tellurium and cadmium-sulfide

Quantum dots (QDs) are one of the first nanotechnologies to be integrated with the biological sciences that used for imaging or tracking macromolecules/cells in cell/tissue. Because of QDs are important in biomedical and biological applications, identify a variety of synthesis methods to produce QDs with different characteristics also is particularly important. Hence, in this review the authors discussed three methods for synthesis of heavy metal chalcogenide-based QDs for use in biomedical field: (i) Organometallic method for synthesis of QDs consists of three components: precursors, organic surfactants and solvents. The authors also discussed water-solubilisation strategies of synthesised QDs including encapsulation and ligand exchange. (ii) Aqueous synthesis technique using short-chain thiols as stabilising agents is a useful alternative to organometallic synthesis of CdSe, CdS and CdTe QDs. (iii) The third method discussed in this article for QDs synthesis involves the utilise of microorganisms to prepare QDs with controlled size, shape, chemical composition and functionality. The authors also discussed recently new methods for the synthesis of the appropriate QDs for use in biology. In addition, attachment of biomolecules such as antibodies, oligonucleotides on the surface of QDs for specific targeting and different opinions about toxicity of QD have been studied.

Topics: Cadmium Compounds; Chalcogens; Colloids; Nanomedicine; Nanoparticles; Particle Size; Peptides; Photochemistry; Photons; Quantum Dots; Selenium Compounds; Semiconductors; Solubility; Solvents; Sulfides; Surface Properties; Tellurium; Water

This work focuses on the synthesis of novel modified core-shell CdTe/CdS quantum dots (QDs) and develops as a fluorescence sensor for glucose determination. The (E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H-[5,5'-bithiazolylidene]-3,3'(4H,4'H)-diyl)bis(3- mercaptopropanoic acid) (DTM) as a new derivative of thiazolidine was synthesized and characterized and used to surface-modification of CdTe/CdS QDs. DTM-capped CdTe/CdS QDs used to immobilization of glucose oxidase (GOD). The intensity fluorescence emission of the CdSe/CdS-DTM/GOD is highly sensitive to the concentration of H

Topics: Biocompatible Materials; Cadmium Compounds; Colloids; Enzymes, Immobilized; Fluorescent Dyes; Glucose; Glucose Oxidase; Molecular Structure; Quantum Dots; Sulfides; Surface Properties; Tellurium; Thiazolidines

The specific identification and elimination of cancer cells has been a great challenge in the past few decades. In this study, the circular dichroism (CD) of cells was measured by a self-designed special system through the folate-conjugated chiral nano-sensor. A novel method was established to recognize cancer cells from normal cells according to the chirality of cells based on their CD signals. After a period of interaction between the nano-sensor and cells, the sharp weakening of CD signals was induced in cancer cells but normal cells remained unchanged. The biocompatibility of the nano-sensor was evaluated and the result showed that it exhibited significant cytotoxic activity against cancer cells while no obvious damage on normal cells. Notably, the research indicated that the nano-sensor may selectively cause apoptosis in cancer cells, and thus, have the potential to act as an antitumor agent.

Topics: Apoptosis; Breast Neoplasms; Cadmium Compounds; Cell Line, Tumor; Circular Dichroism; Female; Folic Acid; Humans; Neoplasms; Quantum Dots; Sulfides; Tellurium

An ultrasensitive label-free photoelectrochemical (PEC) immunosensor was developed to detect amyloid β-protein (Aβ) based on CdS/CdTe-cosensitized SnO2 nanoflowers. Specifically, SnO2 with a flower-like porous nanostructure was utilized as a perfect substrate for the construction of PEC immunosensors, and the SnO2-modified electrode was first coated with CdTe quantum dots (QDs) and then further deposited with CdS by successive ionic layer adsorption and reaction techniques. The formed SnO2/CdS/CdTe-cosensitized structure exhibited excellent photocurrent intensity and was employed as an excellent photoactive matrix to immobilize Aβ antibody to further construct the immunosensor. Under optimal conditions, the as-constructed PEC immunosensor was used to detect Aβ and exhibited a wide linear concentration range from 0.5 pg mL-1 to 10 ng mL-1, with a low limit of detection (LOD, 0.18 pg mL-1, S/N = 3). Meanwhile, it also presented good reproducibility, specificity, and stability and may open a new promising platform for the clinical detection of Aβ or other biomarkers.

Topics: Amyloid beta-Peptides; Antibodies, Monoclonal; Biosensing Techniques; Cadmium Compounds; Electrochemical Techniques; Humans; Immunoassay; Limit of Detection; Photochemical Processes; Quantum Dots; Sulfides; Tellurium; Tin Compounds

A method is described for the simultaneous determination of hepatocellular carcinoma-associated microRNA-122 and microRNA-199a/b-3p. This probe consists of two kinds of nanomaterials. The first comprises CdTe@CdS core-shell quantum dots which, on excitation at 375 nm give two emissions, with peak wavelengths at 543 (g-QDs) and at 627 nm (r-QDs). The second comprises gold nanoparticles acting as a quencher. In the absence of the target, g-QD-N1 and r-QD-N2 are stable due to the fluorescence stability. With the addition of microRNA-122 and microRNA-199a/b-3p, g-QD-N1 and r-QD-N2 are conjugated to the surface of AuNP-S1/S2 through base complementary pairing. As a result, fluorescence resonance energy transfer (FRET) occurs, resulting in a decrease at 550 nm and 635 nm respectively, which can realize the simultaneous detection of two different microRNAs. Detection is achieved within 50 min. The detection limits (3σ/k) are 0.2 nM for microRNA-122 and 0.5 nM for microRNA-199a/b-3p. The clinical applicability of the assay was demonstrated by detecting microRNAs in human serum and different cell lysates. Graphical abstractSchematic for the simultaneous determination of microRNA-122 and microRNA-199a/b-3p by FRET.

Topics: Biosensing Techniques; Cadmium Compounds; Carcinoma, Hepatocellular; Fluorescence Resonance Energy Transfer; Fluorometry; Humans; Limit of Detection; Liver Neoplasms; MicroRNAs; Neoplasms; Nucleic Acid Hybridization; Quantum Dots; Sulfides; Tellurium

Herein, a triple-helix molecular switch photoelectrochemical (PEC) biosensor is developed for ultrasensitive and selective detection of microRNA based on position-controllable CdS//CdTe signal enhancement and switching accompanying the signal amplification of a three-dimensional DNA walking machine. The developed PEC biosensor exhibits excellent analytical performance for microRNA-141 detection with a wide linear range from 5 aM to 100 fM, a low detection limit of 1.3 aM and outstanding selectivity.

Topics: Biosensing Techniques; Cadmium Compounds; DNA; Electrochemical Techniques; Limit of Detection; MicroRNAs; Photochemical Processes; Sulfides; Tellurium

Recent studies reveal a great value of interleukin-8 (IL-8), a pro-inflammatory cytokine, as a potent biomarker for early diagnosis of oral cancer. Herein, a new electrochemical method is proposed to detect IL-8 by facilely incorporating DNA-templated quantum dots (QDs). In principle, target IL-8 is first treated with the reducing agent tris(2-carboxyethyl)phosphine (TCEP) to yield active thiols and then captured by antibody-functionalized magnetic beads (MBs). Thereafter, via the Michael addition reaction between the active thiol and maleimide group, a maleimide-modified DNA probe is linked to the surface of MBs, which can initiate a process of rolling circle amplification. In this way, long-range DNA strands are generated on the MB surface, subsequently recruiting DNA-templated CdTe/CdS QDs (DNA-QDs) to act as electrochemical reporters. By tracing the responses of DNA-QDs, the method allows IL-8 detection in a linear range from 5 to 5000 fg/mL with a detection limit of 3.36 fg/mL. The selectivity, reproducibility, and applicability in complex serum samples are also demonstrated to be favorable, indicating that the method may have a great potential in the future. More importantly, the use of TCEP treatment in the method not only provides a facile way to incorporate DNA-QDs, avoiding the complicated and time-consuming preparation process of antibody-DNA conjugates or functional nanomaterials; but also makes the method capable of being extended to detect other protein biomarkers in view of widespread presence of disulfides, which may hold a broad potential to facilitate efficient biosensing designs.

Topics: Antibodies, Immobilized; Biosensing Techniques; Cadmium Compounds; Electrochemical Techniques; Humans; Immobilized Nucleic Acids; Interleukin-8; Limit of Detection; Mouth Neoplasms; Quantum Dots; Sulfides; Tellurium

Explosive compounds, such as 2,4,6-trinitrotoluene (TNT), pose a great concern in terms of both global public security and environmental protection. There are estimated to be hundreds of TNT contaminated sites all over the world, which will affect the health of humans, wildlife, and the ecosystem. Clearly, the ability to detect TNT in soils, water supplies, and wastewater is important for environmental studies but also important for security, such as in ports and boarders. However, conventional spectroscopic detection is not practical for on-site sensing because it requires sophisticated equipment and trained personnel. We report a rapid and simple chemical sensor for TNT by using TNT binding peptides which are conjugated to fluorescent CdTe/CdS quantum dots (QDs). QDs were synthesized in the aqueous phase, and the peptide was attached directly to the surface of the QDs by using thiol groups. The fluorescent emission from the QDs was quenched in response to the addition of TNT. The response could even be observed by the naked eye. The limit of detection from fluorescence spectroscopic measurement was estimated to be approximately 375 nM. In addition to the rapid response (within a few seconds), selective detection was demonstrated. We believe this label-free chemical sensor contributes to progress for the on-site explosive sensing.

Topics: Cadmium Compounds; Chemistry Techniques, Analytical; Environmental Pollutants; Fluorescent Dyes; Peptides; Quantum Dots; Sulfides; Tellurium; Time Factors; Trinitrotoluene

Topics: Aflatoxin B1; Antibodies, Monoclonal; Cadmium Compounds; Edible Grain; Fluorescence; Fluorescent Dyes; Food Contamination; HEK293 Cells; Humans; Immunoassay; Immunoglobulin Fab Fragments; Limit of Detection; Molecular Docking Simulation; Molecular Dynamics Simulation; Quantum Dots; Sulfides; Tellurium; Zinc Compounds

Topics: Alkaline Phosphatase; Cadmium Compounds; Energy Transfer; Fluorescence; Fluorescent Dyes; Humans; Limit of Detection; Nitrophenols; Organophosphorus Compounds; Quantum Dots; Spectrometry, Fluorescence; Sulfides; Tellurium

Developing methods to determine cell type and cell state has been a significant challenge in the field of cancer diagnosis as well as in typing and quality verification for cultured cells. Herein, we report a cell profiling method based on binding interactions between cell-surface sugar-chain-binding proteins and sugar-chain-immobilized fluorescent nanoparticles (SFNPs), together with a method for cell typing and cell quality verification. Binding profiles of cells against sugar chains were analyzed by performing flow cytometry analysis with SFNPs. Discrimination analysis based on binding profiles could classify cell type and evaluate the quality of cultured cells. By applying our method to differentiated cells originating from conventional cell lines and also to mouse embryotic stem cells, we could detect the cells before and after differentiation. Our method can be utilized not only for the biofunctional analysis of cells but also for diagnosis of cancer cells and quality verification of cultured cells.

