Effect of synthesized cyclohexanol derivatives using L-menthol as a lead compound on the percutaneous absorption of ketoprofen

Citation
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
Citations number
14
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
ISSN journal
03785173 → ACNP
Volume
198
Issue
2
Year of publication
2000
Pages
191 - 200
Database
ISI
SICI code
0378-5173(20000405)198:2<191:EOSCDU>2.0.ZU;2-9
Abstract
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.