Regenerated keratin membrane to match the in vitro drug diffusion through human epidermis

Francesca Selmin , Francesco Cilurzo , Annalisa Aluigi , Silvia Franzè , Paola Minghetti
{"title":"Regenerated keratin membrane to match the in vitro drug diffusion through human epidermis","authors":"Francesca Selmin ,&nbsp;Francesco Cilurzo ,&nbsp;Annalisa Aluigi ,&nbsp;Silvia Franzè ,&nbsp;Paola Minghetti","doi":"10.1016/j.rinphs.2012.10.001","DOIUrl":null,"url":null,"abstract":"<div><p>This work aimed to develop membranes made of regenerated keratin and ceramides (CERs) to match the barrier property of the human stratum corneum in <em>in vitro</em> percutaneous absorption studies. The membrane composition was optimized on the basis of the <em>in vitro</em> drug diffusion profiles of ibuprofen, propranolol and testosterone chosen as model drugs on the basis of their different diffusion and solubility properties. The data were compared to those obtained using human epidermis.</p><p>The ATR-FTIR and SEM analyses revealed that CERs were suspended into the regenerated keratin matrix, even if a partial solubilization occurred. It resulted in the membranes being physically stable after exposure to aqueous buffer and/or mineral oil and the fluxes of ibuprofen and propranolol from these vehicles through membranes and human skin were of the same order of magnitude. The best relationship with human epidermis data was obtained with 180<!--> <!-->μm-thick membrane containing 1% ceramide III and 1% ceramide VI. The data on the testosterone diffusion were affected by the exposure of the membrane to a water/ethanol solution over a prolonged period of time, indicating that such an organic solvent was able to modify the supermolecular organization of keratin and CERs.</p><p>The keratin/CER membranes can represent a simplified model to assay the <em>in vitro</em> skin permeability study of small molecules.</p></div>","PeriodicalId":89718,"journal":{"name":"Results in pharma sciences","volume":"2 ","pages":"Pages 72-78"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rinphs.2012.10.001","citationCount":"33","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in pharma sciences","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211286312000103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 33

Abstract

This work aimed to develop membranes made of regenerated keratin and ceramides (CERs) to match the barrier property of the human stratum corneum in in vitro percutaneous absorption studies. The membrane composition was optimized on the basis of the in vitro drug diffusion profiles of ibuprofen, propranolol and testosterone chosen as model drugs on the basis of their different diffusion and solubility properties. The data were compared to those obtained using human epidermis.

The ATR-FTIR and SEM analyses revealed that CERs were suspended into the regenerated keratin matrix, even if a partial solubilization occurred. It resulted in the membranes being physically stable after exposure to aqueous buffer and/or mineral oil and the fluxes of ibuprofen and propranolol from these vehicles through membranes and human skin were of the same order of magnitude. The best relationship with human epidermis data was obtained with 180 μm-thick membrane containing 1% ceramide III and 1% ceramide VI. The data on the testosterone diffusion were affected by the exposure of the membrane to a water/ethanol solution over a prolonged period of time, indicating that such an organic solvent was able to modify the supermolecular organization of keratin and CERs.

The keratin/CER membranes can represent a simplified model to assay the in vitro skin permeability study of small molecules.

Abstract Image

Abstract Image

Abstract Image

再生角蛋白膜匹配体外药物通过人表皮扩散
本工作旨在开发由再生角蛋白和神经酰胺(CERs)制成的膜,以在体外经皮吸收研究中与人角质层的屏障特性相匹配。以布洛芬、普萘洛尔和睾酮为模型药物,根据其不同的扩散和溶解度特性,对其体外药物扩散谱进行优化。这些数据与使用人表皮获得的数据进行了比较。ATR-FTIR和SEM分析显示,即使发生了部分溶解,cer也悬浮在再生角蛋白基质中。结果表明,在暴露于水性缓冲液和/或矿物油后,膜具有物理稳定性,并且布洛芬和心得安通过膜和人体皮肤的通量在同一数量级上。其中,含有1%神经酰胺III和1%神经酰胺VI的180 μm厚的膜与人体表皮数据的关系最好。长时间暴露于水/乙醇溶液对睾酮扩散数据有影响,表明这种有机溶剂能够修饰角蛋白和cer的超分子组织。角蛋白/CER膜可以作为小分子体外皮肤渗透性研究的简化模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信