journal article·2023-01-27

Nanozymes from Cu(II) Metal–Organic Gel and Melamine for Highly Active Peroxidase-Like Activity to Detect Alkaline Phosphatase

Yunfei Song, Chengzhi Huang, Yuanfang Li

ACS Applied Nano Materials· Volume 6· Issue 2
Publisher page

Abstract

Enzyme-like catalytic activity and efficiency of carbon-based nanomaterials are closely linked to their size, heteroatom composition, and structure, and hence the heteroatom regulation needs to be further explored. In this work, a simple and efficient strategy was proposed to develop Cu-doped 2D carbon material C 3 N 4 (Cu-C 3 N 4 -550) with excellent catalytic performance by pyrolyzing precursors of Cu(II) metal–organic gel (MOG) and melamine directly. Due to its sufficient metal active sites and adequate specific surface areas, the as-prepared Cu-C 3 N 4 -550 was endowed with excellent peroxidase-like activity to promote the oxidation of 3,3′,5,5′-tetramethylbenzidine owing to the generation of • OH in the catalytic reaction. It was amazing to find that the peroxidase mimic activity of the prepared Cu-C 3 N 4 -550 has enhanced 32.3-fold compared with bare C 3 N 4 . High peroxidase-like activity of Cu-C 3 N 4 -550 was influenced severely by the addition of antioxidant ascorbic acid (AA), alkaline phosphatase (ALP) as a typical hydrolase could catalyze substrate 2-phospho- l -ascorbic acid into AA, while AA was capable of capturing • OH generated from the catalytic reaction of Cu-C 3 N 4 -550. Hence, a sensitive, selective, and colorimetric method for the detection of ALP was established, the linear concentration of ALP in this colorimetric sensor from 0.4 to 20 U/L was acquired with a low detection limit of 0.32 U/L. This work not only provides ideas for designing enhanced peroxidase-like activity nanozymes in practical biological analysis but also broadens the MOG derivatives and carbon-based nanomaterials in colorimetric applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Nanomaterials in Catalysis · Electrochemical sensors and biosensors · Advanced biosensing and bioanalysis techniques

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

Affiliations

Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing400715, P. R. China

Key Laboratory of Luminescent and Real-Time Analytical System (Southwest University), Chongqing Science and Technology Bureau, College of Pharmaceutical Sciences, Southwest University, Chongqing400715, P. R. China

Funding

National Natural Science Foundation of China

References (51)

Show source-provided references
1. 10.1021/acs.accounts.9b0014010.1021/acs.accounts.9b00140 ↗
2. 10.1002/admi.20220092810.1002/admi.202200928 ↗
3. 10.1016/j.ccr.2021.21417010.1016/j.ccr.2021.214170 ↗
4. 10.1038/nnano.2007.26010.1038/nnano.2007.260 ↗
5. 10.1007/s11427-016-5044-310.1007/s11427-016-5044-3 ↗
6. 10.1002/chem.20190228810.1002/chem.201902288 ↗
7. 10.1021/acsami.5b0002310.1021/acsami.5b00023 ↗
8. 10.1016/j.bios.2014.03.02310.1016/j.bios.2014.03.023 ↗
9. 10.1039/c7cc09819g10.1039/c7cc09819g ↗
10. 10.1038/s41929-021-00609-x10.1038/s41929-021-00609-x ↗
11. 10.1016/j.bios.2013.03.05710.1016/j.bios.2013.03.057 ↗
12. 10.1002/chem.20090264310.1002/chem.200902643 ↗
13. 10.1039/c1cc11943e10.1039/c1cc11943e ↗
14. 10.1002/adma.20090378310.1002/adma.200903783 ↗
15. 10.1039/d0cc01840f10.1039/d0cc01840f ↗
16. 10.1039/c3nr03693f10.1039/c3nr03693f ↗
17. 10.1007/s12274-017-1426-510.1007/s12274-017-1426-5 ↗
18. 10.1021/acsami.0c0178910.1021/acsami.0c01789 ↗
19. 10.1002/anie.20160480210.1002/anie.201604802 ↗
20. 10.1021/acssuschemeng.1c0263510.1021/acssuschemeng.1c02635 ↗
21. 10.1021/acssuschemeng.1c0072310.1021/acssuschemeng.1c00723 ↗
22. 10.1021/acsanm.9b0103610.1021/acsanm.9b01036 ↗
23. 10.1021/acsabm.9b0088310.1021/acsabm.9b00883 ↗
24. 10.1016/j.snb.2021.12954910.1016/j.snb.2021.129549 ↗
25. 10.1021/acsaem.9b0086710.1021/acsaem.9b00867 ↗
26. 10.1002/cjoc.20210015810.1002/cjoc.202100158 ↗
27. 10.1039/c6cc01955b10.1039/c6cc01955b ↗
28. 10.1039/c2cs35407a10.1039/c2cs35407a ↗
29. 10.1002/ejic.20180081110.1002/ejic.201800811 ↗
30. 10.1021/acssuschemeng.7b0301510.1021/acssuschemeng.7b03015 ↗
31. 10.1002/cssc.20190019410.1002/cssc.201900194 ↗
32. 10.1039/c7cc00665a10.1039/c7cc00665a ↗
33. 10.1039/d0an01846e10.1039/d0an01846e ↗
34. 10.1016/j.jes.2019.06.00610.1016/j.jes.2019.06.006 ↗
35. 10.1021/acssuschemeng.1c0041910.1021/acssuschemeng.1c00419 ↗
36. 10.3390/polym1209196310.3390/polym12091963 ↗
37. 10.1016/j.apcatb.2017.03.04110.1016/j.apcatb.2017.03.041 ↗
38. 10.1021/acssuschemeng.0c0382210.1021/acssuschemeng.0c03822 ↗
39. 10.1016/j.apcatb.2019.11834710.1016/j.apcatb.2019.118347 ↗
40. 10.1016/j.nantod.2020.10097110.1016/j.nantod.2020.100971 ↗
41. 10.1002/adfm.20200109710.1002/adfm.202001097 ↗
42. 10.1021/jacs.7b0651410.1021/jacs.7b06514 ↗
43. 10.1016/j.talanta.2022.12345110.1016/j.talanta.2022.123451 ↗
44. 10.1002/anie.20160550910.1002/anie.201605509 ↗
45. 10.1021/acsami.0c0176310.1021/acsami.0c01763 ↗
46. 10.1021/acs.analchem.9b0051210.1021/acs.analchem.9b00512 ↗
47. 10.1021/acssensors.6b0050010.1021/acssensors.6b00500 ↗
48. 10.1016/j.foodchem.2022.13241210.1016/j.foodchem.2022.132412 ↗
49. 10.1021/acsanm.1c0122010.1021/acsanm.1c01220 ↗
50. 10.1021/acsami.1c2157810.1021/acsami.1c21578 ↗
51. 10.1016/j.snb.2020.12802310.1016/j.snb.2020.128023 ↗