Ferrocene-Encapsulated Zn Zeolitic Imidazole Framework (ZIF-8) for Optical and Electrochemical Sensing of Amyloid-β Oligomers and for the Early Diagnosis of Alzheimer’s Disease
Source abstract
Abstract
In this work, the ferrocene-encapsulated Zn zeolitic imidazole framework (ZIF-8) was prepared by the self-assembly of Zn ions and 2-methylimidazole and used for the dual detection of amyloid-beta oligomers (AβO), which is the main neuropathological hallmark of Alzheimer’s disease. Ferrocene is an optically and electrochemically active signal which was successfully encapsulated inside of the ZIF-8 and released by the competitive coordination between Zn ions and AβO after being treated with AβO. The released ferrocene content was monitored by ultraviolet/visible spectrophotometry and cyclic voltammetry. The dual determination of AβO played a synergetic role in the quick qualitative and precise quantitative analyses in a wide detection range of 10–5 to 102 μM and good feasibility in artificial cerebrospinal fluid.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Molecular Sensors and Ion Detection · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering, Sungkyunkwan University, 16419 Suwon, Korea
Funding
National Research Foundation of Korea
References (28)
Show source-provided references
1. 10.1002/smll.20180267010.1002/smll.201802670 ↗
2. 10.1016/j.biomaterials.2019.01.00110.1016/j.biomaterials.2019.01.001 ↗
3. 10.1021/acsami.8b0786810.1021/acsami.8b07868 ↗
4. 10.1021/ja109900610.1021/ja1099006 ↗
5. 10.1021/ja909263x10.1021/ja909263x ↗
6. 10.1039/c5cs00837a10.1039/c5cs00837a ↗
7. 10.1021/acsami.7b1652210.1021/acsami.7b16522 ↗
8. 10.1021/jacs.7b0122910.1021/jacs.7b01229 ↗
9. 10.1002/smll.20170428210.1002/smll.201704282 ↗
10. 10.1039/c7tb02240a10.1039/c7tb02240a ↗
11. 10.1021/bi011568310.1021/bi0115683 ↗
12. 10.1016/S0162-0134(99)00090-210.1016/S0162-0134(99)00090-2 ↗
13. 10.3390/antib502001310.3390/antib5020013 ↗
14. 10.1021/jp075168m10.1021/jp075168m ↗
15. 10.1039/c0mt00073f10.1039/c0mt00073f ↗
16. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
17. 10.1016/j.bios.2018.04.06110.1016/j.bios.2018.04.061 ↗
18. 10.1002/ejic.20120003810.1002/ejic.201200038 ↗
19. 10.1016/j.jelechem.2014.03.02610.1016/j.jelechem.2014.03.026 ↗
20. 10.1039/b917150a10.1039/b917150a ↗
21. 10.1021/acs.jchemed.7b0036110.1021/acs.jchemed.7b00361 ↗
22. 10.1039/c4mt00016a10.1039/c4mt00016a ↗
23. 10.1002/smll.20140259310.1002/smll.201402593 ↗
24. 10.1038/srep3518610.1038/srep35186 ↗
25. 10.1039/c6ay01910b10.1039/c6ay01910b ↗
26. 10.1016/j.bios.2016.05.06610.1016/j.bios.2016.05.066 ↗
27. 10.1016/j.bios.2015.08.00810.1016/j.bios.2015.08.008 ↗
28. 10.1016/j.snb.2018.07.07810.1016/j.snb.2018.07.078 ↗