Sensitive detection of mercury (II) ion using water-soluble captopril-stabilized fluorescent gold nanoparticles

In our work, a simple, facile, and green method was developed for the synthesis of water-soluble and well-dispersed fluorescent gold nanoparticles (Au NPs) within 5 min, using captopril as a capping agent. The as-prepared Au NPs showed strong emission at 414 nm, with a quantum yield of 5.5%. The fluorescence of the Au NPs can be strongly quenched by mercury (II) ion (Hg^2 +) due to the stronger interactions between thiolates (RS^?) and Hg^2 +. It was applied to the detection of Hg^2 + in water samples in the linear ranges of 0.033–0.133 μM and 0.167–2.500 μM, with a detection limit of 0.017 μM. Therefore, the as-prepared Au NPs can meet the requirement for monitoring Hg^2 + in environmental samples.     

Surface-modified CdS nanoparticles as a fluorescent probe for the selective detection of cysteine

We present a novel method for the selective detection of cysteine, a sulfur-containing amino acid, which plays a crucial role in many important biological functions such as protein folding. Surface-modified colloidal CdS nanoparticles have been used as a fluorescent probe to selectively detect cysteine in the presence of other amino acids in the micromolar concentration range. Cysteine quenches the emission of CdS in the 0.5-10?μM concentration range, whereas the other amino acids do not affect its emission. Among the other amino acids, histidine is most efficient in quenching the emission of the CdS nanoparticles. The sulfur atom of cysteine plays a crucial role in the quenching process in the 0.5-10?μM concentration range. Cysteine is believed to quench the emission of the CdS nanoparticles by binding to their surface via its negatively charged sulfur atom. This method can potentially be applied for its detection in biological samples.     

Highly selective and sensitive magnetic silica nanoparticles based fluorescent sensor for detection of Zn ions

In this work, quinoline group modified multifunctional silica nanoparticles having high magnetization and excellent Zn²⁺ selectivity have been successfully prepared. These multifunctional nanoparticles were characterized by high resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric analysis (TGA), X-ray powder diffraction (XRD) and vibrating sample magnetometer (VSM). The characterization data indicated that the organic ligand was successfully grafted on the surface of the magnetic silica nanoparticles. The fluorescent properties of the nanosensor were characterized and employed to detect Zn²⁺ with excellent selectivity and sensitivity (0.1 μM) toward Zn²⁺ over other cations even in trace amount.     

Preparation of CdS and ZnS nanoparticles using microwave irradiation

Nanoparticles of CdS, ZnS have been prepared by a very simple fast reaction between CdCl₂ or Zn(Ac)₂ and thioacetamide in aqueous solution using microwave irradiation. The nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), reflectance and photoluminescence spectra. The sizes of the sample as prepared were calculated by Debye–Scherrer formula according to XRD spectra to be about 9 and 3 nm for CdS and ZnS, respectively. Similar results can also been obtained in the TEM images.     

Charge-driven selective localization of fluorescent nanoparticles in live cells

Covalent grafting of amino groups onto the carboxylic acid functionalities, naturally covering the surface of fluorescent nanoparticles produced from silicon carbide (SiC NPs), allowed tuning of their surface charge from negative to highly positive. Incubating 3T3-L1 fibroblast cells with differently charged SiC NPs demonstrates the crucial role of the charge in cell fluorescent targeting. Negatively charged SiC NPs concentrate inside the cell nuclei. Close to neutrally charged SiC NPs are present in both cytoplasm and nuclei while positively charged SiC NPs are present only in the cytoplasm and are not able to move inside the nuclei. This effect opens the door for the use of SiC NPs for easy and fast visualization of long-lasting biological processes taking place in the cell cytosol or nucleus as well as providing a new long-term cell imaging tool. Moreover, here we have shown that the interaction between charged NPs and nuclear pore complex plays an essential role in their penetration into the nuclei.     

Detection of ionizing radiation using Ag-doped ZnS nanoparticles

Journal of Materials Science: Materials in Electronics - Fluorescent Ag-doped ZnS nanoparticles have been prepared and used as scintillators for detecting ionizing radiation. Results demonstrate a...     

Sensitive detection of bacterial DNA by magnetic nanoparticles

This work presents sensitive detection of bacterial genomic DNA using a magnetic nanoparticle-based substrate-free method. For the first time, such a method is employed for detection of a clinically relevant analyte by implementing a solid-phase-based molecular probing and amplification protocol that can be executed in 80 min. The molecular detection and amplification protocol is presented and verified on samples containing purified genomic DNA from Escherichia coli cells, showing that as few as 50 bacteria can be detected. This study moves the use of volume-amplified magnetic nanoparticles one step further toward rapid, sensitive, and selective infectious diagnostics.     

