Cadmium Telluride Quantum Dots Research Articles

Low-dose cadmium telluride quantum dots trigger M1 polarization in macrophages through mTOR-mediated transcription factor EB activation

The increasing application of quantum dots (QDs) increases interactions with organisms. The inflammatory imbalance is a significant manifestation of immunotoxicity. Macrophages maintain inflammatory homeostasis. Using macrophages differentiated by phorbol 12-myristate 13-acetate-induced THP-1 cells as models, the study found that low-dose (5 μM) cadmium telluride QDs (CdTe-QDs) hindered monocyte-macrophage differentiation. CD11b is a surface marker of macrophage, and the addition of CdTe-QDs during induction resulted in a decrease in CD11b expression. Moreover, exposure of differentiated THP-1 macrophage (dTHP-1) to 5 μM CdTe-QDs led to the initiation of M1 polarization. This was indicated by the increased surface marker CD86 expression, along with elevated level of NF-κB and IL-1β proteins. The potential mechanisms are being explored. The transcription factor EB (TFEB) plays a significant role in immune regulation and serves as a crucial regulator of the autophagic lysosomal pathway. After exposed to CdTe-QDs, TFEB activation-mediated autophagy and M1 polarization were observed to occur simultaneously in dTHP-1. The mTOR signaling pathway contributed to TFEB activation induced by CdTe-QDs. However, mTOR-independent activation of TFEB failed to promote M1 polarization. These results suggest that mTOR-TFEB is an advantageous target to enhance the biocompatibility of CdTe-QDs.

Portable smartphone-assisted ratiometric fluorescent probe for carbimazole visualization detection

The ratio-based probe improves detection precision and accuracy by minimizing the effects of various experimental conditions. Herein, we constructed a ratio fluorescent probe (Si NPs/TGA-functionalized CdTe) using silicon nanoparticles (Si NPs) as the background signal and mercaptoacetic acid-functionalized cadmium telluride quantum dots (TGA-functionalized CdTe) as the responding unit. The interaction between Carbimazole (CBZ) and sulfhydryl groups on the surface of TGA-functionalized CdTe led to a decrease in the fluorescence intensity of the probe, and the color of the solution turned red and pink turned blue. Meanwhile, a test paper-based detection method integrated with the smartphone sensing platform was established to analyze the red, green, and blue (RGB) values in the images of Si NPs/TGA-functionalized CdTe solution before and after the addition of CBZ based on the change of hue, and an analytical model was constructed based on the R/B value and CBZ concentration, realizing rapid visual detection and analysis of CBZ. In addition, the constructed smartphone sensing platform was applied to the detection of CBZ in human urine, and the limit of detection the fluorescence analysis method and the smartphone sensing platform were 40 nM and 63 nM, with the recoveries of 96.5 %-102.7 % and 90.6 %-107.2 %, and the relative standard deviations of 2.7 %-4.1 % and 3.5 %-6.8 %, respectively. This work provides a significant improvement in the proportional sensing of CBZ in human urine and broadens the use of portable quantitative sensing devices in chemical sensing applications.

Tetrad metal ion mediated molecular switch aptamer sensor for fluorescence assay of plasma IP-10 in clinical tuberculosis

Interferon-γ-inducible protein 10 (IP-10) has demonstrated enormous potential as a novel biomarker for tuberculosis (TB), particularly in the monitoring of patient progression for active or latent tuberculosis infection (LTBI). Herein, we established a tetrad metal ion-mediated molecular switch aptamer sensor for the convenient detection of IP-10 in plasma and the diagnosis of TB. The simple sensor relied on the partially complementary IP-10 aptamer and four DNA hairpin strands rich in cytosine (C), which can form a relatively stable tetrad C-Ag+-C structure when combined with Ag+ without additional modification. Based on the specific recognition of IP-10 and aptamer, a large amount of Ag+ could be released in a short time. Combining with cadmium telluride quantum dots (CdTe QDs) as the signal reporter, we achieved superior analytical performance, with the limits of detection (LOD) reaching 3 fg/mL for IP-10 analysis in 1 h. Clinical practicality was confirmed by evaluating 38 clinical samples (19 TB-positive patients, 14 non-TB patients, and 5 latent TB infection patients). The results showed that the detected IP-10 levels were significantly different between the non-TB and TB/LTBI groups, and the results aligned with clinical computed tomography (CT) results, indicating that the method could represent a reliable diagnostic technique for TB.

