journal article·2017-09-13

Potential-Resolved Electrochemiluminescence for Simultaneous Determination of Triple Latent Tuberculosis Infection Markers

Bin Zhou, Mingyao Zhu, Yan Hao, Peihui Yang

Publisher page

Abstract

A novel electrochemiluminescence (ECL) immunosensor based on the potential-resolved strategy was first developed for simultaneous determination of triple latent tuberculosis infection (LTBI) markers with high sensitivity, interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), and interleukin (IL)-2. In this work, luminol and self-prepared carbon quantum dots and CdS quantum dots were integrated onto gold nanoparticles and magnetic beads in sequence to fabricate potential-resolved ECL nanoprobes with signal amplification. IFN-γ-antibody (Ab)1, TNF-α-Ab1, and IL-2-Ab1 were separately immobilized on three spatially resolved areas of a patterned indium tin oxide electrode to capture the corresponding LTBI markers, which were further recognized by IFN-γ-Ab2, TNF-α-Ab2, and IL-2-Ab2-functionalized ECL nanoprobes. The binding reaction of antibody-functionalized ECL nanoprobes and the captured LTBI markers will generate three sensitive and potential-resolved ECL signals during one potential scanning, and the ECL intensities reflect the concentrations of IFN-γ, TNF-α, and IL-2 in the range of 1.6–200 pg mL –1 . Therefore, the multiplexed ECL immunosensor provided an effective approach for simultaneous detection of triple LTBI markers in human serum, so it will be beneficial to facilitate more accurate and reliable clinical diagnosis for LTBI.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Tuberculosis Research and Epidemiology · Biosensors and Analytical Detection

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

Affiliations

Department of Chemistry, Jinan University, Guangzhou 510632, PR China

Funding

National Natural Science Foundation of China

References (28)

Show source-provided references
1. 10.1016/S0140-6736(10)60359-510.1016/S0140-6736(10)60359-5 ↗
2. 10.1016/S2213-2600(15)00063-610.1016/S2213-2600(15)00063-6 ↗
3. 10.1183/09031936.0021401410.1183/09031936.00214014 ↗
4. WHO · 2016
5. 10.1164/rccm.200606-759OC10.1164/rccm.200606-759OC ↗
6. 10.1016/S1473-3099(04)01206-X10.1016/S1473-3099(04)01206-X ↗
7. 10.1136/thx.2009.12755510.1136/thx.2009.127555 ↗
8. 10.1371/journal.pone.001236510.1371/journal.pone.0012365 ↗
9. 10.1016/j.jinf.2015.04.03210.1016/j.jinf.2015.04.032 ↗
10. 10.1016/j.tube.2016.06.00110.1016/j.tube.2016.06.001 ↗
11. 10.1093/infdis/168.4.105610.1093/infdis/168.4.1056 ↗
12. 10.1164/rccm.200211-1359OC10.1164/rccm.200211-1359OC ↗
13. 10.1016/j.bios.2014.09.08510.1016/j.bios.2014.09.085 ↗
14. 10.1021/acsami.7b0321110.1021/acsami.7b03211 ↗
15. 10.1164/rccm.200402-179OC10.1164/rccm.200402-179OC ↗
16. 10.1021/ac101409t10.1021/ac101409t ↗
17. 10.1016/j.bios.2013.09.04610.1016/j.bios.2013.09.046 ↗
18. 10.1016/j.bios.2014.05.02910.1016/j.bios.2014.05.029 ↗
19. Huang H. X. · Int. J. Electrochem. Sci. · 2015 · 10 · 258010.1016/S1452-3981(23)04869-1 ↗
20. 10.1016/j.bios.2014.08.03410.1016/j.bios.2014.08.034 ↗
21. 10.1007/s10008-015-2936-210.1007/s10008-015-2936-2 ↗
22. 10.1016/j.msec.2015.10.06610.1016/j.msec.2015.10.066 ↗
23. 10.1007/s00604-016-1804-910.1007/s00604-016-1804-9 ↗
24. 10.1016/j.bios.2015.03.03610.1016/j.bios.2015.03.036 ↗
25. 10.1021/acsami.6b1241110.1021/acsami.6b12411 ↗
26. 10.1083/jcb.20021014010.1083/jcb.200210140 ↗
27. 10.1021/ja310317n10.1021/ja310317n ↗
28. 10.1016/j.bios.2013.04.03210.1016/j.bios.2013.04.032 ↗