J4 ›› 2010, Vol. 48 ›› Issue (05): 865-867.
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LI Qingmin1, WANG Xiaozhong2, ZHOU Hongyu2, WEI Wei2, LI Xuwen2, JIN Yongri2
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Abstract:
To establish an HPLC method for the determination of panasenoside [kaempferol-3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside] in the leaves of Panax ginseng C.A.Meyer, the chromatographic separation was performed on a Zorbax Extend C18 column (250 mm×4.6 mm, 5 μm), with V(methanol) ∶V(acetonitrile) ∶ V(0.1% acetic acid/water)=25 ∶5∶70 as mobile phase at a rate of 1.2 mL/min and 25 ℃. The detection wavelength was set at 268 nm. The results show that the linearity of panasenoside was in a range of 0.5~20 μg(r=0.999 9, n=6), and the average recovery and RSD were 98.5% and 064% respectively (n=6).
Key words: Panax ginseng C.A.Meyer, panasenoside, high performance liquid chromatography (HPLC), determination
CLC Number:
LI Qing-Min, WANG Xiao-Zhong, ZHOU Hong-Yu, WEI Wei, LI Xu-Wen, JIN Yong-Ri. Determination of Panasenoside in |Leaves ofPanax ginseng C.A.Meyer by HPLC[J].J4, 2010, 48(05): 865-867.
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