Heit M C, McFarland A, Bock R, Riviere J E
Cutaneous Pharmacology and Toxicology Center, North Carolina State University College of Veterinary Medicine, Raleigh 27606.
J Pharm Sci. 1994 May;83(5):654-6. doi: 10.1002/jps.2600830512.
Iontophoresis is the movement of charged compounds into and through the skin under an external electromotive force. A molecule's charge and size, as well as other factors, will determine its ability to be iontophoresed. One can gain insight into certain electrical aspects of a molecule by determining its isoelectric point as well as its electrophoretic mobility. In the present study, isoelectric focusing and capillary zone electrophoretic studies of luteinizing hormone releasing hormone, (LHRH) and one of its analogs are performed in order to predict their ability to be iontophoresed. The pI of LHRH is determined to be 9.6 while that of its free acid is 6.9. In addition, it is concluded that although the two compounds are chemically similar, the native compound is more mobile at pH > 2.5. These results suggest that the native compound might be better suited for iontophoretic delivery than is the free-acid analog.
离子电渗疗法是指在外部电动势作用下,带电化合物进入并穿透皮肤的过程。分子的电荷、大小以及其他因素将决定其进行离子电渗的能力。通过确定分子的等电点及其电泳迁移率,可以深入了解分子的某些电学特性。在本研究中,进行了促黄体生成素释放激素(LHRH)及其一种类似物的等电聚焦和毛细管区电泳研究,以预测它们进行离子电渗的能力。LHRH的等电点被确定为9.6,而其游离酸的等电点为6.9。此外,得出的结论是,尽管这两种化合物在化学上相似,但天然化合物在pH>2.5时迁移率更高。这些结果表明,与游离酸类似物相比,天然化合物可能更适合离子电渗给药。