Denet Anne-Rose, Ucakar Bernard, Préat Véronique
Unité de Pharmacie Galénique, Université Catholique de Louvain, UCL 7320, 1200 Brussels, Belgium.
Pharm Res. 2003 Dec;20(12):1946-51. doi: 10.1023/b:pham.0000008041.86042.c0.
The purpose of this work was to study the effect of electroporation on iontophoretic transport of two beta-blockers, timolol (lipophilic) and atenolol (hydrophilic), and to have a better understanding of the mechanism of combination.
The transdermal delivery of these beta-blockers through human stratum corneum was studied in three-compartment diffusion cells. The transport of mannitol was evaluated to assess the electroosmotic flow.
The iontophoretic transport of timolol was decreased by electroporation because the high accumulation of the lipophilic cation timolol in the stratum corneum resulted in a decrease of electroosmosis. In contrast, electroosmosis was not affected by atenolol, and the iontophoretic transport of atenolol was increased by electroporation.
Using two different beta-blockers, we showed that lipophilicity and positive charges affect the electrotransport of drugs. Understanding the effect of the physicochemical properties of the drug, as well as the electrical parameters, is thus essential for the optimization of transdermal drug delivery by a combination of electroporation and iontophoresis.
本研究旨在探讨电穿孔对两种β受体阻滞剂(亲脂性的噻吗洛尔和亲水性的阿替洛尔)离子导入转运的影响,并更好地理解联合作用机制。
在三室扩散池中研究这些β受体阻滞剂通过人体角质层的透皮给药情况。评估甘露醇的转运以测定电渗流。
电穿孔降低了噻吗洛尔的离子导入转运,因为亲脂性阳离子噻吗洛尔在角质层中的大量蓄积导致电渗作用减弱。相反,阿替洛尔对电渗作用无影响,电穿孔增加了阿替洛尔的离子导入转运。
通过使用两种不同的β受体阻滞剂,我们表明亲脂性和正电荷会影响药物的电转运。因此,了解药物的理化性质以及电学参数的影响对于通过电穿孔和离子导入联合优化透皮给药至关重要。