Analytical Chemistry Section, CSIR-Indian Institute of Toxicology Research, Mahatma Gandhi Marg, Lucknow 226 001, Uttar Pradesh, India.
J Chromatogr A. 2013 May 24;1291:10-8. doi: 10.1016/j.chroma.2013.03.061. Epub 2013 Mar 27.
A rapid and economical method for the simultaneous determination of 20 amino acids in complex biological and food matrices (hair, urine and soybean seed samples) has been developed using ultrasound assisted dispersive liquid-liquid micro extraction (UA-DLLME). The method involves simultaneous derivatization and extraction followed by gas chromatography-mass spectrometric (GC-MS) analysis of amino acids. The parameters of UA-DLLME were optimized with the aid of design of experiments approach. The procedure involves the rapid injection of mixture of acetonitrile (disperser solvent), trichloroethylene (TCE) (extraction solvent) and ethylchloroformate (derivatization reagent) into the aqueous phase of sample extract containing pyridine. The Plackett-Burman design has indicated that, the factors such as volume of disperser and extraction solvents and pH were found to be significantly affects the extraction efficiency of the method. The optimum conditions of these factors based on central composite design were found to be 250μL of acetonitrile, 80μL of TCE and pH of 10. The limit of detection and limit of quantification were found to be in the range of 0.36-3.68μgL(-1) and 1.26-12.01μgL(-1) respectively. This is the first application of DLLME for the analysis of amino acids in any matrices. The advantages like (i) in situ derivatization and extraction of amino acids without any prior lyophilization and cleanup of sample, (ii) low consumption of extraction solvent, (iii) fast and simple, (iv) cost-effective and (iv) good repeatability make the method amenable for the routine analysis of amino acids in clinical, toxicological, nutritional and quality control laboratories.
已开发出一种快速、经济的方法,用于同时测定复杂生物和食品基质(头发、尿液和大豆种子样品)中的 20 种氨基酸,该方法采用超声辅助分散液-液微萃取(UA-DLLME)。该方法涉及氨基酸的同时衍生化和提取,然后进行气相色谱-质谱(GC-MS)分析。借助实验设计方法优化了 UA-DLLME 的参数。该过程包括将乙腈(分散溶剂)、三氯乙烯(TCE)(萃取溶剂)和氯甲酸乙酯(衍生化试剂)的混合物快速注入含有吡啶的样品萃取物的水相中。Plackett-Burman 设计表明,分散剂和萃取溶剂的体积以及 pH 等因素会显著影响该方法的萃取效率。基于中心复合设计,这些因素的最佳条件被发现为 250μL 的乙腈、80μL 的 TCE 和 pH 值为 10。检测限和定量限的范围分别为 0.36-3.68μgL(-1) 和 1.26-12.01μgL(-1)。这是 DLLME 在任何基质中分析氨基酸的首次应用。该方法具有以下优点:(i) 无需预先冻干和样品净化即可原位衍生化和提取氨基酸,(ii) 萃取溶剂消耗低,(iii) 快速简单,(iv) 经济高效,(iv) 重复性好,使其适用于临床、毒理学、营养和质量控制实验室中氨基酸的常规分析。