| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1220989 | Journal of Pharmaceutical and Biomedical Analysis | 2014 | 6 Pages |
•A novel UFLC-ESI–MS/MS quantitation method was developed.•Gastrodin and HBA were firstly simultaneously determined in dog plasma.•Pharmacokinetics behaviors of the two analytes in dog were studied.
A simple, sensitive and reliable ultra fast liquid chromatography-electrospray ionization–tandem mass spectrometry (UFLC-ESI–MS/MS) method was developed for simultaneously quantifying gastrodin (p-hydroxy-methyl-phenol-β-d-glucoside) and its metabolite p-hydroxybenzyl alcohol (HBA) in dog plasma. Separation was performed on an ultra fast liquid chromatography (UFLC) system. Detection was carried out on a tandem mass spectrometry (MS/MS) in multiple reaction monitoring (MRM) mode via an electrospray ionization (ESI) interface. MRM mode of precursor–product ion transitions was used for gastrodin, HBA and the internal standard (IS, bergeninum) at m/z 285.0 → 123.0, 123.0 → 105.0 and 326.9 → 192.2, respectively. The lower limits of quantification (LLOQ) of this method for both gastrodin and HBA were 1 ng/mL, with their linear concentration ranging from 0.001 to 10 μg/mL. The methods were validated for selectivity, calibration curves, accuracy and precision, extraction recoveries, matrix effects, carry-over, cross talk, dilution integrity, stability and incurred sample reanalysis (ISR). Using this validated method, pharmacokinetic behaviors of gastrodin and HBA after intragastric administration (ig) of gastrodin to dogs were studied for the first time.
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