A new Fe3O4-MWCNTs-reinforced hollow fiber solid/liquid phase microextraction-based natural deep eutectic solvent for determination of trace phthalate esters in aqueous samples using HPLC-DAD

被引:0
|
作者
AL-Hashimi, Nabil N. [1 ]
Alomoush, Qusi K. [2 ]
El-Sheikh, Amjad H. [2 ]
Alsakhen, Nada A. [2 ]
Barri, Thaer [3 ]
Abdelghani, Jafar I. [2 ]
Alqudah, Abdelrahim M. [4 ]
机构
[1] Hashemite Univ, Fac Pharmaceut Sci, Dept Pharmaceut Chem, POB 330127, Zarqa 13133, Jordan
[2] Hashemite Univ, Fac Sci, Dept Phys, POB 330127, Zarqa 13133, Jordan
[3] Univ Petra, Fac Arts & Sci, Dept Chem, POB 961343, Amman, Jordan
[4] Hashemite Univ, Fac Pharmaceut Sci, Dept Clin Pharm & Pharm Practice, POB 330127, Zarqa 13133, Jordan
关键词
Reinforced solid/liquid phase microextraction; Magnetite multi-walled carbon nanotubes; Natural deep eutectic solvent; Diethyl phthalate; Benzyl butyl phthalate; Di-iso-butyl phthalate; HPLC-DAD; Biological fluids and water; LIQUID-LIQUID MICROEXTRACTION; ACID-ESTERS; CARBON NANOTUBES; BAR MICROEXTRACTION; WATER; EXTRACTION;
D O I
10.1007/s11696-024-03752-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we present a new eco-friendly microextraction method based on the magnetite/multi-walled carbon nanotubes reinforced and natural deep eutectic-filled hollow fiber solid/liquid phase microextraction, abbreviated as HF-SLPME, combined with HPLC-DAD analysis. This method has been developed to determine trace levels of phthalate esters, including diethyl phthalate, benzyl butyl phthalate, and di-iso-butyl phthalate in urine, blood plasma, tap water, and groundwater samples. The natural deep eutectic solvents were prepared using terpenoid-derived natural compounds containing menthol and camphor in various ratios. The HF-SLPME device was constructed by reinforcing and immobilizing the synthesized Fe3O4-MWCNTs within the pores of a 2.5 cm segment of hollow fiber microtube through ultrasonication, followed by filling the lumen with the natural deep eutectic solvent with both ends heat sealing. The extraction process was conducted in direct immersion mode. Values of crucial variables for HF-SLPME were optimized through a multivariate methodology based on a central composite design, with 30 extraction tests performed to determine the best conditions. The method exhibited good linearity (correlation coefficients R-2 > 0.996) over a dynamic range lower than 0.927-10(3) mu g L-1. The results show that the limits of detection/quantification for the chosen PEs ranged from 0.19 to 0.27/ 0.65 to 0.92 mu g L-1 with enrichment factor> 37.24. As evidenced by intra- and inter-day precisions, satisfactory reproducibility was achieved with relative standard deviations (RSDs) below 3.7% and 5.1%, respectively. The recoveries of the selected phthalate esters from spiked real samples ranged from 88.4 to 111.1%, with relative standard deviations between 2.3 and 6.5%. This HF-SLPME-HPLC-DAD method offered a new, cost-effective, sensitive microextraction approach for determining and quantifying phthalate esters in aqueous samples with complex matrices.
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页码:9415 / 9433
页数:19
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