Y. Obata et al., Effect of synthesized cyclohexanol derivatives using L-menthol as a lead compound on the percutaneous absorption of ketoprofen, INT J PHARM, 198(2), 2000, pp. 191-200
L-Menthol was selected us a lead compound to synthesize new candidates for
percutaneous absorption enhancers. In a previous study, O-ethylmenthol (MET
) was the most effective compound and caused relatively little skin irritat
ion. To develop more effective compounds, mono- or disubstitute groups of c
yclohexane with an O-ethyl group were synthesized. Some 35 compounds were s
ynthesized and evaluated for their promoting activity and effect on skin. A
n in vivo percutaneous absorption study was performed using rats with hydro
gel containing ketoprofen and each of the synthesized compounds. The plasma
concentration of ketoprofen was determined after the application of hydrog
el to the abdominal al en of rats. The apparent penetration rate (R-p) was
estimated based on the pharmacokinetic model with a constant rate of penetr
ation through the skin after the lag time. The 2-compartment model was appl
ied to the data obtained from the iv administration. As an index to evaluat
e the promoting activity of each enhancer, an enhancement factor (E-t) was
defined as follows. E-r=R-p (with enhancer)/R-p (without enhancer). Irritat
ion to skin was pathologically evaluated. The treated area of rat abdominal
skill was exised after the in vivo experiment using total irritation score
(TIS). The compound having a C-3 positioned iso-butyl group on the chemica
l structure was the most effective and caused relatively little irritation
among mono-substituted compounds. In the case of di-substituted compounds,
all had the same effect as or a stronger effect than MET. Furthermore, the
promoting activity almost corresponded to irritation. To estimate log P, on
e of the physicochemical properties of molecules. a computer program 'CAChe
' was employed. The log P was calculated using the atom typing scheme. Mult
iple regression analysis revealed that the relations between E-r or TIS and
log P were parabolic. It was suggested that the optimum log P value reflec
ts the promoting activity to enhance percutaneous absorption of ketoprofen.
(C) 2000 Elsevier Science B.V. All rights reserved.