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作 者:向文[1] 李琳[1] 刘吉华[1] 余伯阳[1,2]
机构地区:[1]中国药科大学中药复方研究室 [2]中国药科大学现代中药重点实验室,江苏南京210009
出 处:《中国野生植物资源》2012年第4期28-31,共4页Chinese Wild Plant Resources
基 金:教育部博士学科点专项科研基金(20110096130002);江苏高校优势学科建设工程项目(PAPD)
摘 要:目的:建立快速简便检测青蒿素的超高效液相-紫外(UPLC-UV)法,并对不同产地青蒿中青蒿素的含量进行检测。方法:色谱柱Agilent Eclipse Plus C18(2.1 mm×50 mm,1.8μm),流动相乙腈/水(45/55),流速1.0mL/min,柱温28℃,波长200 nm。结果:该方法对青蒿素的分离度较好,保留时间缩短为1.5 min。并且,整个分析过程可以在2 min内完成。线性范围0.101 17~10.117μg,进样量与峰面积线性相关,A=109.4C+6.7026,R2=0.9 993(n=9),加样回收率为99.3%(RSD=2.6%,n=6)。结论:UPLC-UV法分析时间短、样品前处理简单、精密度、稳定性、加样回收率等符合分析检测要求,对于青蒿中青蒿素的含量能进行快速准确的分析。Objective: To establish a simple, rapid and accurate method for the determination of artemisinin in Artemisia annua from different locations by Ultra Performance Liquid Chromatography - Ultraviolet (UPLC -UV). The separation was performed on Agilent Eclipse Plus Ci8 column (2. 1 mm×50 mm, 1.8 μm). Methods:The mobile phase consisted of acetonitrile / water ( 45 / 55 ) at the flow rate of 1.0 mL/min. The detection wavelength was set at 200 nm and column temperature was 28 ℃. Results: Comparing with the other methods, separation of artemisinin is better and retention time ( 1.5 minutes ) is shorter. Furthermore, the determination by UPLC would completed in 2 minutes. The linear rang of ar- temisinin was 0.10 117-10. 117 μg, A = 109.4 C + 6.7 026, R2 = 0.9 993 (n=9) by UPLC Method. The average recovery was 99.3% ( RSD = 2.6 % ,n =6). Conclusion: UPLC - UV is a simple, rapid, accurate and stable method for the determination of artemisinin in Artemisia annua.
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