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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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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 |
Sumario: | 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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