Food Engineering Department, Hacettepe University, Beytepe, Ankara, Turkey.
Anal Bioanal Chem. 2012 Jul;403(10):2915-22. doi: 10.1007/s00216-012-5779-z. Epub 2012 Feb 14.
This study describes a rapid and sensitive analytical method for the determination of amino acids in foods and drinks. The method entailed dilution or extraction of amino acids from foods using the mixture of acetonitrile and 0.1% aqueous formic acid (50:50, v/v). Chromatographic separation of underivatized amino acids was performed using a hydrophilic interaction liquid chromatography within a runtime of 6 min. Both hydrophobicity and charge of the side chain played important roles on the elution order of amino acids under the chromatographic conditions. High-resolution mass spectrometry allowed qualitative and quantitative detection of amino acids in complex food matrices. Its response was found linear over a concentration range of 0.25-10 μg/ml. The method could be successfully applied to various foods and drinks to profile individual amino acids. Mean percentage recoveries of amino acids from different matrices were 88.5% or higher with residual standard deviation of less than 5.0%.
本研究描述了一种快速灵敏的分析方法,用于测定食品和饮料中的氨基酸。该方法采用乙腈和 0.1%甲酸水溶液(50:50,v/v)的混合物从食品中稀释或提取氨基酸。未衍生化氨基酸的色谱分离在 6 分钟的运行时间内使用亲水相互作用液相色谱法进行。在色谱条件下,氨基酸的洗脱顺序主要取决于侧链的疏水性和电荷。高分辨率质谱允许在复杂的食品基质中定性和定量检测氨基酸。其响应在 0.25-10 μg/ml 的浓度范围内呈线性。该方法可成功应用于各种食品和饮料,以分析个体氨基酸。来自不同基质的氨基酸的平均回收率为 88.5%或更高,残留标准偏差小于 5.0%。