Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination

In the present study, acetaminophen (ACT) molecularly imprinted polymer (ACT-MIP) were successfully synthesized via surface imprinting polymerization. The structural and morphological properties of ACT-MIP were characterized using various analytical techniques. ACT-MIP were used as an adsorbent in a...

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Main Authors: Neliswa Mpayipheli, Anele Mpupa, Philiswa Nosizo Nomngongo
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Separations
Subjects:
Online Access:https://www.mdpi.com/2297-8739/8/10/194
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author Neliswa Mpayipheli
Anele Mpupa
Philiswa Nosizo Nomngongo
author_facet Neliswa Mpayipheli
Anele Mpupa
Philiswa Nosizo Nomngongo
author_sort Neliswa Mpayipheli
collection DOAJ
description In the present study, acetaminophen (ACT) molecularly imprinted polymer (ACT-MIP) were successfully synthesized via surface imprinting polymerization. The structural and morphological properties of ACT-MIP were characterized using various analytical techniques. ACT-MIP were used as an adsorbent in a vortex-assisted dispersive molecularly imprinted solid-phase micro-extraction (VA-d-μ-MISPE), coupled with a high-performance liquid chromatography–diode array detector (HPLC-DAD) method for the determination of ACT in water samples. Influential parameters such as the mass of adsorbent, vortex speed, extraction time, desorption volume, and desorption time were optimized using a multivariate approach. Under optimum conditions, the maximum binding capacities of ACT-MIP and NIP (non-imprinted polymers) were 191 mg/g and 71.5 mg/g, respectively. The linearity was attained across concentrations ranging from 0.630 to 500 µg/L, with a coefficient of determination of 0.9959. For ACT-MIP, the limit of detection (LOD) and limit of quantification (LOQ), enhancement factor, and precision of the method were 0.19 ng/L, 0.63 ng/L, 79, and <5%, respectively. The method was applied in the analysis of spiked water samples, and satisfactory percentage recoveries in the range of 95.3–99.8% were obtained.
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spelling doaj.art-fa40da9861004851bc36944b2a50942f2023-11-22T20:00:29ZengMDPI AGSeparations2297-87392021-10-0181019410.3390/separations8100194Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD DeterminationNeliswa Mpayipheli0Anele Mpupa1Philiswa Nosizo Nomngongo2Department of Chemical Sciences, University of Johannesburg, Doornfontein Campus, P.O. Box 17011, Doornfontein 2028, South AfricaDepartment of Chemical Sciences, University of Johannesburg, Doornfontein Campus, P.O. Box 17011, Doornfontein 2028, South AfricaDepartment of Chemical Sciences, University of Johannesburg, Doornfontein Campus, P.O. Box 17011, Doornfontein 2028, South AfricaIn the present study, acetaminophen (ACT) molecularly imprinted polymer (ACT-MIP) were successfully synthesized via surface imprinting polymerization. The structural and morphological properties of ACT-MIP were characterized using various analytical techniques. ACT-MIP were used as an adsorbent in a vortex-assisted dispersive molecularly imprinted solid-phase micro-extraction (VA-d-μ-MISPE), coupled with a high-performance liquid chromatography–diode array detector (HPLC-DAD) method for the determination of ACT in water samples. Influential parameters such as the mass of adsorbent, vortex speed, extraction time, desorption volume, and desorption time were optimized using a multivariate approach. Under optimum conditions, the maximum binding capacities of ACT-MIP and NIP (non-imprinted polymers) were 191 mg/g and 71.5 mg/g, respectively. The linearity was attained across concentrations ranging from 0.630 to 500 µg/L, with a coefficient of determination of 0.9959. For ACT-MIP, the limit of detection (LOD) and limit of quantification (LOQ), enhancement factor, and precision of the method were 0.19 ng/L, 0.63 ng/L, 79, and <5%, respectively. The method was applied in the analysis of spiked water samples, and satisfactory percentage recoveries in the range of 95.3–99.8% were obtained.https://www.mdpi.com/2297-8739/8/10/194acetaminophenmolecularly imprinted polymerselectivityScatchard analysisadsorption isothermssolid-phase microextraction
spellingShingle Neliswa Mpayipheli
Anele Mpupa
Philiswa Nosizo Nomngongo
Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
Separations
acetaminophen
molecularly imprinted polymer
selectivity
Scatchard analysis
adsorption isotherms
solid-phase microextraction
title Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
title_full Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
title_fullStr Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
title_full_unstemmed Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
title_short Vortex-Assisted Dispersive Molecularly Imprinted Polymer-Based Solid Phase Extraction of Acetaminophen from Water Samples Prior to HPLC-DAD Determination
title_sort vortex assisted dispersive molecularly imprinted polymer based solid phase extraction of acetaminophen from water samples prior to hplc dad determination
topic acetaminophen
molecularly imprinted polymer
selectivity
Scatchard analysis
adsorption isotherms
solid-phase microextraction
url https://www.mdpi.com/2297-8739/8/10/194
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AT anelempupa vortexassisteddispersivemolecularlyimprintedpolymerbasedsolidphaseextractionofacetaminophenfromwatersamplespriortohplcdaddetermination
AT philiswanosizonomngongo vortexassisteddispersivemolecularlyimprintedpolymerbasedsolidphaseextractionofacetaminophenfromwatersamplespriortohplcdaddetermination