Highly efficient photoelectrochemical aptasensor based on CdS/CdTe QDs co-sensitized TiO2 nanoparticles designed for thrombin detection.

A photoelectrochemical (PEC) sensor for the sensitive detection of thrombin (TB) was established. Co-sensitized combination of TiO2 nanoparticles combined with modified cadmium sulfide and cadmium telluride quantum dots (CdS/CdTe QDs) was utilized as a photoactive material. Successful growth of CdS/CdTe quantum dots on mesoporous TiO2 films occuredby successive ion-layer adsorption and reaction. This interesting formation of co-sensitive structure is conducive to enhancing the photocurrent response by improving the use rate of light energy. Additionally, the step-level structure of CdS/CdTe QDs and TiO2 NPs shows a wide range of visible light absorption, facilitating the dissociation of excitons into free electrons and holes. Consequently, the photoelectric response of the PEC analysis platform is significantly enhanced. This constructed PEC aptasensor shows good detection of thrombin with a low detection limit (0.033pM) and a widelinear range (0.0001-100nM) in diluted actual human serum samples. In addition, this PEC aptasensor also has the characteristics of good stability and good reproducibility, which provides a novel insight for the quantitative measurement of other similar analytes.

Optimization and performance evaluation of a fluorescent sensor for residual sulfonamide antibiotics in honey samples

AbstractIn the quest to address the mounting concerns over sulfonamide antibiotic residues in food, which pose significant threats to public health and food safety, this study introduces a cutting‐edge detection method. Surface molecular imprinting on silicon nanoparticles is harnessed to fabricate a novel fluorescent sensor that exploits the luminescent properties of cadmium telluride (CdTe) quantum dots. This innovative approach aims to detect residual sulfonamide antibiotics with high specificity and sensitivity. At the heart of this research is the development of a core‐shell nanostructure, where silicon dioxide serves as the core, and a molecularly imprinted polymers (MIPs) layer, tailored to recognize sulfamethazine (SM2), forms the shell. The pivotal advancement in this sensor design is the integration of highly fluorescent CdTe quantum dots within the MIPs layer, which significantly enhances the signal response, enabling the detection of SM2 with remarkable precision. The synthesis of this sensor employs a novel strategy, utilizing 3‐aminopropyltriethoxysilane as the functional monomer, while tetraethyl orthosilicate and ammonium hydroxide act as catalysts to facilitate the polymerization reaction. This meticulous process yields a stable core‐shell structure with active fluorescent properties. Experimental results reveal that under optimal conditions, the sensor exhibits a robust linear response to SM2 concentrations ranging from 10 to 60 μmol L−1, with a detection limit as low as 0.78 μmol L−1. Furthermore, when applied to real food samples, such as honey, the sensor not only demonstrates high recovery rates of 92.3%–98.1%, but also maintains a low relative standard deviation of less than 2.5%. The implications of this study are far‐reaching, offering a promising avenue for the rapid and reliable monitoring of antibiotic residues in the food supply chain, thereby safeguarding consumer health and upholding food safety standards.

Radiolabeled florescent-magnetic graphene oxide nanosheets: probing the biodistribution of a potential PET-MRI hybrid imaging agent for detection of fibrosarcoma tumor.

