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β-Cyclodextrin functionalized persistent luminescence nanoparticle for autofluorescence-free detection of α-glucosidase activity and its inhibitor
A autofluorescence-free sensing strategy based on β-cyclodextrin functionalized persistent luminescence nanoparticle is developed for detection of α-glucosidase activity and its inhibitor with high selectivity and sensitivity. [Display omitted] •A persistent luminescence nanoprobe PLNP-β-CD is prepa...
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Published in: | Microchemical journal 2024-12, Vol.207, p.112211, Article 112211 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | A autofluorescence-free sensing strategy based on β-cyclodextrin functionalized persistent luminescence nanoparticle is developed for detection of α-glucosidase activity and its inhibitor with high selectivity and sensitivity.
[Display omitted]
•A persistent luminescence nanoprobe PLNP-β-CD is prepared.•Nanoprobe leads to sensing without autofluorescence interference.•The detection system provides high selectivity and sensitivity.•The method permits α-glucosidase and its inhibitor detection.
The development of simple, selective and sensitive analytical methods to effectively monitor α-glucosidase (α-Glu) and discover its new inhibitors is very critical for the diagnosis and treatment of diabetes. Herein, an autofluorescence-free sensing method based on β-cyclodextrin (β-CD) functionalized persistent luminescence nanoparticle (PLNP) is established for the detection of α-Glu activity and its inhibitor. The p-nitrophenol (PNP) produced by the hydrolysis of substrate p-nitrobenzene-α-D-glucopyranoside (PNPG) by α-Glu in the system can be selectively captured by the β-CD on the nanoprobe to form adducts through the host guest effect between them, resulting in persistent luminescence quenching due to electron transfer (ET) effect. The proposed method provides a good linear relationship within the range of 5–80 U/L and a low detection limit of 0.9 U/L, and can detect α-Glu in human serum with the recovery rate of 95.4–103.3 %. Furthermore, the detection system can measure the inhibitory ability of acarbose with an IC50 value of 349 μM, proving its good potential for application. |
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ISSN: | 0026-265X |
DOI: | 10.1016/j.microc.2024.112211 |