Kaishun Bi

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Organization: Shenyang Pharmaceutical University
Department: School of Pharmacy
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Co-reporter:Jinting Sui;Yanmei Zhang;Haitao Lv;Xiangcai Meng;Hui Sun;Xijun Wang
Journal of Separation Science 2007 Volume 30(Issue 18) pp:3120-3126
Publication Date(Web):15 NOV 2007
DOI:10.1002/jssc.200700265

An HPLC with SPE method has been developed for analysis of constituents in rat blood after oral administration of the extract of Acanthopanax senticosus (ASE). The plasma sample was prepared by SPE method equipped with Oasis HLB cartridge (3cc, 60 mg). The analysis was performed on a Dikma Diamonsil RP18 column (4.6 mm×150 mm, 5 μm) with the gradient elution of solvent A (ACN) and solvent B (0.1% aqueous phosphoric acid, v/v) and the detection wavelength was set at 270 nm. The calibration curve was linear over the range of 0.156–15.625 μg/mL. The LOD was 60 ng/mL. The intraday precision was less than 5.80%, and the interday precision was less than 6.0%. The recovery was (87.30 ± 1.73)%. As a result, 19 constituents were detected in rat plasma after oral administration of the ASE, including 11 original compounds in ASE and eight metabolites, and three of the metabolites originated from syringin in ASE. Six constituents were identified by comparing with the corresponding reference compounds.

Co-reporter:Yujuan Li, Xinmiao Liang, Hongbin Xiao, Kaishun Bi
Journal of Chromatography B 2003 Volume 787(Issue 2) pp:421-425
Publication Date(Web):25 April 2003
DOI:10.1016/S1570-0232(02)01001-2
A sensitive, simple, and accurate method for determination of spinosin in rat plasma with sulfamethoxazole (SMZ) as internal standard was developed using RP-HPLC with UV detection. Sample preparations were carried out by protein precipitation with acetonitrile, followed by the evaporation of the acetonitrile to dryness. The resultant residue was then reconstituted in mobile phase and injected onto a Hypersil C18 (200×4.6 mm I.D., 5 μm) analytical column. The mobile phase consisted of acetonitrile–water (15:85, v/v) with 1% glacial acetic acid. The assay was shown to be linear over the range of 18.07–903.5 ng/ml (R2=0.995). Mean recovery was determined as 93.6%. Within- and between-day precisions were ≤8.9% RSD. The limit of quantitation was 18.07 ng/ml. The HPLC method developed has been applied to determine the pharmacokinetics of spinosin in rat plasma after having taken Suanzaoren decoction.
(4S)-3-{{{6-O-[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxoprop-2-en-1-yl]-beta-D-glucopyranosyl}oxy}methyl}-4-(hydroxymethyl)-5,5-dimethylcyclohex-2-en-1-one
6''-O-trans-cinnamoylgenipin gentiobioside
6''-O-trans-sinapoyl-(genipin gentiobioside)
6'-O-sinapoyljasminoside A
INDOLO[2',3':3,4]PYRIDO[2,1-B]QUINAZOLIN-5(14H)-ONE, 14-METHYL-
Ginsenoside RK1
Ginsenoside Rk3 standard
Prosta-5,13-dien-1-amide,9,11,15-trihydroxy-N-(2-hydroxyethyl)-, (5Z,9a,11a,13E,15S)-
wuchuyuamide I