Glutathione-capped Gold Nanoparticles Research Articles

A sensitive fluorescence nanoplatform for monitoring benzoyl peroxide in food using carbon dots coupled with glutathione capped gold nanoparticles as FRET probe.

Herein, a sensitive fluorescence nanoplatform for benzoyl peroxide (BPO) detection is constructed from carbon dots (CDs) and glutathione capped gold nanoparticles (GSH-AuNPs). The fluorescence of CDs is first quenched due to the fluorescence resonance energy transfer (FRET) effect in the presence of GSH-AuNPs, and then effectively recovered when adding BPO. The detection mechanism lies in the aggregation of AuNPs in a high salt background due to oxidation of GSH caused by BPO, thus the amount of BPO is reflected by the variations of the recovered signals. The linear range and detection limit in this detection system is found to be 0.05-200μM (R2=0.994) and 0.1µgg-1 (3σ/K), respectively. Several possible interferents with high concentration show little influence on BPO detection. The proposed assay exhibits good performance for BPO determination in wheat flour and noodles, demonstrating its applicability for facile monitoring BPO additive amount in real foods.

Amperometric immunoassay for the carcinoembryonic antigen by using a peroxidase mimic consisting of palladium nanospheres functionalized with glutathione-capped gold nanoparticles on graphene oxide.

A composite nanoenzyme was used in a sandwich-type electrochemical immunoassay for the carcinoembryonic antigen (CEA). Hierarchically porous palladium nanospheres (Pd NPs) were functionalized with glutathione-capped gold nanoparticles (G-Au NPs) and then loaded onto graphene oxide (GO) to obtain a peroxidase mimicking nanoenzyme of type GO-supported G-Au/Pd. The composite can catalyze the oxidation of the substrate tetramethylbenzidine (TMB) by H2O2 to give blue-colored oxidized TMB within only 20s. This strong peroxidase activity, good conductivity and high specific surface area of the material make it a useful label for secondary antibodies (Ab2) for the detection of CEA. The cotton-like electrodeposited gold nanoparticles with good electrical conductivity were used to immobilize primary antibody (Ab1). The amperometric immunoassay has a detection range that extends from 10fg·mL-1 to 100ng·mL-1 at a working potential of -0.4V with addition of 5mmol·L-1 H2O2 as electrochemically active substrate, and the detection limit is as low as 3.2fg·mL-1 (S/N= 3). Graphical abstract Schematic of sandwich electrochemical immunosensor for the carcinoembryonic antigen. Electrodeposited gold used as substrate material, and Graphene oxide supported G-Au NPs functionalized porous Pd nanospheres (GO supported G-Au/Pd) as signal amplification platform, which catalyze the oxidation of tetramethylbenzidine (TMB).

The Effects of Photodynamic Therapy Using Green Laser and Glutathione-Capped-Gold Nanoparticles on Cancer Cells (MCF-7 Cell Line)

Background: Nanotechnology is a discipline that manages, constructs, analyzes and deals with application of materials that have diameter from 1 to 100 nanometers. Gold nanoparticles are defined as stable colloid solutions of clusters of gold atoms with sizes at this minuscule. Objective: The objective of current study was to treat breast cancer using gold nanoparticles capped with drug molecules in specific quantities to reduce the harmful side effects. Method: The gold nanoparticales were prepared by method of Brust-Schiffrin. These nanoparticles were capped with type of drug (Glutathione) used to treat cancerous tumors. These gold nanoparticles were uncapped with drugs at (526nm) when capped with the glutathione drug at (589nm). Results: The resulting evidence suggested that Glutathione-capped Gold nanoparticles were non-toxic up to the maximum recommended dosage. Therefore, the demonstrated biocompatibility offers the potentials of Glutathione-capped with Gold nanoparticles.The candidate is considered as a medicine for cancer therapy.

Gold nanoparticle-based colorimetric sensing of dipicolinic acid from complex samples.

