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作 者:肖晓茹 冯军[2,3,4] 程昊[1,2,3] 黄文艺[1,2,3] 李彦青[1,2,3] 赵彦勇 李利军[1,2,3] XIAO Xiao-ru FENG Jun CHENG Hao HUANG Wen-yi LI Yan-qing ZHAO Yan-yong LI Li-jun(College of Biological and Chemical Engineering, Guangxi University of Science and Technology, Guangxi University of Science and Technology, Liuzhou 545006, China Guangxi Key Laboratory of Green Processing of Sugar Resources, Guangxi University of Science and Technology, Liuzhou 545006, China Key Laboratory for Processing of Sugar Reourees of Guangxi Higher Education Institutes, Guangxi University of Science and Technology, Liuzhou 545006, China Medical College of Pharmacy, Guangxi University of Science and Technology, Liuzhou 545005, China)
机构地区:[1]广西科技大学生物与化学工程学院,广西柳州545006 [2]广西科技大学广西糖资源绿色加工重点实验室,广西柳州545006 [3]广西科技大学广西高校糖资源加工重点实验室,广西柳州545006 [4]广西科技大学医学院药学系,广西柳州545005
出 处:《分析测试学报》2017年第3期388-392,共5页Journal of Instrumental Analysis
基 金:广西自然科学基金项目资助(2014GXNSFAA118402);广西高等学校高水平创新团队及卓越学者计划资助
摘 要:建立了加压毛细管电色谱法(p CEC)检测大黄酸、大黄素、芦荟大黄素、大黄酚、大黄素甲醚5种蒽醌类成分的方法,并对虎杖根中蒽醌类的成分进行分析。该方法采用EP-100-20/45-3-C_(18)毛细管色谱柱(总长度45 cm,有效长度20 cm,直径为100μm,ODS填料3μm)进行分离,流动相为20 mmol/L Na H2PO4(pH 4.7)-乙腈(15∶85),流动相的总流速为0.04 m L/min,分离电压为+5 k V,紫外检测波长为254 nm。结果表明,5种蒽醌类成分的检出限(S/N=3)为0.60~2.54μg/m L,在3.57~162.68μg/m L范围内线性关系良好,相关系数均不小于0.998 2。将所建立的方法用于虎杖中蒽醌类成分的分析,取得良好的实验结果,在低、中、高3个加标浓度下的回收率为91.1%~101.2%,相对标准偏差(RSD)为0.03%~3.6%。A pressurized capillary electrochromatographic(pCEC) method was developed for the determination of the main anthraquinones,including rhein,emodin,aloe emodin,chrysophanol and physcion in root of Polygonum cuspidatum.The separation was performed on a reversed phase EP-100-20/45-3-C18 column(total length of 45 cm,effective length of 20 cm,diameter of 100 μm,ODS packing inside for 3 μm).The mobile phase was composed of 20 mmol/L NaH2PO4(pH 4.7)-acetonitrile(15∶85) at a flow rate of 0.04 mL/min.Under the optimum conditions including running voltage of +5 kV,UV detection wavelength of 254 nm,the limits of detection(S/N=3)were in the range of 0.60-2.54 μg/mL for rhein,aloe emodin,emodin,chrysophanol and physcion,respectively,and the linear detection ranges were 3.57-162.68 μg/mL with correlation coefficients not less than 0.998 2.The established method was used in the analysis of anthraquinones in polygonum cuspidatum with good results.The recoveries at three spiked levels ranged from 91.1% to 101.2%,with relative standard deviations(RSD) of 0.03%-3.6%.
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