Abstract
Purpose: To identify and quantify
anethole in the essential oil of fruits of Illicium
verum Hook (star anise) and in vivo in rat plasma using
reverse-phase liquid chromatography.
Methods: Anethole was identified in
the essential oil of the fruits of Star anise and
determined by gas chromatography-tandem mass
spectrometry (GC-MS), nuclear magnetic resonance (NMR),
ultraviolet visible spectrophotometry (UV-VIS). A
simple, sensitive and validated high performance liguid
chromatography (HPLC) technique with UV-VIS detection
method was developed for the determination of the
compound in rat plasma using: methanol-water (85:15,
v/v) as mobile phase at a flow rate of 0.2 ml/min
Hypersil ODS Thermo (150 mm ´ 2.1 mm ´ 3.0 µM) as column
with wavelength detection at 259 nm.
Results:
GC determination showed that
anethole in the essential oil of star anise exhibited a
retention time of 21.02 min. The validation results for
anethole in plasma were satisfactory, with coefficient
of determination (R2) of 0.9945 and relative
standard deviation of < 3 %. HPLC run time of 4 min with
a retention time of 2.73 min was the faster method to
determine anethole when compared to a previously
reported method which had a run time of 15 min.
Conclusion: Anethole in the essential
oil of Illicium verum Hook can be identified and
determined by GC-MS, NMR and UV-VIS, and a superior HPLC
method has been developed for the determination of the
compound in rat plasma.
Keywords: Anethole,
High performance liguid chromatography, Star anise,
Essential oil, Rat plasma, Illicium verum Hook.