Unmodified gold nanoparticles as a colorimetric probe for visual methamphetamine detection

In recent years, in addition to the classic drugs, addiction to a series of new drug classes known as club drugs has increased significantly. Fast and low-cost bioassay for the detection of amphetamine-based drugs can be an effective strategy towards reducing their abuse. In this study, we designed a sensitive bioassay strategy using gold nanoparticles (GNPs) and the aptamers that possess high affinity toward methamphetamine (MA). It is suggested that the aptamer adopts different tertiary structures in the presence and/or absence of its specific target and GNPs can effectively differentiate between these two states by their characteristic surface plasmon resonance-based colour change. Visual detection of MA and 3,4-methylenedioxy-N-methylamphetamine (MDMA) in the low micromolar range is possible within minutes with the use of this method.     

A facile synthesis of lipid stabilized gold nanoparticles: a step towards biodegradable biosensors

A new class of polylactone was successfully synthesized and utilized for the encapsulation and stabilization of gold nanoparticles. Core/shell nanoparticle architecture, in which a layer of this polymer surrounds the nanoparticle core have been investigated both as a means to improve the stability and surface chemistry and as a way of accessing unique physical properties that are not possible from one nano-material alone. Given the fact that only few systems has so far been developed for the encapsulation of nanoparticles, our success in using a new biodegradable biopolymer with inbuilt functionality reveals the robustness of this work. The biodegradability of this polylactone was evaluated using scanning electron microscopy (SEM). The morphology and stability of these gold-polymer hybrids were evaluated by using the transmission electron microscopy (TEM) and UV-VIS spectroscopy.     

Dendrimer-entrapped gold nanoparticles as a platform for cancer-cell targeting and imaging

We present a general approach for the targeting and imaging of cancer cells using dendrimer-entrapped gold nanoparticles (Au DENPs). Au DENPs were found to be able to covalently link with targeting and imaging ligands for subsequent cancer-cell targeting and imaging. The Au DENPs linked with defined numbers of folic acid (FA) and fluorescein isothiocyanate (FI) molecules are water soluble, stable, and biocompatible. In vitro studies show that the FA- and FI-modified Au DENPs can specifically bind to KB cells (a human epithelial carcinoma cell line) that overexpress high-affinity folate receptors and they are internalized dominantly into lysosomes of target cells within 2 h. These findings demonstrate that Au DENPs may serve as a general platform for cancer imaging and therapeutics.     

Close-packed array of gold nanoparticles and sum frequency generation spectroscopy in total internal reflection: a platform for studying biomolecules and biosensors

An approach is introduced for studying the adsorption and recognition mechanisms of biomolecules, without using any markers. We show for the first time, that the sum frequency generation spectroscopy performed in the total internal reflection (TIR-SFG) geometry, combined with a regular close-packed array of gold nanoparticles allows to probe with a high sensitivity the changes in conformation and orientation induced by the recognition process of avidin by biocytin. This approach represents a new platform with potential use in biosensors, diagnostics and bioactive layers.     

Albumin as a carrier for NO delivery: preparation,physicochemical characterization,and interaction with gold nanoparticles

Background: Nitric oxide (NO) is a gaseous transmitter playing numerous physiological roles and characterized by a short half-life. Its binding to endogenous thiols increases its stability, facilitating its storage and transport. The purpose of this study was to investigate the nitrosated serum albumin (SA-SNO) and to provide a reference for its easy preparation for further use in in vitro studies.

Methods: Serum albumin (SA) was S-nitrosated by reacting with (i) NaNO₂ in acidic medium; (ii) different low-molecular weight S-nitrosothiols (RSNO) (S-nitrosocysteine (CysNO), S-nitrosoglutathione (GSNO), and S,S'-dinitrosobucillamine (Buc(NO)₂)); and (iii) diethylamine NONOate (DEA/NO). SA-SNO was purified by size exclusion chromatography and the S-nitrosation site and the rate were studied by mass spectrometry and Griess–Saville assay, respectively. Then, SA-SNO was characterized by spectrofluorimetry, dynamic light scattering, and circular dichroism. Finally, SA-SNO reactivity with citrate stabilized gold nanoparticles (AuNP-citrate) was investigated via determination of NO release.

Results: S-nitrosation rates of SA were 90.1?±?3.3, 76.8?±?2.7, 80.3?±?3.2, 84.8?±?5.0, and 15.4?±?1.9% (n?=?5), when SA was reacted with acidified NaNO₂, CysNO, GSNO, Buc(NO)₂, and DEA/NO, respectively. The physicochemical characterization indicated that the resulting product corresponded to a mono-S-nitrosothiol (on cysteine-34), and the conformational construction remained unchanged. Stability studies showed that the NO content was preserved over 1 week. AuNP-citrate reacted with SA-SNO with increase of its hydrodynamic diameter but preservation of SNO bond.

Conclusions: SA-SNO prepared and stored under the reported conditions affords a well-defined reference suitable for in vitro studies.     

