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交通工具类型对亲水性、两亲性、亲脂性模型药物经皮渗透效果的影响。

Influence of type of vehicle on dermal penetration efficacy of hydrophilic, amphiphilic, lipophilic model drugs.

机构信息

Department of Pharmaceutics and Biopharmaceutics, Philipps - Universität Marburg, Robert - Koch - Straße 4, 35037 Marburg, Germany.

KliniPharm GmbH, Hauptstr. 23, 65760 Eschborn, Germany.

出版信息

Eur J Pharm Biopharm. 2024 Jul;200:114305. doi: 10.1016/j.ejpb.2024.114305. Epub 2024 Apr 27.

DOI:10.1016/j.ejpb.2024.114305
PMID:38685437
Abstract

The influence of the vehicle on the dermal penetration efficacy of three different active ingredient (AI) surrogates (hydrophilic, amphiphilic, lipophilic model drugs), that were incorporated into these vehicles, was investigated with the ex vivo porcine ear model, which allowed to assess time and space resolved dermal penetration profiles of the AI. Fifteen different vehicles, including classical vehicles (hydrogel, oleogel, o/w cream, w/o ointment, amphiphilic cream) and innovative vehicles were included into the study. Results show tremendous differences in the penetration efficacy of the AI among the different vehicles. The differences in the total amounts of penetrated AI between lowest and highest penetration were about 3-fold for the hydrophilic AI surrogate, 3.5-fold for the amphiphilic AI and almost 5-fold for the lipophilic AI. The penetration depth was also affected by the type of vehicle. Some vehicles allowed the AI to penetrate only into the upper layers of the stratum corneum, whereas others allowed the penetration of the AI into deeper layers of the viable dermis. Data therefore demonstrate that the vehicles in compounding medications cannot be exchanged against each other randomly if a constant and safe medication is desired. The data obtained in the study provide first information on which types of vehicles are exchangeable and which types of vehicles can be used for enhanced dermal penetration of AI, thus providing a first base for a science-based selection of vehicles that can provide both, efficient dermal drug delivery and skin barrier function maintenance/strengthening at the same time.

摘要

本研究采用离体猪耳模型,考察了载体对三种不同(亲水性、两亲性、亲脂性)替代活性成分(AI)的经皮渗透效果的影响,这些 AI 被纳入这些载体中。该模型允许评估 AI 的时间和空间分辨的经皮渗透曲线。研究包括 15 种不同的载体,包括经典载体(水凝胶、油凝胶、o/w 乳膏、w/o 软膏、两亲性乳膏)和创新载体。结果表明,不同载体中 AI 的渗透效果存在巨大差异。亲水性 AI 替代物的总渗透量最低和最高之间的差异约为 3 倍,两亲性 AI 的差异约为 3.5 倍,亲脂性 AI 的差异几乎为 5 倍。载体类型也会影响渗透深度。一些载体仅允许 AI 渗透到角质层的上层,而其他载体则允许 AI 渗透到真皮的更深层。因此,数据表明,如果需要恒定和安全的药物,复方药物中的载体不能随意互换。该研究获得的数据首次提供了关于哪些类型的载体可互换以及哪些类型的载体可用于增强 AI 的经皮渗透的信息,从而为基于科学的载体选择提供了初步依据,这些载体既能有效提供皮肤药物输送,又能同时维持/增强皮肤屏障功能。

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