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A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions

Guanosine-based supramolecular hydrogels are particularly of interest for biomaterial and biomedical purposes, as they are generally biocompatible and stimuli-responsive. We found a strong and long-life transparent hydrogel made by mixing guanosine (G) with 1 equiv. of 2-formylbenzeneboronic acid (2...

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Detalles Bibliográficos
Autores principales: Qiao, Hongwei, Bai, Jiakun, Zhang, Sichun, Li, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055885/
https://www.ncbi.nlm.nih.gov/pubmed/35520041
http://dx.doi.org/10.1039/d0ra05254j
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author Qiao, Hongwei
Bai, Jiakun
Zhang, Sichun
Li, Chao
author_facet Qiao, Hongwei
Bai, Jiakun
Zhang, Sichun
Li, Chao
author_sort Qiao, Hongwei
collection PubMed
description Guanosine-based supramolecular hydrogels are particularly of interest for biomaterial and biomedical purposes, as they are generally biocompatible and stimuli-responsive. We found a strong and long-life transparent hydrogel made by mixing guanosine (G) with 1 equiv. of 2-formylbenzeneboronic acid (2FPB) and KOH. Alkali cations can assist the stacking of individual G-quartet to give extended nanowires, but only K(+) ion induces the formation of a stable and self-supporting network hydrogel for a couple of months. Data from variable temperature NMR indicated that guanosine 2-formylbenzeneborate ester and G are the key components of the self-assembly. Further, G-2FPB-K(+) hydrogel solution can induce berberine (BBR) fluorescence, showing high selectivity to K(+) ion and anti-ion interference capability. A good linear relationship between fluorescent intensity and K(+) concentration allowed us to directly detect K(+) levels in human blood serum.
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spelling pubmed-90558852022-05-04 A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions Qiao, Hongwei Bai, Jiakun Zhang, Sichun Li, Chao RSC Adv Chemistry Guanosine-based supramolecular hydrogels are particularly of interest for biomaterial and biomedical purposes, as they are generally biocompatible and stimuli-responsive. We found a strong and long-life transparent hydrogel made by mixing guanosine (G) with 1 equiv. of 2-formylbenzeneboronic acid (2FPB) and KOH. Alkali cations can assist the stacking of individual G-quartet to give extended nanowires, but only K(+) ion induces the formation of a stable and self-supporting network hydrogel for a couple of months. Data from variable temperature NMR indicated that guanosine 2-formylbenzeneborate ester and G are the key components of the self-assembly. Further, G-2FPB-K(+) hydrogel solution can induce berberine (BBR) fluorescence, showing high selectivity to K(+) ion and anti-ion interference capability. A good linear relationship between fluorescent intensity and K(+) concentration allowed us to directly detect K(+) levels in human blood serum. The Royal Society of Chemistry 2020-08-03 /pmc/articles/PMC9055885/ /pubmed/35520041 http://dx.doi.org/10.1039/d0ra05254j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Qiao, Hongwei
Bai, Jiakun
Zhang, Sichun
Li, Chao
A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title_full A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title_fullStr A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title_full_unstemmed A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title_short A guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to K(+) ions
title_sort guanosine-based 2-formylphenylborate ester hydrogel with high selectivity to k(+) ions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055885/
https://www.ncbi.nlm.nih.gov/pubmed/35520041
http://dx.doi.org/10.1039/d0ra05254j
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