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Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol

Diethylstilbestrol (DES) is considered a representative example of an exogenous endocrine disrupting compound (EDC). It can retard development in infants, lead to serious metabolic regulation disorders, and even result in distortion and cancer in the reproductive system. Therefore, achieving rapid a...

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Autores principales: Zhao, Wen-Rui, Kang, Tian-Fang, Lu, Li-Ping, Cheng, Shui-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079755/
https://www.ncbi.nlm.nih.gov/pubmed/35542503
http://dx.doi.org/10.1039/c8ra01250d
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author Zhao, Wen-Rui
Kang, Tian-Fang
Lu, Li-Ping
Cheng, Shui-Yuan
author_facet Zhao, Wen-Rui
Kang, Tian-Fang
Lu, Li-Ping
Cheng, Shui-Yuan
author_sort Zhao, Wen-Rui
collection PubMed
description Diethylstilbestrol (DES) is considered a representative example of an exogenous endocrine disrupting compound (EDC). It can retard development in infants, lead to serious metabolic regulation disorders, and even result in distortion and cancer in the reproductive system. Therefore, achieving rapid and accurate analysis of trace amounts of DES in complex environments is of great importance to human health and for environmental protection. Novel magnetic molecularly imprinted polymers (MIPs) with excellent molecular recognition ability and super water-compatibility were developed for the selective capture of DES in water samples. Fe(3)O(4)@SiO(2) magnetic nanoparticles (NPs) were synthesized and used as support cores. Molecularly imprinted poly(3-aminophenylboronic acid) (poly(APBA)), synthesized on magnetic cores based on a surface-imprinting strategy, can preferentially bind DES molecules in water samples. The magnetic core–shell MIPs (denoted as Fe(3)O(4)@SiO(2)@APBA/MIPs) exhibited high binding capacity and favorable recognition specificity for DES in water. The adsorption kinetics and experimental isotherm data of DES on magnetic MIPs can be well described by the pseudo-second-order kinetic model and the Langmuir isotherm, respectively. The imprinted nanoparticles were subjected to magnetic solid-phase extraction (MSPE) of DES from water samples. The DES content in the samples was determined by high-performance liquid chromatography (HPLC). The peak area increased linearly with increasing DES concentration over the range 0.08–150 μg L(−1), with a detection limit of 0.03 μg L(−1). The recoveries for spiked lake water samples were in the range 97.1–103.2%, with relative standard deviation (RSD) of 2.8–4.3% (n = 6).
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spelling pubmed-90797552022-05-09 Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol Zhao, Wen-Rui Kang, Tian-Fang Lu, Li-Ping Cheng, Shui-Yuan RSC Adv Chemistry Diethylstilbestrol (DES) is considered a representative example of an exogenous endocrine disrupting compound (EDC). It can retard development in infants, lead to serious metabolic regulation disorders, and even result in distortion and cancer in the reproductive system. Therefore, achieving rapid and accurate analysis of trace amounts of DES in complex environments is of great importance to human health and for environmental protection. Novel magnetic molecularly imprinted polymers (MIPs) with excellent molecular recognition ability and super water-compatibility were developed for the selective capture of DES in water samples. Fe(3)O(4)@SiO(2) magnetic nanoparticles (NPs) were synthesized and used as support cores. Molecularly imprinted poly(3-aminophenylboronic acid) (poly(APBA)), synthesized on magnetic cores based on a surface-imprinting strategy, can preferentially bind DES molecules in water samples. The magnetic core–shell MIPs (denoted as Fe(3)O(4)@SiO(2)@APBA/MIPs) exhibited high binding capacity and favorable recognition specificity for DES in water. The adsorption kinetics and experimental isotherm data of DES on magnetic MIPs can be well described by the pseudo-second-order kinetic model and the Langmuir isotherm, respectively. The imprinted nanoparticles were subjected to magnetic solid-phase extraction (MSPE) of DES from water samples. The DES content in the samples was determined by high-performance liquid chromatography (HPLC). The peak area increased linearly with increasing DES concentration over the range 0.08–150 μg L(−1), with a detection limit of 0.03 μg L(−1). The recoveries for spiked lake water samples were in the range 97.1–103.2%, with relative standard deviation (RSD) of 2.8–4.3% (n = 6). The Royal Society of Chemistry 2018-04-09 /pmc/articles/PMC9079755/ /pubmed/35542503 http://dx.doi.org/10.1039/c8ra01250d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Zhao, Wen-Rui
Kang, Tian-Fang
Lu, Li-Ping
Cheng, Shui-Yuan
Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title_full Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title_fullStr Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title_full_unstemmed Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title_short Magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
title_sort magnetic surface molecularly imprinted poly(3-aminophenylboronic acid) for selective capture and determination of diethylstilbestrol
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079755/
https://www.ncbi.nlm.nih.gov/pubmed/35542503
http://dx.doi.org/10.1039/c8ra01250d
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