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作 者:张海军[1,2] 郭丽[1] 王明泽[1] 车野[1] 侯丽[1] 李泽宇[1] 王殿奎[1]
机构地区:[1]黑龙江省农业科学院大庆分院,黑龙江大庆163316 [2]吉林省种子管理总站,吉林长春130062
出 处:《黑龙江农业科学》2014年第4期97-100,共4页Heilongjiang Agricultural Sciences
基 金:教育部新教师基金资助项目(3M2101936604);国家麻类产业技术体系资助项目(NYCYTX-19-S13);黑龙江省农业科技创新工程重点(青年基金)资助项目
摘 要:为更好地开发和利用拟南芥中总黄酮及相关副产品,研究了检测拟南芥中总黄酮含量的方法。结果表明:以芦丁为标准品,建立了检测拟南芥中总黄酮含量的HPLC法。HPLC法色谱条件:C18色谱柱、35℃柱温、256nm检测波长、35%甲醇:65%水(含0.4%磷酸)流动相、10ML进样量及10mL·min-1流速。标准品芦丁在该色谱条件下,峰型良好,在0.05~1.60mg·mL^-1时峰面积与质量浓度间呈良好线性关系,R2=0.9997,平均加样回收率为99.90%,RSD小于3%(n=6),该方法适用于拟南芥中总黄酮的检测。In order to develop and use the flavonoids and related by-products in Arabidopsis thaliana, the deter- mine method was established for total flavonoids content. The results showed that taking rutin as the standard, high-performance liquid chromatographic method was established, mobile phase consisted on methanol (A)/ 0.4% orthophosphoric acid in distrilled water(B)and each solvent was filtered through a 0.45 μm pore size fil- ter and degassed in an ultrasonic bath before. The analysis of rutin was performed at 35℃ (column oven tem- perature)with 10 mL.min1 flow rate, the injection volume was 10 μL,and solvent A:B of rutin was 35%: 65% ,the chromatogram was detected at 256 nm. The peak area had a good linearity with concentration when R2 : 0. 999 7, the recoveries of standard spiling was 99.90 % with RSD less than 3 %. So the method was suit- able for determination of total flavonoids in Arabidopsis thaliana.
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