Radiolabeled graphene oxide (GO) nanosheets has been one of the most extensively studied nanoplatform for in vivo radioisotope delivery. Herein, we describe the functionalization of the surface of GO nanosheets with Fe3O4 magnetic nanoparticles, cysteine amino acid as an interface ligand, and cadmium telluride quantum dots. To enable In vivo PET imaging, the GO@Fe3O4-cys-CdTe QDs were labeled with 68Ga to yield [68Ga] Ga-Go@ Fe3O4-Cys-CdTe QDs. Furthermore, serum stability tests were performed and the biological behavior of the nanocomposite was evaluated in rats bearing fibrosarcoma tumor. Liver, blood and tumor were the most accumulated sites at 1 h after the injection, and the radiolabeled nanocomposite as a PET/MRI imaging agent showed fast depletion from body and acceptable tumor uptake. Magnetic (Fe3O4) and fluorescent components (CdTe QDs) along with a positron-emitting radionuclide will help to design a multimodal imaging system (PET/MRI/OI) which will offer the advantages of combined imaging techniques and further possible used in localized radionuclide therapy. Overall, [68Ga] Ga-GO@Fe3O4-cys-CdTe QDs nanocomposite shows great promise as a radiolabeled imaging agent owing to high accumulation in tumor region.

Protein corona exacerbated inflammatory response in macrophages elicited by CdTe quantum dots

Nano-bio interface is significant concern in nanomedicine. When nanoparticles (NPs) come into contact with cells, they form complexes with proteins known as protein corona (PC). Cadmium telluride quantum dots (CdTe QDs) have been applied as bioimaging probes and for macrophage theragnostic. However, the impact of protein corona on the behavior of CdTe QDs is not well understood. Macrophages play a crucial role in defending against NPs. In this study, RAW264.7 cells were used to investigated the inflammatory response in macrophages when exposed to CdTe QDs before and after PC formation in fetal bovine serum. The results indicated that protein corona polarized more macrophages towards M1 phenotype. Transcriptomics analysis revealed that PC-CdTe QDs altered a greater number of differentially expressed genes (DEGs) compared to CdTe QDs (177 and 398) at 1.0 μM in macrophages. The DEGs affected by PC-CdTe QDs contained several personalized inflammatory cytokines. The enriched pathways after PC formation included Cytokine-cytokine receptor interaction, NOD-like receptor signaling pathway, and TNF signaling pathway, etc. Furthermore, PC specifically exacerbated the overexpression of CCL2 and IL-1β proteins. Importantly, PC altered the mechanism of CdTe QD-induced pyroptosis, shifting it from activating NLRC4 to both NLRP1 and NLRP3 inflammasomes, and from cleaving GSDMD and GSDMB to GSDMB alone. Overall, protein corona exacerbated the inflammatory response induced by CdTe QDs in macrophages. This study provides valuable insight into the pro-inflammatory effect of protein corona on CdTe QDs, with implications for their use in bioimaging or macrophage theragnostic by either exploiting or eliminating this biological interface effect.

ESPECTROSCOPIA DE FLUORESCÊNCIA: DOS FUNDAMENTOS À INFLUÊNCIA DOS PARÂMETROS INSTRUMENTAIS PARA ANÁLISES DE CORANTES ORGÂNICOS E NANOPARTÍCULAS INORGÂNICAS

FLUORESCENCE SPECTROSCOPY: FROM FUNDAMENTALS TO THE INFLUENCE OF INSTRUMENTAL PARAMETERS FOR ANALYSIS OF ORGANIC DYES AND INORGANIC NANOPARTICLES. Fluorescence spectroscopy is an extremely sensitive analytical technique that has been widely used to elucidate problems that require low detection limits. Although fluorescence spectroscopy is widespread in industry and academia, there is a lack of teaching materials demonstrating its basic principles, as well as the influence of instrumental parameters involved in the technique, which limit its correct use and the full potential of it. For this reason, this work aims to explore the principles of fluorescence spectroscopy and correlate them in function of different instrumental variables to carry out a fluorescence experiment. The spectrofluorometer parameters such as the excitation wavelength, excitation and emission slits, step, integration time, detection geometry as well as concentration of the samples were varied to illustrate how the best resulting spectra can be registered free of artifacts. To do so, two organic dyes with structured vibronic bands (pyrene) and another with unstructured bands (rhodamine 6G) were used. Another study carried out involved the use of 3D spectra, excitation/emission spectra, of cadmium telluride (CdTe) quantum dots. In this case, it was possible to show the excitation spectrum of nanomaterials, collecting emissions at different wavelengths, as well as analyzing the particle size distribution.

