Abstract
The purpose of this study was to investigate dermal pharmacokinetics of terpinen-4-ol
in rats following topical administration of plai oil derived from the rhizomes of
Zingiber cassumunar Roxb. Unbound terpinen-4-ol concentrations in dermal tissue were measured by microdialysis.
The dermal pharmacokinetic study of terpinen-4-ol was performed under non-occlusive
conditions. The oil was topically applied at a dose of 2, 4, and 8 mg/cm2 plai oil corresponding to the amount of 1.0, 1.9, and 3.8 mg/cm2 terpinen-4-ol, respectively. Following topical application of the oil, terpinen-4-ol
rapidly distributed into the dermis and demonstrated linear pharmacokinetics with
no changes in the dose-normalized area under the concentration-time curves across
the investigated dosage range. The mean percentages of free terpinen-4-ol distributed
in the dermis per amount of administered were 0.39 ± 0.06 %, 0.41 ± 0.08 %, and 0.30 ± 0.03 %
for 2, 4, and 8 mg/cm2 doses, respectively. The dermal pharmacokinetics of terpinen-4-ol could provide information
for its further formulation development and therapy schedules.
Key words
terpinen-4-ol -
Zingiber cassumunar
- Zingiberaceae - plai oil - dermal pharmacokinetics - microdialysis