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作 者:吴文玲[1] 陈佳佳[1] 刘守金[1] 俞年军[1] 方成武[1] 张庆庆[1]
机构地区:[1]安徽中医学院药学院安徽现代中药重点实验室,安徽合肥230031
出 处:《中国中药杂志》2009年第9期1121-1123,共3页China Journal of Chinese Materia Medica
基 金:安徽省教育厅自然基金重点课题(2006KJ096A);美国许氏基金会项目
摘 要:目的:建立了用HPLC法对前胡药材中白花前胡甲素、乙素和E素同时定量的方法。方法:高效液相色谱法,色谱柱Agilent TC-C18(4.6 mm×250 mm,5μm);流动相甲醇-水(75∶25);检测波长321 nm;柱温30℃;流速0.8 mL.min^-1;进样量20μL。结果:白花前胡甲素、乙素和E素的浓度与峰面积,分别在3.20-28.80μg(r=0.9999),1.60~14.40μg(r=0.9995),1.64~14.76μg(r=0.9994)呈良好的线性关系;平均加样回收率分别为98.92%,99.66%,99.72%,RSD分别为1.6%,1.5%,1.4%。结论:不同产地前胡所含的香豆素成分含量存在一定的差异,安徽宁国和祈门的前胡中白花前胡甲素含量高于药典的规定,且这3种香豆素含量明显高于其他2个产区。该法适合同时测定前胡样品中3种香豆素成分的含量,分离度好,快速,简便,重现性好。Objective: To develop a reserved-phase HPLC method for the determination of praeruptorin A, praeruptorin B, qianhucoumarin E in roots of Peucedanum praeruptorum. Method: Agilent TC-C18 column (4. 6 mm×250 mm, 5 μm) was used at 30 ℃ with the mobile phase of methanol-water (75:25 ). The flow rate was set at 0. 8 mL .min^-1. The detection wavelength was 321 nm. Result: The linear response ranged from 3.20-28. 80 μg for ± praeruptorin A ( r = 0. 999 9, n = 5), 1.60-14. 40 g for praerup- torin B (r =0. 999 5, n =5) and 1.64-14. 76 g for qianhucoumarin E (r =0. 999 4, n =5), respectively. Recoveries were 98. 92% with RSD 1.6% for praeruptorin A, 99. 66% with RSD 1.5% for praeruptorin B and 99.72% with RSD 1.4% for qianhueoumarin E. Conclusion : The method is quick, simple and repeatable for determination of three coumarin constituents in root of P. praeruptorum.
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