食品科学 ›› 2017, Vol. 38 ›› Issue (14): 144-150.doi: 10.7506/spkx1002-6630-201714022

• 成分分析 • 上一篇    下一篇

高效毛细管区带电泳法同时检测3 个产地沙棘果粉中的活性物质

杨霞,冯锋,,刘荔贞,陈泽忠   

  1. (1.山西师范大学化学与材料科学学院,山西?临汾 041000;2.山西大同大学化学与环境工程学院,山西?大同 037009)
  • 出版日期:2017-07-25 发布日期:2017-09-06
  • 基金资助:
    国家自然科学基金面上项目(21375083)

Simultaneous Determination of Four Active Compounds in Sea Buckthorn Three Different Geographic RegionsHigh Performance Capillary Zone Electrophoresis

YANG Xia, FENG Feng, LIU Lizhen, CHEN Zezhong   

  1. (1. School of Chemistry and Material Science, Shanxi Normal University, Linfen 041000, China;2. School of Chemical and Environmental Engineering, Shanxi Datong University, Datong 037009, China)
  • Online:2017-07-25 Published:2017-09-06

摘要: 利用高效毛细管区带电泳法,对3?个产地沙棘果粉中的芦丁、山柰酚、异鼠李素、槲皮素4?种活性物质进行同时分离测定。考察不同电泳条件对分离效率的影响,得出最佳电泳条件:缓冲溶液20?mmol/L?Na2B4O7-H3BO3(质量浓度为1.5?mg/mL的β-环糊精),pH?9.55,检测波长370?nm,分离电压25?kV,进样时间5?s。在该条件下,芦丁、山柰酚、异鼠李素、槲皮素4?种活性物质在11?min内得到分离,线性范围分别为0.01~0.51、0.05~0.93、0.02~0.65、0.03~0.81?mg/mL,相关系数在0.997?1~0.999?1之间,检出限分别为5.05×10-5、2.10×10-5、3.75×10-5、1.31×10-5?mg/mL(RSN3),各物质线性关系良好。日内及日间精密度范围为0.08%~4.72%,平均回收率在95.51%~104.66%之间,相对标准偏差不大于3.92%(n3)。在优化条件下,对4?种活性物质标准品的混合物进行测定,并用相同方法对3?个产地沙棘果粉中活性物质的提取液进行检测。结果表明:不同产地沙棘中,4?种被检测化合物的含量各不相同。沙棘中被测4?种化合物总量最高的产自新疆乌鲁木齐,最低的产自甘肃武威,而槲皮素含量以产自山西吕梁的最高,山柰酚和异鼠李素以产自新疆乌鲁木齐最高。本方法快速简便、准确可靠,可用于沙棘果粉中多种活性物质的同时检测。

关键词: 高效毛细管区带电泳, 芦丁, 山柰酚, 异鼠李素, 槲皮素, 沙棘

Abstract: A high performance capillary zone electrophoresis (HPCZE) method was developed for the simultaneous separation and determination of rutin, kaempferol, isorhamnetin and quercetin in sea buckthorn. The effects of different electrophoresis conditions on separation efficiency were investigated. The running buffer was 20 mmol/L Na2B4O7-H3BO3 with 1.5 mg/mL β-cyclodextrin at pH 9.55, the detection wavelength was set at 370 nm, applied voltage 25 kV and injection time 5 s. Under these optimal conditions, rutin, kaempferol, isorhamnetin and quercetin could be fully separated each other within eleven minutes with good linearity in the range of 0.01 to 0.51, 0.05 to 0.93, 0.02 to 0.65, and 0.03 to 0.81 mg/mL, respectively and correlation coefficients between 0.997 1 and 0.999 1. The lowest detection limits were 5.05 × 10-5, 2.10 × 10-5, 3.75 × 10-5, and 1.31 × 10-5 mg/mL, respectively (RSN 3). The average recoveries of spiked samples were in the range 95.51% to 104.66%, with a relative standard deviation (RSD) lower than 3.92% (n 3). Under the optimized conditions, a mixture of four standard compounds and four active compounds in extracts of sea buckthorn three different producing areas were determined. The results showed that the total content of active compounds was the highest in seabuckthorn ürümqi, Xinjiang among three different producing regions, and lowest in the sample Wuwei, Gansu. Furthermore, the sample Lüliang, Shanxi had the highest quercetin content while the contents of kaempferol and isorhamnetin were the highest in the sample ürümqi, Xinjiang. This method is rapid, simple, accurate and reliable for the simultaneous detection of active compounds in sea buckthorn.

Key words: high performance capillary zone electrophoresis (HPCZE), rutin, kaempferol, isorhamnetin, quercetin, sea buckthorn

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