Topics: Animals; Cadmium Compounds; Cell Line, Tumor; Embryonic Stem Cells; Flow Cytometry; Humans; Lectins; Ligands; Metal Nanoparticles; Mice; Monosaccharide Transport Proteins; Sulfides; Tellurium; Trisaccharides

We herein report an aqueous synthesis of gelatin stabilized CdTe/CdS/ZnS (CSSG) core/double shell quantum dots (QDs) with improved biocompatibility. The as-synthesized QDs were characterized by ultraviolet-visible (UV-vis) and photoluminescence (PL) spectroscopic techniques, x-ray diffraction technique (XRD), x-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The CSSG QDs revealed high photoluminescence quantum yield (PLQY) with excellent stability over a period of one year and retained 90% of its initial PLQY without any aggregation or precipitation under ambient condition. The cell viability study conducted on HeLa, cervical cancer cell lines indicated that the gelatin stabilization effectively decreased the QDs cytotoxicity by about 50%. The CSSG QDs were conjugated with transferrin (Tf) for the efficient delivery to the cancer cells followed by fluorescence imaging. The results showed that the CSSG QDs illuminates the entire cell which renders the QDs as cell labeling markers. The gelatin stabilized core/double shell QDs are potential candidates for long time fluorescent bio-imaging.

Topics: Biocompatible Materials; Cadmium Compounds; Cell Survival; Gelatin; HeLa Cells; Humans; Luminescent Measurements; Molecular Probes; Optical Imaging; Quantum Dots; Receptors, Transferrin; Sulfides; Tellurium; Transferrin; Zinc Compounds

In this study, semiconducting organic polymer dots (Pdots) and inorganic quantum dots (Qdots) were first utilized to construct the organic-inorganic nanodots heterojunction for the photoelectrochemical (PEC) bioanalysis application. Specifically, n-type CdS Qdots, p-type CdTe Qdots, and tetraphenylporphyrin (TPP)-doped poly[(9,9-dioctylfluorenyl-2,7-diyl)- co-(1,4-benzo-{2,1',3}-thiadazole)] (PFBT) Pdots were fabricated, and their energy levels, that is, their valence band (VB)/conduction band (CB) or lowest unoccupied molecular orbital (LUMO)/highest occupied molecular orbital (HOMO) values, were also determined. Then, these nanodots were integrated to construct four types of p-n and p-p organic-inorganic nanodots heterojunctions, that is, CdS Qdots/TPP-doped PFBT Pdots, TPP-doped PFBT Pdots/CdS Qdots, CdTe Qdots/TPP-doped PFBT Pdots, and TPP-doped PFBT Pdots/CdTe Qdots, on the transparent glass electrode. Upon light irradiation, four heterojunctions exhibited different PEC behaviors with some having prominent photocurrent enhancement. With the model molecule l-cysteine (l-cys) as target, the proposed PEC sensor exhibited good performances. In brief, this work presents the first semiconducting organic-inorganic nanodots heterojunction for PEC bioanalysis application, which could be easily used as a general platform for future PEC bioanalysis building. Besides, it is expected to inspire more interest in the design, development, and implementation of various organic-inorganic heterojunctions for advanced PEC bioanalysis in the future.

Topics: Cadmium Compounds; Electrochemical Techniques; Fluorenes; Light; Photochemical Processes; Polymers; Porphyrins; Quantum Dots; Semiconductors; Sulfides; Tellurium

An ultrasensitive photoelectrochemical (PEC) aptasensor for lead ion (Pb

Topics: Aptamers, Nucleotide; Biosensing Techniques; Cadmium Compounds; Disulfides; Electrochemical Techniques; G-Quadruplexes; Ions; Lead; Manganese; Molybdenum; Nanocomposites; Particle Size; Photochemical Processes; Quantum Dots; Sulfides; Surface Properties; Tellurium

Topics: alpha-Fetoproteins; Antibodies; Biosensing Techniques; Cadmium Compounds; Carcinoembryonic Antigen; Color; Electrochemical Techniques; Immunoassay; Limit of Detection; Luminescent Measurements; Nanoparticles; Sulfides; Tellurium

In this work, we synthesized water-soluble L-cysteine-capped alloyed CdSeTe core quantum dots (QDs) and investigated the structural and optical properties of deposition of each of CdS, CdS/ZnSe and CdS/ZnSe/ZnS shell layers. Photophysical results showed that the overcoating of a CdS shell around the alloyed CdSeTe core [quantum yield (QY) = 8.4%] resulted in effective confinement of the radiative exciton with an improved QY value of 93.5%. Subsequent deposition of a ZnSe shell around the CdSeTe/CdS surface decreased the QY value to 24.7%, but an increase in the QY value of up to 49.5% was observed when a ZnS shell was overcoated around the CdSeTe/CdS/ZnSe surface. QDs with shell layers showed improved stability relative to the core. Data obtained from time-resolved fluorescence measurements provided useful insight into variations in the photophysical properties of the QDs upon the formation of each shell layer. Our study suggests that the formation of CdSeTe/CdS core/shell QDs meets the requirements of quality QDs in terms of high photoluminescence QY and stability, hence further deposition of additional shells are not necessary in improving the optical properties of the core/shell QDs.

Topics: Cadmium Compounds; Fluorescence; Optical Phenomena; Quantum Dots; Selenium Compounds; Solubility; Sulfides; Tellurium; Water; Zinc Compounds

In this paper, a new fluorescence bioassay for Golgi protein-73 (GP73), a promising marker for monitoring liver tumor, was developed by using anti-GP73 antibody (GP73 Ab) capped quantum dots (QDs) coupled with protein A/G agarose beads in an attempt to improve the analysis time, cost and operation. First, carboxylic-functionalized Mn modified CdTe/CdS QDs were synthesized and covalently conjugated with GP73 Ab, then protein A/G agarose beads were specifically combined with the QDs-conjugated Ab to form the QDs-Ab-beads conjugate, which could capture and separate GP73 from the sample through simple centrifugation. It was found that the fluorescence intensity of the above QDs-Ab-beads biosensor could be specifically quenched by GP73 added. A simple, rapid and specific quantitative method for GP73 protein was proposed using the as-prepared QDs-Ab-beads as a biosensor. Under the optimized conditions, the calibration curve of the proposed assay showed good linearity with a correlation coefficient of 0.9935 in the concentration range of 20-150 ng/mL of GP73 protein. The limit of detection (defined as 3σ/K) was 10 ng/mL. The method built exhibited a great potential in the clinic test of GP73.

Topics: Biosensing Techniques; Cadmium Compounds; Humans; Immunoassay; Manganese; Membrane Proteins; Quantum Dots; Sulfides; Tellurium

Ligands used on the surface of colloidal nanoparticles (NPs) have a significant impact on physiochemical properties of NPs and their interaction in biological environments. In this study, we report a one-pot aqueous synthesis of 3-mercaptopropionic acid (MPA)-functionalized CdTe/CdS/ZnS quantum dots (Qdots) in the presence of thiol-terminated methoxy polyethylene glycol (mPEG) molecules as a surface coordinating ligand. The resulting mPEG-Qdots were characterized by using ζ potential, FTIR, thermogravimetric (TG) analysis, and microscale thermophoresis (MST) studies. We investigated the effect of mPEG molecules and their grafting density on the Qdots photophysical properties, colloidal stability, protein binding affinity, and in vitro cellular toxicity. Moreover, cellular binding features of the resulting Qdots were examined by using three-dimensional (3D) tumor-like spheroids, and the results were discussed in detail. Promisingly, mPEG ligands were found to increase colloidal stability of Qdots, reduce adsorption of proteins to the Qdot surface, and mitigate Qdot-induced side effects to a great extent. Flow cytometry and confocal microscopy studies revealed that PEGylated Qdots exhibited distinctive cellular interactions with respect to their mPEG grafting density. As a result, mPEG molecules demonstrated a minimal effect on the ZnS shell deposition and the Qdot fluorescence efficiency at a low mPEG density, whereas they showed pronounced effect on Qdot colloidal stability, protein binding affinity, cytotoxicity, and nonspecific binding at a higher mPEG grafting amount.

Topics: 3-Mercaptopropionic Acid; Animals; Cadmium Compounds; Cattle; Cell Line; Cell Survival; Colloids; Humans; Polyethylene Glycols; Protein Aggregates; Quantum Dots; Serum Albumin, Bovine; Sulfides; Tellurium; Water; Zinc Compounds

A dual-channel optical sensing platform which combines the advantages of dual-wavelength overlapping resonance Rayleigh scattering (DWO-RRS) and fluorescence has been designed for the detection of diminazene aceturate (DA). It is based on the use of thioglycolic acid-wrapped CdTe/CdS quantum dots (Q-dots). In the absence of DA, the thioglycolic acid-wrapped CdTe/CdS Q-dots exhibit the high fluorescence spectrum and low RRS spectrum, so are selected to develop an easy-to-get system. In the presence of DA, the thioglycolic acid-wrapped CdTe/CdS Q-dots and DA form a complex through electrostatic interaction, which result in the RRS intensity getting enhanced significantly with new RRS peaks appearing at 317 and 397 nm; the fluorescence is powerfully quenched. Under optimum conditions, the scattering intensities of the two peaks are proportional to the concentration of DA in the range of 0.0061-3.0 μg mL(-1). The detection limits for the two single peaks are 4.1 ng mL(-1) and 3.3 ng mL(-1), while that of the DWO-RRS method is 1.8 ng mL(-1), indicating that the DWO-RRS method has high sensitivity. Besides, the fluorescence also exhibits good linear range from 0.0354 to 10.0 μg mL(-1) with a detection limit of 10.6 ng mL(-1). In addition, the system has been applied to the detection of DA in milk samples with satisfactory results.

Topics: Animals; Antiprotozoal Agents; Cadmium Compounds; Diminazene; Food Contamination; Limit of Detection; Milk; Quantum Dots; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Sulfides; Tellurium; Thioglycolates

Here we designed a near-infrared electrochemiluminescence (NECL) aptasensor for turn-on ultrasensitive determination of thrombin. It was based on the ECL resonance energy transfer (ECL-RET) of CdTe/CdS coresmall/shellthick quantum dots (QDs) to gold nanorods (AuNRs). AuNRs which functioned as ECL acceptors were assembled onto CdTe/CdS film by DNA hybridization between aptamers and their complementary oligonucleotides. In the absence of thrombin, the NECL of QDs was quenched as a result of the ECL-RET of QDs to AuNRs. In the presence of thrombin, the NECL of the system was "turned on" because thrombin can replace the AuNRs onto the QDs film, owing to the specific aptamer-protein affinity interactions. In this way, the increment of ECL intensity and the concentration of thrombin showed a logarithmic linear correlation in the range of 100 aM to 10 fM with a detection limit of 31 aM (S/N=3). Importantly, the developed aptasensor was successfully applied to thrombin sensing in real serum samples.

