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罗每乐甲涂剂——一种治疗甲真菌病新药剂学方法的实现。

Loceryl nail lacquer--realization of a new galenical approach to onychomycosis therapy.

作者信息

Pittrof F, Gerhards J, Erni W, Klecak G

机构信息

Pharma Division Preclinical Development, F. Hoffmann-La Roche Ltd, Basel, Switzerland.

出版信息

Clin Exp Dermatol. 1992 Sep;17 Suppl 1:26-8. doi: 10.1111/j.1365-2230.1992.tb00273.x.

DOI:10.1111/j.1365-2230.1992.tb00273.x
PMID:1458660
Abstract

Loceryl nail lacquer was developed to provide the effective antifungal drug, amorolfine, in a once-weekly dosage regimen combined with a convenient mode of application. Traditional formulations such as creams and nail solutions do not fulfil these requirements because they are wiped or washed off very rapidly. Amorolfine nail lacquer builds a non-water-soluble film on the nail plate, and this film remains in place for 1 week. The film contains a high concentration of amorolfine and forms a depot from which the drug is delivered and which allows the drug to permeate the nail plate. The film-forming polymer and the solvent were optimized for drug release, stability, and convenience of application (drying time, no gloss, transparency). In preclinical development, porcine hoof horn was used as a screening model to differentiate between formulations and dosage strengths with respect to the penetration rate. A high drug concentration of 11.72 micrograms/specimen (10 mm in diameter) was reached in the hoof horn after 6 h, increasing to 39.5 micrograms/specimen within 7 days, the maximum duration of the investigation. The drug concentration achieved was far above its minimum inhibitory concentration. Furthermore, the penetration model clearly indicated that amorolfine crossed the horn barrier and was found in the moistened gauze which simulated the nail bed. After a 7-day penetration period, 1.8% of the applied dose (500 micrograms) was available under the nail.

摘要

罗每乐搽剂的研发目的是提供有效抗真菌药物阿莫罗芬,采用每周一次的给药方案并结合便捷的应用方式。传统剂型如乳膏和指甲液剂无法满足这些要求,因为它们会很快被擦掉或冲洗掉。阿莫罗芬搽剂可在指甲板上形成非水溶性薄膜,该薄膜能保持一周。该薄膜含有高浓度的阿莫罗芬,形成一个储库,药物从该储库中释放,并使药物渗透指甲板。成膜聚合物和溶剂针对药物释放、稳定性及应用便利性(干燥时间、无光泽、透明度)进行了优化。在临床前研发中,猪蹄角被用作筛选模型,以区分不同剂型和剂量强度的渗透速率。给药6小时后,蹄角中的药物浓度达到11.72微克/样本(直径10毫米),在7天的最长研究时间内增加到39.5微克/样本。所达到的药物浓度远高于其最低抑菌浓度。此外,渗透模型清楚地表明,阿莫罗芬穿过角质屏障,并在模拟甲床的湿润纱布中被发现。经过7天的渗透期后,在指甲下有1.8%的给药剂量(500微克)可用。

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