2013•Yiyao daobaoRequires access

Determination of Five Saponins From Sanqi Capsule by Ultra Fast Liquid Chromatography

Bilian Chen

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Abstract

Objective To establish an ultra fast liquid chromatography(UFLC) method for determining five saponins in sanqi capsule.Methods Chromatography was performed on an shimadzu C18 column(75 mm×2.0 mm,2.2 μm) at 25 ℃.The gradient elution was acetonitrile-water at a flow rate of 0.3 mL·min-1.The detection wavelength was at 203 nm.Results The linear ranges for notoginsenoside R1,ginsenoside Rg1,ginsenoside Re,ginsenoside Rb1 and ginsenoside Rd were 9.38-351.62 ng(R2=1),52.11-1 954.12 ng(R2=0.999 9),6.85-152.17 ng(R2=0.999 6),44.99-1 687.25 ng(R2=1),9.96-221.27 ng(R2=1),respectively.The average recoveries were 96.6% for notoginsenoside R1(RSD=0.9%),97.1% for ginsenoside Rg1(RSD=1.4%),101.0% for ginsenoside Re(RSD=1.4%),97.9% for ginsenoside Rb1(RSD=2.4%),98.2% for ginsenoside Rd(RSD=1.8%),respectively(n=6).Conclusion The method is simple,rapid and suitable for determination of five saponins in sanqi capsule.

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What this paper is about

Objective To establish an ultra fast liquid chromatography(UFLC) method for determining five saponins in sanqi capsule.Methods Chromatography was performed on an shimadzu C18 column(75 mm×2.0 mm,2.2 μm) at 25 ℃.The gradient elution was acetonitrile-water at a flow rate of 0.3 mL·min-1.The detection wavelength was at 203 nm.Results The linear ranges for notoginsenoside R1,ginsenoside Rg1,ginsenoside Re,ginsenoside Rb1 and ginsenoside Rd were 9.38-351.62 ng(R2=1),52.11-1 954.12 ng(R2=0.999 9),6.85-152.17 ng(R2=0.999 6),44.99-1 687.25 ng(R2=1),9.96-221.27 ng(R2=1),respectively.The average recoveries were 96.6% for notoginsenoside R1(RSD=0.9%),97.1% for ginsenoside Rg1(RSD=1.4%),101.0% for ginsenoside Re(RSD=1.4%),97.9% for ginsenoside Rb1(RSD=2.4%),98.2% for ginsenoside Rd(RSD=1.8%),respectively(n=6).Conclusion The method is simple,rapid and suitable for determination of five saponins in sanqi capsule.

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Available abstract

Objective To establish an ultra fast liquid chromatography(UFLC) method for determining five saponins in sanqi capsule.Methods Chromatography was performed on an shimadzu C18 column(75 mm×2.0 mm,2.2 μm) at 25 ℃.The gradient elution was acetonitrile-water at a flow rate of 0.3 mL·min-1.The detection wavelength was at 203 nm.Results The linear ranges for notoginsenoside R1,ginsenoside Rg1,ginsenoside Re,ginsenoside Rb1 and ginsenoside Rd were 9.38-351.62 ng(R2=1),52.11-1 954.12 ng(R2=0.999 9),6.85-152.17 ng(R2=0.999 6),44.99-1 687.25 ng(R2=1),9.96-221.27 ng(R2=1),respectively.The average recoveries were 96.6% for notoginsenoside R1(RSD=0.9%),97.1% for ginsenoside Rg1(RSD=1.4%),101.0% for ginsenoside Re(RSD=1.4%),97.9% for ginsenoside Rb1(RSD=2.4%),98.2% for ginsenoside Rd(RSD=1.8%),respectively(n=6).Conclusion The method is simple,rapid and suitable for determination of five saponins in sanqi capsule.

Key concepts: Ginsenoside Rg1, Chromatography, Gradient elution, Ginsenoside, Chemistry, Capsule, High-performance liquid chromatography, Ginseng

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