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中国精品科技期刊2020

HPLC法测定姜黄根茎及姜黄素饮料中姜黄素类化合物的含量

孙鹏尧, 李丹丹, 牟德华

孙鹏尧, 李丹丹, 牟德华. HPLC法测定姜黄根茎及姜黄素饮料中姜黄素类化合物的含量[J]. 食品工业科技, 2016, (21): 313-317. DOI: 10.13386/j.issn1002-0306.2016.21.052
引用本文: 孙鹏尧, 李丹丹, 牟德华. HPLC法测定姜黄根茎及姜黄素饮料中姜黄素类化合物的含量[J]. 食品工业科技, 2016, (21): 313-317. DOI: 10.13386/j.issn1002-0306.2016.21.052
SUN Peng-yao, LI Dan-dan, MO De-hua. High-performance liquid chromatography method for quantitative determination of curcuminoids in rhizomes of Curcuma Longa L.and curcumin beverage[J]. Science and Technology of Food Industry, 2016, (21): 313-317. DOI: 10.13386/j.issn1002-0306.2016.21.052
Citation: SUN Peng-yao, LI Dan-dan, MO De-hua. High-performance liquid chromatography method for quantitative determination of curcuminoids in rhizomes of Curcuma Longa L.and curcumin beverage[J]. Science and Technology of Food Industry, 2016, (21): 313-317. DOI: 10.13386/j.issn1002-0306.2016.21.052

HPLC法测定姜黄根茎及姜黄素饮料中姜黄素类化合物的含量

详细信息
    作者简介:

    孙鹏尧(1990-),女,在读硕士研究生,研究方向:食品科学与工程,E-mail:spy_yao@163.com。;

    牟德华(1960-),男,本科,教授,研究方向:农产品加工,E-mail:dh_mou@163.com。;

  • 中图分类号: R284.1;TS207.3

High-performance liquid chromatography method for quantitative determination of curcuminoids in rhizomes of Curcuma Longa L.and curcumin beverage

  • 摘要: 建立高效液相色谱(HPLC)测定姜黄根茎以及姜黄素饮料中姜黄素类化合物的含量。样品用乙醇辅助超声波提取,以DIKMA Platisil ODS(4.6 mm×250 mm,5μm)柱为分析柱,乙腈和水(磷酸调p H为3.0)为流动相进行梯度洗脱,流速:1.0 m L/min,检测波长:425 nm,柱温:30℃。姜黄素、去甲氧基姜黄素、双去甲氧基姜黄素分别在1.00~200.00,0.96~192.00,0.96~192.00 mg/L范围内线性关系良好,相关系数R2>0.999。平均回收率分别为106.87%(RSD=1.24%)、105.28%(RSD=0.48%)、96.86%(RSD=0.26%)。本方法操作简单、快速、重复性好,可用于姜黄根茎及饮料中的姜黄素类化合物的检测。 
    Abstract: A HPLC method was established for the determination of curcuminoids content in rhizomes of Curcuma Longa L. and curcumin beverage.The samples were extracted in ethanol by ultrasonic treatment.The determination by RP-HPLC was carried out using DIKMA Platisil ODS column( 4.6 mm × 250 mm,5 μm) and acetonitrile-water( p H = 3.0 adjusted by phosphoric acid) with gradient elution at a flow rate of 1 m L/min. The UV detection wavelength was 425 nm and the column temperature was set at 30 ℃.The calibration curves were linear in the range of 1.00 ~ 200.00,0.96 ~ 192.00,0.96 ~ 192.00 mg / L( R2> 0.999) for curcumin,demethoxycurcumin and bisdemethoxycurcumin.The average recoveries were 106.87%( RSD = 1.24%),105.28%( RSD = 0.48%) and 96.86%( RSD = 0.26%),respectively. The method was simple,rapid and reproducible,and can be used for the determination of curcuminoids in rhizomes of Curcuma longa L.and curcumin beverage.
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  • 收稿日期:  2016-04-24

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