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机构地区:[1]江西省药物研究所,南昌330029
出 处:《江西中医药大学学报》2016年第1期68-70,共3页Journal of Jiangxi University of Chinese Medicine
摘 要:目的:建立大黄总蒽醌胶囊中5种蒽醌苷元及5种游离蒽醌的高效液相色谱法含量测定方法。方法:采用Alltima C18柱,(4.6mm×250mm,5μm)色谱柱,流动相:甲醇-0.1%磷酸溶液(85∶15),检测波长:440nm。结果:芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚等5种游离蒽醌线性关系良好,水解后5种蒽醌苷元及总游离蒽醌回收率为100.54%和101.58%,RSD分别为1.4%和1.1%。结论:本方法操作快速、准确,可作为大黄总蒽醌胶囊中蒽醌的质量控制方法。Objective: To establish an HPLC method for the determination of 5 hydrolysis anthraquinone glycosides and 5 free anthraquinones in rhubarb total anthraquinones capsule by HPLC. Method: Alltima C18column( 4. 6mm × 200 mm,5μm) was used in HPLC with mobile phase methanol-0. 1% phosphoric acid solutions( 85 ∶ 15),the detection wavelength at 440 nm. Results: the calibration curve was good for the aloe-emodin,rhein,emodin,chrysophanol,physcione content. The average recovery ratio of 5 hydrolysis anthraquinone glycosides and 5 free anthraquinones were 100. 54% and 101. 58%. The relative standard deviation were 1. 4% and 1. 1%. Conclusion: This method is rapid and accurate. It can be used for quality control on anthraquinones of Rhubarb total anthraquinones capsule.
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