Efficient sensitization of CdTe QDs towards PTCDA for sensitive photoelectrochemical Hg2+ assay.

Herein, a sensitive photoelectrochemical (PEC) biosensor was designed for the detection of mercury ions (Hg2+) on the basis of the efficient sensitization of cadmium telluride quantum dots (CdTe QDs) towards 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) and the significant quenching ability of a thymine-Hg2+-thymine (T-Hg2+-T) structure. The proposed CdTe QD/PTCDA sensitized structure was successfully constructed via continuous incubation of PTCDA and CdTe QDs on the glassy carbon electrode (GCE) interface, which embraced strong light absorption capacity and high carrier separation efficiency, giving rise to a remarkably improved initial photocurrent response. Notably, the PEC signal generated from the CdTe QD/PTCDA sensitized structure was almost fivefold higher than that of PTCDA owing to the efficient sensitization of CdTe QDs towards PTCDA. Once target Hg2+ ions were added, a T-rich S1 strand modified on the surface of 1-hexanethiol (HT)/S1/gold nanoparticles (Au NPs)/CdTe QDs/PTCDA/GCE immediately reacted with Hg2+ to produce multiple stable T-Hg2+-T structures. Therefore, the initial PEC signal would be considerably quenched by a high steric hindrance effect derived from the T-Hg2+-T structures. As a result, a quenched PEC response could achieve the detection of Hg2+ in concentrations ranging from 100 fM to 1000 nM. More importantly, the combination of the CdTe QDs/PTCDA sensitization structure and the T-Hg2+-T structure paves a promising pathway to developing a novel PEC biosensing platform for Hg2+ detection and also provides a favorable strategy for monitoring environmental pollution related to Hg2+.

Rapid determination of histamine in cheese by employing fluorescence enhancement of quantum dots-molecularly imprinted polymer

A fluorescent surface imprinted polymer was prepared by grafting Cadmium Telluride (CdTe) quantum dots into the methacrylic acid polymerization on the surface of silica. And a rapid turn-on fluorescence biosensor based on fluorescence enhancement effect was developed for the rapid and sensitive detection of histamine, which only took 8 min with a sensitive detection limit of 14.3 μmol/L. The cheese samples were tested by employing the fluorescent imprinted polymer, and the recovery was obtained in the range of 92.1–102%. The proposed histamine biosensing method shows great advantages, including no need for derivatization and reduced consumption of organic reagents. This has an important guiding role in the rapid detection of biological amines and other fluorescent responsive substances in complex systems.

Synthesis of a dual-emission fluorescent probe using graphitic carbon nitride as a carrier for the rapid detection of mesosulfuron-methyl

Pesticides play an irreplaceable role in ensuring increased food production and income, but the overuse of pesticides can also pose a threat to food and environmental safety. A novel dual-emission fluorescent probe was developed for the facile and accurate detection of sulfonylurea herbicides. A Förster resonance energy transfer system, based on N-doped carbon dots (N-CDs) and thioglycolic acid-capped cadmium telluride quantum dots (TGA-CdTe QDs) as energy donor–acceptor pairs, was established using graphitic carbon nitride (g-C3N4) as a substrate and successfully applied for the micro-detection of mesosulfuron-methyl (Mes). The CDs-CdTe/C3N4 probe exhibits emission peaks at 445 and 593 nm with strong fluorescence intensity under single-wavelength excitation. Mes was shown to significantly decrease the fluorescence intensity of each emission peak via different quenching mechanisms, and the degree of quenching was proportional to Mes concentration. The linear range of fluorescence measurement was 0–90 µM, with limits of detection at 1.3 µM (445 nm) and 0.8 µM (593 nm). The dual-emission fluorescent probe exhibited excellent selectivity for Mes compared with the other eleven herbicides. The fluorescent probe has a satisfying detection performance in environmental water samples and wheat samples, and has potential application in the portable detection of pesticide residues.

