Comparison of skin transport and metabolism of ethyl nicotinate in various species

被引:19
作者
Ngawhirunpat, T
Opanasopit, P
Prakongpan, S
机构
[1] Silpakorn Univ, Fac Pharm, Nakhon Pathom 73000, Thailand
[2] Mahidol Univ, Dept Pharm, Bangkok 10700, Thailand
关键词
species difference; skin transport; skin metabolism;
D O I
10.1016/j.ejpb.2004.05.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The skin transport and metabolism characteristics of ethyl nicotinate (EN) in rabbit, rat, guinea-pig, pig, shed snake skin and human were compared. In vitro skin transport using excised skin and hydrolysis experiments using skin homogenate were carried out. Flux of EN, a metabolite, nicotinic acid (NA), and the total (EN + NA), as well as kinetic parameters (V-max and K-m) for hydrolysis of EN were determined and compared among various species. The enzymatic conversion of EN to NA was observed for all skin permeation experiments. Total flux from EN-saturated solution between rabbit, rat, guinea-pig and human was significantly different (P < 0.05). A great difference between species was observed in skin esterase activity. The NA/total flux ratio of human was significantly lower than that of rabbit, rat or guinea-pig but lower than that of shed snake skin (P < 0.05). There is no significant difference in skin permeation and metabolism between human and pig (P > 0.05). Total flux increased linearly with an increase in EN donor concentration for all species. For pig, shed snake skin and human, NA flux increased with an increase in EN donor concentration and reached a plateau, suggesting the metabolic saturation was taking place in the skin. NA flux at plateau and EN donor concentration in which the NA flux reached a plateau were also affected by species difference. These findings indicated that the discrepancy in transdermal profiles of EN among species tested was predominantly due to the difference in the esterase activity in the skin. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:645 / 651
页数:7
相关论文
共 26 条
[1]  
CHAN SY, 1987, INT J PHARMACEUT, V55, P1
[2]   THE INFLUENCE OF DIFFERENT STRAINS AND AGE ON INVITRO RAT SKIN PERMEABILITY TO WATER AND MANNITOL [J].
DICK, IP ;
SCOTT, RC .
PHARMACEUTICAL RESEARCH, 1992, 9 (07) :884-887
[3]   PERMEATION OF HAIRLESS MOUSE SKIN .1. EXPERIMENTAL METHODS AND COMPARISON WITH HUMAN EPIDERMAL PERMEATION BY ALKANOLS [J].
DURRHEIM, H ;
FLYNN, GL ;
HIGUCHI, WI ;
BEHL, CR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1980, 69 (07) :781-786
[4]   DODECYL N,N-DIMETHYLAMINO ACETATE AND AZONE ENHANCE DRUG PENETRATION ACROSS HUMAN, SNAKE, AND RABBIT SKIN [J].
HIRVONEN, J ;
RYTTING, JH ;
PARONEN, P ;
URTTI, A .
PHARMACEUTICAL RESEARCH, 1991, 8 (07) :933-937
[5]   USE OF SHED SNAKE SKIN AS A MODEL MEMBRANE FOR INVITRO PERCUTANEOUS PENETRATION STUDIES - COMPARISON WITH HUMAN SKIN [J].
ITOH, T ;
XIA, J ;
MAGAVI, R ;
NISHIHATA, T ;
RYTTING, JH .
PHARMACEUTICAL RESEARCH, 1990, 7 (10) :1042-1047
[6]  
KAO J, 1984, TOXICOL APPL PHARM, V725, P289
[7]  
KASTING BB, 1992, PRODRUG TOPICAL OCUL, P117
[8]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[9]  
MACREESH AH, 1965, TOXICOL APPL PHARM, V7, P20
[10]   SKIN METABOLISM OF TOPICALLY APPLIED COMPOUNDS [J].
MARTIN, RJ ;
DENYER, SP ;
HADGRAFT, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1987, 39 (1-2) :23-32