Search

Rapid and sensitive detection of tumor biomarkers and cancer cells is of crucial importance for the early diagnosis and prognosis prediction of cancer. The present report describes a target-induced fluorescence enhancement immunosensor that utilizes the optical property of carbon dots (CDs) and the metal-enhanced fluorescence effect (MEF) property of silver nanoparticles (AgNPs) for the sensitive detection of the cancer biomarker human epididymis protein 4 (HE4) and ovarian cancer cells. Nitrogen and sulfur co-doped CDs with a quantum yield of 85.6% were prepared and served as the fluorophore in MEF. The HE4 antibody (Ab) specific to the HE4 antigen was linked covalently to the surface of the synthesized CDs as the capture. The HE4 Ab-conjugated AgNPs (AgNPs-Ab) were prepared and utilized as signal amplification elements. In the presence of the target HE4, composite sandwich structures were formed between the labeled CDs-Ab and AgNPs-Ab, which brought the CDs and AgNPs into proximity, resulting in the fluorescence of CDs enhancement owing to MEF. The intensity of fluorescence enhancement was positively correlated with the HE4 concentration in the clinically important range of 0.01-200 nM with a limit detection of 2.3 pM. Moreover, the immunosensor was also successfully applied to specific fluorescence labeling and quantitative determination of HE4-positive ovarian cancer cells. The proposed target-triggered MEF sensor platform demonstrated high sensitivity, excellent anti-interference ability, along with successful validation in complex biological matrices, providing a new approach for HE4 detection in early diagnosis and therapeutic monitoring., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)

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 Fe(3+) with a linear range of 0.5μM to 2mM and a detection limit of 13.6nM due to Fe(3+)-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/Fe(3+) 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 Fe(3+) ions and apoferritin in living cells suggest that this sensing system has great potential applications in biosensing, bioimaging, and many other fields., (Copyright © 2016 Elsevier B.V. All rights reserved.)

A new fluorescence "turn-on" nanosensor for carbonate determination was reported based on CdSe quantum dots (QDs) modified with thio ligands containing urea groups: N-(5-mercapto-1,3,4-thiadiazol-2-ylcarbamoyl)-2-(o-tolyloxy)acetamide (AASH-CdSe QDs). The AASH-CdSe QDs were prepared through a ligand exchange process and characterized by transmission electron microscopy (TEM), fluorescence spectroscopy, UV-vis spectroscopy and FT-IR spectroscopy. The synthesized AASH-CdSe QDs allowed a selective fluorescence "turn-on" response towards carbonate. Under optimal conditions, the relative fluorescence intensity increases linearly with carbonate concentration in the range 1 x 10(-7)-1 x 10(-4) M with a detection limit of 2.3 x 10(-8) M. A Langmuir-type binding model was highly effective in describing the carbonate concentration dependence of the luminescence intensity of the AASH-CdSe QDs. The possible mechanism was discussed.

"Host" molecules, containing a binding site that is highly specific for an analyte "guest," are used as sensors to register analyte binding through a variety of mechanisms such as colorimetric, fluorescent, or electrochemical signals. There is increasing interest in the host-guest chemistry on the surface of quantum dots (QDs) and in the changes that it produces in the luminescent properties of QDs. The bulk of this study focuses on those QDs with bound host molecules (crown ether, cyclodextrin, calixarene, and porphyrin) and the selectivity they display toward metal ions and small organic molecules.

A new fluorescence “turn-on” nanosensor for carbonate determination was reported based on CdSe quantum dots (QDs) modified with thio ligands containing urea groups: N-(5-mercapto-1,3,4-thiadiazol-2-ylcarbamoyl)-2-(o-tolyloxy)acetamide (AASH-CdSe QDs). The AASH-CdSe QDs were prepared through a ligand exchange process and characterized by transmission electron microscopy (TEM), fluorescence spectroscopy, UV-vis spectroscopy and FT-IR spectroscopy. The synthesized AASH-CdSe QDs allowed a selective fluorescence “turn-on” response towards carbonate. Under optimal conditions, the relative fluorescence intensity increases linearly with carbonate concentration in the range 1 × 10−7–1 × 10−4M with a detection limit of 2.3 × 10−8M. A Langmuir-type binding model was highly effective in describing the carbonate concentration dependence of the luminescence intensity of the AASH-CdSe QDs. The possible mechanism was discussed. [ABSTRACT FROM AUTHOR]

Abstract Gadolinium doped carbon dots (Gd-CDs) were prepared as a dual-modal imaging agent for enhanced MR imaging and cell fluorescence imaging. The Gd-CDs were synthesized via one-step solvent free technique with Gd-DTPA and l -arginine as the Gd and carbon sources with a quantum yield of 57.78%. The Gd-CDs exhibited good crystal structure, excellent aqueous dispersity, high colloidal stability, intense fluorescence and low cytotoxicity. The bio-TEM images revealed that the Gd-CDs could be easily internalized by cancer cells and escape from the endosomes. Furthermore, the Gd-CDs demonstrated wonderful multi-color fluoresence cell labeling ability at various excitation wavelength and much better MR contrast effect compared with commercial Gd-DTPA with a high r 1 relaxivity value 6.27 mM−1s−1. In addition, Gd-CDs exhibited brighter MR signal than Gd-DTPA in the animal MR imaging test. Finally, the Gd-CDs also indicated low long-term toxicity by the serum biochemistry analysis. Thus, these results indicated that Gd-CDs would be an excellent dual-modal imaging probe for enhanced MR imaging and fluorescence imaging. Highlights • The Gd-CDs were prepared with high quantum yield and excellent colloidal stability. • Gd-CDs could be taken up and exhibited good multi-fluorescence labeling ability. • Gd-CDs revealed wonderful MR cell imaging and in vivo animal imaging ability. [ABSTRACT FROM AUTHOR]