Abstract
A rapid and simple high-performance liquid chromatographic (HPLC) method was developed
and validated to simultaneously analyze the diastereomers of (+)-licarin A and isolicarin
A in rat plasma after intravenous administration. The analytes were extracted from
the plasma by solid-phase extraction (SPE). Diastereomeric separation and determination
were successfully achieved using a Diamonsil™ ODS C18 reversed-phase column (250 mm × 4.6 mm i. d., 5 μm) with an RP18 guard column (8 mm × 4.6 mm
i. d., 5 μm) and a mobile phase of MeOH-H2 O (4 : 1, v/v). UV detection was at 270 nm. The linear ranges of the standard curves
were 0.25 – 150.00 μg/mL for (+)-licarin A and 0.10 – 75.00 μg/mL for isolicarin A.
The lower limits of detection and quantification were 0.05 and 0.25 μg/mL for (+)-licarin
A, and 0.05 and 0.10 μg/mL for isolicarin A, respectively. This assay method was successfully
applied to study the pharmacokinetics of diastereomers (+)-licarin A and isolicarin
A in rat plasma.
Abbreviations
HPLC:high-performance liquid chromatography
LLOD:lower limits of detection
LLOQ:lower limits of quantification
QC:quality control
R.S.D.:relative standards deviation
SD:Sprague-Dawley
SPE:solid-phase extraction
UV:ultraviolet
Key words
Myristica fragrans
- Myristicaceae - (+)-licarin A - isolicarin A - diastereomers - pharmacokinetics
- HPLC
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Prof. Xiu-Wei Yang
State Key Laboratory of Natural and Biomimetic Drugs
Department of Natural Medicines
School of Pharmaceutical Sciences
Peking University
Beijing 100083
People’s Republic of China
Telefon: +86/10/8280/5106
Fax: +86/10/8280/2724
eMail: xwyang@bjmu.edu.cn