Ultrasonic-assisted magnetic solid phase extraction of morphine in urine samples by new imprinted polymer-supported on MWCNT-Fe3O4-NPs: Central composite design optimization

[Display omitted] •UA magnetic solid phase extraction followed by UV–vis spectrophotometer for MO detection.•UA synthesis of morphine imprinted polymer-coated MWCNT-Fe3O4-NPs.•Extraction process of MO was performed in short sonication time (8min).•Optimization of extraction process parameters using...

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Veröffentlicht in:Ultrasonics sonochemistry 2016-11, Vol.33, p.240-248
Hauptverfasser: Kolaei, Milad, Dashtian, Kheibar, Rafiee, Zahra, Ghaedi, Mehrorang
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Sprache:eng
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Zusammenfassung:[Display omitted] •UA magnetic solid phase extraction followed by UV–vis spectrophotometer for MO detection.•UA synthesis of morphine imprinted polymer-coated MWCNT-Fe3O4-NPs.•Extraction process of MO was performed in short sonication time (8min).•Optimization of extraction process parameters using central composite design. Multiwalled carbon nanotubes (MWCNTs) were magnetized with Fe3O4 nanoparticles (MWCNTs-Fe3O4-NPs) and subsequently coated by vinyl end groups (Vinyltrimethoxysilane). MWCNT-Fe3O4-NPs were used as support for a new morphine (MO) molecularly imprinted polymer (MWCNT-Fe3O4-NPs@MO-MIP) by surface imprinting polymerization method. The MWCNT-Fe3O4-NPs@MO-MIP was characterized by FTIR, VSM and SEM techniques and successfully used for determination of MO. Ultrasonic-assisted magnetic solid phase extraction followed by UV–vis spectrophotometer (UAMSPE-UV–vis) was investigated for MWCNT-Fe3O4-NPs@MO-MIP and compared with non-imprinted polymer (NIP) using batch method. Central composite design under response surface methodology was used for the evaluation of the effect of variables, individually, as well as their possible interaction effects on the adsorption process. The variables such as sonication time, MWCNT-Fe3O4-NPs@MO-MIP mass, initial concentration of MO and pH were investigated in this study. At optimum experimental conditions, UAMSPE-UV–vis method was exhibited a linear range of 0.8–8.7mgL−1 of the MO concentration with a detection limit of 0.18mgL−1. The relative standard deviation for the analyte was found to be lower than 2.32%. The MWCNT-Fe3O4-NPs@MO-MIP adsorption capacity was found to be 37.01mgg−1. The enrichment and preconcentration factors were found to be 107.01 and 98.21, respectively. The developed method was finally applied successfully to the determination of MO in urine and wastewater samples with the recoveries ranged from 96.40 to 105.6%.
ISSN:1350-4177
1873-2828
DOI:10.1016/j.ultsonch.2016.05.003