Development and Validation of a Routine Multi-Residue Method for the Quantitative Determination of Pesticide Residues in Fruits, Vegetables, and Rice Using UPLC-MS/MS

Applications | 2019 | WatersInstrumentation
LC/MS, LC/MS/MS, LC/QQQ
Industries
Food & Agriculture
Manufacturer
Waters

Importance of the Topic


Multi-residue pesticide analysis in fruits, vegetables, and rice is essential for ensuring food safety, regulatory compliance, and facilitating global trade. The combination of simplified QuEChERS extraction with UPLC-MS/MS offers rapid, sensitive, and cost-effective monitoring of hundreds of pesticide residues.

Objectives and Study Overview


This work aimed to develop and validate a robust, quantitative method for 204 LC-amenable pesticides in commodity group 1 (high-water matrices) and group 5 (high-starch matrices) following a DisQuE QuEChERS protocol coupled to a Waters ACQUITY UPLC I-Class PLUS System with Xevo TQ-S cronos Tandem Quadrupole MS.

Methodology and Instrumentation


Samples of cucumber, tomato, red and green pepper, and brown rice were extracted using a CEN QuEChERS procedure (acidified MeCN, salting out, dispersive SPE with MgSO4 and PSA), diluted with aqueous mobile phase, and analyzed by UPLC-MS/MS. A 19 min gradient on an ACQUITY UPLC HSS T3 column (2.1 × 100 mm, 1.8 μm) at 45 °C with polarity switching enabled high-throughput data acquisition. Mass parameters (MRM transitions, cone voltage, collision energy) were sourced from the Quanpedia database and manually verified for representative compounds.

Instrumentation Used


  • Waters ACQUITY UPLC I-Class PLUS System
  • Xevo TQ-S cronos Tandem Quadrupole Mass Spectrometer
  • MassLynx 4.2 and TargetLynx XS software
  • ACQUITY UPLC HSS T3 column

Key Results and Discussion


  • Linearity: R2 ≥ 0.99 over 0.001–0.1 mg/kg; residuals < 20%
  • Sensitivity: LOQs ≤ 0.01 mg/kg for all targets; 93% ≤ 0.005 mg/kg
  • Matrix Effects: ± 20% response deviation for > 80% of pesticides across all matrices
  • Precision: inter-day RSD ≤ 20% at default MRL levels; instrument robustness RSD ≤ 3% over > 200 injections
  • Specificity: no significant interferences in blanks

Benefits and Practical Applications


This validated method supports routine quality control and regulatory monitoring, offering high sensitivity, wide dynamic range, fast analysis, and reduced downtime. It enables laboratories to efficiently screen diverse commodities against EU MRLs and adapt to global trade requirements.

Future Trends and Opportunities


Advancements may include automation of sample preparation, expansion to high-resolution MS for non-target screening, integration with data analytics for trend monitoring, and extension to metabolite and degradation product analysis.

Conclusion


The DisQuE QuEChERS and UPLC-MS/MS workflow on the Xevo TQ-S cronos platform delivers a reliable, high-throughput multi-residue pesticide method, meeting stringent validation criteria and offering robust performance for routine food safety testing.

References


  • Regulation (EU) 2017/660 on coordinated multiannual control program of the Union for 2018–2020
  • SANTE/11813/2017: Method Validation and Quality Control Procedures for Pesticide Residues
  • Waters LC Multiresidue Pesticide Standards Kit Care and Use Manual, 720005342EN
  • Rapid Alert System for Food and Feed (RASFF) portal, European Commission

Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.

Downloadable PDF for viewing
 

Similar PDF

DEVELOPMENT AND VALIDATION OF MULTI-RESIDUE PESTICIDES METHOD FOR  ROUTINE ANALYSIS OF FOOD SAMPLES USING UPLC-MS/MS
LC-MS/MS Analysis of Pesticide Residues in Rice and Unexpected Detection of Residues in an Organic Rice Sample
UPLC and APGC Multi Residue Pesticide Analysis on a Single Tandem Quadrupole Mass Spectrometer Platform
Waters Application Notes - Food Testing