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Content determination and stability study of polydatin and resveratrol in Fuzheng Shengxue Capsules |
ZHANG Ming ZHAO Xianmei YI Rong ZHAO Bingjing ZHANG Yuqin WU Xuechai LIU Linsen YU Botao |
Department of Pharmacy, the General Hospital of Western Theater Command Chinese People’s Liberation Army, Sichuan Province, Chengdu 610083, China
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Abstract Objective To study the content determination method of Fuzheng Shengxue Capsules and to investigate its stability. Methods The contents of polydatin and resveratrol in Fuzheng Shengxue Capsules were determined by high performance liquid chromatograph. Agilent YMC-Triart C18 (250 mm×4.6 mm, 5 μm) was used as the column, and acetonitrile∶water (25∶75) was used as the eluent; elution time was 15 min; the wavelength was 312 nm, the flow rate was 1.1 ml/min, the column temperature was 27℃, and the sample size was 10 μl. The stability of Fuzheng Shengxue Capsules was investigated according to the 2020 edition of Pharmacopoeia of the People’s Republic of China. Results The linear relationships of polydatin and resveratrol were good in the concentration ranges of 16.81-168.81 μg/ml and 4.52-45.23 μg/ml, respectively, and the regression equations were Y=115.2X+101.91 (r=0.999 9), Y=2.75X+28.59 (r=0.999 9) respectively. The average recoveries were 99.23% and 99.84%. The contents of polydatin and resveratrol were 551.0-555.3 μg/g and 136.9-140.4 μg/g, respectively. Fuzheng Shengxue Capsules was stable in two years. Conclusion The content determination method of the preparation is simple, easy, and repeatable; and the validity period is tentatively set to be two years.
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