Topics: Aptamers, Nucleotide; Biosensing Techniques; Cadmium Compounds; Electrochemical Techniques; Gold; Humans; Infrared Rays; Limit of Detection; Luminescent Measurements; Nanotubes; Quantum Dots; Sulfides; Tellurium; Thrombin

Fluorescent nanoparticles or quantum dots (QDs) have been intensely studied for basic and applied research due to their unique size-dependent properties. There is an increasing interest in developing ecofriendly methods to synthesize these nanoparticles since they improve biocompatibility and avoid the generation of toxic byproducts. The use of biological systems, particularly prokaryotes, has emerged as a promising alternative. Recent studies indicate that QDs biosynthesis is related to factors such as cellular redox status and antioxidant defenses. Based on this, the mixture of extreme conditions of Antarctica would allow the development of natural QDs producing bacteria.. In this study we isolated and characterized cadmium and tellurite resistant Antarctic bacteria capable of synthesizing CdS and CdTe QDs when exposed to these oxidizing heavy metals. A time dependent change in fluorescence emission color, moving from green to red, was determined on bacterial cells exposed to metals. Biosynthesis was observed in cells grown at different temperatures and high metal concentrations. Electron microscopy analysis of treated cells revealed nanometric electron-dense elements and structures resembling membrane vesicles mostly associated to periplasmic space. Purified biosynthesized QDs displayed broad absorption and emission spectra characteristic of biogenic Cd nanoparticles.. Our work presents a novel and simple biological approach to produce QDs at room temperature by using heavy metal resistant Antarctic bacteria, highlighting the unique properties of these microorganisms as potent natural producers of nano-scale materials and promising candidates for bioremediation purposes.

Topics: Antarctic Regions; Bacteria; Cadmium Compounds; Drug Resistance, Bacterial; Fluorescent Dyes; Metabolome; Metals, Heavy; Microscopy, Electron, Transmission; Nanoparticles; Quantum Dots; RNA, Ribosomal, 16S; Spectrometry, Fluorescence; Sulfides; Tellurium

CdSe/CdS/ZnS and CdTe quantum dots (QDs) were synthesized by successive ion layer adsorption and reaction (SILAR) technique and direct aqueous synthesis respectively using thiol stabilizers. Synthesized CdSe/CdS/ZnS and CdTe QDs stabilized with 3-mercaptopropionic acid (MPA) and mercaptosuccinic acid (MSA) were used as fluorescent labels after conjugation with folic acid (FA) and anti-HER2 antibodies. Photoluminescence quantum yield of folated CdSe/CdS/ZnS-MPA and CdTe-MSA QDs was 59% and 77% than that of non-folated hydrophilic QDs. The folate receptor-mediated delivery of folic acid-conjugated CdTe-MSA and CdSe/CdS/ZnS-MPA QDs showed higher cellular internalization as observed by confocal laser scanning microscopic studies. Folated and non-folated CdTe-MSA QDs were highly toxic and exhibited only 10% cell viability as compared to > 80% cell viability with CdSe/CdS/ZnS-MPA QDs over the concentration ranging from 3.38 to 50 pmoles. Immunohistochemistry (IHC) results of human breast cancer tissue samples showed positive results with anti-HER2 antibody conjugated CdSe/CdS/ZnS-MPA QDs with better sensitivity and specificity as compared to conventional IHC analysis using diaminobenzedene staining.

Topics: 3-Mercaptopropionic Acid; Animals; Antibodies, Neoplasm; Breast Neoplasms; Cadmium Compounds; Drug Delivery Systems; Female; Folic Acid; Humans; Mice; Mice, Inbred BALB C; Quantum Dots; Receptor, ErbB-2; Selenium Compounds; Succinates; Sulfides; Tellurium; Zinc Compounds

We report an efficient method to biosynthesize biocompatible cadmium telluride and cadmium sulphide quantum dots from the fungus Rhizopus stolonifer. The suspension of the quantum dots exhibited purple and greenish-blue luminescence respectively upon UV light illumination. Photoluminescence spectroscopy, X-ray diffraction, and transmission electron microscopy confirms the formation of the quantum dots. From the photoluminescence spectrum the emission maxima is found to be 424 and 476nm respectively. The X-ray diffraction of the quantum dots matches with results reported in literature. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay for cell viability evaluation carried out on 3-days transfer, inoculum 3×10

Topics: Animals; Biotechnology; Cadmium Compounds; Chalcogens; Green Chemistry Technology; Humans; MCF-7 Cells; Mice; Nanotechnology; NIH 3T3 Cells; Quantum Dots; Rhizopus; Sulfides; Tellurium

Water-soluble thioglycolic acid (TGA)-capped core/shell CdTe/CdS quantum dots (QDs) were synthesized. The interactions of rhein and emodin with TGA-CdTe/CdS QDs were evaluated by fluorescence and ultraviolet-visible absorption spectroscopy. Experimental results showed that the high fluorescence intensity of TGA-CdTe/CdS QDs could be effectively quenched in the presence of rhein (or emodin) at 570 nm, which may have resulted from an electron transfer process from excited TGA-CdTe/CdS QDs to rhein (or emodin). The quenching intensity was in proportion to the concentration of both rhein and emodin in a certain range. Under optimized conditions, the linear ranges of TGA-CdTe/CdS QDs fluorescence intensity versus the concentration of rhein and emodin were 0.09650-60 µg/mL and 0.1175-70 µg/mL with a correlation coefficient of 0.9984 and 0.9965, respectively. The corresponding detection limits (3σ/S) of rhein and emodin were 28.9 and 35.2 ng/mL, respectively. This proposed method was applied to determine rhein and emodin in human urine samples successfully with remarkable advantages such as high sensitivity, short analysis time, low cost and easy operation. Based on this, a simple, rapid and highly sensitive method to determine rhein (or emodin) was proposed.

Topics: Anthraquinones; Cadmium Compounds; Emodin; Humans; Molecular Structure; Particle Size; Quantum Dots; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Sulfides; Surface Properties; Tellurium; Thioglycolates

Although many studies reporting the organ-level biodistribution of nanoparticles (NPs) in animals, very few have addressed the fate of NPs in organs at the cellular level. The liver appears to be the main organ for accumulation of NPs after intravenous injection. In this study, for the first time, the in vivo spatiotemporal disposition of recently developed mercaptosuccinic acid (MSA)-capped cadmium telluride/cadmium sulfide (CdTe/CdS) quantum dots (QDs) is explored in rat liver using multiphoton microscopy (MPM) coupled with fluorescence lifetime imaging (FLIM), with subcellular resolution (∼1 μm). With high fluorescence efficiency and largely improved stability in the biological environment, these QDs show a distinct distribution pattern in the liver compared to organic dyes, rhodamine 123 and fluorescein. After intravenous injection, fluorescent molecules are taken up by hepatocytes and excreted into the bile, while negatively charged QDs are retained in the sinusoids and selectively taken up by sinusoidal cells (Kupffer cells and liver sinusoidal endothelial cells), but not by hepatocytes within 3 h. The results could help design NPs targeting the specific types of liver cells and choose the fluorescent markers for appropriate cellular imaging.

Topics: Animals; Cadmium Compounds; Liver; Mice; Microscopy; Photons; Quantum Dots; Rats; Sulfides; Tellurium

The impact of strain on the optical properties of semiconductor quantum dots (QDs) is fundamentally important while still awaiting detailed investigation. CdTe/CdS core/shell QDs represent a typical strained system due to the substantial lattice mismatch between CdTe and CdS. To probe the strain-related effects, aqueous CdTe/CdS QDs were synthesized by coating different sized CdTe QD cores with CdS shells upon the thermal decomposition of glutathione as a sulfur source under reflux. The shell growth was carefully monitored by both steady-state absorption and fluorescence spectroscopy and transient fluorescence spectroscopy. In combination with structural analysis, the band alignments as a consequence of the strain were modified based on band deformation potential theory. By further taking account of these strain-induced band shifts, the effective mass approximation (EMA) model was modified to simulate the electronic structure, carrier spatial localization, and electron-hole wave function overlap for comparing with experimentally derived results. In particular, the electron/hole eigen energies were predicted for a range of structures with different CdTe core sizes and different CdS shell thicknesses. The overlap of electron and hole wave functions was further simulated to reveal the impact of strain on the electron-hole recombination kinetics as the electron wave function progressively shifts into the CdS shell region while the hole wave function remains heavily localized in CdTe core upon the shell growth. The excellent agreement between the strain-modified EMA model with the experimental data suggests that strain exhibits remarkable effects on the optical properties of mismatched core/shell QDs by altering the electronic structure of the system.

Topics: Cadmium Compounds; Electrons; Kinetics; Models, Molecular; Molecular Conformation; Optical Phenomena; Quantum Dots; Quantum Theory; Sulfides; Tellurium

We investigate the effects of the excitation power on the photoluminescence spectra of aqueous CdTe/CdS core-shell quantum dots. We have focused our efforts on nanoparticles that are drop-cast on a silicon nitride substrate and dried out. Under such conditions, the emission intensity of these nanocrystals decreases exponentially and the emission center wavelength shifts with the time under laser excitation, displaying a behavior that depends on the excitation power. In the low-power regime a blueshift occurs, which we attribute to photo-oxidation of the quantum dot core. The blueshift can be suppressed by performing the measurements in a nitrogen atmosphere. Under high-power excitation the nanoparticles thermally expand and aggregate, and a transition to a redshift regime is then observed in the photoluminescence spectra. No spectral changes are observed for nanocrystals dispersed in the solvent. Our results show a procedure that can be used to determine the optimal conditions for the use of a given set of colloidal quantum dots as light emitters for photonic crystal optical cavities.

Topics: Cadmium Compounds; Light; Luminescent Measurements; Quantum Dots; Sulfides; Tellurium; Water

Aldo-ketoreductase family 1 member B10 (AKR1B10) is a novel prognostic predictor and therapeutic target for colorectal cancer (CRC), and enzyme-linked immunosorbent assays (ELISAs) and electrochemiluminescence (ELC) assays are sample-consuming and high-cost methods. Therefore, it is very necessary to develop a new, simple, and fast yet highly sensitive and specific method for the detection of AKR1B10 in serum. Semiconducting quantum dots (QDs) possess a high fluorescence quantum yield, stability against photobleaching, and size-controlled luminescence properties; thus, they are suitable for photoelectrochemical tumor marker detection, especially in complex biological samples. However, CdTe/CdS QDs have not been applied for the detection of AKR1B10 in serum.. AKR1B10 in peripheral blood has been established using anti-AKR1B10-conjugated CdTe/CdS QDs and measurements. The assay sensitivity was determined by measuring the quenched fluorescence intensity of AKR1B10 at 0.5, 1, 2, 5, or 10 ng/mL in phosphate-buffered solution (PBS) or 0.25%, 0.5%, 1.0%, 2.0%, or 5% human serum diluted in PBS. The assay was optimized under different pH values (7.00 - 7.40) for different reaction durations (10 - 60 minutes). The specificity of anti-AKR1B10-QDs was determined by testing the inhibition of AKR1B10 activity with carcinoembryonic antigen (CEA), immunoglobulin G (IgG), or alpha-fetoprotein (AFP), each at 1 ng/mL.. Under the optimized incubation time (30 minutes) at room temperature and optimal pH (7.1 - 7.2), a correlation between the decreased fluorescence intensity of anti-AKR1B10-conjugated CdTe/CdS QDs and the concentration of AKR1B10 in the range from 0.05 to 100 ng/mL was established. The assay was sensitive for the detection of AKR1B10 in the range from 0.05 to 100 ng/mL, and the detection limit was 0.02 ng/mL. The assay presented a high specificity because the anti-AKR1B10-conjugated CdTe/CdS QDs only reacted with AKR1B10 in the sera in the presence of CEA, IgG, or AFP.. In conclusion, the immunofluorescence assay to detect AKR1B10 in serum using anti-AKR1B10-conjugated CdTe/CdS QDs was simple and fast yet presented high sensitivity and specificity. Our findings provide a promising tool for the early prediction of CRC.

