食品科学

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液相色谱-质谱法和高效液相色谱法定性定量测定籽瓜中的L-瓜氨酸

席冬华1,李维霞1,高 晶2,阿塔吾拉•铁木尔3,李 玲1,吴 斌3,*   

  1. 1.新疆大学化学化工学院,新疆 乌鲁木齐 830046;2.新疆大学理化测试中心,新疆 乌鲁木齐 830046;
    3.新疆农业科学院农产品贮藏加工研究所,新疆 乌鲁木齐 830091
  • 出版日期:2014-12-25 发布日期:2014-12-29
  • 通讯作者: 吴 斌
  • 基金资助:

    新疆维吾尔自治区级公益性科研院所基本科研业务费专项(KY2013045;KY2014038)

Identification and Quantitation of L-Citrulline in Seeding Watermelon by Liquid Chromatography- Tandem Mass Spectrometry and Rapid High Performance Liquid Chromatography

XI Dong-hua1, LI Wei-xia1, GAO Jing2, ATAWULLA•Tiemur3, LI Ling1, WU Bin3,*   

  1. 1. College of Chemistry and Chemical Engineering, Xinjiang University, Ürümqi 830046, China;
    2. Center for Physics and Chemistry Analysis, Xinjiang University, Ürümqi 830046, China;
    3. Institute of Agro-Products Storage and Processing, Xinjiang Academy of Agricultural Sciences, Ürümqi 830091, China
  • Online:2014-12-25 Published:2014-12-29
  • Contact: WU Bin

摘要:

建立一种非衍生化样品前处理的液相色谱-质谱和高效液相色谱方法,对籽瓜中的L-瓜氨酸进行定性、定量分析,通过单因素试验和正交试验优化提取条件。液相色谱-质谱条件:Acuity C18(50 mm×2.1 mm,1.7 μm)色谱柱;流动相:10%乙腈和90%甲醇溶液(甲醇-水体积比1∶1);流速0.2 mL/min;柱温:40 ℃;进
样量10 μL。在电喷雾离子源正模式、多反应监测扫描方式下分析,L-瓜氨酸的定性离子对为m/z 176.09/158.9,m/z 176.09/112.9,定量离子对为m/z 176.09/158.9。高效液相色谱条件:Platisil ODS C18 (250 mm×4.6 mm,5 μm)色谱柱,以0.03 mmol/L磷酸为流动相,流速0.7 mL/min,柱温30 ℃,检测波长202 nm。结果表明:L-瓜氨酸标准品在0.5~100 μg/mL范围内线性关系良好(R2=0.999 9),平均回收率在95.12%~104.21%之间,相对标准偏差为1.86%~4.75%(n=3)。籽瓜中含有丰富的L-瓜氨酸,本方法测得籽瓜样品中L-瓜氨酸的平均含量为0.656~2.563 mg/g。

关键词: 籽瓜, L-瓜氨酸, 非衍生化, 液相色谱-质谱法, 高效液相色谱法

Abstract:

In this work, certification of L-citrulline in seeding watermelon extract by liquid chromatography-tandem
mass spectrometry (LC-MS-MS), and rapid determination of underivatized L-citrulline in seeding watermelon by high
performance liquid chromatography (HPLC) were established. Single factor and orthogonal experiments were used to
optimize the extraction conditions. LC-MS-MS analysis was carried out using Acuity C18 (50 mm × 2.1 mm, 1.7 μm) as the
stationary phase and a mixture of 10% acetonitrile and 90% methanol-water (50:50, V/V) as the mobile phase at a flow rate
of 0.2 mL/min with a column temperature of 40 ℃. The electrospray ionization (ESI) source was applied and operated in
a positive ion mode. The diagnostic product ions of L-citrulline were m/z 176.09/158.9 and m/z 176.09/112.9. Moreover,
the ion pair of m/z 176.09/158.9 was used for quantification. HPLC separation was performed suing Platisil ODS C18
(250 mm × 4.6 mm, 5 μm) as the stationary phase and 0.03 mmol/L phosphoric acid as the mobile phase at a flow rate of
0.7 mL/min with a column temperature of 30 ℃, and the detection wavelength was set at 202 nm. The results showed that
a good linear relationship was obtained for L-citrulline in the concentration range of 0.5–100 μg/mL with R2 = 0.999 9.
Average recoveries varied from 95.12% to 104.21% with RSD of 1.86%–4.75% (n = 3). The content of L-citrulline in
seeding watermelon was determined to be 0.656–2.563 mg/g.

Key words: seeding watermelon, L-citrulline, non-derivatization, liquid chromatography coupled to tandem mass spectrometry (LC-MS-MS), high performance liquid chromatography (HPLC)

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