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[Determination of puerarin in plasma by high performance liquid chromatography].

Jin Xl, Xiaoyun Zhu, Wang Wj, Cheng Gf

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Abstract

A high performance liquid chromatography with fluorescence detection has been developed for determination of puerarin in plasma using a column of YWG-C16 (10 microns) and mobile phase of methanol (450 ml)-water (522.5 ml)-0.1 mol.L-1 phosphate buffer (pH 7.4, 27.5 ml). The preparation of samples was as follows: Transfer 0.1 ml of plasma into a 1 ml stoppered glass tube containing daidzein as internal standard, add 0.4 ml of absolute alcohol to deproteinize the plasma, vortex for 2 min, centrifuge for 15 min at 2800 r.min-1 and inject 20 microliters of the supernatant into the HPLC column. Linear calibration curve was obtained by plotting concentration vs peak height ratio over the range 0.03-12.00 micrograms.ml-1 with a correlation coefficient of 0.999. The average recovery of puerarin was 95.3% and the average RSD was 4.8%. The minimum detectable quantity of puerarin was 0.04 ng, equivalent to 10 ng.ml-1 plasma. This method is highly sensitive, specific, simple and rapid. The plasma concentration-time course of puerarin given i.v. 2.25 mg.kg-1 to two dogs determined by this method was found to fit a two-compartments open model with T1/2 alpha of 6.0 min and T1/2 beta of 57.4 min.

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What this paper is about

A high performance liquid chromatography with fluorescence detection has been developed for determination of puerarin in plasma using a column of YWG-C16 (10 microns) and mobile phase of methanol (450 ml)-water (522.5 ml)-0.1 mol.L-1 phosphate buffer (pH 7.4, 27.5 ml). The preparation of samples was as follows: Transfer 0.1 ml of plasma into a 1 ml stoppered glass tube containing daidzein as internal standard, add 0.4 ml of absolute alcohol to deproteinize the plasma, vortex for 2 min, centrifuge for 15 min at 2800 r.min-1 and inject 20 microliters of the supernatant into the HPLC column. Linear calibration curve was obtained by plotting concentration vs peak height ratio over the range 0.03-12.00 micrograms.ml-1 with a correlation coefficient of 0.999. The average recovery of puerarin was 95.3% and the average RSD was 4.8%. The minimum detectable quantity of puerarin was 0.04 ng, equivalent to 10 ng.ml-1 plasma. This method is highly sensitive, specific, simple and rapid. The plasma concentration-time course of puerarin given i.v. 2.25 mg.kg-1 to two dogs determined by this method was found to fit a two-compartments open model with T1/2 alpha of 6.0 min and T1/2 beta of 57.4 min.

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Available abstract

A high performance liquid chromatography with fluorescence detection has been developed for determination of puerarin in plasma using a column of YWG-C16 (10 microns) and mobile phase of methanol (450 ml)-water (522.5 ml)-0.1 mol.L-1 phosphate buffer (pH 7.4, 27.5 ml). The preparation of samples was as follows: Transfer 0.1 ml of plasma into a 1 ml stoppered glass tube containing daidzein as internal standard, add 0.4 ml of absolute alcohol to deproteinize the plasma, vortex for 2 min, centrifuge for 15 min at 2800 r.min-1 and inject 20 microliters of the supernatant into the HPLC column. Linear calibration curve was obtained by plotting concentration vs peak height ratio over the range 0.03-12.00 micrograms.ml-1 with a correlation coefficient of 0.999. The average recovery of puerarin was 95.3% and the average RSD was 4.8%. The minimum detectable quantity of puerarin was 0.04 ng, equivalent to 10 ng.ml-1 plasma. This method is highly sensitive, specific, simple and rapid. The plasma concentration-time course of puerarin given i.v. 2.25 mg.kg-1 to two dogs determined by this method was found to fit a two-compartments open model with T1/2 alpha of 6.0 min and T1/2 beta of 57.4 min.

Key concepts: Puerarin, Chromatography, Chemistry, High-performance liquid chromatography, Calibration curve, Standard curve, Coefficient of variation, Plasma

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