张变, 常佳丽, 余琼芳, 陈卫东. 高效液相色谱法测定A549细胞内新藤黄酸含量方法的建立[J]. 蚌埠医科大学学报, 2017, 42(11): 1439-1442. DOI: 10.13898/j.cnki.issn.1000-2200.2017.11.003
    引用本文: 张变, 常佳丽, 余琼芳, 陈卫东. 高效液相色谱法测定A549细胞内新藤黄酸含量方法的建立[J]. 蚌埠医科大学学报, 2017, 42(11): 1439-1442. DOI: 10.13898/j.cnki.issn.1000-2200.2017.11.003
    ZHANG Bian, CHANG Jia-li, YU Qiong-fang, CHEN Wei-dong. Establishment of HPLC method measuring the gambogenic acid in A459 cells[J]. Journal of Bengbu Medical University, 2017, 42(11): 1439-1442. DOI: 10.13898/j.cnki.issn.1000-2200.2017.11.003
    Citation: ZHANG Bian, CHANG Jia-li, YU Qiong-fang, CHEN Wei-dong. Establishment of HPLC method measuring the gambogenic acid in A459 cells[J]. Journal of Bengbu Medical University, 2017, 42(11): 1439-1442. DOI: 10.13898/j.cnki.issn.1000-2200.2017.11.003

    高效液相色谱法测定A549细胞内新藤黄酸含量方法的建立

    Establishment of HPLC method measuring the gambogenic acid in A459 cells

    • 摘要: 目的:建立高效液相色谱法测定肿瘤细胞内新藤黄酸含量的方法。方法:应用高效液相色谱法测定细胞内新藤黄酸的含量。色谱柱为COSMOSIL C18柱,流动相为甲醇-0.1%磷酸水溶液(90:10 V:V),流速为1.0 mL/min,柱温为30℃,检测波长为360 nm,进样量为20 μL。结果:在0.05~30 μg/mL内新藤黄酸样品溶液质量浓度与峰面积比线性关系良好(P<0.01)。精密度、稳定性的RSD<10%,准确度均在实测值的10%以内,特异性良好,同一浓度的新藤黄酸孵育相同时间样品测定结果重复性好。结论:该方法简单方便,准确度高,适用于定量测定肿瘤细胞内新藤黄酸的含量。

       

      Abstract: Objective:To establish an HPLC method for the content determination of gambogenic acid in tumor cells.Methods:The gambogenic acid in cells was measured using HPLC.The chromatographic column was COSMOSIL C18 column,the mobile phase was 90% methanol:0.1% aqueous phosphoric acid(90:10,V:V),the flow rate was 1.0 mL/min,the column temperature was 30℃,the detection wavelength was 360 nm,and the injection volume was 20 μL.Results:The linear relationship between the 0.05 to 30 μg/mL of gambogenic acid and peak area was good(P<0.01).The precision and stability of RSD was lower than 10%.The accuracy of the measure value was less than 10%,the specificity was good.The repeatability of sample determination at the same time and concentration of gambogenic acid was good.Conclusions:The method is simple,convenient and accurate,which is suit for the determination of gambogenic acid in tumor cells.

       

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