CALCULATION OF SKIN PERMEABILITY COEFFICIENT FOR IONIZED AND UNIONIZED SPECIES OF INDOMETHACIN

被引:18
作者
HAYASHI, T [1 ]
SUGIBAYASHI, K [1 ]
MORIMOTO, Y [1 ]
机构
[1] JOSAI UNIV, FAC PHARMACEUT SCI, 1-1 KEYAKIDAI, SAKADO, SAITAMA 35002, JAPAN
关键词
INDOMETHACIN; WEAK ELECTROLYTE; PERMEABILITY COEFFICIENT; PERMEATION PATHWAY; HAIRLESS RAT SKIN;
D O I
10.1248/cpb.40.3090
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The contribution of ionized and unionized species to the overall permeation of weak electrolytes through the skin was investigated to determine the effect of pH in the vehicle on the permeability of indomethacin (IDM), as a model drug, through hairless rat skin. The permeability of IDM through polydimethylsiloxane (silicone) and poly(2-hydroxyethyl methacrylate) (pHEMA) membranes which may reflect lipid and aqueous pathway, respectively, was also measured for comparison. As the pH in the vehicle increased, there was an exponential increase in the skin permeation rate of IDM. The permeation rate of IDM through the silicone membrane was constant independent of pH, whereas that through the pHEMA membrane increased with increasing pH, similar to the skin permeation. The permeability coefficients of ionized and unionized species through the skin estimated using the skin permeation rates and solubilities of IDM at various pHs were 1.50 x 10(-7) and 2.79 x 10(-5) cm/s, respectively. These results indicated that the permeation of ionized species greatly contributed to the total permeation of IDM at higher pH, and that the total permeation rate of IDM was determined by the permeation of unionized species at lower pH. These contributions depend on the pH and pK(a) values and the ratio of permeability coefficient of each species. It was also confirmed that the skin has at least two kinds of permeation pathways and these two species permeate through a different pathway.
引用
收藏
页码:3090 / 3093
页数:4
相关论文
共 14 条
[1]   ETHER WATER PARTITIONING AND PERMEABILITY THROUGH NUDE-MOUSE SKIN INVITRO .2. HYDROCORTISONE 21-NORMAL-ALKYL ESTERS, ALKANOLS AND HYDROPHILIC COMPOUNDS [J].
ACKERMANN, C ;
FLYNN, GL ;
SMITH, WM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 36 (01) :67-71
[2]  
BARRY B W, 1987, Journal of Controlled Release, V6, P85, DOI 10.1016/0168-3659(87)90066-6
[3]  
BUDAVARI S, 1989, MERCK INDEX, P1324
[4]   LIPIDS AND THE EPIDERMAL PERMEABILITY BARRIER [J].
ELIAS, PM .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1981, 270 (01) :95-117
[5]  
GHANEM A-H, 1987, Journal of Controlled Release, V6, P75, DOI 10.1016/0168-3659(87)90065-4
[6]   PREDICTION OF SKIN PERMEABILITY OF DRUGS .1. COMPARISON WITH ARTIFICIAL MEMBRANE [J].
HATANAKA, T ;
INUMA, M ;
SUGIBAYASHI, K ;
MORIMOTO, Y .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1990, 38 (12) :3452-3459
[7]  
HATANAKA T, 1992, INT J PHARM, V79, P21
[8]  
Higuchi T, 1960, J SOC COSMET CHEM, V11, P85
[9]   DRUG PERMEATION THROUGH HUMAN SKIN - THEORY AND INVITRO EXPERIMENTAL MEASUREMENT [J].
MICHAELS, AS ;
CHANDRASEKARAN, SK ;
SHAW, JE .
AICHE JOURNAL, 1975, 21 (05) :985-996
[10]  
MORIMOTO Y, 1986, INT J PHARM, V32, P31