色谱

色谱 ›› 2015, Vol. 33 ›› Issue (10): 1040-1045.DOI: 10.3724/SP.J.1123.2015.06010

• 研究论文 • 上一篇    下一篇

高效液相色谱-四极杆/静电场轨道阱高分辨质谱测定奶粉中的低聚果糖

刘芸1, 丁涛1, 徐素丽2, 吴斌1, 沈崇钰1, 张睿1, 王艳1, 费晓庆1   

  1. 1. 江苏出入境检验检疫局动植物与食品检测中心, 江苏 南京 210001;
    2. 南京医科大学公共卫生学院, 江苏 南京 210001
  • 收稿日期:2015-06-08 出版日期:2015-10-08 发布日期:2012-05-09
  • 通讯作者: 丁涛
  • 基金资助:

    江苏出入境检验检疫局科技计划项目(2015KJ29);国家科技支撑计划课题(2014BAK19B00,2014BAK19B02).

Determination of fructo-oligosaccharides in milk powder by high performance liquid chromatography- quadrupole/electrostatic field orbitrap high resolution mass spectrometry

LIU Yun1, DING Tao1, XU Suli2, WU Bin1, SHEN Chongyu1, ZHANG Rui1, WANG Yan1, FEI Xiaoqing1   

  1. 1. Animal, Plant and Food Inspection Center, Jiangsu Entry-Exit Inspection and Quarantine Bureau, Nanjing 210001, China;
    2. School of Public Health, Nanjing Medical University, Nanjing 210001, China
  • Received:2015-06-08 Online:2015-10-08 Published:2012-05-09

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103

被引次数

3

摘要：

建立了高效液相色谱-四极杆/静电场轨道阱高分辨质谱法测定奶粉中低聚果糖的方法。奶粉样品用水溶解,加乙酸锌沉淀蛋白,经离心、0.22 μm粒径的微孔膜过滤后,采用Carbohydrate色谱柱(100 mm×2.1 mm, 2.6 μm)进行分离,以乙腈与0.1%乙酸水溶液为流动相进行梯度洗脱。质谱采用正离子Target-MS/MS模式,在分离窗口为m/z 4.0和碰撞能为30 eV的条件下,提取响应值较高且在待测样品中无干扰的目标子离子的精确质量数,此方法能够很好地排除样品中的基质干扰。在所建立的色谱-质谱条件下,蔗果三糖(GF2)、蔗果四糖(GF3)和蔗果五糖(GF4)能够得到较好的分离,高分辨质谱提取的质量准确度小于5×10-6(5 ppm),整个分析时间只需10 min。该方法对GF2和GF3的检出限可达100 μg/kg,对GF4的检出限可达55 μg/kg。待测物质采用外标法定量,线性关系良好,相关系数均大于0.998。通过加标验证,在5、10和20 mg/kg 3个加标水平下,奶粉中GF2、GF3和GF4的平均回收率在75.8%~107.3%范围内,相对标准偏差(RSD)在1.6%~8.3%范围内。该方法样品前处理过程简单,只需沉淀蛋白质,通过二级子离子的选择即可排除基质干扰,分析时间短,测定结果准确、可靠,适用于任何奶粉的高通量测定。

关键词: 低聚果糖, 高分辨质谱, 高效液相色谱-四极杆/静电场轨道阱质谱, 奶粉

Abstract:

A method of high performance liquid chromatography-quadrupole/electrostatic field Orbitrap high resolution mass spectrometry (HPLC-Q/Orbitrap MS) was developed to determine fructo-oligosaccharides in milk powder. The milk powder samples were dissolved in deionized water. Subsequently, an aqueous solution of zinc acetate was used to precipitate protein. After centrifugation, the final aqueous solution was filtered by a polytetrafluoroethylene (PTFE) membrane with pore size of 0.22 μm. The analytes were separated on a Carbohydrate column (100 mm×2.1 mm, 2.6 μm) through gradient elution with the combination of acetonitrile and 0.1% formic acid aqueous solution. The target-MS/MS templates were performed at isolation window of m/z 4.0 and collision energy of 30 eV in positive mode to extract the accurate product ion mass of analytes. Under the optimal condition, 1-kestose (GF2), nystose (GF3) and 1-F-β-fructofuranosyl nystose (GF4) were well separated and the accuracy of extracted mass routinely detected was below 5×10-6 (5 ppm). The whole analysis time is only ten minutes. The detection limits for GF2 and GF3 were 100 μg/kg, and the detection limit for GF4 was 55 μg/kg. Good linearities were obtained in their respective linear ranges with correlation coefficients higher than 0.998. The average recoveries at three spiked levels (5, 10 and 20 mg/kg) were in the range of 75.8%-107.3% and the relative standard deviations (RSDs) were in the range of 1.6%-8.3%. The proposed method is simple, sensitive, fast and only in need of precipitation of proteins. The interference of matrix can be eliminated through the selection of product ion. The results were convenient and reliable and thus can be used in the large batch determination of any milk powder.

Key words: fructo-oligosaccharides, high performance liquid chromatography-quadrupole/electrostatic field orbitrap mass spectrometry (HPLC-Q/Orbitrap MS), high resolution mass spectrometry (HRMS), milk powder

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