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渗透促进剂和离子导入对猪皮肤超微结构及胆囊收缩素-8透过性的影响。

Effect of penetration enhancers and iontophoresis on the ultrastructure and cholecystokinin-8 permeability through porcine skin.

作者信息

Bhatia K S, Gao S, Freeman T P, Singh J

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, North Dakota State University, Fargo 58105, USA.

出版信息

J Pharm Sci. 1997 Sep;86(9):1011-5. doi: 10.1021/js970023k.

Abstract

The present study explores the effect of chemical penetration enhancers and iontophoresis on the in vitro permeability of cholecystokinin-8 (CCK-8) through porcine epidermis and on the ultrastructural changes in stratum corneum as observed by transmission electron microscopy (TEM). Enhancer [i.e., ethanol (EtOH), and 10% oleic acid in combination with ethanol (OA/EtOH)] pretreatment significantly increased (p < 0.01) the permeability coefficient of CCK-8 in comparison with the control (pretreated epidermis without enhancer). Iontophoresis further increased the permeability of CCK-8 (p < 0.01) through the enhancer-pretreated epidermis in comparison with the control. These results showed the synergistic effect of iontophoresis and enhancers such as OA/EtOH that provides an additional driving force to maintain and control the target flux of CCK-8. The ultrastructure of stratum corneum treated with ethanol demonstrated a loss of structural components in the superficial stratum corneum cell layers. OA/EtOH transformed the highly compact cells of stratum corneum into a looser network of filaments, creating an increased free volume and greater intracellular surface area. Treatment of stratum corneum with OA/EtOH followed by iontophoresis resulted in further swelling of stratum corneum cell layers. In conclusion, OA/EtOH in combination with iontophoresis increased the permeability of CCK-8 by loosening and swelling of stratum corneum cell layers.

摘要

本研究探讨了化学渗透促进剂和离子导入对胆囊收缩素-8(CCK-8)经猪表皮的体外通透性以及透射电子显微镜(TEM)观察到的角质层超微结构变化的影响。与对照(未用促进剂预处理的表皮)相比,促进剂[即乙醇(EtOH)以及10%油酸与乙醇的组合(OA/EtOH)]预处理显著提高(p < 0.01)了CCK-8的渗透系数。与对照相比,离子导入进一步提高了CCK-8通过促进剂预处理表皮的通透性(p < 0.01)。这些结果表明离子导入和诸如OA/EtOH等促进剂具有协同作用,为维持和控制CCK-8的目标通量提供了额外的驱动力。用乙醇处理的角质层超微结构显示角质层浅层细胞层的结构成分丢失。OA/EtOH将角质层高度紧密的细胞转变为更松散的细丝网络,增加了自由体积并增大了细胞内表面积。先用OA/EtOH处理角质层然后进行离子导入导致角质层细胞层进一步肿胀。总之,OA/EtOH与离子导入相结合通过使角质层细胞层疏松和肿胀增加了CCK-8的通透性。

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