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作 者:石冬琴[1,2] 王荣[2] 田薇[1] 谢华[2]
机构地区:[1]浙江农林大学林业与生物技术学院,浙江临安311300 [2]兰州军区兰州总医院临床药理基地,兰州730050
出 处:《解放军医药杂志》2013年第4期65-67,70,共4页Medical & Pharmaceutical Journal of Chinese People’s Liberation Army
基 金:全军"十二五"面上项目(BWS2012JO12)
摘 要:目的建立同时测定白术中白术内酯Ⅱ、Ⅲ的毛细管电泳紫外检测方法,并测定白术样品中白术内酯Ⅱ、Ⅲ的含量。方法采用毛细管区带电泳法,紫外检测波长254 nm,缓冲液硼酸-硼砂体积比为5∶1,分离电压15 kV,柱温20℃,电动进样10 s。结果在最优条件下,白术内酯Ⅱ、Ⅲ完全分离;在线性范围内与峰面积线性关系良好,白术内酯Ⅱ线性方程为Y=2724.5X-54.078(r=0.9958),白术内酯Ⅲ的线性方程为Y=244.65X+201.8(r=0.9995),检测限(S/N=3)为0.2和1.0μg/ml。结论毛细管电泳紫外检测法可用于白术中白术内酯Ⅱ、Ⅲ的含量测定。Objective To establish a capillary electrophoresis with ultraviolet detection (CE-UV) method for simultaneous determination of butenolide Ⅱ and Ⅲ in atractylodes macrocephala, and to detect contents of butenolide Ⅱ and Ⅲ in atractylodes macrocephala koidz. Methods The method was used by capillary zone eleetrophoresis, whose system included a 254 nm ultraviolet wavelength, the 5 : 1 volume ratio of boric acid-borax buffer solution, 15 kV running voltage, 15℃ of column temperature and the 10 s of electrokinetic injection. Results In the optimization condition, butenolide Ⅱ was completely separated from butenolide Ⅲ; and in linear range with peak area had good liner relationship, linear equation of butenolide Ⅱ was Y = 2724.5X - 54. 078 ( r = 0. 9958) , and linear equation of butenolide m was Y =244.65×+201.8 (r =0. 9995) , two detection limits (S/N =3) for butenolide Ⅱ and Ⅲ were 0.2 μg/ml and 0. 1 μg/ml respectively. Conclusion The capillary electrophoresis with ultraviolet detection method may apply to quantitate butenolide Ⅱ and Ⅲ in atractylodes macrocephala koidz.
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