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Updated: Jun 19, 2026

Fabrication of a Dipole-assisted Solid Phase Extraction Microchip for Trace Metal Analysis in Water Samples
Published on: August 7, 2016
Liquid-liquid-solid microextraction based on membrane-protected molecularly imprinted polymer fiber for trace
Yuling Hu1, Yangyang Wang, Yufei Hu
1School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou, 510275, China. ceshyl@mail.sysu.edu.cn
A new liquid-liquid-solid microextraction (LLSME) method uses a special fiber to efficiently extract triazine herbicides from complex samples. This technique improves accuracy and sensitivity for trace analysis in water, milk, and urine.
Area of Science:
- Analytical Chemistry
- Environmental Science
- Materials Science
Background:
- Traditional sample preparation methods for trace analysis often face challenges with complex matrices and analyte recovery.
- Molecularly imprinted polymers (MIPs) offer high selectivity but can be affected by direct exposure to aqueous samples.
- Hollow fiber liquid-phase microextraction (HF-LPME) provides enrichment and sample cleanup but may lack specificity.
Purpose of the Study:
- To develop and validate a novel liquid-liquid-solid microextraction (LLSME) technique for enhanced sample preparation.
- To integrate the selectivity of MIPs with the enrichment and cleanup capabilities of HF-LPME.
- To overcome limitations of existing microextraction methods, particularly water interference in MIP-based techniques.
Main Methods:
- A porous membrane-protected molecularly imprinted polymer (MIP)-coated silica fiber was designed for LLSME.
- The technique involves a three-phase extraction process: aqueous sample, organic phase within a membrane, and MIP fiber.
- Extraction parameters (organic solvent, time) were optimized, and the method was coupled with High-Performance Liquid Chromatography (HPLC).
Main Results:
- The LLSME technique demonstrated high selectivity and efficiency for extracting terbutylazine.
- Optimized parameters led to low limits of detection (0.006-0.02 µg L⁻¹) and good recoveries in real samples.
- Repeatability was satisfactory, with relative standard deviations (RSD) ranging from 1.2% to 9.6% for real samples (n=5).
Conclusions:
- The developed LLSME method is a fast, selective, and sensitive pretreatment technique for trace analysis of triazines in complex aqueous samples.
- LLSME effectively combines the advantages of MIP-SPME and HF-LPME, offering a robust solution for challenging sample matrices.
- The method shows significant potential for real-world applications in environmental monitoring and food safety analysis.
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