Zwitterionic covalent organic nanosheets for selective analysis of domoic acid in marine environment.

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Main Authors: Xu, Jinhua, Yu, Zhenli, Zhang, Wenmin, Xie, Shiye, Liao, Baodi, Zhang, Lan
Format: Artículo científico
Language:en
Published: Analytica chimica acta 2024
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author Xu, Jinhua
Yu, Zhenli
Zhang, Wenmin
Xie, Shiye
Liao, Baodi
Zhang, Lan
author_facet Xu, Jinhua
Yu, Zhenli
Zhang, Wenmin
Xie, Shiye
Liao, Baodi
Zhang, Lan
Xu, Jinhua
Yu, Zhenli
Zhang, Wenmin
Xie, Shiye
Liao, Baodi
Zhang, Lan
collection PubMed - marine biology
contents Zwitterionic covalent organic nanosheets for selective analysis of domoic acid in marine environment. Xu, Jinhua Yu, Zhenli Zhang, Wenmin Xie, Shiye Liao, Baodi Zhang, Lan Kainic Acid Nanostructures Adsorption Metal-Organic Frameworks Water Pollutants, Chemical Density Functional Theory Limit of Detection Domoic acid (DA) is a neurotoxic compound causing amnesic shellfish poisoning, secreted by red algae and diatoms. As a glutamate analogue, DA accumulates in filter-feeding marine organisms, posing significant health risks to humans upon consumption. Detecting DA in marine environments remains challenging due to its low concentration and interference from complex matrices. Effective detection and removal require materials with high efficiency and selectivity, which traditional inorganic ionic materials lack due to their limited adsorption capacity and selectivity. Ionic covalent organic frameworks (iCOFs) expected to become highly efficient DA adsorbents due to tunable ionic sites. Thus, a zwitterionic covalent organic nanosheet (TGDB-iCONs) was synthesized to selectively capture DA. TGDB-iCONs was prepared by one-step Schiff-base reaction of the charged monomer triaminoguanidine hydrochloride. It uniformly distributed positively charged guanidinium and negatively charged chloride ions on the surface, forming zwitterionic binding sites. The self-peeling of TGDB-iCONs facilitated the exposure of active sites and improved the adsorption efficiency. Several binding forces were generated between TGDB-iCONs and DA, including complementary electrostatic hydrophilic interactions, which were verified by density functional theory (DFT) calculation. TGDB-iCONs exhibited ultra-fast adsorption kinetics (7 min) and relatively high adsorption capacity (66.48 mg/g) for DA. Furthermore, TGDB-iCONs exhibit strong salt resistance, which is attributed to the charge "shielding" effect of the zwitterionic ions present in TGDB-iCONs. TGDB-iCONs could highly selectively enrich DA and detect trace DA from marine environment including seawater, algae and marine organisms and the limit of detection as low as 0.3 ng/kg. This comprehensive study not only sheds light on the vast potential of ionic covalent organic frameworks nanosheets (iCONs) in supporting early warning, control, and traceability of DA, but also lays a solid foundation for future research endeavors aimed at designing and harnessing the unique properties of iCONs.
format Artículo científico
id pubmed_39532426
institution PubMed
language en
publishDate 2024
publisher Analytica chimica acta
record_format pubmed
spellingShingle Zwitterionic covalent organic nanosheets for selective analysis of domoic acid in marine environment.
Xu, Jinhua
Yu, Zhenli
Zhang, Wenmin
Xie, Shiye
Liao, Baodi
Zhang, Lan
Kainic Acid
Nanostructures
Adsorption
Metal-Organic Frameworks
Water Pollutants, Chemical
Density Functional Theory
Limit of Detection
Zwitterionic covalent organic nanosheets for selective analysis of domoic acid in marine environment. Xu, Jinhua Yu, Zhenli Zhang, Wenmin Xie, Shiye Liao, Baodi Zhang, Lan Kainic Acid Nanostructures Adsorption Metal-Organic Frameworks Water Pollutants, Chemical Density Functional Theory Limit of Detection Domoic acid (DA) is a neurotoxic compound causing amnesic shellfish poisoning, secreted by red algae and diatoms. As a glutamate analogue, DA accumulates in filter-feeding marine organisms, posing significant health risks to humans upon consumption. Detecting DA in marine environments remains challenging due to its low concentration and interference from complex matrices. Effective detection and removal require materials with high efficiency and selectivity, which traditional inorganic ionic materials lack due to their limited adsorption capacity and selectivity. Ionic covalent organic frameworks (iCOFs) expected to become highly efficient DA adsorbents due to tunable ionic sites. Thus, a zwitterionic covalent organic nanosheet (TGDB-iCONs) was synthesized to selectively capture DA. TGDB-iCONs was prepared by one-step Schiff-base reaction of the charged monomer triaminoguanidine hydrochloride. It uniformly distributed positively charged guanidinium and negatively charged chloride ions on the surface, forming zwitterionic binding sites. The self-peeling of TGDB-iCONs facilitated the exposure of active sites and improved the adsorption efficiency. Several binding forces were generated between TGDB-iCONs and DA, including complementary electrostatic hydrophilic interactions, which were verified by density functional theory (DFT) calculation. TGDB-iCONs exhibited ultra-fast adsorption kinetics (7 min) and relatively high adsorption capacity (66.48 mg/g) for DA. Furthermore, TGDB-iCONs exhibit strong salt resistance, which is attributed to the charge "shielding" effect of the zwitterionic ions present in TGDB-iCONs. TGDB-iCONs could highly selectively enrich DA and detect trace DA from marine environment including seawater, algae and marine organisms and the limit of detection as low as 0.3 ng/kg. This comprehensive study not only sheds light on the vast potential of ionic covalent organic frameworks nanosheets (iCONs) in supporting early warning, control, and traceability of DA, but also lays a solid foundation for future research endeavors aimed at designing and harnessing the unique properties of iCONs.
title Zwitterionic covalent organic nanosheets for selective analysis of domoic acid in marine environment.
topic Kainic Acid
Nanostructures
Adsorption
Metal-Organic Frameworks
Water Pollutants, Chemical
Density Functional Theory
Limit of Detection
url https://pubmed.ncbi.nlm.nih.gov/39532426/