Topics: Aldehyde Reductase; Aldo-Keto Reductases; Cadmium Compounds; Fluorescent Antibody Technique; Humans; Quantum Dots; Sensitivity and Specificity; Sulfides; Tellurium

A novel flow-injection chemiluminescence (FI-CL) method was described for the determination of sinomenine hydrochloride (SIN). The method was based on the inhibitory effect of SIN on the CL reaction of luminol and K3Fe(CN)6 in an alkaline solution, which was sensitized by CdTe/CdS quantum dots (QDs). Under the optimized conditions, the linear range for the determination of SIN was 1.0 × 10(-8) to 1.4 × 10(-6) mol/L. The detection limit was 7.5 × 10(-9) mol/L, and the relative standard deviation was 2.47% (n = 11). The current CL method was applied to determine SIN in pharmaceutical formulations and biological fluids with satisfactory results. The possible CL reaction mechanism was discussed briefly.

Topics: Cadmium Compounds; Ferricyanides; Flow Injection Analysis; Kinetics; Limit of Detection; Luminescent Measurements; Luminol; Morphinans; Quantum Dots; Sulfides; Tellurium

A fluorescence polarization homogenous system based on CdTe/CdS QDs that employed a K(+)-mediated G-quadruplex as an enhancer was identified for sensitive and selective detection of Hg(2+) and biothiols in complex samples.

Topics: Cadmium Compounds; Fluorescence Polarization; G-Quadruplexes; Mercury; Potassium; Quantum Dots; Sulfhydryl Compounds; Sulfides; Tellurium

We compared the effects of several ligands frequently used in aqueous synthesis, including L-cysteine, L-cysteine hydrochloride, N-acetyl-L-cysteine (NAC), glutathione and 3-mercaptopropionic acid, for microwave synthesis of CdTe quantum dots (QDs) in a sealed vessel with varied temperatures and times, and then developed a rapid microwave-assisted protocol for preparing highly luminescent, photostable and biocompatible CdTe/CdS/ZnS core-multishell QDs. The effects of molecular structures of these ligands on QD synthesis under high temperatures were explored. Among these ligands, NAC was found to be the optimal ligand in terms of the optical properties of resultant QDs and reaction conditions. The emission wavelength of NAC-capped CdTe QDs could reach 700 nm in 5 min by controlling the reaction temperature, and the resultant CdTe/CdS/ZnS core-multishell QDs could achieve the highest quantum yields up to 74% with robust photostability. In addition, the effects of temperature, growth time and shell-precursor ratio on shell growth were examined. Finally, cell culturing indicated the low cytotoxicity of CdTe/CdS/ZnS core-multishell QDs as compared to CdTe and CdTe/CdS QDs, suggesting their high potential for applications in biomedical imaging and diagnostics.

Topics: Biocompatible Materials; Cadmium Compounds; Cell Survival; Dose-Response Relationship, Drug; HEK293 Cells; Humans; Ligands; Luminescence; Microwaves; Molecular Structure; Particle Size; Quantum Dots; Structure-Activity Relationship; Sulfides; Surface Properties; Tellurium; Temperature; Zinc Compounds

We report herein the facile surface-functionalization of one type of biocompatible, oligomeric nanoparticles 1-NPs with NIR-emitting CdTe/CdS QDs and folate for tumor-targeted imaging in vivo. The -NH2 and -SH groups of cysteine residues on the 1-NPs were utilized to covalently conjugate CdTe/CdS QDs and Mal-FA to prepare the hybrid nanoparticles 1-NPs-QDs-FA. As-prepared 1-NPs-QDs-FA showed NIR-fluorescence emission at 734 nm, selective uptake by FR-overexpressing tumor cells in vitro, and selective FR-overexpressing tumor-targeted imaging in vivo. This first example of oligomeric/inorganic hybrid nanoparticles provides people with new type of biomaterials for tumor-targeted imaging with high selectivity.

Topics: Animals; Cadmium Compounds; Diagnostic Imaging; Fluorescence; Folic Acid; Mice, Nude; Nanoparticles; Neoplasms; Optical Imaging; Organ Specificity; Quantum Dots; Spectroscopy, Near-Infrared; Sulfides; Tellurium

Lattice-strained CdTe/CdS:Cu quantum dots (QDs) with a widely tunable near-infrared (NIR) fluorescence emission spectrum (700-910 nm) and long lifetime (up to 1 μs) are synthesized. Based on the multiemission and multi-lifetime of the well-defined QDs, NIR-emitting two-dimensional (2D) codes are achieved by embedding as-prepared QDs into agarose beads. This provides a new strategy for fluorescent 2D codes.

Topics: Cadmium Compounds; Light; Materials Testing; Quantum Dots; Spectroscopy, Near-Infrared; Sulfides; Tellurium

The substrate-overlayer approach has been used to acquire surface enhanced Raman spectra (SERS) during and after electrochemical atomic layer deposition (ECALD) of CdSe, CdTe, and CdS thin films. The collected data suggest that SERS measurements performed with off-resonance (i.e. far from the surface plasmonic wavelength of the underlying SERS substrate) laser excitation do not introduce perturbations to the ECALD processes. Spectra acquired in this way afford rapid insight on the quality of the semiconductor film during the course of an ECALD process. For example, SERS data are used to highlight ECALD conditions that yield crystalline CdSe and CdS films. In contrast, SERS measurements with short wavelength laser excitation show evidence of photoelectrochemical effects that were not germane to the intended ECALD process. Using the semiconductor films prepared by ECALD, the substrate-overlayer SERS approach also affords analysis of semiconductor surface adsorbates. Specifically, Raman spectra of benzenethiol adsorbed onto CdSe, CdTe, and CdS films are detailed. Spectral shifts in the vibronic features of adsorbate bonding suggest subtle differences in substrate-adsorbate interactions, highlighting the sensitivity of this methodology.

Topics: Cadmium Compounds; Electrochemistry; Selenium Compounds; Spectrum Analysis, Raman; Sulfides; Surface Properties; Tellurium

A TiO2/CdS:Mn hybrid structure cosensitized with two different sizes of CdTe quantum dots (QDs) was designed to develop a novel and ultrasensitive photoelectrochemical DNA assay. In this protocol, TiO2/CdS:Mn hybrid structure was prepared by successive adsorption and reaction of Cd(2+)/Mn(2+) and S(2-) ions on the surface of TiO2 film and then was employed as matrix for immobilization of hairpin DNA probe, whereas large-sized CdTe-COOH QDs and small-sized CdTe-NH2 QDs as signal amplification elements were successively labeled on the terminal of hairpin DNA probe. The target DNA detection was based upon the photocurrent change originated from conformation change of the hairpin DNA probe after hybridization with target DNA. In the absence of target DNA, the immobilized DNA probe was in the hairpin form and the anchored different sizes of CdTe-COOH and CdTe-NH2 QDs were close to the TiO2/CdS:Mn electrode surface, which led to a very strong photocurrent intensity because of the formation of the cosensitized structure. However, in the presence of target DNA, the hairpin DNA probe hybridized with target DNA and changed into a more rigid, rodlike double helix, which forced the multianchored CdTe QDs away from the TiO2/CdS:Mn electrode surface, resulting in significantly decreased photocurrent intensity because of the vanished cosensitization effect. By using this cosensitization signal amplification strategy, the proposed DNA assay could offer an ultrasensitive and specific detection of DNA down to 27 aM, and it opened up a new promising platform to detect various DNA targets at ultralow levels for early diagnoses of different diseases.

Topics: Biosensing Techniques; Cadmium Compounds; DNA; Electrochemical Techniques; Limit of Detection; Manganese; Microscopy, Electron, Transmission; Photochemical Processes; Quantum Dots; Sulfides; Tellurium; Titanium

The marriage of energy transfer with electrochemiluminescence has produced a new technology named electrochemiluminescence energy transfer (ECL-ET), which can realize effective and sensitive detection of biomolecules. To obtain optimal ECL-ET efficiency, perfect energy overlapped donor/acceptor pair is of great importance. Herein, we present a sensitive ECL-ET based immunosensor for the detection of tumor markers, using energy tunable CdSeTe/CdS/ZnS double shell quantum dots (QDs) and gold nanorods (GNRs) as the donor and acceptor, respectively. Firstly a facile microwave-assisted strategy for the synthesis of green- to near-infrared-emitting CdSeTe/CdS/ZnS QDs with time- and component-tunable photoluminescence was proposed. And, on the basis of the adjustable optical properties of both CdSeTe/CdS/ZnS QDs and GNRs, excellent overlap between donor emission and acceptor absorption can be obtained to ensure effective ECL-ET quenching, thus improving the sensing sensitivity. This method represents a novel approach for versatile detection of biomolecules at low concentrations.

Topics: Biomarkers, Tumor; Biosensing Techniques; Cadmium; Cadmium Compounds; Carcinoembryonic Antigen; Electrochemical Techniques; Energy Transfer; Humans; Immunoassay; Luminescent Measurements; Nanotubes; Quantum Dots; Selenium; Sulfides; Tellurium; Zinc Compounds

This study explored a simple and fast method utilizing ultraviolet (UV) irradiation to synthesize CdTe/CdS/ZnS QDs in aqueous solution. Based on the reaction of photolysis and chemical deposition, the CdS and ZnS shell can be successively deposited around the thiol-capped CdTe cores through the interaction of Cd²⁺/Zn²⁺ and S²⁻ produced by UV irradiation. The effect of the UV irradiation time, the ratios of thioglycolic acid (TGA)/Cd and TGA/Zn on the shell formation, shell stability, and the photoluminescence (PL) intensity of the QDs, was systematically investigated. Keeping the ratio of TGA/Cd, increasing UV irradiation time from 30 to 120 s, the blue-shift of the fluorescence emission peak position of CdTe/CdS QDs was observed. As the irradiation time increased continuously from 120 to 300 s, the red-shift of the emission peak position was observed. In the total irradiation time, the PL intensity of all the samples was enhanced. By applying 300 s irradiation on the samples, the emission peak was blue-shifted at a fixed TGA/Cd ratio of 1:1 and red-shifted at the ratios of 2:1, 4:1, 8:1, and 13:1. The PL intensity reached its highest value at the ratio of 2:1. The effect of TGA/Zn ratio on ZnS shell formation showed a similar progress. Under an optimum synthesized reaction condition, the particle sizes of CdTe core, CdTe/CdS core-shell and CdTe/CdS/ZnS core-shell-shell QDs were 2.6 nm, 3.4 nm, and 4.6 nm respectively. This study confirmed that with the core-shell-shell structure, CdTe/CdS/ZnS QDs had high anti-oxidability, photostability, and low toxicity. Therefore they can be further used in cell imaging efficiently.

Topics: Biocompatible Materials; Cadmium Compounds; Cell Line; Cell Survival; Fluorescent Dyes; Humans; Microscopy, Confocal; Quantum Dots; Spectrometry, Fluorescence; Sulfides; Tellurium; Ultraviolet Rays; Water; Zinc Compounds

The increasing use of products derived from nanotechnology has raised concern about their potential toxicity to aquatic life. This study sought to examine the comparative immunotoxicity of capped cadmium sulphide/cadmium telluride (CdS/CdTe) quantum dots (QDs) and possible impact of particle/aggregate size on two bivalves (Mytilus edulis and Elliptio complanata) and a fish (Oncorhynchus mykiss). The QDs were dispersed in sterile water and fractionated using a series of micro/ultrafiltration membranes of decreasing pore size: 450 nm, 100 nm, 50 nm, 25 nm, 100 kDa (6.8 nm), 30 kDa (4.6 nm), 10 kDa (3.2 nm) and 1 kDa (1.5 nm). The total concentrations of cadmium and tellurium were determined for the filtered material and for that retained on the filters (retentate). The immunotoxicity was determined by measuring cell viability and phagocytosis. Results revealed that nanoparticles retained on the ultrafilters had a higher Cd/Te ratio compared to the permeate fraction (ratio of 5 and 2 respectively) which could indicate that the CdS core was not associated with the permeable fraction of Cd. Our results demonstrate that the toxicity of CdS/CdTe QDs was concentration and size dependent. Large CdS/CdTe QD aggregates (25 nm < size < 100 nm) reduced phagocytosis more than did smaller nanoparticles (<25 nm). Moreover, our results revealed that the different species responded differently to these fractions. Mytilus edulis hemocytes were less sensitive to CdS/CdTe QDs than the Oncorhynchus mykiss macrophage and Elliptio complanata hemocytes.