Dual‐emission ratiometric fluorescence sensors based on silica, molecularly imprinted polymers and carbon quantum dots for high‐sensitivity and high‐selectivity detection of sulfadiazine

AbstractIn this work, a dual‐emission ratiometric fluorescence sensor was prepared and used for the detection of sulfadiazine (SDZ) drug. The hydrothermal method was used to synthesize carbon quantum dots (CQD) (fluorescence response signal) and sulfhydryl‐modified cadmium telluride quantum dots (fluorescence reference signal), and a molecularly imprinted polymer was subsequently synthesized. After eluting the template molecule SDZ, the blot recognition site remains on the surface of the imprinted polymer. During the process of detection, due to electron transfer between SDZ and CQDs, holes of stimulated electrons are filled. This leads to fluorescence quenching at around 430 nm, which greatly improves sensor selection performance. Compared with traditional single‐emission fluorescence sensors, ratiometric fluorescence sensors have a wider linear range and higher detection accuracy. Under the optimal conditions, the sensor exhibited excellent performance in terms of low detection limit (4.2 nmol L−1) and satisfactory linear range (2–20 μmol L−1). This intelligent response change mode also provides prospect for detection of other sulfonamide antibiotics and offers a reference to signal transform for other molecular imprinting technologies. © 2023 Society of Industrial Chemistry.

Functionalized graphene, quantum dots, and PEDOT:PSS based screen-printed electrode for the endocrine disruptor bisphenol A determination

Strategies aimed for the monitoring the endocrine disruptor bisphenol A (BPA) become essential due to the high toxicity that this substance can cause in the environment. In this sense, a screen-printed electrode with functionalized graphene, cadmium telluride quantum dots, and polymer (PEDOT:PSS) was manufactured for the determination of the BPA in environmental matrices. The materials that compose the sensor were characterized by fluorescence spectroscopy, X-ray diffraction, FEG-SEM, TEM and FTIR. The electrochemical behavior of the analyte was performed by cyclic voltammetry and the quantification by square-wave voltammetry, respectively. The electroanalytical method showed a linear response in the BPA concentration range from 0.020 to 9.0 µmol L−1 with a limit of detection of 3.4 nmol L−1. Finally, the electroanalytical method was successfully applied to environmental samples for the determination of BPA, with a recovery close to 100%. This demonstrates its good applicability and sensitivity for this type of sample.

Enzyme-free nucleic acid and luminescent material cascade amplifications enable urinary dual miRNAs assay for non-invasive bladder cancer diagnosis

We presented a facile biosensing strategy for the detection of dual microRNAs (miRNA-21 and miRNA-126) in urine samples from bladder cancer (BC) patients. The fluorescent homogeneous detection of miRNAs was achieved by elaborate parallel catalytic hairpin assembly (CHA) integrated with material cascade amplifications. The continuous release of G-quadruplex (G4) sequences and Hg2+ was attributed to the specific recognition between the miRNAs and the corresponding hairpin oligonucleotides. Assisted by the streptavidin-(T-Hg2+-T-biotin)4 structures, more Hg2+ emission was obtained, and the spatial site block effect was used to order its distribution, significantly improving the selective recognition performance of cadmium telluride quantum dots (CdTe QDs) (1.4–2.9 times). Furthermore, the peroxidase-like activity of G4-hemin was used to catalyze the oxidation of dopamine (DA) to fluorescence-enhanced polydopamine (PDA). The generated PDA signal and the Hg2+-quenched CdTe QDs signal completed the synchronous detection to achieve a high-sensitivity analysis of the dual miRNAs. The limit of detection (LOD) of both miRNAs was as low as the fM level. Eventually, 56 clinical urine samples were quantified. The results showed satisfying specificity (100%) and sensitivity (92%) with a strong clinical agreement, including computed tomography (CT) and pathology findings, indicating a rapid non-invasive solution for early diagnosis of BC.

