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作 者:张丽娜[1] 肖艺[1] 魏双[1] 明有山 吴秀红[1]
机构地区:[1]辽宁科技大学化学工程学院,辽宁鞍山114051
出 处:《辽宁科技大学学报》2015年第5期355-357,共3页Journal of University of Science and Technology Liaoning
基 金:辽宁科技大学大学生创新创业训练计划项目(201510146050)
摘 要:利用反相-高效液相色谱法(RP-HPLC)建立了快速测定人参皂苷Re和Rh2含量方法。色谱柱为Agilent Extend C18(4.6×150 mm,5μm),流动相为乙腈-0.05%乙酸梯度洗脱溶液,流速1.00 m L/min,波长203 nm,柱温30.0℃。人参皂苷Re和Rh2的线性范围分别为0.17~456.6 mg/L和6.00~449.4 mg/L;人参皂苷Re和人参皂苷Rh2的平均加标回收率分别为99.60%和99.78%。本方法快速、灵敏、准确性好,可用于测定人参和西洋参提取物中人参皂苷Re和人参皂苷Rh2的含量。A method for determination ginsedoside Re and Rh2 has been developed by RP-HPLC. Agilent Extend C18(4.6 mm× 150 mm, 5 μm)served as the stationary phase. The mobile phase consists of actonitrile and 0.05% acetic acid in term of gradient operation. Detection wavelength was 203 nrn, column temperature 30.0 ℃, flow rate, 1.00 mL/min. The analytical linearity range of ginsenoside Re and Rh2 were 0.17~456.6 mglL and 6.00-449.4 mg/L, respectively .The recoveries of ginsenoside Re and Rh2 were 99.60% and 99.78%, respectively. The method developed is rapid, simple and accurate and can be used to determine the ginsenoside Re and Rh2 of Radix et Rhizoma Ginseng and Panax quinquefolium L extraction product.
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