A hydrophilic interaction chromatography-tandem mass spectrometry method for amino acid profiling in mussels

作者：Tsochatzis Emmanouil D; Begou Olga; Gika Helen G; Karayannakidis Panayotis; Kalogiannis Stavros^*

来源：Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, 2017, 1047: 197-206.

DOI：10.1016/j.jchromb.2016.05.018

• HILIC
• Tandem mass spectrometry
• Free amino acids
• Total amino acids
• Mussels

A UHPLC-HILIC-tandem MS method has been developed and validated for the quantification of 21 amino acids (20 protein amino acids and cystine) in their free form (FAA) and as protein constituents (total amino acids, TAA) in a rich protein food matrix such as lyophilized mussels (Mytilus galloprovincialis) samples. FAA were analyzed after suspending the samples in the presence of trichloroacetic acid in order to prevent dissolving the proteins, while TAA were determined after acid hydrolysis with 6 M HCI in the presence of 4% v/v thioglycolic acid as a reducing agent. In hydrolysed samples 17 amino acids could be determined since tryptophan, cysteine, cystine and asparagine were degraded during acid hydrolysis. Linear regression coefficients (R-2) were above 0.99 for all amino acids. Accuracy and precision, expressed as recovery (%) and relative standard deviation (RSD, %) were in acceptable levels, ranging from 78.2 to 123.3% and below 15%, respectively for both FAA and TM. Uncertainty was also below 12% for FM and below 22% for TAA. Sensitivity of the method was high with LOD values ranging from 0.003 to 0.034 g/100 g for FAA and 0.001 to 0.004 g/100 g for TM, while LOQ, ranged from 0.009 to 0.104 g/100 g for FM and 0.002 to 0.011 g/100 g for TM. The method proved to be a fast and reliable tool for acquiring information on free and total amino acids profile in high protein content foodstuffs such as mussels.

• 出版日期2017-3-15