Dipicolinic acid (DPA) can cause neurotoxicity and is abundant in bacterial spores. Although analytical methods have been reported for DPA detection with high sensitivity, their selectivity toward DPA is declined greatly in the presence of phosphates in the samples. In this study, we developed an approach for DPA detection that is not affected by the presence of phosphates. A colorimetric method based on the use of gold nanoparticles (AuNP) complexed with Ca2+ as sensing agents was explored for DPA detection. Calcium ions and glutathione-capped gold nanoparticles (AuNPs@GSH) can easily form complexes (Ca2+-AuNP@GSH) through GSH-Ca2+ chelation, leading to the aggregation of AuNPs@GSH. The aggregation resulting from the complexes of AuNPs@GSH and Ca2+ can be reversed with the addition of DPA owing to the high formation constant (log Kf = 4.4) between DPA and Ca2+. Furthermore, the color of AuNPs@GSH changes from red to purple when complexed with Ca2+, returning to red upon addition of DPA. The limit of detection of this sensing method toward DPA was estimated to be as low as ~ 2μM. The feasibility of using the sensing method for quantitative detection of DPA in soil and Bacillus cereus spore samples was also demonstrated. Graphical abstract A AuNP-based colorimetric sensing method against dipicolinic acid is developed.

Thiols-Induced Rapid Photoluminescent Enhancement of Glutathione-Capped Gold Nanoparticles for Intracellular Thiols Imaging Applications.

The rapid detection and imaging of intracellular thiols is of great importance during the occurrence and development of some chronic diseases. Here we demonstrate the rapid thiols-induced photoluminescence (PL) enhancement of the low luminescent glutathione (GSH) stabilized Au nanoparticles, AuGSH (low). The dynamic PL investigation reveals that the PL enhancement fits a first-order reaction model. The X-ray photoelectron spectroscopic and mass spectroscopic results indicate that AuGSH (low) are mainly comprised of "thiols-insufficient" Au species and the additional thiols can efficiently attach to the "unsaturated" surface of Au nanoparticles, accompanied by significant PL enhancement. The noncytotoxic AuGSH (low) probe can be successfully applied for imaging of intracellular thiols. Generally, this work illustrates the great prospects of facile-prepared AuGSH (low) as a candidate for thiols labeling and imaging.

Graphene oxide-promoted reshaping and coarsening of gold nanorods and nanoparticles.

This paper describes thermally induced reshaping and coarsening behaviors of gold nanorods and nanoparticles immobilized on the surface of graphene oxide. Cetyltrimethylammonium bromide-stabilized gold nanorods with an aspect ratio of ∼3.5 (54:15 nm) and glutathione-capped gold nanoparticles with an average core size of ∼3 nm were synthesized and self-assembled onto the surface of graphene oxide. The hybrid materials were then heated at different temperatures ranging from 50 to 300 °C. The effects of heat treatments were monitored using UV-vis spectroscopy and transmission electron microscopy (TEM). These results were directly compared with those of heat-treated free-standing gold nanorods and nanoparticles without graphene oxide to understand the heat-induced morphological changes of the nanohybrids. The obtained results showed that the gold nanorods would undergo a complete reshaping to spherical particles at the temperature of 50 °C when they are assembled on graphene oxide. In comparison, the complete reshaping of free-standing gold nanorods to spherical particles would ultimately require a heating of the samples at 200 °C. In addition, the spherical gold nanoparticles immobilized on graphene oxide would undergo a rapid coarsening at the temperature of 100-150 °C, which was lower than the temperature (150-200 °C) required for visible coarsening of free-standing gold nanoparticles. The results indicated that graphene oxide facilitates the reshaping and coarsening of gold nanorods and nanoparticles, respectively, during the heat treatments. The stripping and spillover of stabilizing ligands promoted by graphene oxide are proposed to be the main mechanism for the enhancements in the heat-induced transformations of nanohybrids.

Hydroxyl radical-induced etching of glutathione-capped gold nanoparticles to oligomeric AuI–thiolate complexes

Fenton reagent reacted with glutathione-capped gold nanoparticles to form oligomeric Au(i)–thiolate complexes.

PH-dependent immobilization of urease on glutathione-capped gold nanoparticles.

