Application of microwave technique to analysis with HPLC to Rupixiao tablets
Bin Chen
Abstract
Bin Chen
Abstract
Objective:To determine the content of notoginsenoside R1 and ginsenoside Rg1 in Rupixiao tablets by HPLC after applying microwave technique to deal with the sample.Methods:The distilled water as the solvent,to extract notoginsenoside R1 and ginsenoside Rg1 in Rupixiao tablets with the microwave circumfluence,and receiving the sample solution,an Agilent Eclipse XDB-C18 column(4.6 mm×150 mm,5 μm)was adopted with a mixture of acetonitrile and 0.05% phosphoric acid solution(20∶80)as the mobile phase at a flow rate of 0.72 mL·min-1 and the column temperature of 20 ℃ with the detection wavelength at 203 nm,the reference wavelength of 360 nm,and the whole wavelength scanning between 400 nm and 190 nm.Results:With this chromatographic condition,notoginsenoside R1 and ginsenoside Rg1 can be separated completely.The calibration curve was linear in the range of 49.25-492.5 μg·mL-1 for notoginsenoside R1 with r=0.9999 and 53.00-530.0 μg·mL-1 for ginsenoside Rg1 with r=0.9999;The average recoveries(n=6)of notoginsenoside R1 and ginsenoside Rg1 were 98.19% and 101.5%,respectively.Conclusion:The method is simple,accurate,and reproducible,the primary characteristic is fast,saving on the energy and the solvent,and the contamination is fewer,so it can reduce the labor intensity and improve the work circumstance.
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Objective:To determine the content of notoginsenoside R1 and ginsenoside Rg1 in Rupixiao tablets by HPLC after applying microwave technique to deal with the sample.Methods:The distilled water as the solvent,to extract notoginsenoside R1 and ginsenoside Rg1 in Rupixiao tablets with the microwave circumfluence,and receiving the sample solution,an Agilent Eclipse XDB-C18 column(4.6 mm×150 mm,5 μm)was adopted with a mixture of acetonitrile and 0.05% phosphoric acid solution(20∶80)as the mobile phase at a flow rate of 0.72 mL·min-1 and the column temperature of 20 ℃ with the detection wavelength at 203 nm,the reference wavelength of 360 nm,and the whole wavelength scanning between 400 nm and 190 nm.Results:With this chromatographic condition,notoginsenoside R1 and ginsenoside Rg1 can be separated completely.The calibration curve was linear in the range of 49.25-492.5 μg·mL-1 for notoginsenoside R1 with r=0.9999 and 53.00-530.0 μg·mL-1 for ginsenoside Rg1 with r=0.9999;The average recoveries(n=6)of notoginsenoside R1 and ginsenoside Rg1 were 98.19% and 101.5%,respectively.Conclusion:The method is simple,accurate,and reproducible,the primary characteristic is fast,saving on the energy and the solvent,and the contamination is fewer,so it can reduce the labor intensity and improve the work circumstance.
Key concepts: Chemistry, Chromatography, Ginsenoside Rg1, Phosphoric acid, High-performance liquid chromatography, Calibration curve, Ginsenoside, Microwave