HPLC Analysis of the Composition of Albiflorin, Paeoniflorin, 2,3,5,4'-Tetrahydro Xystilbene-2--Glucoside and Penta--Galloyl--Glucoside in Kundan Capsule
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HPLC Analysis of the Composition of Albiflorin, Paeoniflorin, 2,3,5,4'-Tetrahydro Xystilbene-2--Glucoside and Penta--Galloyl--Glucoside in Kundan Capsule
Chinese Journal of Experimental Traditional Medical FormulaeVol. 18, Issue 7, Pages: 112-116(2012)
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Published:2012
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FENG Bing, Chen Ting, ZHAO Rui-zhi, et al. HPLC Analysis of the Composition of Albiflorin, Paeoniflorin, 2,3,5,4'-Tetrahydro Xystilbene-2--Glucoside and Penta--Galloyl--Glucoside in Kundan Capsule[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(7): 112-116.
DOI:
FENG Bing, Chen Ting, ZHAO Rui-zhi, et al. HPLC Analysis of the Composition of Albiflorin, Paeoniflorin, 2,3,5,4'-Tetrahydro Xystilbene-2--Glucoside and Penta--Galloyl--Glucoside in Kundan Capsule[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(7): 112-116.DOI:
HPLC Analysis of the Composition of Albiflorin, Paeoniflorin, 2,3,5,4'-Tetrahydro Xystilbene-2--Glucoside and Penta--Galloyl--Glucoside in Kundan Capsule
Objective: To establish an HPLC method for the simultaneous determination of albiflorin
paeoniflorin
2
3
5
4'-tetrahydroxystilbene-2-O-β-D-glucoside and penta-O-galloyl-β-D-glucoside in Kundan Capsule. Method: The analysis was carried out on an Agilent TC-C18 column (4.6 nm×250 mm
5 μm). The mobile phase was composed of acetonitrile (A)-methanol (B)-0.1% phosphoric acid aqueous (C) with gradient elution; the detection wavelength was set at 230 nm; the column temperature was at 30 ℃; the flow rate was 1.0 mL·min-1. Result: The calibration curves of albiflorin
paeoniflorin
2
3
5
4'-tetrahydroxystilbene-2-O-β-D-glucoside and penta-O-galloyl-β-D-glucoside were linear in the ranges of 0.02-1.84
0.03-1.65
0.03-3.44
0.01-0.81 mg (r>0.999 9) respectively. The mean recoveries of low
middle and high concentration of the four components were among 99.5%-102.6% (RSD 1.3%-2.1%)
98.5%-103.5% (RSD 0.5%-2.4%)
98.3%-104.2% (RSD 0.5%-2.2%). Conclusion: The method is accurate and sensitive
which can be used in the quality control of Kundan capsule.