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Determination of Notoginsenoside R1,Ginsenoside Rg1 and Ginsenoside Rb1 in Compound Huanggen Gran-ules by HPLC / 中国药师
China Pharmacist ; (12): 55-57,58, 2015.
Article in Zh | WPRIM | ID: wpr-671104
Responsible library: WPRO
ABSTRACT

Objective:

To set up a method for simultaneously determining the content of notoginsenoside R1 , ginsenoside Rg1 and ginsenoside Rb1 in compound Huanggen granules ( sugar free) .

Methods:

The HPLC method was carried out on an Agilent ZORBAX SB-C18(250 mm ×4.6 mm,5 μm)column. The mobile phase was acetonitrile-water with gradient elution. The flow rate was 1.0 ml· min-1 . The detection wavelength was at 203 nm. The column temperature was set at 25℃ and the sample size was 10 μl.

Results:

The linearity of notoginsenoside R1, ginsenoside Rg1 and ginsenoside Rb1 was within the range of 1. 6-10. 0 μg·ml-1(r=0. 999 6), 6. 3-39. 3 μg·ml-1(r=0. 999 8) and 6. 3-39. 7 μg·ml-1(r=0. 999 7), respectively. The average recovery was 98. 81%(RSD=1. 20%),99. 93%(RSD=0. 93%) and 99. 22%(RSD=0. 87%)(n=6) , respectively.

Conclusion:

The method is simple, repro-ducible and specific, which can be used in the quality control of the preparation.
Key words
Full text: 1 Index: WPRIM Language: Zh Journal: China Pharmacist Year: 2015 Type: Article
Full text: 1 Index: WPRIM Language: Zh Journal: China Pharmacist Year: 2015 Type: Article