2014Pharmaceutical Journal of Chinese People's Liberation ArmyRequires access

Simultaneous Determination of Contents of Matrine and Oxymatrine in Sophora tonkinensis Gagnep. by HPLC

Li K

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Abstract

Objective To purificate matrine and oxymatrine in Sophora tonkinensis Gagnep. by ion exchange resin and to establish a method for determining the two components by RP-HPLC. Methods The separation was performed on a C 18 column with a mobile phase composed of acetonitrile-0. 2 % phosphoric acid solution-triethanolamine( 8∶ 92∶ 0. 01; V / V / V) after the sample was extracted and purified with ion exchange resin. The detection wavelength was set at 208 nm. Results Matrine and oxymatrine had a retention time of approximately 5. 5 min and 8. 1 min,respectively. The peak shape was clear and symmetrical,and the analysis time was about 10 min per injection. Good linear correlations were observed when the amount of injection ranged from 1. 0 to 300. 0 μg·ml- 1for matrine( r2= 0. 9996) and 2. 0 to 600. 0 μg·ml- 1for oxymatrine( r2=0. 9998). The average recovery of matrine and oxymatrine was 90. 5% and 91. 6% respectively for the Sophora tonkinensis Gagnep. samples. Conclusion A simple HPLC method has been established and validated for simultaneous analysis of matrine and oxymatrine in Sophora tonkinensis Gagnep.

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Objective To purificate matrine and oxymatrine in Sophora tonkinensis Gagnep. by ion exchange resin and to establish a method for determining the two components by RP-HPLC. Methods The separation was performed on a C 18 column with a mobile phase composed of acetonitrile-0. 2 % phosphoric acid solution-triethanolamine( 8∶ 92∶ 0. 01; V / V / V) after the sample was extracted and purified with ion exchange resin. The detection wavelength was set at 208 nm. Results Matrine and oxymatrine had a retention time of approximately 5. 5 min and 8. 1 min,respectively. The peak shape was clear and symmetrical,and the analysis time was about 10 min per injection. Good linear correlations were observed when the amount of injection ranged from 1. 0 to 300. 0 μg·ml- 1for matrine( r2= 0. 9996) and 2. 0 to 600. 0 μg·ml- 1for oxymatrine( r2=0. 9998). The average recovery of matrine and oxymatrine was 90. 5% and 91. 6% respectively for the Sophora tonkinensis Gagnep. samples. Conclusion A simple HPLC method has been established and validated for simultaneous analysis of matrine and oxymatrine in Sophora tonkinensis Gagnep.

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Available abstract

Objective To purificate matrine and oxymatrine in Sophora tonkinensis Gagnep. by ion exchange resin and to establish a method for determining the two components by RP-HPLC. Methods The separation was performed on a C 18 column with a mobile phase composed of acetonitrile-0. 2 % phosphoric acid solution-triethanolamine( 8∶ 92∶ 0. 01; V / V / V) after the sample was extracted and purified with ion exchange resin. The detection wavelength was set at 208 nm. Results Matrine and oxymatrine had a retention time of approximately 5. 5 min and 8. 1 min,respectively. The peak shape was clear and symmetrical,and the analysis time was about 10 min per injection. Good linear correlations were observed when the amount of injection ranged from 1. 0 to 300. 0 μg·ml- 1for matrine( r2= 0. 9996) and 2. 0 to 600. 0 μg·ml- 1for oxymatrine( r2=0. 9998). The average recovery of matrine and oxymatrine was 90. 5% and 91. 6% respectively for the Sophora tonkinensis Gagnep. samples. Conclusion A simple HPLC method has been established and validated for simultaneous analysis of matrine and oxymatrine in Sophora tonkinensis Gagnep.

Key concepts: Oxymatrine, Matrine, Chromatography, Chemistry, High-performance liquid chromatography, Sophora, Sophora flavescens, Phosphoric acid

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