4 research outputs found
General Strategy to Fabricate Electrochemiluminescence Sandwich-Type Nanoimmunosensors Using CdTe@ZnS Quantum Dots as Luminescent Labels and Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> Nanoparticles as Magnetic Separable Scaffolds
This
work aims to develop universal sandwich-type electrochemiluminescence
(ECL) nanoimmunosensors for quantitative detection of biomarkers.
A series of low-toxic CdTe@ZnS QDs with different core sizes have
been synthesized via hydrothermal method and characterized by UV–vis
spectra, photoluminescence spectra, TEM, EDS, and XRD. Especially,
the ECL behaviors of CdTe@ZnS QDs have been investigated carefully.
The CdTe@ZnS QDs with the highest ECL quantum yields have been chosen
as ECL labels for conjugation with secondary antibodies. The QDs-labeled
antibodies have been characterized by agarose gel electrophoresis.
Meanwhile, Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> magnetic nanoparticles
were utilized as nanocarriers for the immobilization of primary antibodies
due to magnetic separation ability, large specific surface area, and
ease of amination for biofunctionalization. Successful fabrication
of the nanoimmunosensor was confirmed by SEM and electrochemical impedance
spectroscopy. Carcinoembryonic antigen was detected as a model to
prove the feasibility of the above strategy. Under the optimal conditions,
the proposed nanoimmunosensor exhibited a wide linear range of 0.01
to 125 ng mL<sup>–1</sup> for carcinoembryonic antigen determination
with a low detection limit of 3.0 pg mL<sup>–1</sup> (S/N =
3). Moreover, the nanoimmunosensor also displayed excellent selectivity,
good stability, and acceptable reproducibility, indicating its potential
applications in clinical diagnostics and immune research
One-Pot Green Synthesis of High Quantum Yield Oxygen-Doped, Nitrogen-Rich, Photoluminescent Polymer Carbon Nanoribbons as an Effective Fluorescent Sensing Platform for Sensitive and Selective Detection of Silver(I) and Mercury(II) Ions
This
work reports on a facile, economical, and green preparative strategy
toward water-soluble, fluorescent oxygen-doped, nitrogen-rich, photoluminescent
polymer carbon nanoribbons (ONPCRs) with a quantum yield of approximately
25.61% by the hydrothermal process using uric acid as a carbon–nitrogen
source for the first time. The as-prepared fluorescent ONPCRs showed
paddy leaf-like structure with 80–160 nm length and highly
efficient fluorescent quenching ability in the presence of mercuryÂ(II)
(Hg<sup>2+</sup>) or silver (Ag<sup>+</sup>) ions due to the formed
nonfluorescent metal complexes via robust Hg<sup>2+</sup>-O or Ag<sup>+</sup>-N interaction with the O and N of fluorescent ONPCRs, which
allowed the analysis of Hg<sup>2+</sup> and Ag<sup>+</sup> ions in
a very simple method. By employing this sensor, excellent linear relationships
existed between the quenching degree of the ONPCRs and the concentrations
of Hg<sup>2+</sup> and Ag<sup>+</sup> ions in the range of 2.0 nM
to 60 μM and 5.0 nM to 80 μM, respectively. By using ethylenediaminetetraacetate
and ammonia as the masking agent of Hg<sup>2+</sup> and Ag<sup>+</sup> ions, respectively, Hg<sup>2+</sup> or Ag<sup>+</sup> ions were
exclusively detected in coexistence with Ag<sup>+</sup> or Hg<sup>2+</sup> ions with high sensitivity, and the detection limits as
low as 0.68 and 1.73 nM (3σ) were achieved, respectively, which
also provided a reusable detection method for Hg<sup>2+</sup> and
Ag<sup>+</sup> ions. Therefore, the easily synthesized fluorescent
ONPCRs may have great potential applications in the detection of Hg<sup>2+</sup> and Ag<sup>+</sup> ions for biological assay and environmental
protection
Determination of Thiols by Fluorescence using Au@Ag Nanoclusters as Probes
<div><p>A simple and label-free fluorescent assay for the sensitive determination of biological thiols was developed using Au@Ag nanoclusters. The sensing approach was based on the strong affinity of thiols to silver on the surface of the nanoclusters. In the presence of thiol-containing amino acids, the fluorescence of the Au@Ag nanoclusters was quenched due to the formation of a non-fluorescent coordination complex via the robust Ag-S bond, which allowed the determination of thiol-containing amino acids in a very simple and rapid way. Under the optimal conditions, an excellent linear relationship was present due to quenching of the Au@Ag nanoclusters over cysteine concentrations between 20 nM and 80 µM with a low detection limit of 5.87 nM. Glutathione was determined between 2 µM and 70 µM with a detection limit of 1.01 µM. In addition, the results reveal that the fluorescent assay has excellent selectivity toward thiol-containing amino acids compared to non-thiol containing amino acids. Moreover, the assay was successfully used to determine cysteine in human plasma, and thus Au@Ag nanoclusters are a suitable fluorescent probe for biological applications.</p></div
Nonenzymatic Amperometric Aptamer Cytosensor for Ultrasensitive Detection of Circulating Tumor Cells and Dynamic Evaluation of Cell Surface N‑Glycan Expression
Dynamic assessment of glycan expression
on the cell surface and
accurate determination of circulating tumor cells are increasingly
imperative for cancer diagnosis and therapeutics. Herein, a unique
and versatile nonenzymatic sandwich-structured electrochemical cytosensor
was developed. The cytosensor was constructed based on a cell-specific
aptamer, the lectin-functionalized porous core–shell palladium
gold nanoparticles (Pd@Au NPs). To establish the cytosensor, amine-modified-SYL3C
aptamer was first attached to the surface of aminated Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> nanoparticles (Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>–NH<sub>2</sub> NPs) through cross-linked
reaction via glutaraldehyde. Besides, in terms of noncovalent assembly
of concanavalin A on Pd@Au NPs, a lectin-functionalized nanoprobe
was established. This nanoprobe had the capabilities of both the specific
carbohydrate recognition and the current signal amplification in view
of the Pd@Au NPs as the electrocatalyst for the reduction of hydrogen
peroxide (H<sub>2</sub>O<sub>2</sub>). Herein, we used MCF-7 cells
as a model target, and the constructed cytosensor showed a low detection
limit (down to three cells), a wide linear detection ranging from
100 to 1 × 10<sup>6</sup> cells mL<sup>–1</sup>. The established
method sensitively realized the detection of the amount of cell and
exact evaluation of glycan expression on cell surface, demonstrating
great application prospects