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Highly fluorescent carbon dots as selective and sensitive “on-off-on” probes for iron(III) ion and apoferritin detection and imaging in living cells
Highly blue luminescent nitrogen-doped carbon dots (N-CDs) with a fluorescence quantum yield of 42.3% were prepared by an efficient one-step pyrolytic route from ethylenediaminetetraacetic acid and urea. The as-synthesized N-CDs were demonstrated as an effective fluorescent probe for label-free, sel...
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Published in: | Biosensors & bioelectronics 2016-09, Vol.83, p.229-236 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Highly blue luminescent nitrogen-doped carbon dots (N-CDs) with a fluorescence quantum yield of 42.3% were prepared by an efficient one-step pyrolytic route from ethylenediaminetetraacetic acid and urea. The as-synthesized N-CDs were demonstrated as an effective fluorescent probe for label-free, selective and sensitive recognition of Fe3+ with a linear range of 0.5μM to 2mM and a detection limit of 13.6nM due to Fe3+-quenched fluorescence (turn-off). The quenched fluorescence could be turned on after the addition of apoferritin owing to the removal of ferric species from the surface of N-CDs by apoferritin, making complex N-CDs/Fe3+ a selective apoferritin probe with a linear range of 0.1–25μM and a detection limit as low as 2.6nM. In addition, the application of this novel N-CDs-based probe for imaging Fe3+ ions and apoferritin in living cells suggest that this sensing system has great potential applications in biosensing, bioimaging, and many other fields.
•Highly luminescent N-doped carbon dots were prepared by an efficient one-step pyrolytic route.•Sensitive and selective sensing of Fe3+ and apoferritin was achieved.•The mechanism of the Fe3+ and apoferritin sensing was studied.•The probe is applied to fluorescence imaging for cellular Fe3+ and apoferritin successfully. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2016.04.066 |