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快速高效液相色谱法测定烟草中的多酚

Determination of polyphenols in tobacco samples by ultra-fast HPLC

  • 摘要: 为实现烟草中多酚类物质的高通量准确测定,设计了具有固相萃取功能的样品萃取瓶,并将其作为前处理装置,建立了测定烟草中5-O-咖啡酰奎宁酸、绿原酸、4-O-咖啡酰奎尼酸、咖啡酸、莨菪葶、芦丁、山柰酚-3-O-芸香糖苷和槲皮素等8种多酚的快速高效液相色谱方法。结果表明:①设计的样品萃取瓶可以集样品提取、固相萃取净化、过滤和转移为一体,大大提高了样品前处理制备速度;②以0.1%(体积比)甲酸水溶液和乙腈为流动相,C18色谱柱(50 mm×4.6 mm,1.8 μm)为色谱分离柱,8种多酚类物质在0.05~350 μg/mL范围内具有较好的线性关系(r>0.999);检出限为0.35~1.03 μg/g;不同添加水平下的平均回收率为91.1%~101.5%,日内和日间RSD均小于5%。③5个烟草样品中8种多酚的含量在0.43~15.22 mg/g之间,与行业标准方法检测结果基本一致。该方法前处理简单快捷,灵敏度高,重复性较好,可以满足烟草样品中多酚类物质的高通量检测要求。

     

    Abstract: In order to achieve high-throughput and accurate determination of polyphenols in tobacco, a sample extraction vial with a solid-phase extraction(SPE)function was designed and used as a pre-treatment device to establish an ultra-fast high performance liquid chromatography (HPLC) method for determining eight polyphenols, including neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, caffeic acid, scopoletin, rutin, kaempferol-3-O-rutinoside and quercetin. The results showed that:1)The sample extraction vial integrated the functions of sample extraction, SPE purification, filtration and transfer, which significantly improved the preparation speed. 2)The prepared sample was separated on a C18 column(50 mm×4.6 mm, 1.8 μm)by using 0.1% formic acid aqueous solution and acetonitrile as the mobile phase. The eight analytes were separated smoothly with good linearity in the range of 0.05-350 μg/mL and the correlation coefficients larger than 0.999. The limits of detection(LODs)were 0.35-1.03 μg/g. The mean recoveries ranged from 91.1% to 101.5%, and the intra-day and inter-day precision was less than 5%. 3)The contents of the eight polyphenols in five tobacco samples were between 0.43 and 15.22 mg/g, which were consistent with the results obtained using the tobacco industry standard method. This new method is simple, rapid, sensitive, reproducible, and suitable for the high-throughput detection of polyphenols in tobacco samples.

     

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