Iontophoretic transport pathways: Dependence on penetrant physicochemical properties

被引:45
作者
Turner, NG
Guy, RH
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT BIOPHARMACEUT SCI,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT PHARMACEUT CHEM,SAN FRANCISCO,CA 94143
关键词
D O I
10.1021/js970046z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The objective of this work was to investigate how the preferred iontophoretic transport pathways of a molecule depend on its physicochemical properties. Laser scanning confocal microscopy (LSCM) was used to visualize in hairless mouse skin the distribution of two fluorescent penetrants: calcein, a multiply charged (-4), hydrophilic molecule; and nile red, a lipophilic, neutral compound, lontophoresis and passive delivery of nile red showed that the percutaneous transport of this compound occurred via (inter-and intracellular) pathways that were clearly distinct from those followed by calcein. Although the distribution of nile red was influenced somewhat by the passage of current relative to the passive control, there was relatively little enhancement of the penetration of this compound into the skin. Calcein, on the other hand, did not passively enter the skin. However, with iontophoresis, greatly enhanced transport, with an important contribution from follicular structures, was observed. Sequential (dual) transport of the two fluorophores illustrated clearly the different pathways followed and reflected the transport and visualization studies of the individual species. It may be concluded, therefore, that the iontophoretic pathways followed across the skin are dictated by the physicochemical properties of the penetrant and by its affinity for the different environments available.
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页码:1385 / 1389
页数:5
相关论文
共 16 条
[1]  
ABRAMSON HA, 1942, ARCH DERMATOL SYPHIL, V44, P190
[2]  
Allen T.M., 1984, LIPOSOME TECHNOLOGY, P177
[3]   METHODS FOR INVITRO PERCUTANEOUS-ABSORPTION STUDIES .2. ANIMAL-MODELS FOR HUMAN-SKIN [J].
BRONAUGH, RL ;
STEWART, RF ;
CONGDON, ER .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 62 (03) :481-488
[4]   PENETRATION ENHANCEMENT FOR POLYPEPTIDES THROUGH EPITHELIA .D. ROUTES OF DELIVERY - CASE-STUDIES .6. TRANSDERMAL DELIVERY OF PEPTIDES AND PROTEINS [J].
CULLANDER, C ;
GUY, RH .
ADVANCED DRUG DELIVERY REVIEWS, 1992, 8 (2-3) :291-329
[5]   VISUALIZATION OF IONTOPHORETIC PATHWAYS WITH CONFOCAL MICROSCOPY AND THE VIBRATING PROBE ELECTRODE [J].
CULLANDER, C ;
GUY, RH .
SOLID STATE IONICS, 1992, 53 :197-206
[6]  
DAYLIGHT I, 1990, CHEM INFORMATION SYS
[7]   A NEW SYSTEM FOR INVITRO STUDIES OF IONTOPHORESIS [J].
GLIKFELD, P ;
CULLANDER, C ;
HINZ, RS ;
GUY, RH .
PHARMACEUTICAL RESEARCH, 1988, 5 (07) :443-446
[8]  
GREENSPAN P, 1985, J LIPID RES, V26, P781
[9]   NILE RED - A SELECTIVE FLUORESCENT STAIN FOR INTRACELLULAR LIPID DROPLETS [J].
GREENSPAN, P ;
MAYER, EP ;
FOWLER, SD .
JOURNAL OF CELL BIOLOGY, 1985, 100 (03) :965-973
[10]  
GRIMNES S, 1984, ACTA DERM-VENEREOL, V64, P93