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作 者:邬国栋[1] 张佳[1] 杨丹[1] 王振旺[1] 李旻辉[1]
机构地区:[1]内蒙古科技大学包头医学院,内蒙古包头014060
出 处:《中国实验方剂学杂志》2012年第6期69-71,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(81060372;81160504);教育部科学技术研究重点项目(211033)
摘 要:目的:利用反相高效液相色谱法对尖叶假龙胆中norswertianolin成分进行含量测定。方法:采用Shim-pack VP-ODS-C18柱(4.6 mm×150 mm,5μm),流动相0.1%磷酸水溶液(A)-乙腈(B)(80:20),流速1.0 mL.min-1,柱温25℃,紫外检测波长254 nm。结果:尖叶假龙胆中norswertianolin在9.6~192 mg.L-1线性关系良好(r=0.999 5);仪器精密度RSD0.67%(n=6);方法重复性RSD 1.88%(n=6);样品在12 h内稳定;平均回收率为99.8%(RSD 1.31%)。结论:本法快速、准确、重复性好,可用于蒙药尖叶假龙胆中norswertianolin成分的含量测定。Objective: To determine norswertianolin of Gentianella acuta by reverse-phase HPLC method. Method: The determination of norswertianolin was performed on a shim-pack VP-ODS-C18 column (4 mm× 150 mm, 5 μm). The mobil phase was 0. 1% phosphoric acid solution (A) -aeetonitrile (B) (80:20 The flow rate was 1.0 mL. min-1. Ultraviolet absorption detector was set at 254 nm and column temperature at ℃ Norswertianolin of G. acuta was separated well. Result: The result indicated that the linear range norswertianolin of G. acutawas between 9.6-192 mg· L -1 (r = 0. 999 5) ; the relative Standard deviations instrument precision was 0. 67% (n = 6) ; the relative standard deviations of method reproducibility was 1.88% =6); the relative standard deviations for stability was 1.68%; the average recovery was 99.8% (n = 6 Conclusion: The results indicated that this developed assay method was rapid, accurate, and reliable and could readily used as a quality control method for the norswertianolin. .6 ). 25 of of (n ). be
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