Direct determination of glyphosate, glufosinate, and AMPA in soybean and corn by liquid chromatography/tandem mass spectrometry

• Published in: Analytical and bioanalytical chemistry 2016-07, Vol.408 (18), p.4995-5004
• Main Authors: Chamkasem, Narong, Harmon, Tiffany
• Format: Article
• Language: English
• Subjects: Acetic acid; Acids; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - analysis; Aminobutyrates - analysis; Analytical Chemistry; Biochemistry; Cations; Characterization and Evaluation of Materials; Chemical properties; Chemistry; Chemistry and Materials Science; Chromatography; Chromatography, Liquid - methods; Complex Mixtures - analysis; Composition; Corn; Detectors; Food Science; Glycine - analogs & derivatives; Glycine - analysis; Glycine max - chemistry; Glyphosate; Herbicides; Identification and classification; Laboratory Medicine; Linearity; Liquid chromatography; Mass spectrometry; Methods; Monitoring/Environmental Analysis; Pesticides; Plant Extracts - analysis; Plant Extracts - chemistry; Reproducibility of Results; Research Paper; Scientific imaging; Sensitivity and Specificity; Solvents; Soybeans; Suspended particulate matter; Tandem Mass Spectrometry - methods; Toxicity; Zea mays - chemistry
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-016-9597-6

Glyphosate, glufosinate, and aminomethylphosphonic acid (AMPA) are amphoteric, low mass, high water soluble, and do not have chromophore. They are very difficult to be retained on a reversed phase HPLC and detected by UV or fluorescence detectors. A liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed to determine these analytes in soybean and corn using a reversed phase with weak anion-exchange and cation-exchange mixed-mode Acclaim™ Trinity™ Q1 column. The sample was shaken with water containing ethylenediaminetetraacetic acid disodium salt (Na 2 EDTA) and acetic acid for 10 min to precipitate protein and extract the analytes into the solution. The supernatant was passed thru an Oasis HLB SPE to retain suspended particulates and non-polar interferences. The sample was directly injected and analyzed in 6 min by LC-MS/MS with no sample concentration or derivatization steps. Three isotopically labeled internal standards corresponding to each analyte were used to counter matrix suppression effect. Linearity of the detector response with a minimum coefficient of determination ( R 2 ) of more than 0.995 was demonstrated in the range of 10 to 1000 ng/mL for each analyte. Accuracy (recovery %) and precision (relative standard deviation or RSD %) were evaluated at the fortification levels of 0.1, 0.5, and 2 μg/g in seven replicates in both soybean and corn samples.