THE ROLE OF ELECTROOSMOTIC FLOW ON IN-VITRO TRANSDERMAL IONTOPHORESIS

Authors
Citation
Ry. Lin et al., THE ROLE OF ELECTROOSMOTIC FLOW ON IN-VITRO TRANSDERMAL IONTOPHORESIS, Journal of controlled release, 43(1), 1997, pp. 23-33
Citations number
31
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
ISSN journal
01683659
Volume
43
Issue
1
Year of publication
1997
Pages
23 - 33
Database
ISI
SICI code
0168-3659(1997)43:1<23:TROEFO>2.0.ZU;2-J
Abstract
Amino acids and their amino or carboxyl group blocked derivatives were selected to investigate the relative importance of the electroosmotic flow as comparing with the passive and electrical flows in transderma l iontophoresis. Specifically, the effects of the solute's hydrophobic ity, the solute's charge, the buffer's salt concentration, and the ele ctrical current density on the electroosmotic flow of transdermal were clearly demonstrated. In a summary, the electroosmotic flow direction enhanced the permeability of the positively charged solutes (anodic d elivery), and the enhancements were diminished as the buffer's salt co ncentration increases; however, for anionic solutes and neutral solute s, the permeability reduced by increasing the buffer salt concentratio n was not as apparent as for cationic solutes since the negative effec t of electroosmotic flow on anionic solutes was lessened as buffer con centration increases. Also, the increase in the electrical current den sity pushes up the permeability of cationic solutes by both increasing the electrical and electroosmotic flow; but for anionic solutes, the favor of the electrical flow in a higher electrical field was weakened by increasing negative electroosmotic flow. Furthermore, in the molec ular weight range of the solutes under this investigation (89-300 g/mo l), experimental results indicated that the hydrophobicity of solutes plays a more prominent role than molecular weight in passive diffusion , and the results allow to eliminate the argument of the permeability differences caused by the different molecular weights of the anionic s olutes and the cationic solutes of this study.