An Integrated QuEChERS LC–MS/MS Method for Screening, Confirmation, and Quantification of Nitroimidazole Residues in Food

Clicks: 2
ID: 315604
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #348 of 359 articles by views in journal of aoac international

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 359 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
BACKGROUND: Nitroimidazoles are prohibited veterinary drugs, for which sensitive and reliable analytical methods are required for regulatory residue control in food, particularly across diverse and complex matrices. OBJECTIVE: This study aimed to develop an integrated QuEChERS-LC-MS/MS method for screening, confirmatory identification, and quantitative determination of nitroimidazole residues within a single harmonized analytical workflow. METHODS: Samples were prepared using a unified QuEChERS procedure followed by dispersive solid-phase clean-up and LC-MS/MS analysis with isotope-labelled internal standards. Screening was conducted using a predefined screening target concentration (STC) as a validation reference level. Samples meeting relative retention time requirements and exhibiting responses exceeding a conservative screening cut-off were classified as suspected positives and subjected to confirmatory evaluation based on ion ratio criteria, followed by quantitative determination within the same analytical run. The method was validated for muscle, offal, fat, milk, egg, and aquatic products. Decision limits (CCα) and detection capabilities (CCβ) were established in accordance with regulatory guidelines. RESULTS: Excellent linearity was obtained (r2 ≥ 0.99) over the range of 0-2.5 µg/L. Mean recoveries ranged from 84 to 116%, with RSDs 0.1-8.1%. Limits of quantification were 0.2-0.4 µg/kg across all matrices, and matrix effects were adequately controlled (91-110%). CONCLUSION: The validated method provides a robust and harmonized analytical workflow suitable for screening, confirmation, and quantification of nitroimidazole residues across a wide range of food matrices, supporting regulatory residue control. HIGHLIGHTS: A single harmonized QuEChERS-LC-MS/MS workflow was developed for the screening, confirmatory identification, and quantitative determination of four nitroimidazoles and their metabolites in animal and aquatic foods. The method applies an STC-based decision strategy with confirmatory identification criteria and was validated across multiple matrices, achieving low LOQs. Performance was evaluated in accordance with Commission Implementing Regulation (EU) 2021/808 and verified through international proficiency testing.
Reference Key
openalex_W7163131535 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Hoi-yan Fiona Shiu, Kong-Chi Lau, Ho-pan Michael Yau
Journal journal of aoac international
Year 2026
DOI
10.1093/jaoacint/qsag047
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.