Topics: Animals; Bivalvia; Cadmium Compounds; Cell Survival; Hemocytes; Macrophages; Oncorhynchus mykiss; Particle Size; Phagocytosis; Quantum Dots; Sulfides; Tellurium

An octachlorostyrene (OCS) photoelectrochemical (PEC) immunosensor was developed by cross-linking anti-OCS antibody onto a CdTe/CdS-sensitized TiO2 nanotube arrays (NTAs). The anti-OCS polyclonal antibody was developed in rabbit as a result of immunization with BSA-OCS hapten conjugate. TiO2 NTAs were immobilized firstly with hydrothermally synthesized CdTe quantum dots (QDs), and then CdS which filled the spaces within the CdTe-TiO2 composite and encapsulated the CdTe QDs, forming an ideal stepwise bandedge structure, which benefited the light harvesting. The PEC immunosensor therefore shows high specificity and high sensitivity with a limit of detection of 2.58 pM, and a linear range from 5 pM to 50 nM. The testing time is 4 min. The analysis of river water reveals that the proposed sensor can be applied in the analysis of OCS in real water samples without complicated pre-treatments.

Topics: Animals; Cadmium Compounds; Electrochemical Techniques; Environmental Monitoring; Equipment Design; Immunoassay; Limit of Detection; Nanotubes; Quantum Dots; Rabbits; Rivers; Styrenes; Sulfides; Tellurium; Titanium; Water Pollutants, Chemical

Near-infrared (NIR, 700-900 nm) fluorescent quantum dots are highly promising as NIR bioprobes for high-resolution and high-sensitivity bioimaging applications. In this article, we present a class of NIR-emitting CdTe/CdS/ZnS core-shell-shell quantum dots (QDs), which are directly prepared in aqueous phase via a facile microwave synthesis. Significantly, the prepared NIR-emitting QDs possess excellent aqueous dispersibility, strong photoluminescence, favorable biocompatibility, robust storage-, chemical-, and photo-stability, and finely tunable emission in the NIR range (700-800 nm). The QDs are readily functionalized with antibodies for use in immunofluorescent bioimaging, yielding highly spectrally and spatially resolved emission for in vitro and in vivo imaging. In comparison to the large size of 15-30 nm of the conventional NIR QDs, the extremely small size (≈ 4.2 nm or 7.5 nm measured by TEM or DLS, respectively) of our QDs offers great opportunities for high-efficiency and high-sensitivity targeted imaging in cells and animals.

Topics: Animals; Cadmium Compounds; HeLa Cells; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasms; Optical Imaging; Quantum Dots; Solubility; Sulfides; Tellurium; Water; Zinc Compounds

Novel CdTe/CdS/SiO2 core/multishell fluorescent composite nanoparticles were prepared by reverse microemulsion method in this paper. Water-soluble CdTe/CdS core/shell quantum dots (QDs) were synthesized with 3-mercaptopropionic acid as the stabilizers and thiourea as the sulphur source in aqueous solution. CdTe/CdS/SiO2 fluorescent nanoparticles were obtained by hydrolysis of tetraethyl orthosilicate (TEOS) at room temperature in cyclohexane solution when polyethylene glycol tert-octylphenyl ether (Triton X-100) as the surfactant and n-hexanol as the co-surfactant. The resultant core/multishell fluorescent composite nanoparticles were inert and chemically stable in harsh environments because of the silica layer. In this paper, the diameter of these particles was about 64 nm, and the maximum emission was about 678 nm. The coating of silica could provide a great convenience for the biological functionalization of the surface of luminescent QDs and be useful to label biological molecules in vitro and vivo in the biological analyses.

Topics: Cadmium Compounds; Microscopy, Electron, Transmission; Nanoparticles; Silicon Dioxide; Sulfides; Tellurium

Water-soluble CdTe/CdS quantum dots (QDs) with tuneable emissions were prepared in aqueous solution at pH=6-7 via refluxing and hydrothermal treatment. The resultant CdTe/CdS QDs are stabilized with mercaptosuccinic acid (MSA) and show high fluorescence quantum yields (maximum QY is 84%). Characterization with UV-Vis, PL, XPS, XRD and TEM demonstrates a core (CdTe)-shell (CdS) structure, which leads to high fluorescence quantum yields. The effective protection from CdS shell and MSA enables CdTe QDs to be chemically stable in a pH range of 6-9 and less toxic. These merits make our CdTe/CdS QDs very promising for bio-imaging applications, as exemplified by labelling HEK 293 cells.

Topics: Cadmium Compounds; HEK293 Cells; Humans; Hydrogen-Ion Concentration; Materials Testing; Quantum Dots; Sulfides; Tellurium

This paper describes the development of a simplified and rapid method for the aqueous synthesis of quantum dots (QDs) with CdTe cores and gradient CdS external shells (CdTe/CdS QDs) aided by microwave irradiation. Several synthesis parameters, such as molar ratio of reagents, pH, reaction temperature, and reaction time, were studied in details. Under the optimized conditions, highly effective CdTe/CdS QDs could be synthesized in aqueous phase in only 15 min. In order to improve the biocompatibility of the CdTe/CdS QDs, these QDs were then interacted with carboxymethyl chitosan (CMC) so as they could be used as fluorescent probes in the aqueous phase. With the incorporation of CMC, the stability of modified QDs was found to have improved significantly (from 4 months to more than 10 months at room temperature). The photoluminescence quantum yield (PLQY) of the modified QDs could reach 75%, other parameters include a full width at half maximum of the emission (FWHM) spectrum as 40 ~ 60 nm, and an average size, estimated from electron microscopic images, as 3.5 nm. As fluorescent probes, these modified QDs were successfully used for imaging live Madin-Darby canine kidney (MDCK) cells, in which the preliminary results indicated that these modified QDs demonstrated good biocompatibility and showed promising applications for bio-labeling and imaging.

Topics: Animals; Cadmium Compounds; Cell Line; Cell Survival; Chitosan; Dogs; Fluorescent Dyes; Microwaves; Molecular Imaging; Optical Phenomena; Quantum Dots; Spectrometry, Fluorescence; Sulfides; Tellurium; Water

A novel dual-fluorescence quantum dots (QD) nanocomposite with tuning emission wavelength and fluorescence intensity was synthesized, in which CdS and CdTe were the internal standard and probe, respectively. This nanocomposite exhibited good photobleaching and pH stability, and exhibited selective sensing for Hg(2+) with a detection limit (3SD/k) of 5.6 nM. Based on the blue background emitted by the internal standard CdS, a novel visual fluorescence detection method has been established, and can be used for the qualitative and semi-quantitative colorimetric analysis of Hg(2+).

Topics: Cadmium Compounds; Environmental Pollutants; Fluorescent Dyes; Mercury; Nanocomposites; Quantum Dots; Reference Standards; Spectrometry, Fluorescence; Sulfides; Tellurium; Thioglycolates

To be able to label a gene and monitor its migration are key important approaches for the clinical application of cancer suicide gene therapy. Photonic nanomaterials are introduced in this work. One of the most promised suicide genes - herpes simplex virus thymidine kinase (HSV-TK) gene - is successfully linked with CdTe/CdS core/shell quantum dots (QDs) via EDC/NHS coupling method. From confocal microscopy it was demonstrated that plasmid TK intracellular trafficking can be effectively and distinctly traced via monitoring the luminescence of the QDs up to 96 h after transfection of QDs-TK conjugates into Hela cells. MTT results show that the QDs-TK conjugates have a high efficient cytotoxicity after adding GCV into Hela cells, whereas the QDs exert no detectable deleterious effects on the cellular processes. The apoptosis induced by QDs-TK conjugates with GCV is distinctly traced partly due to the strong luminescence of the QDs. Our results indicate that photonic nanomaterials, e.g. QDs, provide a tool for monitoring TK gene delivery and anti-cancer activity.

Topics: Antineoplastic Agents; Cadmium Compounds; Cell Death; Cell Shape; Cell Survival; Electrophoresis, Agar Gel; Ganciclovir; Genes, Transgenic, Suicide; Genetic Therapy; HeLa Cells; Humans; Neoplasms; Quantum Dots; Reproducibility of Results; Simplexvirus; Solubility; Sulfides; Tellurium; Thymidine Kinase; Transfection; Water

CdTe/CdS core(small)/shell(thick) quantum dots (QDs) with tunable near-infrared fluorescence were directly synthesized in aqueous phase through a facile one-step strategy. The QDs possessed bright fluorescence, ultrasmall size, excellent photostability and good biocompatibility. Their applicability for biological imaging was demonstrated with the in vivo active tumor targeting of nude mice.

Topics: Animals; Cadmium Compounds; Fluorescent Dyes; Mice; Mice, Nude; Neoplasms; Quantum Dots; Sulfides; Tellurium

Here we demonstrate the aqueous synthesis of colloidal nanocrystal heterostructures consisting of the CdTe core encapsulated by CdS/ZnS or CdSe/ZnS shells using glutathione (GSH), a tripeptide, as the capping ligand. The inner CdTe/CdS and CdTe/CdSe heterostructures have type-I, quasi-type-II, or type-II band offsets depending on the core size and shell thickness, and the outer CdS/ZnS and CdSe/ZnS structures have type-I band offsets. The emission maxima of the assembled heterostructures were found to be dependent on the CdTe core size, with a wider range of spectral tunability observed for the smaller cores. Because of encapsulation effects, the formation of successive shells resulted in a considerable increase in the photoluminescence quantum yield; however, identifying optimal shell thicknesses was required to achieve the maximum quantum yield. Photoluminescence lifetime measurements revealed that the decrease in the quantum yield of thick-shell nanocrystals was caused by a substantial decrease in the radiative rate constant. By tuning the diameter of the core and the thickness of each shell, a broad range of high quantum yield (up to 45%) nanocrystal heterostructures with emission ranging from visible to NIR wavelengths (500-730 nm) were obtained. This versatile route to engineering the optical properties of nanocrystal heterostructures will provide new opportunities for applications in bioimaging and biolabeling.

