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定量预测电离效应对人体皮肤渗透性的影响。

Quantitative prediction of ionization effect on human skin permeability.

机构信息

Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29, Yoshida-shimoadachicho, Sakyo-ku, Kyoto 606-8501 Japan; Drug Discovery Research Laboratories, Kyoto R&D Center, Maruho Co., Ltd., 93 Awata-cho, Chudoji, Shimogyo-ku, Kyoto, Japan.

Drug Development Research Laboratories, Kyoto R&D Center, Maruho Co., Ltd., 93 Awata-cho, Chudoji, Shimogyo-ku, Kyoto, Japan.

出版信息

Int J Pharm. 2017 Apr 30;522(1-2):222-233. doi: 10.1016/j.ijpharm.2017.03.009. Epub 2017 Mar 7.

DOI:10.1016/j.ijpharm.2017.03.009
PMID:28279739
Abstract

Although skin permeability of an active ingredient can be severely affected by its ionization in a dose solution, most of the existing prediction models cannot predict such impacts. To provide reliable predictors, we curated a novel large dataset of in vitro human skin permeability coefficients for 322 entries comprising chemically diverse permeants whose ionization fractions can be calculated. Subsequently, we generated thousands of computational descriptors, including LogD (octanol-water distribution coefficient at a specific pH), and analyzed the dataset using nonlinear support vector regression (SVR) and Gaussian process regression (GPR) combined with greedy descriptor selection. The SVR model was slightly superior to the GPR model, with externally validated squared correlation coefficient, root mean square error, and mean absolute error values of 0.94, 0.29, and 0.21, respectively. These models indicate that Log D is effective for a comprehensive prediction of ionization effects on skin permeability. In addition, the proposed models satisfied the statistical criteria endorsed in recent model validation studies. These models can evaluate virtually generated compounds at any pH; therefore, they can be used for high-throughput evaluations of numerous active ingredients and optimization of their skin permeability with respect to permeant ionization.

摘要

尽管药物在剂量溶液中的离解会严重影响其皮肤渗透性,但大多数现有的预测模型都无法预测这种影响。为了提供可靠的预测因子,我们精心整理了一个包含 322 种具有不同化学结构的透皮物质的新型大型体外人类皮肤渗透率数据集,这些物质的离解分数可以计算出来。随后,我们生成了数千个计算描述符,包括 LogD(特定 pH 值下的辛醇-水分配系数),并使用非线性支持向量回归(SVR)和高斯过程回归(GPR)结合贪婪描述符选择对数据集进行了分析。SVR 模型略优于 GPR 模型,外部验证的平方相关系数、均方根误差和平均绝对误差值分别为 0.94、0.29 和 0.21。这些模型表明 LogD 对于综合预测离解对皮肤渗透性的影响是有效的。此外,所提出的模型满足了最近模型验证研究中支持的统计标准。这些模型可以在任何 pH 值下评估虚拟生成的化合物;因此,它们可用于高通量评估大量活性成分,并针对透皮物质的离解优化其皮肤渗透性。

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