Utility of Three-Dimensional Skin From Human-Induced Pluripotent Stem Cells as a Tool to Evaluate Transdermal Drug Permeation

被引:6
作者
Naito, Chihiro [1 ]
Yamaguchi, Tomoko [2 ]
Katsumi, Hidemasa [1 ]
Kimura, Suyo [1 ]
Kamei, Sachi [1 ]
Morishita, Masaki [1 ]
Sakane, Toshiyasu [1 ,3 ]
Kawabata, Kenji [2 ]
Yamamoto, Akira [1 ]
机构
[1] Kyoto Pharmaceut Univ, Dept Biopharmaceut, Yamashina Ku, Kyoto 6078414, Japan
[2] Natl Inst Biomed Innovat Hlth & Nutr, Lab Stem Cell Regulat, Osaka 5670085, Japan
[3] Kobe Pharmaceut Univ, Dept Pharmaceut Technol, Higashinada Ku, Kobe, Hyogo 6588558, Japan
关键词
transdermal; skin; drug delivery system(s); absorption; MOLECULAR-WEIGHT DEPENDENCE; EPIDERMIS MODELS; PENETRATION; KERATINOCYTES; DELIVERY; BARRIER;
D O I
10.1016/j.xphs.2019.07.006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Transdermal drug delivery is an attractive route for administration of drugs, and it offers several advantages such as painless administration. To accurately predict the rate of human skin permeation for new transdermal drug formulations, we developed a novel assessment system using induced pluripotent stem cells (iPSCs). Skin was generated from iPSC-derived keratinocytes and fibroblasts. In the histological and immunohistochemical examination, cellular markers (keratin 14 and keratin 10) for the epidermal basal and suprabasal layers were clearly detected within the multilayer structures produced in the human iPSC-based three-dimensional skin model. The results from our permeation study indicate that an initial lag time exists during permeation of 5(6)-carboxyfluorescein and fluorescein isothiocyanate dextran 4000. Furthermore, the permeation for these model drugs in human iPSC-based skin was inversely proportional to the molecular weight of the drugs. These results of the present iPSC-based skin are useful basic information as a first step for developing a new assessment system to predict the efficacy of drug permeation in human skin by using iPSC-based skin. (c) 2019 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:3524 / 3527
页数:4
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