Biomedical Chromatography · 2019 · 13 citations · 16 references
PharmacyPharmaceutical AnalysisPharmacologyBiochemical PharmacologyChromatographic AnalysisMass Spectrometric AnalysisAnalytical ChromatographyBioanalytical Method ValidationChromatographic CouplingChromatographyInstrumental AnalysisLiquid ChromatographyAssay DeterminationExtraction RecoveryLiquid Chromatography-mass SpectrometryLiquid Chromatography-mass Spectrometry AnalysisPharmacokinetic ParametersTandem Mass SpectrometryUltra-performance Liquid Chromatography Method DevelopmentUltra-performance Liquid Chromatography-mass Spectrometry
Abstract In this study, an accurate and reliable method of ultra‐performance liquid chromatography coupled with a triple‐quadrupole tandem mass spectrometry was firstly developed and fully validated for the simultaneous determination of epicatechin, neoastilbin, astilbin, isoastilbin, engeletin and resveratrol in rat plasma after administration of Smilacis glabrae Roxb. extract. Naringenin was used as an internal standard (IS). The analyte and IS were separated on a C 18 column by gradient elution with a mobile phase of acetonitrile–0.3% acetic acid at a flow rate of 0.25 mL/min for a total run time of 8 min. The method was validated in terms of selectivity, linearity, precision, accuracy, extraction recovery, matrix effect and stability. The developed method was successfully applied to determine the main pharmacokinetic parameters of six components in rat plasma.
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HIGH ABSORPTION BUT VERY LOW BIOAVAILABILITY OF ORAL RESVERATROL IN HUMANS
Thomas Walle, Faye Hsieh, Mark H. DeLegge et al. · Drug Metabolism and Disposition · 2004 · 1.8K citations
Jean‐Francois Marier, Pascal Vachon, Ari Gritsas et al. · Journal of Pharmacology and Experimental Therapeutics · 2002 · 478 citations
Inhibition of cancer growth by resveratrol is related to its low bioavailability
Miguel Asensi, Ignacio Medina, Ángel Ortega et al. · Free Radical Biology and Medicine · 2002 · 388 citations
Medicine, Oncology, Pharmacology +10