3 results match your criteria: "Guangdong Provincial Hospital of Chinese Medicine Affiliated to Guangzhou University of Chinese Medicine[Affiliation]"
J Chromatogr B Analyt Technol Biomed Life Sci
August 2019
Second Clinical Medical College of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine Affiliated to Guangzhou University of Chinese Medicine, 111 Dade Road, Guangzhou 510120, China. Electronic address:
A simple, accurate, and reliable liquid chromatography-mass spectrometry (LC-MS/MS) method was developed and validated for the determination of mangiferin in rat plasma and tissue homogenates using rutin as an internal standard (IS). Chromatographic separation was achieved on a Shiseido CAPCELL PAK C column (150 × 2.0 mm, 5 μm) using a gradient elution of 1% acetic acid in water and methanol at a flow rate of 300 μL·min.
View Article and Find Full Text PDFJ Chromatogr B Analyt Technol Biomed Life Sci
January 2016
Guangdong Provincial Hospital of Chinese Medicine Affiliated to Guangzhou University of Chinese Medicine, 111 Dade Road, Guangzhou 510120, China. Electronic address:
A rapid, specific and sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous determination of strychnine, brucine, strychnine N-oxide and brucine N-oxide in rat plasma. Plasma samples were pretreated via simple protein precipitation with methanol and ephedrine hydrochloride was used as internal standard. Chromatographic separation was carried out on an ZORBAX Eclipse XDB-C18 column (2.
View Article and Find Full Text PDFJ Chromatogr B Analyt Technol Biomed Life Sci
August 2014
Guangdong Provincial Hospital of Chinese Medicine Affiliated to Guangzhou University of Chinese Medicine, 111 Dade Road, Guangzhou 510120, China. Electronic address:
A rapid, specific and sensitive liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and validated for the simultaneous determination of timosaponin B-II (TB-II) and A-III (TA-III) in rat plasma. Plasma samples were pretreated via simple protein precipitation with acetonitrile and ginsenoside Rg2 was used as internal standard. Chromatographic separation was carried out on an Agilent XDB-C8 (150 mm × 2.
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