Sensitive and selective detection of mercury (II) based on the aggregation of gold nanoparticles stabilized by riboflavin

Gold nanoparticles (AuNPs) can be stabilized by riboflavin against tris buffer-induced aggregation. However, in the presence of mercury (II) (Hg2+), riboflavin can be released from the AuNPs surface and the riboflavin-Hg2+ complex formed, leading to the aggregation of AuNPs in tris buffer. The aggregation extent depends on the concentration of Hg2+. Based on the aggregation extent, a simple and sensitive method of determining Hg2+ is developed. The method enables the detection of Hg2+ over the concentration range of 0.02-0.8 microM, with a detection limit (3sigma) of 14 nM, and shows excellent selectivity for Hg2+ over other metal ions (Cu2+, Co2+, Cd2+, Pb2+, Mg2+, Zn2+, Ag+, Ce3+, Ca2+, Al3+, K+). More importantly, the method avoids complicated surface modifications and tedious separation processes.     

Highly selective colorimetric detection of hydrochloric acid using unlabeled gold nanoparticles and an oxidizing agent

We report a colorimetric system for the detection of HCl in aqueous environments using unlabeled gold nanoparticle (AuNP) probes. This nonaggregation-based detection system relies on the ability of chloro species to cause rapid leaching of AuNPs in an aqueous dispersion containing a strong oxidizing agent, such as HNO(3) or H(2)O(2). The leaching process leads to remarkable damping of the surface plasmon resonance peak of the AuNP dispersion. This method works only with AuNPs of a particular size (～30 nm diameter). It is highly selective for HCl over several common mineral acids, salts, and anions. This simple and cost-effective sensing system provides rapid and simple detection of HCl at concentrations as low as 500 ppm (far below the hazard limit) in natural water systems.     

DNA sequence detection using selective fluorescence quenching of tagged oligonucleotide probes by gold nanoparticles

Simple, fast, economical, and sensitive detection of specific DNA sequences is crucial to pathogen detection and biomedical research. We have designed a novel fluorescent assay for DNA hybridization based on the electrostatic properties of DNA. We exploit the ability to create conditions where single-stranded DNA adsorbs on negatively charged gold nanoparticles while double-stranded DNA does not. Dye-tagged probe sequences have their fluorescence efficiently quenched when they are mixed with gold nanoparticles unless they hybridize with components of the analyte. Subfemtomole amounts of untagged target are detected in minutes using commercially available materials. Target sequences in complex mixtures of DNA and single-base mismatches in DNA sequences are easily detected.     

Aptamer-conjugated nanoparticles for selective collection and detection of cancer cells

We have developed a method for the rapid collection and detection of leukemia cells using a novel two-nanoparticle assay with aptamers as the molecular recognition element. An aptamer sequence was selected using a cell-based SELEX strategy in our laboratory for CCRF-CEM acute leukemia cells that, when applied in this method, allows for specific recognition of the cells from complex mixtures including whole blood samples. Aptamer-modified magnetic nanoparticles were used for target cell extraction, while aptamer-modified fluorescent nanoparticles were simultaneously added for sensitive cell detection. Combining two types of nanoparticles allows for rapid, selective, and sensitive detection not possible by using either particle alone. Fluorescent nanoparticles amplify the signal intensity corresponding to a single aptamer binding event, resulting in improved sensitivity over methods using individual dye-labeled probes. In addition, aptamer-modified magnetic nanoparticles allow for rapid extraction of target cells not possible with other separation methods. Fluorescent imaging and flow cytometry were used for cellular detection to demonstrate the potential application of this method for medical diagnostics.     

Protein discrimination using fluorescent gold nanoparticles on plasmonic substrates

Fluorescent gold nanoparticle (GNP) is an easily synthesized and biocompatible optical platform for sensing and imaging with tunable near-infrared (NIR) emission. However, the relatively low fluorescence (FL) quantum yield limits the further improvement of sensitivity and application. Here, we find that, on plasmonic substrates, the FL intensity of protein-directed synthesized GNPs can be enhanced significantly (~20-fold). Moreover, protein analytes can interact with GNPs and influence the enhanced fluorescence process so that we can obtain distinct FL image patterns. Then, using the array-based sensing strategy, protein discrimination can be achieved. In our present experiment, five GNPs were used as sensing elements and 10 kinds of proteins at three concentrations (0.2, 0.5, and 1 μM) were successfully identified. This array-based sensing strategy using enhanced-fluorescence from GNPs is highly sensitive and differentiable, expanding the application field of GNPs.     

