journal article·2019-11-08

“Turn-On” Fluorescence Determination of β-Glucosidase Activity Using Fluorescent Polymer Nanoparticles Formed from Polyethylenimine Cross-Linked with Hydroquinone

Jinshui Liu, Huijuan Bao, Chenfu Liu, Fangfei Wu, Feng Gao

ACS Applied Polymer Materials· Volume 1· Issue 11
Publisher page

Abstract

β-Glucosidase is associated with many diseases, so it is important to be able to accurately determine β-glucosidase activity. Here, we describe a turn-on fluorescence method for sensitively determining β-glucosidase activity. The method involves the formation of water-soluble fluorescent polymer nanoparticles. β-Glucosidase initially hydrolyzes the β-arbutin substrate to release hydroquinone (1,4-dihydroxybenzene). The hydroquinone then forms cross-links between branched polyethylenimine molecules to give fluorescent water-soluble polymer nanoparticles. The polymer nanoparticles were found to fluoresce with excitation and emission peaks at 373 and 510 nm, respectively, and the fluorescence intensity was related to the β-glucosidase activity. The fluorescence intensity could therefore be used to determine the β-glucosidase activity. The lowest β-glucosidase activity that could be determined was 0.4 U L–1, and the dynamic linear range was 1.0–36.0 U L–1. The method was very selective for β-glucosidase activity and was not sensitive to other proteins. The method was successfully used to determine β-glucosidase in spiked samples containing human serum albumin at a concentration of 0.5%, and the recoveries were 95.2%–104.5%.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Electrochemical sensors and biosensors · Neonatal Health and Biochemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Chemistry and Materials Science, Anhui Key Laboratory of Chemo/Biosensing, The Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-based Materials, Anhui Normal University, Wuhu 241000, China

School of Pharmaceutical Sciences, Gannan Medical University, Ganzhou 341000, China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Anhui Province

References (40)

Show source-provided references
1. 10.1039/C8TB03230K10.1039/C8TB03230K ↗
2. 10.1021/acssensors.6b0034110.1021/acssensors.6b00341 ↗
3. 10.1021/acssensors.8b0113010.1021/acssensors.8b01130 ↗
4. 10.1021/acssensors.8b0047110.1021/acssensors.8b00471 ↗
5. 10.1021/acs.bioconjchem.9b0039110.1021/acs.bioconjchem.9b00391 ↗
6. 10.4067/S0718-9516201700030001810.4067/S0718-95162017000300018 ↗
7. 10.1016/j.bios.2015.12.09410.1016/j.bios.2015.12.094 ↗
8. 10.1016/j.bios.2015.07.02310.1016/j.bios.2015.07.023 ↗
9. 10.1039/C6RA06062E10.1039/C6RA06062E ↗
10. 10.1016/j.biopha.2017.04.11310.1016/j.biopha.2017.04.113 ↗
11. 10.1016/j.ejbt.2017.08.01010.1016/j.ejbt.2017.08.010 ↗
12. 10.1002/jib.41810.1002/jib.418 ↗
13. 10.1016/j.bios.2014.09.02310.1016/j.bios.2014.09.023 ↗
14. 10.1016/j.snb.2016.04.08610.1016/j.snb.2016.04.086 ↗
15. 10.1021/ac102095j10.1021/ac102095j ↗
16. 10.1021/acsnano.6b0594910.1021/acsnano.6b05949 ↗
17. 10.1021/acs.accounts.8b0024210.1021/acs.accounts.8b00242 ↗
18. 10.1007/s12274-018-2135-410.1007/s12274-018-2135-4 ↗
19. 10.1039/C7PY01579H10.1039/C7PY01579H ↗
20. 10.1039/C6NR01909A10.1039/C6NR01909A ↗
21. 10.1016/j.polymer.2017.02.03910.1016/j.polymer.2017.02.039 ↗
22. 10.1039/C4CC05806B10.1039/C4CC05806B ↗
23. 10.1016/j.bios.2018.03.02810.1016/j.bios.2018.03.028 ↗
24. 10.1002/anie.20150495110.1002/anie.201504951 ↗
25. 10.1021/acs.jpcc.6b1269510.1021/acs.jpcc.6b12695 ↗
26. 10.1007/s00604-016-1747-110.1007/s00604-016-1747-1 ↗
27. 10.1016/j.talanta.2015.06.01410.1016/j.talanta.2015.06.014 ↗
28. 10.1021/ja300724x10.1021/ja300724x ↗
29. 10.1039/C6GC01820C10.1039/C6GC01820C ↗
30. 10.1016/j.bios.2016.04.04710.1016/j.bios.2016.04.047 ↗
31. 10.1021/acsami.6b0740710.1021/acsami.6b07407 ↗
32. 10.1039/C7GC01236E10.1039/C7GC01236E ↗
33. 10.1039/C7TC03314A10.1039/C7TC03314A ↗
34. 10.1016/j.mtchem.2017.09.00110.1016/j.mtchem.2017.09.001 ↗
35. 10.1002/chem.20180271210.1002/chem.201802712 ↗
36. 10.1016/j.molliq.2017.08.11910.1016/j.molliq.2017.08.119 ↗
37. 10.1007/s00604-018-3149-z10.1007/s00604-018-3149-z ↗
38. 10.1021/acsapm.8b0016210.1021/acsapm.8b00162 ↗
39. 10.1631/jzus.B180041610.1631/jzus.B1800416 ↗
40. 10.6023/cjoc20180301110.6023/cjoc201803011 ↗