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Peer-reviewedCC BYScientific Reports

A novel hydrophobic deep eutectic solvent-based paired-drop microextraction method for the trace determination of metribuzin in urine samples

  1. 1Health and Environment Research Center, Zanjan University of Medical Sciences (ZUMS)
  2. 2Department of Occupational Health Engineering, School of Public Health, Tehran University of Medical Sciences (TUMS)

Abstract

A hydrophobic deep eutectic solvent (DES) was molecularly tailored from tributylphosphine oxide and octanoic acid via hydrogen-bonding and employed as an efficient extractant in a novel ultrasound-assisted paired-drop microextraction (UAE-PDME) method for metribuzin determination in urine. The DES structure was confirmed by FTIR analysis. The innovative paired-drop design addresses a key practical challenge: while ultrasound efficiently disperses the extractant, quantitatively retrieving a minute volume (e.g., 2 µL) of dispersed solvent from an aqueous sample is nearly impossible. This method solves this by using a second, hanging DES droplet that coalesces with the dispersed microdroplets during gentle stirring, enabling efficient, complete, and centrifugation-free collection of the enriched phase. After optimization of key parameters, the method was rigorously validated using spiked urine samples. It demonstrated excellent performance: a wide linear range of 5–500 µg/L, low limits of detection and quantification of 0.20 and 0.67 µg/L, respectively, high precision (RSD < 3.6%), quantitative recoveries (99.5–103.1%) with negligible matrix effect (− 4.2%) and high solvent phase recovery (98.5%). The high extraction efficiency is attributed to the DES’s rational molecular design. The DES-UAE-PDME method represents a green, rational, and effective sample preparation strategy for trace pesticide monitoring using conventional HPLC–UV instrumentation.

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BibTeX
@article{pourhossein2026novel,
  title = {{A novel hydrophobic deep eutectic solvent-based paired-drop microextraction method for the trace determination of metribuzin in urine samples}},
  author = {Mehran Pourhossein and Seyed Jamaleddin Shahtaheri},
  journal = {Scientific Reports},
  year = {2026},
  month = jul,
  doi = {10.1038/s41598-026-61712-2},
  url = {https://doi.org/10.1038/s41598-026-61712-2},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - A novel hydrophobic deep eutectic solvent-based paired-drop microextraction method for the trace determination of metribuzin in urine samples
AU  - Mehran Pourhossein
AU  - Seyed Jamaleddin Shahtaheri
PY  - 2026
DA  - 2026/07/01
JO  - Scientific Reports
DO  - 10.1038/s41598-026-61712-2
UR  - https://doi.org/10.1038/s41598-026-61712-2
AB  - A hydrophobic deep eutectic solvent (DES) was molecularly tailored from tributylphosphine oxide and octanoic acid via hydrogen-bonding and employed as an efficient extractant in a novel ultrasound-assisted paired-drop microextraction (UAE-PDME) method for metribuzin determination in urine. The DES structure was confirmed by FTIR analysis. The innovative paired-drop design addresses a key practical challenge: while ultrasound efficiently disperses the extractant, quantitatively retrieving a minute volume (e.g., 2 µL) of dispersed solvent from an aqueous sample is nearly impossible. This method solves this by using a second, hanging DES droplet that coalesces with the dispersed microdroplets during gentle stirring, enabling efficient, complete, and centrifugation-free collection of the enriched phase. After optimization of key parameters, the method was rigorously validated using spiked urine samples. It demonstrated excellent performance: a wide linear range of 5–500 µg/L, low limits of detection and quantification of 0.20 and 0.67 µg/L, respectively, high precision (RSD < 3.6%), quantitative recoveries (99.5–103.1%) with negligible matrix effect (− 4.2%) and high solvent phase recovery (98.5%). The high extraction efficiency is attributed to the DES’s rational molecular design. The DES-UAE-PDME method represents a green, rational, and effective sample preparation strategy for trace pesticide monitoring using conventional HPLC–UV instrumentation.
SN  - 2045-2322
ER  -