# Construction and Comparison of UPLC-QE-Orbitrap-MS and UPLC-MS/MS Methods for the Detection of Diazepam Residues in Complex Aquatic Matrices

**Authors:** Yuanhao Yang, Yi Li, Qiangbing Tian, Juanning Yang, Yiming Xu, Wen Su, Fei Wang, Siyao Qu, Sien Wen, Wei Cao

PMC · DOI: 10.3390/foods14193296 · Foods · 2025-09-23

## TL;DR

This paper presents a reliable method for detecting diazepam and its metabolites in aquatic samples using two advanced mass spectrometry platforms.

## Contribution

A dual-platform detection system for accurate trace quantification of diazepam in complex aquatic matrices is developed and validated.

## Key findings

- Both UPLC-QE-Orbitrap-MS and UPLC-MS/MS showed excellent linearity and low detection limits.
- Strong inter-platform agreement was observed with Pearson r > 0.990 and p < 0.001.
- Recoveries ranged from 73.8% to 117.9%, indicating high accuracy and reproducibility.

## Abstract

A standardized pretreatment protocol was established for simultaneous determination of diazepam and its metabolites—nordazepam, oxazepam, and temazepam—in aquatic products using liquid chromatography–mass spectrometry. Samples were extracted with 0.2% formic acid in acetonitrile (solid–liquid ratio 1:5, m/v), purified via MCX solid-phase extraction, eluted with 5% ammoniated methanol, and concentrated under reduced pressure. The residue was reconstituted in 0.2% formic acid–50% acetonitrile aqueous solution. Chromatographic and mass spectrometric conditions were optimized on two platforms: UPLC-QE-Orbitrap-MS and UPLC-MS/MS, with quantification based on internal standards. Both platforms showed excellent linearity across 0.2–200 ng/mL (R2 > 0.997), with detection and quantification limits as low as 0.1 μg/kg and 0.2 μg/kg, respectively. Following Codex Alimentarius guidelines (CAC/GL-71), 330 matrix samples (intra-batch n = 6, inter-batch n = 5) were validated, showing strong inter-platform agreement (Pearson r > 0.990, p < 0.001). Intra-batch RSDs ranged from 1.86% to 14.64%, and inter-batch RSDs from 1.10% to 11.41%. Recoveries ranged from 73.8% to 117.9% (p > 0.05). The dual-platform detection system developed herein demonstrates high sensitivity, strong matrix interference resistance, and excellent reproducibility, enabling accurate trace quantification of diazepam and its metabolites in heterogeneous aquatic samples.

## Linked entities

- **Chemicals:** diazepam (PubChem CID 3016), nordazepam (PubChem CID 2997), oxazepam (PubChem CID 4616), temazepam (PubChem CID 5391), formic acid (PubChem CID 284), acetonitrile (PubChem CID 6342)

## Full-text entities

- **Chemicals:** acetonitrile (MESH:C032159), methanol (MESH:D000432), MCX (-), Diazepam (MESH:D003975), nordazepam (MESH:D003708), oxazepam (MESH:D010076), formic acid (MESH:C030544), temazepam (MESH:D013693)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12524225/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12524225/full.md

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Source: https://tomesphere.com/paper/PMC12524225