Topics: Cadmium Compounds; Glutathione; Molecular Structure; Nanoparticles; Particle Size; Sulfides; Surface Properties; Tellurium; Water; Zinc Compounds

This work reports an ECL immunoassay method for ultrasensitive detection of prostate protein antigen (PSA), by remarkably efficient energy-transfer induced electrochemiluminescence (ECL) quenching from the CdS nanoparticles (NPs) sensitized TiO(2) nanotube array (CdS-TiO(2) NTs) to the activated CdTe NPs functionalized multi-wall carbon nanotubes (CdTe-MWNTs) composite. The coupling of TiO(2) and CdS NPs results in a cathodic ECL intensity 14.7 times stronger than that of the pure TiO(2) NTs electrode, which could be efficiently quenched by the CdTe-MWNTs. The enhanced mechanism of TiO(2) NTs ECL by CdS NPs was studied in detail by cyclic voltammetry and ECL spectroscopy. The strong absorption of the CdTe-MWNTs in the wavelength range of 400-800 nm renders them highly efficient for ECL quenching labeled on anti-PSA antibody. Based on a sandwich structure, we developed an ECL immunoassay method for the sensitive and selective detection of PSA. The ECL intensity decrement was logarithmically related to the concentration of the PSA in the range of 1.0 fg mL(-1) to 10 pg mL(-1) with a detection limit of 1 fg mL(-1). Human serum samples were then tested using the proposed immunoassay with excellent correlations, suggesting that the proposed immunoassay method is of great promise in clinical screening of cancer biomarkers.

Topics: Antigens; Cadmium Compounds; Electrochemical Techniques; Humans; Male; Microscopy, Electron, Transmission; Nanotubes, Carbon; Prostate; Sulfides; Tellurium; Titanium

A novel and portable strategy based on fluorescence polarization immunoassay (FPIA) using quantum dots (QDs) was described in this study for simple, rapid, and sensitive detection of carcinoembryonic antigen (CEA). Under optimal conditions, the sensor has a wide dynamic range (from 0.5 ng/mL to 200 ng/mL) and a good correlation. The limit of detection (LOD) is 0.21 ng/mL (S/N = 3). The sensor has been applied for detection of carcinoembryonic antigen in 10 human serum samples with the range of recovery from 92.1 % to 103.6 %. Furthermore, bioconjugation of the core-shell QDs with streptavidin (SA) has been successfully applied in immunofluorescent imaging of the human hepatocellular carcinoma (HEPG2) cell line. The experimental results demonstrated the successful application of QDs-based fluorescence polarization immunoassay for detection of target proteins of biomedical importance. This strategy shows great promise for clinical diagnoses and basic discovery with high sensitivity, good specificity, simple procedures and short analysis time.

Topics: Antibodies; Biophysical Phenomena; Cadmium Compounds; Calibration; Carcinoembryonic Antigen; Fluorescence Polarization Immunoassay; Hep G2 Cells; Humans; Molecular Imaging; Sulfides; Tellurium; Time Factors

Quantum dots (QDs) show promise as novel nanomaterials for sentinel lymph node (SLN) mapping through their use in noninvasive in vivo fluorescence imaging, and they have provided remarkable results. However, in vivo fluorescence imaging has limitations mainly reflected in the strong autofluorescence and low deepness of tissue penetration associated with this technique. Here, we report on the use of self-illuminating 3-mercaptopropionic acid-capped CdTe/CdS QDs for mouse axillary SLN mapping by bioluminescence resonance energy transfer, which was found to overcome these limitations [corrected]. We used CdTe/CdS QDs synthesized in aqueous solution to conjugate a mutant of the bioluminescent protein, Renilla reniformis luciferase. The nanobioconjugates obtained had an average hydrodynamic diameter of 19 nm, and their luminescence catalyzed by the substrate (coelenterazine) could penetrate into at least 20 mm of hairless pigskin, which could be observed using an in vivo imaging system equipped with a 700 nm emission filter. Conversely, the fluorescence of the nanobioconjugates penetrated no more than 10 mm of pigskin and was observed with a strong background. When 80 μL of the nanobioconjugates (containing about 0.5 μmol/L of QDs) and 5 μL of coelenterazine (1 μg/μL) were intradermally injected into a mouse paw, the axillary SLN could be imaged in real time without external excitation, and little background interference was detected. Furthermore, the decayed luminescence of QD-Luc8 in SLNs could be recovered after being intradermally reinjected with the coelenterazine. Our data showed that using self-illuminating QDs, as opposed to fluorescence QDs, has greatly enhanced sensitivity in SLN mapping, and that the SLN could be identified synchronously by the luminescence and fluorescence of the self-illuminating QDs.

Topics: 3-Mercaptopropionic Acid; Animals; Cadmium Compounds; Fluorescent Dyes; Injections, Intradermal; Luminescent Measurements; Lymph Nodes; Mice; Nanoconjugates; Optical Imaging; Quantum Dots; Sentinel Lymph Node Biopsy; Skin; Skin Absorption; Spectrometry, Fluorescence; Sulfides; Swine; Tellurium; Whole Body Imaging

A novel fluorescent probe for Cu(2+) determination based on the fluorescence quenching of glyphosate (Glyp)-functionalized quantum dots (QDs) was firstly reported. Glyp had been used to modify the surface of QDs to form Glyp-functionalized QDs following the capping of thioglycolic acid on the core-shell CdTe/CdS QDs. Under the optimal conditions, the response was linearly proportional to the concentration of Cu(2+) between 2.4×10(-2)μg mL(-1) and 28μg mL(-1), with a detection limit of 1.3×10(-3)μg mL(-1) (3δ). The Glyp-functionalized QDs fluorescent probe offers good sensitivity and selectivity for detecting Cu(2+). The fluorescent probe was successfully used for the determination of Cu(2+) in environmental samples. The mechanism of reaction was also discussed.

Topics: Cadmium Compounds; Copper; Environmental Monitoring; Fluorescence; Fluorescent Dyes; Glycine; Glyphosate; Ions; Limit of Detection; Microscopy, Electron, Transmission; Molecular Probe Techniques; Quantum Dots; Sensitivity and Specificity; Sulfides; Tellurium; Thioglycolates; Wastewater

The assembly and isolation of DNA oligonucleotide-functionalized gold nanoparticles (AuNPs) has become a well-developed technology that is based on the strong bonding interactions between gold and thiolated DNA. However, achieving DNA-functionalized semiconductor quantum dots (QDs) that are robust enough to withstand precipitation at high temperature and ionic strength through simple attachment of modified DNA to the QD surface remains a challenge. We report the synthesis of stable core/shell (1-20 monolayers) QD-DNA conjugates in which the end of the phosphorothiolated oligonucleotide (5-10 nucleotides) is "embedded" within the shell of the QD. These reliable QD-DNA conjugates exhibit excellent chemical and photonic stability, colloidal stability over a wide pH range (4-12) and at high salt concentrations (>100 mM Na(+) or Mg(2+)), bright fluorescence emission with quantum yields of up to 70%, and broad spectral tunability with emission ranging from the UV to the NIR (360-800 nm).

Topics: Cadmium Compounds; DNA; Fluorescence; Gold; Infrared Rays; Metal Nanoparticles; Quantum Dots; Semiconductors; Sulfides; Tellurium; Ultraviolet Rays

Colloidal CdTe quantum wires are reported having ensemble photoluminescence efficiencies as high as 25% under low excitation-power densities. High photoluminescence efficiencies are achieved by formation of a monolayer CdS shell on the CdTe quantum wires. Like other semiconductor nanowires, the CdTe quantum wires may contain frequent wurtzite-zinc-blende structural alternations along their lengths. The present results demonstrate that the optical properties, emission-peak shape and photoluminescence efficiencies, are independent of the presence or absence of such structural alternations.

Topics: Cadmium Compounds; Colloids; Quantum Dots; Semiconductors; Sulfides; Tellurium

An easy process was developed to synthesize TiO(2) nanowires sensitized with CdS and CdTeS quantum dots (QDs) requiring no pretreatment of the TiO(2) nanowires prior to nanoparticle generation. CdS and CdTeS nanoparticles were firstly grown by an in situ colloidal method directly onto the TiO(2) surface, hence not requiring subsequent functionalization of the QDs. The resulting nanostructure assembly and composition was confirmed by transmission electron microscopy (TEM), x-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Successful decoration of the TiO(2) nanowires by the QDs was observed by TEM, while XPS spectra provided clear evidence for the coexistence of CdS and CdTeS QDs and TiO(2) nanowires. The electronic structure of the TiO(2) nanowires was preserved as indicated by Raman spectroscopy. Preliminary photocurrent measurements showed that inclusion of Te in CdS QDs improved the photocurrent efficiency. Compared to bare TiO(2) nanowires, CdS/TiO(2) nanoassemblies showed an enhancement in photocurrent efficiency of 300% while CdTeS/TiO(2) presented an improvement of 350%. This study indicates that the generation of strongly anchored CdS and CdTeS QDs on a TiO(2) nanowire surface is achievable without introduction of a linker molecule, whose presence is known to decrease the electron injection efficiency.

Topics: Cadmium Compounds; Nanowires; Particle Size; Photochemical Processes; Quantum Dots; Spectrum Analysis, Raman; Sulfides; Tellurium; Titanium; X-Ray Diffraction

In this study, we design a FRET system consisting of gold nanorod (AuNR) and quantum dots (QDs) for turn-on fluorescent sensing of 2,4,6-trinitrotoluene (TNT) in near-infrared region. The amine-terminated AuNR and carboxyl-terminated QDs first form a compact hybrid assembly through amine-carboxyl attractive interaction, which leads to a high-efficiency (>92%) FRET from QDs to AuNRs and an almost complete emission quenching. Next, added TNT molecules break the preformed assembly because they can replace the QDs around AuNRs, based on the specific reaction of forming Meisenheimer complexes between TNT and primary amines. Thus, the FRET is switched off, and a more than 10 times fluorescent enhancement is obtained. The fluorescence turn-on is immediate, and the limit of detection for TNT is as low as 0.1 nM. Importantly, TNT can be well distinguished from its analogues due to their electron deficiency difference. The developed method is successfully applied to TNT sensing in real environmental samples.

Topics: Cadmium Compounds; Chemistry Techniques, Analytical; Fluorescence Resonance Energy Transfer; Gold; Infrared Rays; Nanotubes; Quantum Dots; Sulfides; Tellurium; Trinitrotoluene

A simple one-pot polymer encapsulation method is developed for group II-VI semiconductor quantum dots (QDs) synthesized in aqueous solution. The micelles of amphiphilic polymers, such as octadecylamine-modified poly(acrylic acid), capture and encapsulate the QDs when the original hydrophilic ligands, namely 3-mercaptopropionic acid (MPA), capped on the CdTe/CdS core/shell QDs are partially or fully exchanged by the hydrophobic ligands, 1-dodecanethiol. The molar ratio of the amphiphilic polymer to QDs plays a crucial role in determining the final morphology of the encapsulated structures, including the number of QDs encapsulated in one polymeric micelle. Importantly, the polymer coating significantly improves the optical properties of the QDs, which enhances the photoluminescence quantum yield by about 50%. Furthermore, the photostability of the amphiphilic polymer-coated QDs is much better than that of the synthesized QDs capped with MPA.

