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寡核苷酸经离子电渗法透过人表皮膜的研究:能斯特-普朗克模型研究

Iontophoretic transport of oligonucleotides across human epidermal membrane: a study of the Nernst-Planck model.

作者信息

Li S K, Ghanem A H, Teng C L, Hardee G E, Higuchi W I

机构信息

Department of Pharmaceutics and Pharmaceutical Chemistry, College of Pharmacy, University of Utah, Salt Lake City, Utah 84112, USA.

出版信息

J Pharm Sci. 2001 Jul;90(7):915-31. doi: 10.1002/jps.1043.

Abstract

The objective of this study was to investigate the transport behavior of a series of oligonucleotides with human epidermal membrane (HEM) and to examine the applicability of the modified NERNST-PLANCK model to transdermal iontophoresis of these macromolecules. Iontophoretic transport experiments were first carried out in a synthetic model membrane system (Nuclepore membranes) with a four-electrode potentiostat to examine the baseline modified NERNST-PLANCK model. The modified NERNST-PLANCK model derived from the Einstein relation and the Stokes-Einstein equation taken from previous work did not hold for the oligonucleotides. Results obtained in the Nuclepore studies were, however, consistent with predictions of the modified NERNST-PLANCK model using the experimentally determined electromobilities and diffusion coefficients. The electromobilities of the oligonucleotides (determined by capillary electrophoresis) were found to be more than a factor of two smaller than expected from the Einstein relation between electromobilities and diffusion coefficients (the latter determined in diffusion cell experiments). A correlation between these electromobilities and the theoretical electromobilities estimated by considering the effects of counterion binding and the effects of mobility reduction according to colloid theory was also observed. These results suggest that the modified NERNST-PLANCK model predictions are satisfactory only when the electromobilities and the effective molecular size of the oligonucleotides are known and are used directly to predict the iontophoretically enhanced transport. Results with the HEM experiments generally agreed with model predictions based on the experimental electromobilities. The oligonucleotide HEM flux data also suggest the existence of pores with effective pore radii greater than the effective radii estimated in previous studies with small molecular weight model permeants.

摘要

本研究的目的是研究一系列寡核苷酸在人表皮膜(HEM)中的转运行为,并检验修正的能斯特 - 普朗克模型对这些大分子经皮离子电渗疗法的适用性。首先在具有四电极恒电位仪的合成模型膜系统(核孔膜)中进行离子电渗转运实验,以检验基线修正的能斯特 - 普朗克模型。源自爱因斯坦关系和先前工作中的斯托克斯 - 爱因斯坦方程的修正能斯特 - 普朗克模型不适用于寡核苷酸。然而,在核孔研究中获得的结果与使用实验测定的电迁移率和扩散系数的修正能斯特 - 普朗克模型的预测一致。发现寡核苷酸的电迁移率(通过毛细管电泳测定)比根据电迁移率与扩散系数之间的爱因斯坦关系预期的小两倍多(后者在扩散池实验中测定)。还观察到这些电迁移率与通过考虑反离子结合效应和根据胶体理论的迁移率降低效应估计的理论电迁移率之间的相关性。这些结果表明,只有当寡核苷酸的电迁移率和有效分子大小已知并直接用于预测离子电渗增强转运时,修正的能斯特 - 普朗克模型预测才令人满意。HEM实验的结果总体上与基于实验电迁移率的模型预测一致。寡核苷酸HEM通量数据还表明存在有效孔径大于先前用小分子模型渗透物研究中估计的有效半径的孔。

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