Mercaptosuccinic acid capped cadmium telluride quantum dots as luminescent thermometer over a wide temperature range of −100 to 60℃

Thermal-sensitive photoluminescence (PL) properties of cadmium telluride quantum dots capped with mercaptosuccinic acid (MSA-CdTe QDs) were investigated by collecting QDs’ PL steady-state spectra and decay curves from a cryogenic temperature of −100℃ to 60℃. These QDs display peak wavelength redshift and shorten fluorescence lifetime with the increase of temperature. In situ XRD patterns showed that the QDs’ grain size increases due to thermal expansion induced by the increasement of temperature, which further leads to the redshift of luminescence peak wavelength position. The results prove MSA-CdTe QDs are excellent candidates for luminescence thermometry over a broad temperature range of −100 to 60℃.

Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line.

Nanoparticles have shown promising potential for efficient drug delivery, circumventing biological interferences like immunological and renal clearance and mechanical and enzymatic destruction. However, a handful of research papers have questioned the biomedical use of metal-based nanoparticles like cadmium telluride quantum dots (CdTe-QDs) for their cytotoxic, genotoxic, and carcinogenic potential. Herein, we examined the effects of CdTe-QD NPs on gene expression profile of hepatocellular carcinoma (Huh-7) cell line. Huh-7 cells were treated with CdTe-QD NPs (10μg/ml for 6, 12, and 24hours, and 25μg/ml for 6 and 12hours), and transcriptomic analysis was performed using microarray to evaluate the global gene expression profile. Differential expressed genes (DEGs) were observed for both the doses (10 and 25μg/ml) of CdTe-QD NPs at different time points. Gene ontology (GO) analysis revealed that genes involved in molecular function of cell cycle, organizational injury and abnormalities, cell death and survival, gene expression, cancer, organismal survival, and cellular development were differentially expressed. Overall, we have demonstrated differential expression of several genes, involved in maintaining cell survival, metabolism, and genome integrity. These findings were confirmed by RT-qPCR study for some canonical pathway genes signifying possible implication in NP toxicity-mediated cell survival and inhibition of cell death.

Application of CdTe quantum dots sensitized titanate nanotubes in photocatalytic degradation of organic pollutants under visible light irradiation

The use of solar-driven photocatalysis for the degradation of recalcitrant organic waste from water is a promising and environmentally friendly technology to meet the challenge of mitigating increasing global pollution. This paper presents a new composite of layered H2Ti3O7 hydrothermal nanotubes (TNT) with cadmium telluride quantum dots prepared by the simple mixing suspensions of both components in TNT/CdTe-QDs ratios in the range of 1:0.005–1:0.03. The products were characterized by X-ray diffraction, spectroscopic techniques such as Fourier transform infrared, Raman scattering, UV–visible diffuse reflectance, photoluminescence, and X-ray photoelectron spectroscopy, as well as by scanning and transmission electron microscopy. The photocatalytic performance of the products was tested by photocatalytic degradation of two molecular models of contaminants, methyl orange (MO) and 4-chlorophenol (4-CP). Nearly 100 % removal of organic contaminants was achieved and the degradation rate of MO and 4-CP under simulated sunlight in the presence of QDs was approximately five and four times faster than using TNT alone, respectively. The degradation rate response in the presence of specific radical scavengers corresponds to a direct Z-scheme photocatalysis. Recycling experiments demonstrated a structurally stable catalyst that maintains its efficiency after five irradiation cycles. Photoelectrochemical and photocurrent measurements validated the synergistic effect observed, reflecting that heterojunction promotes the transfer of photogenerated electrons and holes, decreasing recombination changes and improving photocatalytic activity.

An investigation on the structural and optical properties of mercaptosuccinic acid capped cadmium telluride quantum dots