Topics: Acrylic Resins; Amines; Cadmium Compounds; Electrophoresis, Polyacrylamide Gel; Luminescence; Nanotechnology; Polymers; Quantum Dots; Solutions; Spectrophotometry, Ultraviolet; Sulfides; Surface-Active Agents; Tellurium

A fluorescent magnetic hybrid imaging nanoprobe (HINP) was fabricated by the conjugation of superparamagnetic Fe3O4 nanoparticles and visible light emitting (∼600 nm) fluorescent CdTe/CdS quantum dots (QDs). The assembly strategy used the covalent linking of the oxidized dextran shell of magnetic particles to the glutathione ligands of QDs. The synthesized HINP formed stable water-soluble colloidal dispersions. The structure and properties of the particles were characterized by transmission electron and atomic force microscopy, energy dispersive x-ray analysis and inductively coupled plasma optical emission spectroscopy, dynamic light scattering analysis, optical absorption and photoluminescence spectroscopy, and fluorescent imaging. The luminescence imaging region of the nanoprobe was extended to the near-infrared (NIR) (∼800 nm) by conjugation of the superparamagnetic nanoparticles with synthesized CdHgTe/CdS QDs. Cadmium, mercury based QDs in HINP can be easily replaced by novel water-soluble glutathione stabilized AgInS2/ZnS QDs to present a new class of cadmium-free multimodal imaging agents. The observed NIR photoluminescence of fluorescent magnetic nanocomposites supports their use for bioimaging. The developed HINP provides dual-imaging channels for simultaneous optical and magnetic resonance imaging.

Topics: Absorption; Cadmium Compounds; Ferric Compounds; Fluorescence; Hydrodynamics; Ligands; Magnetic Resonance Imaging; Magnetics; Molecular Probes; Nanoparticles; Particle Size; Phantoms, Imaging; Quantum Dots; Spectrometry, Fluorescence; Sulfides; Tellurium; Ultraviolet Rays

This work reports an aptasensor for ultrasensitive detection of thrombin based on remarkably efficient energy-transfer induced electrochemiluminescence (ECL) quenching from CdS:Mn nanocrystals (NCs) film to CdTe QDs-doped silica nanoparticles (CdTe/SiO(2) NPs). CdTe/SiO(2) NPs were synthesized via the Stöber method and showed black bodies' strong absorption in a wide spectral range without excitonic emission, which made them excellent ECL quenchers. Within the effective distance of energy scavenging, the ECL quenching efficiency was dependent on the number of CdTe QDs doped into the silica NPs. Using ca. 200 CdTe QDs doped silica NPs on average of 40 nm in diameter as ECL quenching labels, attomolar detection of thrombin was successfully realized. The protein detection involves a competition binding event, based on thrombin replacing CdTe/SiO(2) NPs labeled probing DNA which is hybridized with capturing aptamer immobilized on a CdS:Mn NCs film modified glassy carbon electrode surface by specific aptamer-protein affinity interactions. It results in the displacement of ECL quenching labels from CdS:Mn NCs film and concomitant ECL signal recovery. Owing to the high-content CdTe QDs in silica NP, the increment of ECL intensity (ΔI(ECL)) and the concentration of thrombin showed a double logarithmic linear correlation in the range of 5.0 aM∼5.0 fM with a detection limit of 1aM. And, the aptasensor hardly responded to antibody, bovine serum albumin (BSA), haemoglobin (Hb) and lysozyme, showing good detection selectivity for thrombin. This long-distance energy scavenging could have a promising application perspective in the detection of biological recognition events on a molecular level.

Topics: Cadmium Compounds; DNA; Luminescent Measurements; Manganese; Nanoparticles; Quantum Dots; Silicon Dioxide; Sulfides; Tellurium; Thrombin

We first reported an ultrasensitive hydrogen peroxide biosensor in this work. The biosensor was fabricated by coating graphene-gold nanocomposite (G-AuNP), CdTe-CdS core-shell quantum dots (CdTe-CdS), gold nanoparticles (AuNPs) and horseradish peroxidase (HRP) in sequence on the surface of gold electrode (GE). Cyclic voltammetry and differential pulse voltammetry were used to investigate electrochemical performances of the biosensor. Since promising electrocatalytic synergy of G-AuNP, CdTe-CdS and AuNPs towards hydrogen peroxide was achieved, the biosensor displayed a high sensitivity, low detection limit (S/N=3) (3.2×10(-11) M), wide calibration range (from 1×10(-10) M to 1.2×10(-8) M) and good long-term stability (20 weeks). Moreover, the effects of omitting G-AuNP, CdTe-CdS and AuNP were also examined. It was found that sensitivity of the biosensor is more 11-fold better if G-AuNP, CdTe-CdS and AuNPs are used. This could be ascribed to improvement of the conductivity between graphene nanosheets in the G-AuNP due to introduction of the AuNPs, ultrafast charge transfer from CdTe-CdS to the graphene sheets and AuNP due to unique electrochemical properties of the CdTe-CdS, and good biocompatibility of the AuNPs for horseradish peroxidase. The biosensor is of best sensitivity in all hydrogen peroxide biosensors based on graphene and its composites up to now.

Topics: Armoracia; Biosensing Techniques; Cadmium Compounds; Calibration; Electrochemical Techniques; Gold; Graphite; Horseradish Peroxidase; Hydrogen Peroxide; Limit of Detection; Nanocomposites; Quantum Dots; Sulfides; Tellurium

In order to properly assess the environmental risk of engineered nanoparticles (ENP), it is necessary to determine their fate (including dissolution, aggregation, and bioaccumulation) under representative environmental conditions. CdTe/CdS quantum dots (QD), such as those used in medical imaging, are known to release Cd(2+) due (mainly) to the dissolution of their outer shell. In this study, Chlamydomonas reinhardtii was exposed to either a soluble Cd salt or QD at similar concentrations of total Cd. Free Cd concentrations were measured using the Absence of Gradients and Nernstian Equilibrium Stripping technique. QD dissolution increased with decreasing pH and with increasing QD concentration. When exposed to QD, bioaccumulation was largely accounted for by dissolved Cd. Nonetheless, QD were shown to be taken up by the cells and to provoke unique biological effects. Whole transcriptome screening using RNA-Seq analysis showed that the free Cd and the QD had distinctly different biological effects.

Topics: Cadmium; Cadmium Compounds; Chlamydomonas reinhardtii; Gene Expression Profiling; Gene Expression Regulation, Plant; Hydrogen-Ion Concentration; Nanoparticles; Particle Size; Quantum Dots; Solubility; Sulfides; Tellurium

We report here a new electrochemiluminescence (ECL) approach for detection of single nucleotide polymorphisms (SNPs) based on isothermal cycle-assisted triple-stem probe labeled with Au nanoparticles (NPs) and CdTe NPs. The system is composed of a CdS nanocrystals (NCs) film on glassy carbon electrode (GCE) as ECL emitter attached a double-stem DNA probe labeled with Au NPs. Then, the third stem labeled with CdTe NPs hybridizes with the double-stem DNA to form a triple-stem probe with the two labels near the CdS NCs film. A dual-quenched ECL of CdS NCs film is achieved due to energy transfer (ET) from CdS NCs to Au NPs and CdTe NPs, which makes the sensor exhibit relatively low background. Once the one base mutant DNA (mDNA) sequence as target of SNPs analysis displaces the third stem and hybridizes with the double-stem probe, forcing Au NPs away from the CdS NCs film, an ECL enhancement by the ECL-induced surface plasmon resonance of Au NPs is observed. Furthermore, after an isothermal cycle induced by primer, polymerase, and nicking endonuclease (NEase), a further enhancement of ECL is obtained. Taking advantages of the isothermal circular amplification system and the triple-stem probe architecture which enables turning its high selectivity toward specific target sequences, the reported biosensor shows excellent discrimination capabilities of SNPs with high selectivity and low detection limit (35 aM).

Topics: Biosensing Techniques; Cadmium Compounds; DNA, Mitochondrial; Electrochemical Techniques; Electrodes; Gold; Humans; Luminescent Measurements; Metal Nanoparticles; Mutation; Polymorphism, Single Nucleotide; Sulfides; Tellurium

Ion exchange of ionic semiconductor nanoparticles (NPs) is a facile method for the synthesis of type-II semiconductor heterostructured NPs with staggered alignment of band edges for photoelectric applications. Through consideration of the crystallographic orientation and strain at the heterointerface, well-designed heterostructures can be constructed through ion exchange reactions. Here we report the selective synthesis of anisotropically phase-segregated cadmium sulfide (CdS)/ cadmium telluride (CdTe) heterodimers via a novel anion exchange reaction of CdS NPs with an organic telluride precursor. The wurtzite-CdS/zinc blende-CdTe heterodimers in this study resulted from spontaneous phase segregation induced by the differences in the crystal structures of the two phases, accompanying a centrosymmetry breaking of the spherical CdS NPs. The CdS/CdTe heterodimers exhibited photoinduced spatial charge separation because of their staggered band-edge alignment.

Topics: Anions; Cadmium Compounds; Dimerization; Nanoparticles; Particle Size; Semiconductors; Sulfides; Surface Properties; Tellurium; Zinc

We experimentally investigate carrier multiplication (CM) in type II CdTe/CdSe quantum dot (QD) heterostructures by the means of a simple and robust subnanosecond transient photoluminescence spectroscopy setup. Experimental conditions were set to minimize the blurring of the CM signature by extraneous effects. The extracted photon energy threshold for CM is consistent with previous studies in CdSe and CdTe QDs (around 2.65 times the type II energy band gap) and we can infer an upper bound to CM yield. This study indicates that, while CM is probably present in type II QD heterostructures below the CM threshold for each constituent separately, it exhibits only a modest yield.

Topics: Cadmium Compounds; Colloids; Crystallization; Light; Luminescent Measurements; Nanotechnology; Photochemistry; Photons; Quantum Dots; Selenium Compounds; Sulfides; Surface Properties; Tellurium; Zinc Compounds

The collective properties of nanoparticles manifest in their ability to self-organize into complex microscale structures. Slow oxidation of tellurium ions in cadmium telluride (CdTe) nanoparticles results in the assembly of 1- to 4-micrometer-long flat ribbons made of several layers of individual cadmium sulfide (CdS)/CdTe nanocrystals. Twisting of the ribbons with an equal distribution of left and right helices was induced by illumination with visible light. The pitch lengths (250 to 1500 nanometers) varied with illumination dose, and the twisting was associated with the relief of mechanical shear stress in assembled ribbons caused by photooxidation of CdS. Unusual shapes of multiparticle assemblies, such as ellipsoidal clouds, dog-bone agglomerates, and ribbon bunches, were observed as intermediate stages. Computer simulations revealed that the balance between attraction and electrostatic repulsion determines the resulting geometry and dimensionality of the nanoparticle assemblies.

Topics: Cadmium Compounds; Computer Simulation; Light; Metal Nanoparticles; Microscopy, Electron; Oxidation-Reduction; Quantum Dots; Spectrometry, X-Ray Emission; Sulfides; Tellurium

We demonstrate the synthesis of near-IR-emitting zinc blende CdTe/CdS tetrahedral-shaped nanocrystals with a magic-sized (approximately 0.8 nm radius) CdTe core and a thick CdS shell (up to 5 nm). These high-quality water-soluble nanocrystals were obtained by a simple but reliable aqueous method at low temperature. During the growth of the shell over the magic core, the core/shell nanocrystals change from type I to type II, as revealed by their enormous photoluminescence (PL) emission peak shift (from 480 to 820 nm) and significant increase in PL lifetime (from approximately 1 to approximately 245 ns). These thick-shell nanocrystals have a high PL quantum yield, high photostability, compact size (hydrodynamic diameter less than 11.0 nm), and reduced blinking behavior. The magic-core/thick-shell nanocrystals may represent an important step toward the synthesis and application of next-generation colloidal nanocrystals from solar cell conversion to intracellular imaging.