Sensitive carbohydrate detection using surface enhanced Raman tagging

Glycomic analysis is an increasingly important field in biological and biomedical research as glycosylation is one of the most important protein post-translational modifications. We have developed a new technique to detect carbohydrates using surface enhanced Raman spectroscopy (SERS) by designing and applying a Rhodamine B derivative as the SERS tag. Using a reductive amination reaction, the Rhodamine-based tag (RT) was successfully conjugated to three model carbohydrates (glucose, lactose, and glucuronic acid). SERS detection limits obtained with a 633 nm HeNe laser were ～1 nM in concentration for all the RT-carbohydrate conjugates and ～10 fmol in total sample consumption. The dynamic range of the SERS method is about 4 orders of magnitude, spanning from 1 nM to 5 μM. Ratiometric SERS quantification using isotope-substituted SERS internal references allows comparative quantifications of carbohydrates labeled with RT and deuterium/hydrogen substituted RT tags, respectively. In addition to enhancing the SERS detection of the tagged carbohydrates, the Rhodamine tagging facilitates fluorescence and mass spectrometric detection of carbohydrates. Current fluorescence sensitivity of RT-carbohydrates is ～3 nM in concentration while the mass spectrometry (MS) sensitivity is about 1 fmol, achieved with a linear ion trap electrospray ionization (ESI)-MS instrument. Potential applications that take advantage of the high SERS, fluorescence, and MS sensitivity of this SERS tagging strategy are discussed for practical glycomic analysis where carbohydrates may be quantified with a fluorescence and SERS technique and then identified with ESI-MS techniques.     

Economical, green synthesis of fluorescent carbon nanoparticles and their use as probes for sensitive and selective detection of mercury(II) ions

The present article reports on a simple, economical, and green preparative strategy toward water-soluble, fluorescent carbon nanoparticles (CPs) with a quantum yield of approximately 6.9% by hydrothermal process using low cost wastes of pomelo peel as a carbon source for the first time. We further explore the use of such CPs as probes for a fluorescent Hg(2+) detection application, which is based on Hg(2+)-induced fluorescence quenching of CPs. This sensing system exhibits excellent sensitivity and selectivity toward Hg(2+), and a detection limit as low as 0.23 nM is achieved. The practical use of this system for Hg(2+) determination in lake water samples is also demonstrated successfully.     

Imaging breast cancer cells and tissues using peptide-labeled fluorescent silica nanoparticles

The imaging of tumor cells and tumor tissue samples is very important for cancer detection and therapy. We have taken advantages of fluorescent silica nanoparticles (FSiNPs) coupled with a molecular recognition element that allows for effective in vitro and ex vivo imaging of tumor cells and tissues. In this study, we report on the targeting and imaging of MDA-MB-231 human breast cancer cells using arginine-glycine-aspartic acid (RGD) peptide-labeled FSiNPs. When linked with RGD peptide using the cyanogen bromide (CNBr) method, the FSiNPs exhibited high target binding to alphavbeta3 integrin receptor (ABIR)-positive MDA-MB-231 breast cancer cells in vitro. Further study regarding the ex vivo imaging of tumor tissue samples was also carried out by intravenously injecting RGD peptide-labeled FSiNPs into athymic nude mice bearing the MDA-MB-231 tumors. Tissue images demonstrated that the high integrin alphavbeta3 expression level of the MDA-MB-231 tumors was clearly visible due to the special targeting effects of the RGD peptide-labeled FSiNPs, and the tumor fluorescence reached maximum intensity at 1 h postinjection. Our results break new ground for using FSiNPs to optically image tumors, and may also broaden the applications of silica nanoparticles in biomedicine.     

Dc conductivity of nanoparticles of CdS and ZnS

The dc conductivity of consolidated nanoparticles of ZnS and CdS has been studied over the temperature range from 300 to 525 K and the conductivity has been found to be much larger than that of single crystals. Nanoparticles of Ag of different concentration were dispersed in nanoparticles of ZnS and CdS and the conductivity of composite pellets was also studied. The conductivity has been found to be drastically enhanced compared to that of pellets not containing Ag and that of bulk crystals. The enhancement in conductivity may be attributed to a reversal of the size-induced metal-insulator transition of Ag nanoparticles permitting charges to pass through them thereby increasing the conductivity.