Synthesis of magnetic molecular imprinted polymer with a new functional monomer for dispersive micro solid phase extraction of captopril from wastewater and biological samples and determination by UV-Vis spectrophotometry

被引:8
|
作者
Sabbaghi, Najmeh [1 ]
Shabani, Ali Mohammad Haji [1 ]
Dadfarnia, Shayessteh [1 ]
Farsadrooh, Majid [2 ]
机构
[1] Yazd Univ, Fac Sci, Dept Chem, Yazd 89195741, Iran
[2] Univ Sistan & Baluchestan, Fac Sci, Dept Chem, Renewable Energies Res Lab, POB 98135 674, Zahedan, Iran
关键词
Captopril; Dispersive magnetic micro solid phase extraction; Magnetic molecularly imprinted polymer; N-(allylcarbamothioyl)-2-chlorobenzamide; UV-Vis spectrophotometry; PERFORMANCE LIQUID-CHROMATOGRAPHY; HUMAN PLASMA; INJECTION-ANALYSIS; DRUG; MICROEXTRACTION; SEPARATION;
D O I
10.1007/s00604-023-05746-7
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A magnetic molecularly imprinted polymer (MMIP) was fabricated for captopril by surface polymerization of Fe3O4@SiO2 nanoparticles using a new functional monomer of N-( allylcarbamothioyl)-2-chlorobenzamide. It was then employed as a selective nanosorbent for dispersive magnetic micro solid phase extraction ( DM-mu-SPE) of captopril from biological and wastewater samples. To characterize the physicochemical properties of the MMIP, different analytical methods such as the vibrating sample magnetometer, field emission scanning electron microscopy, Brunauer-Emmett-Teller, and Fourier transform infrared spectroscopy were utilized. To gain the maximum extraction recovery of captopril, the influence of various operating conditions was investigated and experimental settings optimized. After the extraction step, the concentration of captopril was measured by UV-Vis spectrophotometer at 245 nm. The assessments demonstrated that the MMIP provides higher extraction efficiency in comparison to magnetic non-imprinted polymer, suggesting the establishment of selective recognition binding sites at the MMIP surface. The method depicted desirable figures of merit of a low detection limit of 0.16 mu g L-1, a limit of quantification of 0.50 mu g L-1, a linear dynamic range of 0.50-22.0 mu g L-1, and an acceptable preconcentration factor of 333. The magnetic MIP was successfully employed for preconcentration and extraction of trace amounts of captopril in real samples, such as human blood serum, urine, and wastewater samples, with recoveries in the range 95.7 to 102.6% and relative standard deviations < 5%.
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页数:11
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