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Oligosaccharide Sensing Using Fluorophore-Probed Curdlans in Aqueous Media AITranslate

Osaka University; Tokyo Institute of Technology; Kyoto Prefectural University; Tokyo Institute of Technology
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Publisher: ACS
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Abstract AITranslate

Saccharide sensing in aqueous media has recently garnered considerable attention in supramolecular and analytical chemistry; however, it still faces significant challenges. Herein, we report oligosaccharide sensing using the designed and synthesized fluorophore-probed curdlans. Aggregation-induced emission of the tetraphenylethylene (TPE) chromophore is a powerful candidate for outputting fluorescence signals upon the addition of the target oligosaccharide acarbose. Among the saccharides tested, the TPE-Cur chemosensors simultaneously exhibited high sensitivity and excellent selectivity toward acarbose. Morphological studies using atomic force microscopy, dynamic light scattering, fluorescence spectroscopy, and lifetime measurements revealed the importance of globule-to-coaggregation conversion upon oligosaccharide incorporation into the dynamic hydrogen-bonding networks of the curdlan string. This study provides perspectives for saccharide-responsive materials that are an attractive alternative to conventional chemosensors, which are difficult to sense in aqueous media.

KeyWords AITranslate

oligosaccharide sensing curdlan aggregationinduced emission tetraphenylethylene fluorescence chemosensor
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.2c02251

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Citation Information:

Saccharide sensing in aqueous media has recently garnered considerable attention in supramolecular and analytical chemistry; however, it still faces significant challenges. Herein, we report oligosaccharide sensing using the designed and synthesized fluorophore-probed curdlans. Aggregation-induced emission of the tetraphenylethylene (TPE) chromophore is a powerful candidate for outputting fluorescence signals upon the addition of the target oligosaccharide acarbose. Among the saccharides tested, the TPE-Cur chemosensors simultaneously exhibited high sensitivity and excellent selectivity toward acarbose. Morphological studies using atomic force microscopy, dynamic light scattering, fluorescence spectroscopy, and lifetime measurements revealed the importance of globule-to-coaggregation conversion upon oligosaccharide incorporation into the dynamic hydrogen-bonding networks of the curdlan string. This study provides perspectives for saccharide-responsive materials that are an attractive alternative to conventional chemosensors, which are difficult to sense in aqueous media.

quote

GB/T 7714-2015 [1] Hiroki Kurohara, Yumiko Hori, Munenori Numata, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.2c02251.
MLA [1] Hiroki Kurohara, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.2c02251.
APA [1] Hiroki Kurohara, Yumiko Hori, Munenori Numata, & Gaku Fukuhara. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.2c02251
IEEE [1] Hiroki Kurohara, Yumiko Hori, Munenori Numata, and Gaku Fukuhara, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.2c02251. keywords: {oligosaccharide sensing;curdlan;aggregationinduced emission;tetraphenylethylene;fluorescence chemosensor}