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Hexagonal Cobalt Oxyhydroxide–Carbon Dots Hybridized Surface: High Sensitive Fluorescence Turn-on Probe for Monitoring of Ascorbic Acid in Rat Brain Following Brain Ischemia
Abstract
In this study, we report a novel and efficient fluorescence probe synthesized by Tris(hydroxymethyl)aminomethane-derived carbon dots (CDs)-modified hexagonal cobalt oxyhydroxide(CoOOH) nanoflakes (Tris-derived CDs-CoOOH) for monitoring of cerebral ascorbic acid (AA) in brain microdialysate. The as-prepared Tris-derived CDs with the fluorescence quantum yield of 7.3% are prepared by a one-step pyrolysis strategy of the sole precursor and used as the signal output. After being hybridized with CoOOH nanoflakes to form Tris-derived CDs-CoOOH, the luminescence of the Tris-derived CDs can be efficiently quenched by CoOOH via fluorescence resonance energy transfer (FRET). Due to the specific redox reaction between the enediol group of AA and hexagonal CoOOH nanoflakes, AA can reduce the hexagonal CoOOH nanoflakes in the Tris-derived CDs-CoOOH and lead to collapse of the hybrized structure, then the release of Tris-derived CDs, and thus finally the fluorescence recovery. Moreover, cobalt ions (II), generated by CoOOH nanoflakes oxidizing AA, almost have no obvious interference on the fluorescence probe, i.e., Tris-derived CDs, which could be ascribed to the surface of Tris-derived CDs containing a few strong chelation groups such as amino/carboxyl/thiol groups, instead of plenty of -OH groups with weak chelation with Co(2+). On the basis of this feature, the Tris-derived CDs-CoOOH fluorescent probe demonstrates a linear range from 100 nM to 20 μM with the detection limit of ∼50 nM, i.e., with an improved sensitivity toward AA detection. Compared with other turn-on fluorescent methods using convenient fluorophore-nitroxide fluorescent probes for detection of AA, the method demonstrated here possesses a facial synthesis route, lower limit of detection, and wider linear range, which validates sensing of AA in the cerebral systems during the calm/ischemia process. This study provides a fluorescence assay for the simple yet facial detection of AA in the cerebral systems and assists in the understanding of the biological processes in the physiological and pathological study.
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Cites
Applications of Nanoparticles in Biology
De, M., Ghosh, P. S., & Rotello, V. M. (2008) · Advanced Materials · doi:10.1002/adma.200703183 · Cited by 1,547
Gazdik, Z., Zitka, O., Petrlova, J., Adam, V., Zehnalek, J., Horna, A., Reznicek, V., Beklova, M., & Kizek, R. (2008) · Sensors · doi:10.3390/s8117097 · Cited by 170
Cited by
The quenching of the fluorescence of carbon dots: A review on mechanisms and applications
Zu, F., Yan, F., Bai, Z., Xu, J., Wang, Y., Huang, Y., & Zhou, X. (2017) · Microchimica Acta · doi:10.1007/s00604-017-2318-9 · Cited by 1,602
Self-citationQi, H., Teng, M., Liu, M., Liu, S., Li, J., Yu, H., Teng, C., Huang, Z., Liu, H., Shao, Q., et al. (2019) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2018.12.047 · Cited by 640
Li, L., & Dong, T. (2018) · Journal of Materials Chemistry C · doi:10.1039/c7tc05878k · Cited by 452
Self-citationZhu, X., Zhao, T., Nie, Z., Liu, Y., & Yao, S. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b02167 · Cited by 265
Zhang, Q., He, D., Li, X., Feng, W., Lyu, C., & Zhang, Y. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2019.121350 · Cited by 264
Metadata
- Authors
- Li, L., Wang, C., Liu, K., Wang, Y., Liu, K., & Lin, Y.
- Venue
- Analytical Chemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 2015-03-04
- Volume
- 87
- Issue
- 6
- Pages
- 3404-3411
- ISSN
- 0003-2700 (ISSN-L)
- 1520-6882
- OpenAlex
- W2322859667
- Cited by
- 186
- References
- 2
- FWCI
- 9.06
- Type
- journal article
- Language
- en
- Open access
- closed
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- Li, L., Wang, C., Liu, K., Wang, Y., Liu, K., & Lin, Y. (2015). Hexagonal Cobalt Oxyhydroxide–Carbon Dots Hybridized Surface: High Sensitive Fluorescence Turn-on Probe for Monitoring of Ascorbic Acid in Rat Brain Following Brain Ischemia. Analytical Chemistry. https://doi.org/10.1021/ac5046609
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