Bimetallic Cu@Co-MOFs Mimic Peroxidase for Colorimetric Detection of Glutathione
Source abstract
Abstract
Nanozyme possess the advantages of high enzyme simulation activity, low cost, and excellent stability. As a substitute for natural enzymes, nanozyme have demonstrated significant potential in various fields. In this study, a bimetallic organometallic framework Cu@Co-MOFs was synthesized via the hydrothermal method using terephthalic acid (H 2 BDC) as a ligand and characterized. Cu@Co-MOFs exhibits outstanding peroxidase activity (POD) by catalyzing the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) and other color-developing substrates through •OH formation. A simple, rapid, and reliable colorimetric method for quantitatively detecting glutathione (GSH) was developed based on the Pod-like activity of Cu@Co-MOFs. The linear range of this method was 1–1200 μM with a detection limit of 0.72 μM. This work not only proposes a bimetallic organic framework with high POD as a straightforward and practical platform for visually detecting GSH but also provides a strategy to enhance the performance of nanomaterials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Nanomaterials in Catalysis · Advanced biosensing and bioanalysis techniques · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Public Health, General Hospital of Ningxia Medical University
Ningxia Medical University
Funding
Key Research and Development Program of Ningxia · Chunhui Project Foundation of the Education Department of China
References (54)
Show source-provided references
1. 10.1016/bs.vh.2022.09.00210.1016/bs.vh.2022.09.002 ↗
2. 10.1016/0304-3940(92)90355-B10.1016/0304-3940(92)90355-B ↗
3. 10.1016/S0891-5849(01)00530-510.1016/S0891-5849(01)00530-5 ↗
4. 10.1016/S1043-6618(02)00320-110.1016/S1043-6618(02)00320-1 ↗
5. 10.1016/j.jphotochem.2022.11426410.1016/j.jphotochem.2022.114264 ↗
6. 10.1002/slct.20170084510.1002/slct.201700845 ↗
7. 10.1039/c4cc03329a10.1039/c4cc03329a ↗
8. 10.1016/j.talanta.2017.11.04410.1016/j.talanta.2017.11.044 ↗
9. 10.1039/C6AY01575A10.1039/C6AY01575A ↗
10. 10.3390/foods1313212710.3390/foods13132127 ↗
11. 10.1016/j.cej.2024.15061210.1016/j.cej.2024.150612 ↗
12. 10.1021/acs.accounts.9b0014010.1021/acs.accounts.9b00140 ↗
13. 10.1002/INMD.2023002010.1002/INMD.20230020 ↗
14. 10.1016/j.snb.2023.13490310.1016/j.snb.2023.134903 ↗
15. 10.1016/j.mtbio.2023.10063810.1016/j.mtbio.2023.100638 ↗
16. 10.1007/s40820-023-01047-z10.1007/s40820-023-01047-z ↗
17. 10.1016/j.ijhydene.2023.03.18510.1016/j.ijhydene.2023.03.185 ↗
18. 10.3390/ijms2409781910.3390/ijms24097819 ↗
19. 10.1039/C9QI01564G10.1039/C9QI01564G ↗
20. 10.1039/D2NJ01994A10.1039/D2NJ01994A ↗
21. 10.1021/ic400844v10.1021/ic400844v ↗
22. 10.1002/chem.20140609810.1002/chem.201406098 ↗
23. 10.1039/C9RA02372K10.1039/C9RA02372K ↗
24. 10.1002/elan.20206056610.1002/elan.202060566 ↗
25. 10.1016/j.cej.2021.12866910.1016/j.cej.2021.128669 ↗
26. 10.1016/j.foodchem.2024.13878810.1016/j.foodchem.2024.138788 ↗
27. 10.1039/C9RA01143A10.1039/C9RA01143A ↗
28. 10.1039/D1NJ05569K10.1039/D1NJ05569K ↗
29. 10.1016/j.cej.2018.09.17410.1016/j.cej.2018.09.174 ↗
30. 10.1016/j.bios.2014.07.05810.1016/j.bios.2014.07.058 ↗
31. 10.1016/j.ceramint.2015.12.10110.1016/j.ceramint.2015.12.101 ↗
32. 10.1016/j.snb.2020.12941210.1016/j.snb.2020.129412 ↗
33. 10.1007/s11581-020-03651-010.1007/s11581-020-03651-0 ↗
34. 10.1016/j.jhazmat.2016.06.05810.1016/j.jhazmat.2016.06.058 ↗
35. 10.1016/j.apcatb.2016.09.00510.1016/j.apcatb.2016.09.005 ↗
36. 10.1002/adfm.20170345510.1002/adfm.201703455 ↗
37. 10.1021/acsanm.2c0453310.1021/acsanm.2c04533 ↗
38. 10.1038/nnano.2007.26010.1038/nnano.2007.260 ↗
39. 10.1007/s00604-022-05311-810.1007/s00604-022-05311-8 ↗
40. 10.1016/j.bios.2019.11145010.1016/j.bios.2019.111450 ↗
41. 10.1016/j.colsurfb.2023.11358910.1016/j.colsurfb.2023.113589 ↗
42. 10.1021/acsami.9b0300410.1021/acsami.9b03004 ↗
43. 10.1021/acs.analchem.3c0107010.1021/acs.analchem.3c01070 ↗
44. 10.1016/j.inoche.2023.11101110.1016/j.inoche.2023.111011 ↗
45. 10.1155/2018/197968410.1155/2018/1979684 ↗
46. 10.1021/acs.analchem.8b0447810.1021/acs.analchem.8b04478 ↗
47. 10.1016/j.jssc.2018.11.03210.1016/j.jssc.2018.11.032 ↗
48. 10.1016/j.cej.2021.13307910.1016/j.cej.2021.133079 ↗
49. 10.1016/j.snb.2020.12911510.1016/j.snb.2020.129115 ↗
50. 10.1039/C1AN15718C10.1039/C1AN15718C ↗
51. 10.1021/acsami.0c0176310.1021/acsami.0c01763 ↗
52. 10.1021/ac400770510.1021/ac4007705 ↗
53. 10.1016/j.snb.2021.12963810.1016/j.snb.2021.129638 ↗
54. 10.1016/j.snb.2018.07.09110.1016/j.snb.2018.07.091 ↗