超高效液相色谱质谱联用法测定保健食品中褪黑素的不确定度评定

Uncertainty evaluation for the determination of melatonin in dietary supplements by ultra high performance liquid chromatography tandem mass spectrometry

  • 摘要:
    目的 评定超高效液相色谱质谱联用(液质联用)技术测定保健食品中褪黑素的方法的不确定度来源,探讨各分量的影响,以提高测定方法的准确性。
    方法 分析液质联用测定保健食品中褪黑素过程中不确定度的来源,主要包括不均匀性、天平称量、样品测试的重复性、溶液配制、标准曲线拟合及仪器允许误差等方面,并对这些不确定度进行合成。
    结果 对不确定度贡献较大的因素主要是样品制备和曲线拟合的过程,规格为500 mg的褪黑素片剂在含量测定时的扩展不确定度为15.624 ng·mL-1(置信区间P=95%,k=2)。
    结论 液质联用法测定褪黑素含量的不确定度主要由标准曲线拟合、溶液配制和样本前处理引入,应严格规范实验流程,简化步骤,提高实验测定结果的准确性。

     

    Abstract:
    Objective To evaluate the sources of uncertainty in determination of melatonin in dietary supplements using ultra-high performance liquid chromatography-mass spectrometry (LC-MS) technology, to explore the effects of each component, and to improve the accuracy of the determination method.
    Methods The sources of uncertainty in establishment of a method for determining melatonin in dietary supplements using liquid chromatography-mass spectrometry were analyzed. These sources mainly included non-uniformity, balance weighing, repeatability of sample testing, solution preparation, standard curve fitting, and instrument tolerance error, etc, and the synthesis of these uncertainties was also discussed.
    Results The factors that contributed significantly to uncertainty were mainly the process of sample preparation and curve fitting. The expanded uncertainty for 500 mg melatonin tablets in content determination was 15.624 ng·mL-1 (P=95%, k=2).
    Conclusion The uncertainty of measuring melatonin content by liquid chromatography-mass spectrometry is mainly introduced in the context of standard curve fitting, solution preparation, and sample pretreatment. The experimental process should be strictly standardized, steps should be simplified, and the accuracy of experimental measurement results should be improved.

     

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