In this work, a sonication induced modified wet chemical approach is adopted to synthesize highly luminescent and water soluble cadmium telluride (CdTe) quantum dots (QDs). The morphology, size, crystal structural, and optical properties of CdTe QDs are investigated for different refluxing time (1–4 h). The refluxing time-dependent optical constants viz. band gap energy and Urbach energy of the QDs are estimated from UV–Visible absorption spectra. The optical band gap energy decreased from ~ 2.12 to 1.92 eV and the Urbach energy increased from ~ 361 to 487 meV, with the increase in refluxing time. CdTe QDs are found to be uniform in size. The average size of the QDs estimated from the High Resolution Transmission Electron Microscope image analysis is about 5.8 and 8.2 nm for refluxing times 1 and 4 h, respectively. The growth mechanism of the QDs as a function of refluxing time has also been discussed. The fluorescence spectra of the QDs, revealed emission peaks having wavelength from ~ 534 to 585 nm, under the excitation wavelength of 320 nm. The fluorescence emission peaks showed a bathochromic shift with increasing refluxing time. CdTe QDs also exhibit excitation-dependent fluorescence behaviour. Two crystalline phases of the CdTe QDs, namely hexagonal and cubic are confirmed from the High Resolution Transmission Electron Microscope images and Selected Area Electron Diffraction patterns analysis. The phase transformation from hexagonal to cubic is successfully achieved by tuning the refluxing time from 1 to 4 h.

A fluorescence nanoprobe of N-Acetyl-L-Cysteine capped CdTe QDs for sensitive detection of nitrofurazone

A method was established for detecting the content of nitrofurazone (NFZ) by fluorescence quenching of N-Acetyl-L-Cysteine (NAC) coated cadmium telluride quantum dots (CdTe QDs). By means of transmission electron microscopy (TEM) and multispectral methods such as fluorescence and ultraviolet visible spectra (UV–vis), the synthesized CdTe QDs were characterized. The quantum yield (φ) of CdTe QDs was measured as 0.33 by reference method. The CdTe QDs had a better stability, the RSD of fluorescence intensity was 1.51% in three months. NFZ quenching the emission light of CdTe QDs was observed. The analyses of Stern-Volmer and time-resolved fluorescence suggested the quenching was static. The binding constants (Ka) between NFZ and CdTe QDs were 1.14 × 104 (293 K), 0.74 × 104 (303 K) and 0.51 × 104 (313 K) L mol−1. The hydrogen bond or van der Waals force was the dominated binding force between NFZ and CdTe QDs. The interaction was further characterized by UV–vis absorption as well as Fourier transform infrared spectra (FT-IR). Using fluorescence quenching effect, a quantitative determination of NFZ was carried out. The optimal experimental conditions were studied and determined as following: pH was 7 and contact time was 10 min. The effects of reagent addition sequence, temperature and the foreign substances including some metals (Mg2+; Zn2+; Ca2+; K+; Cu2+), glucose, bovine serum albumin (BSA) and furazolidone on the determination were studied. There was a high correlation between the concentration of NFZ (0.40 – 39.63 μg mL−1) and F0/F with the standard curve F0/F = 0.0262c + 0.9910 (r = 0.9994). The detection limit (LOD) reached 0.04 μg mL−1 (3S0/S). The contents of NFZ in beef and bacteriostatic liquid were detected. The recovery of NFZ was 95.13% – 103.03% and RSD was 0.66% – 1.37% (n = 5).

Fluorescent probe of quantum dots and zinc oxide in ahighly selective polymer simultaneously determined florfenicol and sparfloxacin.

A nanocomposite fluorescent probe was fabricated for the simultaneous determination of florfenicol and sparfloxacin based on fluorescence quenching. The probe was synthesized by integrating nitrogen-doped graphene quantum dots (N-GQDs), cadmium telluride quantum dots (CdTe QDs) and zinc oxide nanoparticles (ZnO) into a molecularly imprinted polymer (MIP). The determination was based on the quenching of fluorescence emissions from N-GQDs by florfenicol, detected at 410nm, and the quenching of fluorescence emissions from CdTe QDs by sparfloxacin, detected at 550nm. The fluorescent probe was highly sensitive and specific with good linear relationships for florfenicol and sparfloxacin in the range 0.10 to 100.0μg L-1. The limits of detection for florfenicol and sparfloxacin were 0.06 and 0.10μg L-1, respectively. The fluorescent probe was used to determine florfenicol and sparfloxacin in food samples and the results agreed well with the results of chromatographic determination. Recoveries of spikedmilk, egg and chicken samplesreached 93.3-103.4% with good precision (RSD < 6%). The advantages of the nano-optosensor include high sensitivity and selectivity, simplicity, rapidity, convenience, good accuracy and precision.