Urease is a nickel-dependent metalloenzyme that catalyzes the hydrolysis of urea to form ammonia and carbon dioxide. Although the enzyme serves a significant role in several detoxification and analytical processes, its usability is restricted due to high cost, availability in small amounts, instability, and a limited possibility of economic recovery from a reaction mixture. Hence, there is a need to develop an efficient, simple, and reliable immobilization strategy for the enzyme. In this study, the carboxyl terminated surface of glutathione-capped gold nanoparticles have been utilized as a solid support for the covalent attachment of urease. The immobilization has been carried out at different pH conditions so as to elucidate its effect on the immobilization efficiency and enzyme bioactivity. The binding of the enzyme has been quantitatively and qualitatively analyzed through techniques like ultraviolet-visible spectroscopy, intrinsic steady state fluorescence, and circular dichorism. The bioactivity of the immobilized enzyme was investigated with respect to the native enzyme under different thermal conditions. Recyclability and shelf life studies of the immobilized enzyme have also been carried out. Results reveal that the immobilization is most effective at pH of 7.4 followed by that in an acidic medium and is least in alkaline environment. The immobilized enzyme also exhibits enhance activity in comparison to the native form at physiological temperature. The immobilized urease (on gold glutathione nanoconjugates surface) can be effectively employed for biosensor fabrication, immunoassays and as an in vivo diagnostic tool in the future.

PH dependent immobilization of Urease on glutathione capped gold nanoparticles

pH dependent immobilization of Urease on glutathione capped gold nanoparticles

Conjugates of low-symmetry Ge, Sn and Ti carboxy phthalocyanines with glutathione caped gold nanoparticles: An investigation of photophysical behaviour

This work reports on conjugation of low symmetry Ge (GeMCPc), Ti (TiMCPc) and Sn (SnMCPc) carboxy phthalocyanines with glutathione capped gold nanoparticles (GSH-AuNPs). The photophysical behaviour of the novel phthalocyanines–GSH-AuNPs conjugate was investigated and compared to the monocarboxy Pcs and to the mixture of Pc with GSH-AuNPs without a chemical bond. Blue shifting of Q band of the phthalocyanines was observed on linking to GSH-AuNPs. An improvement in triplet lifetimes was obtained for all the MPcs–GSH-AuNPs-linked conjugates compared to the MPcs alone. The highest triplet quantum yield of 0.75 and the longest triplet lifetime of 130 μs were obtained for the GeMCPc–GSH-AuNPs-linked conjugate. Fluorescence quantum yields and lifetimes were low for the conjugates due to quenching by the nanoparticles.

Effect of buried potential barrier in label-less electrochemical immunodetection of glutathione and glutathione-capped gold nanoparticles

The influence of potential barriers, introduced to the immunoglobulin-based sensory films, on voltammetric signals of a redox ion probe has been investigated. Films with positive and negative barriers have been examined by depositing charged self-assembled thiol monolayers as the basal layers of a sensory film. The studies performed with monoclonal anti-glutathione antibody-based sensors using ferricyanide ion probe have shown stronger sensor response to the layer components, as well as to the glutathione-capped gold nanoparticles acting as the antigen, for films with positive potential barrier buried deep in the film than for negative barrier films. The larger changes in differential resistance, peak separation and peak heights observed for films with positive barrier have been attributed to different depth and width of the charge distributions in these films. A buried positive barrier with narrow charge distribution width provides the best conditions for film stability and prevents fouling (less ion-exchanges with the medium). This conclusion has been confirmed by calculations of the electric field distribution and potential profiles in immunosensing films performed by numerical integration of Poisson equation for Gaussian distributions of fixed charges of covalently bound components. The proposed fixed-charge model can aid in rapid evaluation of sensory films in sensor development work. The implications of potential barriers in sensory film design are discussed.

Fluorescent gold nanoparticles-based fluorescence sensor for Cu2+ ions

A new fluorescence sensor for the highly selective detection of Cu2+ ion with a detection limit of 3.6 nM based on the aggregation-induced fluorescence quenching of the highly fluorescent glutathione-capped gold nanoparticles is reported.