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中国精品科技期刊2020
HPLC-MS法测定食品中生物碱的研究[J]. 食品工业科技, 2012, (16): 73-75. DOI: 10.13386/j.issn1002-0306.2012.16.028
引用本文: HPLC-MS法测定食品中生物碱的研究[J]. 食品工业科技, 2012, (16): 73-75. DOI: 10.13386/j.issn1002-0306.2012.16.028
Study on determination of alkaloids in food by high performance liquid chromatography mass spectrometry[J]. Science and Technology of Food Industry, 2012, (16): 73-75. DOI: 10.13386/j.issn1002-0306.2012.16.028
Citation: Study on determination of alkaloids in food by high performance liquid chromatography mass spectrometry[J]. Science and Technology of Food Industry, 2012, (16): 73-75. DOI: 10.13386/j.issn1002-0306.2012.16.028

HPLC-MS法测定食品中生物碱的研究

Study on determination of alkaloids in food by high performance liquid chromatography mass spectrometry

  • 摘要: 建立了一种高效液相色谱电喷雾质谱(HPLC-ESI-MS)法同时测定食品中六种生物碱的方法。采用ZORBAX SB-C8(2.1mm×150mm,3.5μm)色谱柱,乙腈(A)和pH5的4mmol/L乙酸铵溶液(B)为流动相,梯度洗脱使所有分析物均达到基线分离。采用ESI+一级质谱扫描模式得到甜菜碱、胆碱、苦参碱、阿托品、马钱子碱和乌头碱的定性离子,分别为m/z118.2、104.2、249.5、290.3、395.4和646.4,结合质谱保留时间检测六种生物碱。结果表明,采用1.0mg/mL混合标准溶液,准确性好,RSD<0.59%。该方法应用于检测实际样品荒漠肉苁蓉、山药、宁夏枸杞,添加回收率分别为81.7%112.9%、80.8%117.5%、96.9%119.3%,说明建立的方法可以快速准确的检测实际样品中的生物碱成分。 

     

    Abstract: An high-performance liquid chromatographic electrospray ionization mass spectrometry (HPLC-ESI-MS) method was developed for the identification of 6 alkaloids in food. A mixture of acetonitrile (A) and pH5 4mmol/L ammonium acetate aqueous solution (B) were used as the mobile phase for the chro-matographic separation on ZORBAX SB-C8 (2.1mm×150mm, 3.5μm) column in the gradient elution mode. Under positive electrospray ionization mode, the protonated molecularM+H+ions for betaine (m/z 118.2) , choline (m/z 104.2) , matrine (m/z 249.5) , atropine (m/z 290.3) , brucine (m/z 395.4) and aconitine (m/z 646.4) and retain time were obtained as qualitative analysis. The experiment results indicated that RSD of the precision was less than 0.59% for adding 1.0mg/mL of spike standard. This method was used in the actual sample Herba Cistanche, Rhizoma Dioscoreae, Lycium bar-barum L testing and the average extraction recoveries were in the range of 81.7%112.9%, 80.8%117.5%, 96.9%119.3%. A simple, rapid and accurate identification of 6 alkaloids was successfully achieved using the method.

     

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