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经皮离子电渗疗法:多肽对电渗作用的调节

Transdermal iontophoresis: modulation of electroosmosis by polypeptide.

作者信息

Hirvonen J, Guy R H

机构信息

Department of Biopharmaceutical Sciences, University of California, San Francisco 94143-0446, USA.

出版信息

J Control Release. 1998 Jan 2;50(1-3):283-9. doi: 10.1016/s0168-3659(97)00150-8.

Abstract

The objective of this research was to further evaluate the relative importance of electrorepulsion and electroosmosis to the mechanism of enhanced transport across the skin during iontophoresis. Specifically, the impact of iontophoresing into the skin positively and negatively charged polypeptides (poly-L-lysines and poly-L-glutamic acids, respectively) on the membrane's permselectivity and hence on the quantity and direction of electroosmotic flow, was examined. Experiments were performed in vitro at pH 7.4 using conventional methodology; electroosmosis during the iontophoresis of the polypeptides into and across the skin was tracked in the usual way via the movement of the polar, uncharged, non-metabolizable marker, D-mannitol. Electrotransport of the cationic polypeptides attenuated electroosmotic flow in the normal anode-to-cathode direction; the degree of inhibition was correlated both with the initial concentration of poly-L-lysine in the anodal chamber and with the molecular weight of the polypeptide employed (from 1 to 25 kilodaltons). Iontophoresis of the anionic poly-L-glutamic acids from the cathode provoked a slight increase in electroosmotic flow in the 'reverse' direction (i.e. from the receptor phase beneath the skin towards the cathode chamber located on the epidermal side of the membrane); this effect, however, was much less dramatic than that produced in the opposite sense by the cationic polypeptides. The results suggest that driving large positively-charged polypeptide molecules into the skin leads to neutralization of the membrane's negativity, a subsequent loss of permselectivity and a concomitant attenuation of electroosmosis in the conventional anode-to-cathode direction. Presumably, the relatively poor iontophoretic permeability of these species (which becomes more and more evident with increasing molecular weight) results in a sufficiently important association of the polypeptide with the skin during the period of current passage. Much less significant effects are realized by the cathodal iontophoresis of poly-anions due to the difficulty of 'pushing' negative ions into an already negatively-charged membrane.

摘要

本研究的目的是进一步评估电排斥和电渗作用对离子电渗疗法中经皮增强转运机制的相对重要性。具体而言,研究了分别向皮肤中离子电渗带正电荷和负电荷的多肽(聚-L-赖氨酸和聚-L-谷氨酸)对膜的选择透过性的影响,进而对电渗流的数量和方向的影响。实验在体外pH 7.4条件下采用传统方法进行;通过极性、不带电荷、不可代谢的标记物D-甘露醇的移动,以常规方式跟踪多肽离子电渗进入皮肤和穿过皮肤过程中的电渗作用。阳离子多肽的电转运减弱了正常阳极到阴极方向的电渗流;抑制程度与阳极室中聚-L-赖氨酸的初始浓度以及所用多肽的分子量(1至25千道尔顿)均相关。从阴极进行阴离子聚-L-谷氨酸的离子电渗引发了“反向”电渗流的轻微增加(即从皮肤下方的接受相朝向位于膜表皮侧的阴极室);然而,这种效应远不如阳离子多肽在相反方向产生的效应显著。结果表明,将大的带正电荷多肽分子驱入皮肤会导致膜的负电荷中和,随后选择透过性丧失,并伴随着传统阳极到阴极方向电渗作用的减弱。据推测,这些物质相对较差的离子电渗通透性(随着分子量增加越来越明显)导致在电流通过期间多肽与皮肤有足够重要的结合。由于难以将负离子“推入”已经带负电荷的膜中,聚阴离子的阴极离子电渗产生的影响要小得多。

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