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作 者:陈英
出 处:《海峡药学》2013年第9期84-86,共3页Strait Pharmaceutical Journal
摘 要:目的建立HPLC法测定绞股蓝总甙片中人参皂苷Rbl的含量。方法色谱柱为AgilentExtend—c18(5μm,4.6mmx250mm),流动相为乙腈-水线性梯度洗脱,流速为I.OmL·Min-1。紫外检测波长为203nm,柱温35℃。结果人参皂苷Riol在0.422—2.5321μg.mL-1。范围内线性良好,平均回收率为97.56%,RSD为1.05%(n=6)。结论该方法结果准确、重复性好,可用于绞股蓝总甙片的质量控制。OBJECTIVE To estabilish an HPLC method for quantitative determining of ginsenoside Rbl in Gypenoside Tablets. METHODS Separation was accomplished on the Agilent Extend-Cls column(51m,4. 6mm x 250mm) ,with aeetonitrile-water as mobile phase by gradient elution. The flow rate was 1.0mL min -1 and the de-tection wavelength was set at 203nm. The column temperature was at 35~C. RESULTS The method offered good linearity 0. 422 ~2. 5321xg. mL-1 for ginsenoside RbI ( r =0. 9997). The average recovery rate was 97.56% ( RSD = 1.05% ,n = 6). CONCLUSION The method was accurate and repeatable, and can be used for quality control of Gypenoside tablets.
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