2013•Unpublished venueRequires access

Determination of paeoniflorin and baicalin in Qizhixiangfu Pills by HPLC

Liu Fen

Open publisher page 1 citations

Abstract

Objective To establish an HPLC method for the determination of paeoniflorin and baicalin in Qizhixiangfu pills. Methods The analysis was carried out on a Capcell PAK C18column( 4. 6 mm × 250 mm,5μm). The mobile phase was acetonitrile( A)- 0. 2% phosphoric acid( B) with gradient elution and the detection wavelength was 230 nm( 0 ~ 5 min,80% B;5 ~ 15 min,80% B→50%);280 nm(15 ~22 min,50% B→20%;22 ~26 min,20%B) and the flow rate was 1 mL·min- 1;The column temperature was 30 ℃. Results The linear ranges of paeoniflorin and baicalin were 0. 40 ~ 4. 76 μg and 0. 66~ 7. 97 μg,respectively. The average recoveries were 98. 42%( RSD = 0. 83%) for paeoniflorin and 99. 10%( RSD =1. 16%) for baicalin. Conclusion The method was simple,stable accurate and repeatability,and can be used for determining paeoniflorin and baicalin in Qizhixiangfu pills.

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Objective To establish an HPLC method for the determination of paeoniflorin and baicalin in Qizhixiangfu pills. Methods The analysis was carried out on a Capcell PAK C18column( 4. 6 mm × 250 mm,5μm). The mobile phase was acetonitrile( A)- 0. 2% phosphoric acid( B) with gradient elution and the detection wavelength was 230 nm( 0 ~ 5 min,80% B;5 ~ 15 min,80% B→50%);280 nm(15 ~22 min,50% B→20%;22 ~26 min,20%B) and the flow rate was 1 mL·min- 1;The column temperature was 30 ℃. Results The linear ranges of paeoniflorin and baicalin were 0. 40 ~ 4. 76 μg and 0. 66~ 7. 97 μg,respectively. The average recoveries were 98. 42%( RSD = 0. 83%) for paeoniflorin and 99. 10%( RSD =1. 16%) for baicalin. Conclusion The method was simple,stable accurate and repeatability,and can be used for determining paeoniflorin and baicalin in Qizhixiangfu pills.

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Available abstract

Objective To establish an HPLC method for the determination of paeoniflorin and baicalin in Qizhixiangfu pills. Methods The analysis was carried out on a Capcell PAK C18column( 4. 6 mm × 250 mm,5μm). The mobile phase was acetonitrile( A)- 0. 2% phosphoric acid( B) with gradient elution and the detection wavelength was 230 nm( 0 ~ 5 min,80% B;5 ~ 15 min,80% B→50%);280 nm(15 ~22 min,50% B→20%;22 ~26 min,20%B) and the flow rate was 1 mL·min- 1;The column temperature was 30 ℃. Results The linear ranges of paeoniflorin and baicalin were 0. 40 ~ 4. 76 μg and 0. 66~ 7. 97 μg,respectively. The average recoveries were 98. 42%( RSD = 0. 83%) for paeoniflorin and 99. 10%( RSD =1. 16%) for baicalin. Conclusion The method was simple,stable accurate and repeatability,and can be used for determining paeoniflorin and baicalin in Qizhixiangfu pills.

Key concepts: Paeoniflorin, Baicalin, Chromatography, Chemistry, Repeatability, Phosphoric acid, High-performance liquid chromatography, Organic chemistry

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