 2, and at monthly intervals during the treatment phase of the study. Patients considered clinically cured or improved also participated in a 6-month follow-up study. During this phase, patients were monitored and samples taken every 2 months.

RESULTS

Significant amounts of fluconazole were detected in the earliest fingernail samples taken (after 2 weeks of treatment). After two weekly doses, 30% to 33% of steady-state concentrations had been achieved in healthy nails and 22% to 29% in affected nails. Steady state was achieved in 3 to 5 months. Fluconazole concentration in nails as well as plasma followed dose-proportional pharmacokinetics. Nail:plasma ratios in affected nails were 0.4 to 0.6 at 2 weeks and 1.7 to 1.8 at 6 months. Fluconazole concentrations fell slowly after drug discontinuation and were still detectable 4 months after end of treatment. A statistically significant correlation was found between steady-state concentration and clinical and global outcomes.

CONCLUSION

Fluconazole rapidly penetrates the fingernail, where it is retained at detectable levels for at least 4 months after drug discontinuation. A significant correlation exists between fluconazole concentration in the fingernails and clinical and global outcomes.

摘要

背景

氟康唑已被证明对多种浅表和全身性真菌感染安全有效。对广泛的III期研究的初步分析表明,它对甲癣的治疗非常有效。其药代动力学特性,包括低分子量和高水溶性,表明它具有穿透指甲的独特能力。这一特性可能部分解释了氟康唑治疗甲癣的有效性。

目的

作为一项更大规模研究的一部分,测定了氟康唑的血浆和指甲浓度,该研究比较了每周一次服用氟康唑(150、300和450毫克)与安慰剂治疗由皮肤癣菌引起的指甲远端甲下甲癣的安全性和有效性。还研究了氟康唑浓度与疗效之间的关系。

方法

药代动力学研究通过采集133例患者的血浆和指甲样本进行,这133例患者是参与一项双盲、安慰剂对照临床试验的349例患者的子集,该试验中氟康唑以每周一次的剂量150、300或450毫克给药,直至甲癣治愈或最长治疗9个月。在研究的治疗阶段,于基线、第2周以及每月采集一次用于药代动力学分析的血液和指甲样本。临床治愈或改善的患者也参与了一项为期6个月的随访研究。在此阶段,对患者进行监测并每2个月采集一次样本。

结果

在最早采集的指甲样本(治疗2周后)中检测到了大量氟康唑。每周服用两次后,健康指甲达到了稳态浓度的30%至33%,患病指甲达到了22%至29%。3至5个月达到稳态。指甲和血浆中的氟康唑浓度遵循剂量比例药代动力学。患病指甲在2周时的指甲:血浆比值为0.4至0.6,6个月时为1.7至1.8。停药后氟康唑浓度下降缓慢,治疗结束后4个月仍可检测到。在稳态浓度与临床和总体结果之间发现了统计学上的显著相关性。

结论

氟康唑能迅速穿透指甲,停药后在指甲中至少4个月可检测到其留存水平。指甲中的氟康唑浓度与临床和总体结果之间存在显著相关性。

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