Simultaneous determination of three pesticide adjuvant residues in plant-derived agro-products using liquid chromatography-tandem mass spectrometry


Li H., Jiang Z., Cao X., Su H., Shao H., Jin F., ...Daha Fazla

JOURNAL OF CHROMATOGRAPHY A, cilt.1528, ss.53-60, 2017 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1528
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1016/j.chroma.2017.10.075
  • Dergi Adı: JOURNAL OF CHROMATOGRAPHY A
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.53-60
  • Anahtar Kelimeler: Pesticide adjuvant, Plant-derived agro-product, Isotope-labelled internal standard, Liquid chromatography tandem mass, spectrometry, QuEChERS, GAS-CHROMATOGRAPHY, EXTRACTION PROCEDURE, METABOLITES, URINE, N-ETHYL-2-PYRROLIDONE, N-METHYL-2-PYRROLIDONE, SEDIMENTS, STEROIDS, PLASMA, QUICK
  • Atatürk Üniversitesi Adresli: Hayır

Özet

Herein, an accurate and reliable isotope-labelled internal standard method was developed and validated for simultaneous determination of three polar pesticide adjuvants, namely 2-pyrrolidone, N-methyl-2-pyrrolidone, and N-ethyl-2-pyrrolidone in plant-derived agro-products. Matrices, including apple, cabbage, tomato, cucumber, rice, and wheat were extracted with a modified quick, easy, cheap, effective, rugged, and safe "QuEChERS" method and purified with a new clean-up sorbent (Z-Sep). A hydrophilic interaction liquid chromatography column (HILIC), exhibiting a lipophilic-hydrophilic character, was used to separate the three analytes over 10 min using liquid chromatography tandem mass spectrometry (LC-MS/MS). Matrix effects in various matrices were evaluated and an isotope-labelled internal standard method was employed to compensate for ion enhancement/suppression effects. At three fortification levels (2.0, 5.0, and 20.0 mu g/kg), the mean recoveries ranged from 78.5 to 112.1% with relative standard deviations (RSDs) < 11.0% for all tested analytes. The limits of detection (LODs) and quantification (LOQs) were 0.04-0.45 and 0.12-1.58 mu g/kg in various matrices, respectively. The developed experimental protocol was successfully applied to monitor different samples purchased from local markets in Beijing, China. In conclusion, the developed method exhibited both high sensitivity and satisfactory accuracy and is suitable for the simultaneous determination of the three tested pesticide adjuvant residues in agro-products of plant origin. (C) 2017 Elsevier B.V. All rights reserved.