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A sensitive and accurate liquid chromatography–tandem mass spectrometry method was developed and validated for the determination of dryocrassin ABBA, a potential active component isolated from Dryopteris crassirhizoma, in rat plasma. Chromatographic separation was achieved on a Zorbax SB-C18 column (50 × 2.1 mm, 1.8 µm), with elution consisting of eluent (A) 10 mm ammonium acetate in methanol containing 0.1% formic acid and (B) 10 mm ammonium acetate in water containing 0.1% formic acid (A:B = 99:1, v/v) at a flow rate of 0.3 mL/min. Multiple reaction monitoring mode was used to monitor the precursor–product ion transitions of m/z 819.3 403.4 for dryocrassin ABBA and m/z 426.2 409.2 for internal standard. This assay exhibited a good linearity with a correlation coefficient >0.99 and showed no endogenous interference with the analyte and internal standard. The lower limit of quantification of dryocrassin ABBA was 4 ng/mL in 50 μL of rat plasma. The method was successfully applied in the pharmacokinetic study of dryocrassin ABBA in rats after intravenous (2.35 mg/kg) and oral (23.5 mg/kg) doses of dryocrassin ABBA. The oral bioavailability (F) of dryocrassin ABBA was estimated to be 50.1%. Our study is the first to clarify the pharmacokinetic behaviors of dryocrassin ABBA in animals. Copyright © 2014 John Wiley & Sons, Ltd.

GdVO4 was synthesized by solid state reaction at high temperature and characterized by XRD, UVvisible DRS, BET and SEM. XRD analysis of GdVO4 showed its structure was of tetragonal type. When GdVO4 was loaded with 0.3 wt% Pt, it showed the better photocatalytic activity for water splitting under simulated solar irradiation, and the amounts of the produced hydrogen in pure water were about 9.33 μmol under the irradiation of simulated solar for 6 h. Furthermore, photodegradation of Rhodamine B (Rh B ) on the samples were investigated under simulated solar irradiation.