Selective extraction and determination of catecholamines in urine samples by using a dopamine magnetic molecularly imprinted polymer and capillary electrophoresis. Bouri, M., Lerma-García, M., Salghi, R., Zougagh, M., & Ríos, A. Talanta, 99:897-903, Elsevier B.V., 2012. cited By 85
Selective extraction and determination of catecholamines in urine samples by using a dopamine magnetic molecularly imprinted polymer and capillary electrophoresis [link]Paper  doi  abstract   bibtex   
A rapid and selective method for the extraction and determination of catecholamines (CLs) from urine samples has been successfully developed using a magnetic molecularly imprinted polymer (MMIP) as a sorbent material. The MMIP has been prepared using dopamine hydrochloride (DA) as template molecule, methacrylic acid (MAA) as functional monomer, ethylene glycol dimethacrylate (EDMA) as cross-linking agent and Fe3O4 magnetite as magnetic component. The extraction was carried out by stirring urine samples with the magnetic polymer. When the extraction was completed, the MMIP, together with the captured analytes, was easily separated from the sample matrix by an adscititious magnet. The analytes desorbed from the MMIP were determined by capillary electrophoresis (CE). It was shown that the MMIP had high affinity and selectivity toward DA and other structurally related CLs such as 3-methoxytyramine hydrochloride (MT), DL-normetanephrine hydrochloride (NME), DL-norephinephrine hydrochloride (NE) and (±) epinephrine (E). Different parameters affecting the extraction efficiency were evaluated in order to achieve the optimal pre-concentration of the analytes and to reduce non-specific interactions. Under the optimal conditions, the CL limits of detection were at the 0.04-0.06 μM range. The relative standard deviations of migration time and response ranged from 0.7% to 1.4% and from 2.9% to 5.5%, respectively. The proposed method was successfully applied to determine CLs, including MT, NME, DA, NE and E in human urine samples. © 2012 Elsevier B.V.
@ARTICLE{Bouri2012897,
author={Bouri, M. and Lerma-García, M.J. and Salghi, R. and Zougagh, M. and Ríos, A.},
title={Selective extraction and determination of catecholamines in urine samples by using a dopamine magnetic molecularly imprinted polymer and capillary electrophoresis},
journal={Talanta},
year={2012},
volume={99},
pages={897-903},
doi={10.1016/j.talanta.2012.07.053},
note={cited By 85},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-84866126707&doi=10.1016%2fj.talanta.2012.07.053&partnerID=40&md5=fbbc10783fe268f82ea22c6c0c746054},
affiliation={Department of Analytical Chemistry and Food Technology, University of Castilla-La Mancha, Av. Camilo José Cela 10, E-13004, Ciudad Real, Spain; Laboratoire d'Ingénieries des Procédés de l'Energie et de l'Environnement, ENSA, B.P. 1136, Agadir, Morocco; Regional Institute for Applied Chemistry Research, IRICA, Av. Camilo José Cela 10, E-13004, Ciudad Real, Spain; Albacete Science and Technology Park, E-02006 Albacete, Spain},
abstract={A rapid and selective method for the extraction and determination of catecholamines (CLs) from urine samples has been successfully developed using a magnetic molecularly imprinted polymer (MMIP) as a sorbent material. The MMIP has been prepared using dopamine hydrochloride (DA) as template molecule, methacrylic acid (MAA) as functional monomer, ethylene glycol dimethacrylate (EDMA) as cross-linking agent and Fe3O4 magnetite as magnetic component. The extraction was carried out by stirring urine samples with the magnetic polymer. When the extraction was completed, the MMIP, together with the captured analytes, was easily separated from the sample matrix by an adscititious magnet. The analytes desorbed from the MMIP were determined by capillary electrophoresis (CE). It was shown that the MMIP had high affinity and selectivity toward DA and other structurally related CLs such as 3-methoxytyramine hydrochloride (MT), DL-normetanephrine hydrochloride (NME), DL-norephinephrine hydrochloride (NE) and (±) epinephrine (E). Different parameters affecting the extraction efficiency were evaluated in order to achieve the optimal pre-concentration of the analytes and to reduce non-specific interactions. Under the optimal conditions, the CL limits of detection were at the 0.04-0.06 μM range. The relative standard deviations of migration time and response ranged from 0.7% to 1.4% and from 2.9% to 5.5%, respectively. The proposed method was successfully applied to determine CLs, including MT, NME, DA, NE and E in human urine samples. © 2012 Elsevier B.V.},
author_keywords={Capillary electrophoresis;  Catecholamines;  Extraction;  Human urine;  Magnetic molecularly imprinted polymer},
keywords={Amines;  Body fluids;  Capillary electrophoresis;  Crosslinking;  Ethylene;  Ethylene glycol;  Hormones;  Iron oxides;  Magnetism;  Magnetite;  Neurophysiology, Catecholamines;  Ethylene glycol dimethacrylate;  Extraction efficiencies;  Human urine;  Molecularly Imprinted Polymer;  Non-specific interactions;  Relative standard deviations;  Selective extraction, Extraction},
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correspondence_address1={Ríos, A.; Department of Analytical Chemistry and Food Technology, Av. Camilo José Cela 10, E-13004, Ciudad Real, Spain; email: angel.rios@uclm.es},
publisher={Elsevier B.V.},
issn={00399140},
coden={TLNTA},
pubmed_id={22967640},
language={English},
abbrev_source_title={Talanta},
document_type={Article},
source={Scopus},
}

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