Topics: Cadmium Compounds; Infrared Rays; Luminescent Measurements; Microscopy, Electron, Transmission; Nanostructures; Semiconductors; Sulfides; Tellurium; Temperature; Water; Zinc

Topics: Cadmium Compounds; Light; NAD; Nanoparticles; Particle Size; Selenium Compounds; Spectrometry, Fluorescence; Sulfides; Tellurium; Time Factors

We report the imaging of hepatocellular carcinoma cells and the immunoassay for alpha fetoprotein (AFP) using CdTe/CdS/ZnS core-shell-shell QDs. Stable and high PLQY (20%-48%) CdTe/CdS/ZnS core-shell-shell QDs were synthesized by a stepwise process. Bioconjugation of the core-shell-shell QDs with streptavidin (SA) was successfully applied in immunofluorescent imaging of the human hepatocellular carcinoma (HCC) cell line HepG2.2.15. Furthermore, the thioglycolic acid (TGA)-capped CdTe/CdS/ZnS core-shell-shell QDs fluorescence lifetime is longer than fluorescein, so it was first engaged to conjugate with antigen for the determination of protein (AFP) by fluorescence polarization immunoassay.

Topics: alpha-Fetoproteins; Cadmium Compounds; Carcinoma, Hepatocellular; Cell Line, Tumor; Chromatography, High Pressure Liquid; Diagnostic Imaging; Fluorescein-5-isothiocyanate; Humans; Immunoassay; Liver Neoplasms; Microscopy, Fluorescence; Quantum Dots; Spectrophotometry, Ultraviolet; Sulfides; Tellurium; Zinc Compounds

Tailor-designed Au/SiO(2) core/shell nanoparticles are employed to enhance the efficiency of fluorescence resonance energy transfer based on quantum dots and R-phycoerythrin in solution.

Topics: Cadmium Compounds; Fluorescence Resonance Energy Transfer; Gold; Phycoerythrin; Quantum Dots; Silicon Dioxide; Solutions; Sulfides; Tellurium

In this report, we evaluated the cytotoxicity of a series of quantum dots (QDs) directly synthesized in aqueous phase, i.e., thiols-stabilized CdTe, CdTe/CdS core-shell structured and CdTe/CdS/ZnS core-shell-shell structured QDs, with a variety of cell lines including K562 and HEK293T. We have demonstrated that the CdTe QDs are highly toxic for cells due to the release of cadmium ions. Epitaxial growth of a CdS layer reduces the cytotoxicity of QDs to a small extent. However, the presence of a ZnS outlayer greatly improves the biocompatibility of QDs, with no observed cytotoxicity even at very high concentration and long-time exposure in cells. Our systematic investigation clearly shows that the cytotoxicity of QDs can be modulated through elaborate surface coatings and that the CdTe/CdS/ZnS core-shell-shell structured QDs directly synthesized in aqueous phase are highly promising biological fluorescent probes for cellular imaging.

Topics: Cadmium Compounds; Cell Death; Cell Survival; Humans; K562 Cells; Quantum Dots; Sulfhydryl Compounds; Sulfides; Surface Properties; Tellurium; Water; Zinc Compounds

Supersaturation was found to play a pivotal role during nanoparticle-synthesis and its subtle variation helped achieve two prime objectives: (a) high photoluminescence quantum efficiency (PLQE) and (b) narrow size distribution, thereby obviating the need for post-preparative treatments. Degree of supersaturation of initial synthetic mixture was varied by changing the concentration of reagents while keeping their molar ratio constant at 1:2.5:0.5 for [Cd(2+)]:[cysteine]:[chalcogenide]. An eight-fold increase in supersaturation caused a sharp focusing of size distribution by 64% for CdS quantum dots (QDs). The as-prepared CdS and CdTe QDs were found to have size distribution as low as 4% at higher supersaturation. For a four-fold increase in supersaturation, PLQE of as-prepared CdTe QDs (4.3 nm) rose by 5 times to a remarkably high value of 54%. The focusing of size distribution with increasing supersaturation was found to work well even in the absence of any stabilizer. A substantial overlap of nucleation and growth was found at low supersaturation (0.5S(CdTe)), whereas a good separation of the two events is achieved at a higher supersaturation (4S(CdTe)). This study provides a simplified aqueous route for producing highly monodisperse, photoluminescent and biocompatible nanoparticles.

Topics: Biocompatible Materials; Cadmium Compounds; Luminescence; Particle Size; Quantum Dots; Sulfides; Surface Properties; Tellurium; Time Factors; Water

We present and discuss results and features related to the synthesis of water-soluble semiconductor quantum dots and their application as fluorescent biomarkers in cancer diagnostics. We have prepared and applied different core-shell quantum dots, such as cadmium telluride-cadmium sulfide, CdTe-CdS, and cadmium sulfide-cadmium hydroxide, CdS/Cd(OH)(2), in living healthy and neoplastic cells and tissues samples. The CdS/Cd(OH)(2) quantum dots presented the best results, maintaining high levels of luminescence as well as high photostability in cells and tissues. Labeled tissues and cells were analyzed by their resulting fluorescence, via conventional fluorescence microscopy or via laser scanning confocal microscopy. The procedure presented in this work was shown to be efficient as a potential tool for fast and precise cancer diagnostics.

Topics: Cadmium Compounds; Cell Line, Tumor; Cells, Cultured; Cervix Uteri; Female; Fluorescence; Glioma; Humans; Microscopy, Confocal; Microscopy, Fluorescence; Nanotechnology; Neoplasms; Neuroglia; Quantum Dots; Sulfides; Tellurium; Uterine Cervical Dysplasia

Selective quenching of luminescence of quantum dots (QDs) by Cu2+ ions vis-à-vis other physiologically relevant cations has been reexamined. In view of the contradiction regarding the mechanism, we have attempted to show why Cu2+ ions quench QD-luminescence by taking CdS and CdTe QDs with varying surface groups. A detailed study of the solvent effect and also size dependence on the observed luminescence has been carried out. For a 13% decrease in particle diameter (4.3 nm -->3.7 nm), the quenching constant increased by a factor of 20. It is established that instead of surface ligands of QDs, conduction band potential of the core facilitates the photo-induced reduction of Cu (II) to Cu (I) thereby quenching the photoluminescence. Taking the advantage of biocompatibility of dendrimer and its high affinity towards Cu2+ ions, we have followed interaction of Cu2+-PAMAM and also dendrimer with the CdTe QDs. Nanomolar concentration of PAMAM dendrimer was found to quench the luminescence of CdTe QDs. In contrast, Cu2+-PAMAM enhanced the fluorescence of CdTe QDs and the effect has been attributed to the binding of Cu2+-PAMAM complex to the CdTe particle surface. The linear portion of the enhancement plot due to Cu2+-PAMAM can be used for determination of Cu2+ ions with detection limit of 70 nM.

Topics: Cadmium Compounds; Copper; Dendrimers; Fluorescent Dyes; Ions; Ligands; Luminescence; Particle Size; Polyamines; Quantum Dots; Sulfides; Surface Properties; Tellurium

Topics: Anisotropy; Cadmium Compounds; Crystallization; Electronics; Metal Nanoparticles; Microscopy, Electron, Scanning; Microscopy, Electron, Transmission; Nanoparticles; Nanotechnology; Optics and Photonics; Sulfides; Tellurium; Ultraviolet Rays; X-Ray Diffraction

Topics: Cadmium; Cadmium Compounds; Crystallization; Electrochemistry; Metal Nanoparticles; Microscopy, Electron, Transmission; Nanoparticles; Nanotechnology; Quantum Dots; Selenium; Semiconductors; Spectrophotometry; Sulfides; Tellurium

Ultrasonic irradiation of core/shell structures was shown to lead to low toxicity and high quantum yields relative to thermal methods for bio-application.

Topics: Animals; Antibodies; Cadmium Compounds; Cell Survival; Chlorocebus aethiops; HeLa Cells; Herpesvirus 1, Human; Humans; Luminescent Agents; Luminescent Measurements; Microscopy, Confocal; Nanostructures; Particle Size; Quantum Theory; Semiconductors; Solubility; Sonication; Sulfides; Tellurium; Thioglycolates; Thymidine Kinase; Ultrasonics; Vero Cells

In this work we used a setup consisting of an optical tweezers combined with a nonlinear microspectroscopy system to perform scanning microscopy and obtain emission spectra using two photon excited (TPE) luminescence of captured single living cells labeled with core-shell fluorescent semiconductor quantum dots (QDs). The QDs were obtained via colloidal synthesis in aqueous medium with an adequate physiological resulting pH. Sodium polyphosphate was used as the stabilizing agent. The results obtained show the potential presented by this system as well as by these II-VI fluorescent semiconductor quantum dots to perform spectroscopy in living trapped cells in any neighborhood and dynamically observe the cell chemical reactions in real time.

Topics: Animals; Cadmium Compounds; Macrophages, Peritoneal; Mice; Mice, Inbred BALB C; Microscopy, Confocal; Microspectrophotometry; Optical Tweezers; Quantum Dots; Selenium Compounds; Silicon; Spectrometry, Fluorescence; Spectrum Analysis, Raman; Sulfides; Tellurium; Titanium; Zinc Compounds

Commercially available quantum dots (QDs) were characterized using CE. The CE instruments were laboratory-built, each being capable of both electrokinetic and hydrodynamic injection. Modes of detection include UV absorption and LIF. The CE-LIF system was further modified to handle microliter sample volumes during injection. Sodium phosphate (5-25 mM, pH 7.5-11) was found to be a good buffer electrolyte. Sodium mercaptoproprionate CdTe/CdS (ADS620) QDs and carboxylic acid CdSe/ZnS (T2-Evitag) QDs yielded high separation efficiencies of N = 1.5x10(6) plates at t(M) = 10 min and N = 1.0x10(5) plates at t(M) = 3.8 min, respectively. Apparently the EDC/sulfo-NHS bioconjugation chemistry worked well with the neutral T2-Evitag QDs, but not so well with the negatively charged ADS620 QDs. This preliminary knowledge will serve as a basis for new CE immunoassay studies of QD-biomolecule conjugates and their immunocomplexes with target analytes.

Topics: Animals; Cadmium Compounds; Cattle; Electrophoresis, Capillary; Equipment Design; Quantum Dots; Selenium Compounds; Serum Albumin, Bovine; Sulfides; Tellurium; Zinc Compounds

Four different types of solar cells prepared in different laboratories have been characterized by impedance spectroscopy (IS): thin-film CdS/CdTe devices, an extremely thin absorber (eta) solar cell made with microporous TiO2/In(OH)xSy/PbS/PEDOT, an eta-solar cell of nanowire ZnO/CdSe/CuSCN, and a solid-state dye-sensitized solar cell (DSSC) with Spiro-OMeTAD as the transparent hole conductor. A negative capacitance behavior has been observed in all of them at high forward bias, independent of material type (organic and inorganic), configuration, and geometry of the cells studied. The experiments suggest a universality of the underlying phenomenon giving rise to this effect in a broad range of solar cell devices. An equivalent circuit model is suggested to explain the impedance and capacitance spectra, with an inductive recombination pathway that is activated at forward bias. The deleterious effect of negative capacitance on the device performance is discussed, by comparison of the results obtained for a conventional monocrystalline Si solar cell showing the positive chemical capacitance expected in the ideal IS model of a solar cell.

Topics: Cadmium Compounds; Computer Simulation; Crystallization; Electric Capacitance; Electric Power Supplies; Electrochemistry; Equipment Design; Equipment Failure Analysis; Light; Materials Testing; Models, Chemical; Nanostructures; Solar Energy; Sulfides; Tellurium