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机构地区:[1]新疆维吾尔自治区中药民族药研究所,乌鲁木齐830002 [2]新疆大学生命科学与技术学院,乌鲁木齐830046
出 处:《西北药学杂志》2014年第2期127-129,共3页Northwest Pharmaceutical Journal
基 金:国家药品(维药)标准提高项目(编号:535)
摘 要:目的:建立维吾尔药材白花丹中白花丹醌含量测定方法。方法采用反相高效液相色谱法,色谱柱为Waters XTerra RP C18(250 mm ×4.6 mm ,5μm);流动相为甲醇-水溶液;体积流量为1.0 mL ·183; min-1;检测波长为270 nm ;柱温25℃。结果在上述条件下,白花丹醌进样量在0.0286~0.4576μg范围内呈良好的线性关系,加样回收率为100.4%,RSD为1.2%。结论该方法简便、准确、灵敏度高、重复性好,能有效测定白花丹药材中白花丹醌的含量。Objective To establish a method for the determination of plumbagin in Plumbago zeylanica L ..Methods Plumbagin was determined by RP-HPLC on a Waters XTerra RP C18 (250 mm × 4 .6 mm ,5μm) column with methanol-water as the mobile phase . The flow rate was 1 .0 mL · min-1 ,the detection wavelength was 270 nm ,and the column temperature was 25 ℃ .Results The cal-ibration curve of plumbagin was linear within the range of 0 .028 6-0 .457 6 μg and the average recovery was 100 .4% (RSD=1.2% ) .Conclusion The method is simple ,accurate ,sensitive and reproducible .It could be used for the determination of plumba-gin in Plumbago zeylanica L ..
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