Soybeans as a phytochemical reservoir for the production and stabilization of biocompatible gold nanoparticles

The present study demonstrates an unprecedented green process for the production of gold nanoparticles by simple treatment of gold salts with soybean extracts. Reduction capabilities of antioxidant phytochemicals present in soybean and their ability to reduce gold salts chemically to nanoparticles with subsequent coating of proteins and a host of other phytochemicals present in soybean on the freshly generated gold nanoparticles are discussed. The new genre of green nanoparticles exhibit remarkable in vitro stability in various buffers including saline, histidine, HSA, and cysteine solutions. MTT assays reveal that the green gold nanoparticles are nontoxic and thus provide excellent opportunities for their applications in nanomedicine for molecular imaging and therapy. The overall strategy described herein for the generation of gold nanoparticles meets all 12 principles of green chemistry, as no "man-made" chemicals, other than the gold salts, are used in the green nanotechnological process.     

Gum arabic as a phytochemical construct for the stabilization of gold nanoparticles: in vivo pharmacokinetics and X-ray-contrast-imaging studies

Gold nanoparticles (AuNPs) have exceptional stability against oxidation and therefore will play a significant role in the advancement of clinically useful diagnostic and therapeutic nanomedicines. Despite the huge potential for a new generation of AuNP-based nanomedicinal products, nontoxic AuNP constructs and formulations that can be readily administered site-specifically through the intravenous mode, for diagnostic imaging by computed tomography (CT) or for therapy via various modalities, are still rare. Herein, we report results encompassing: 1) the synthesis and stabilization of AuNPs within the nontoxic phytochemical gum-arabic matrix (GA-AuNPs); 2) detailed in vitro analysis and in vivo pharmacokinetics studies of GA-AuNPs in pigs to gain insight into the organ-specific localization of this new generation of AuNP vector, and 3) X-ray CT contrast measurements of GA-AuNP vectors for potential utility in molecular imaging. Our results demonstrate that naturally occurring GA can be used as a nontoxic phytochemical construct in the production of readily administrable biocompatible AuNPs for diagnostic and therapeutic applications in nanomedicine.     

Myoglobin/gold nanoparticles/carbon spheres 3-D architecture for the fabrication of a novel biosensor

A novel biosensor based on a myoglobin/gold nanoparticles/carbon spheres (Mb-AuNPs-CNs) 3-D architecture bioconjunction has been fabricated for the determination of hydrogen peroxide (H₂O₂). Cyclic voltammetry (CV), Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM) were used to characterize the bioconjunction of the AuNPs-CNs with Mb. Experimental results demonstrate that the AuNPs-CNs hybrid material is more effective in facilitating electron transfer of the immobilized enzyme than CNs alone, which can be attributed to the unique nanostructure and larger surface area of the bioconjunction. The biosensor displayed good performance for the detection of H₂O₂ with a wide linear range from 0.28 μmol/L to 116.5 μmol/L and a detection limit of 0.12 μmol/L. The Michaelis-Menten constant K _M^app value was estimated to be 0.3 mmol/L. The resulting biosensor exhibited fast amperometric response, and good stability, reproducibility, and selectivity to H₂O₂. This article is published with open access at Springerlink.com     

X-ray computed tomography imaging of a tumor with high sensitivity using gold nanoparticles conjugated to a cancer-specific antibody via polyethylene glycol chains on their surface

Contrast agents are often used to enhance the contrast of X-ray computed tomography (CT) imaging of tumors to improve diagnostic accuracy. However, because the iodine-based contrast agents currently used in hospitals are of low molecular weight, the agent is rapidly excreted from the kidney or moves to extravascular tissues through the capillary vessels, depending on its concentration gradient. This leads to nonspecific enhancement of contrast images for tissues. Here, we created gold (Au) nanoparticles as a new contrast agent to specifically image tumors with CT using an enhanced permeability and retention (EPR) effect. Au has a higher X-ray absorption coefficient than does iodine. Au nanoparticles were supported with polyethylene glycol (PEG) chains on their surface to increase the blood retention and were conjugated with a cancer-specific antibody via terminal PEG chains. The developed Au nanoparticles were injected into tumor-bearing mice, and the distribution of Au was examined with CT imaging, transmission electron microscopy, and elemental analysis using inductively coupled plasma optical emission spectrometry. The results show that specific localization of the developed Au nanoparticles in the tumor is affected by a slight difference in particle size and enhanced by the conjugation of a specific antibody against the tumor.     

Green synthesis of gold nanoparticles: Its effect on cocoon and silk traits of mulberry silkworm (Bombyx mori L.)

In the present century the small particles are unique phenomenon which can be developed by bottom-up and top-down processes. These small particles may be considered as nanoparticles which help to build up a technology called nanotechnology. Nanomaterials are those materials which possess the length scales below 100 nm and quite often they make a comparison with a human hair, which is about 80,000 nm wide. We have introduced this technology, specially the green synthesis of gold (Au) nanoparticles in silkworm (Bombyx mori L.). The gold nanoparticles clearly indicate that they have a tremendous effect on enhancement of silk proteins and thus the enhancement of the cocoon weight in silkworms. Gold nanoparticles were prepared from onion, Allium cepa L. The extracted green gold nanomaterials from A. cepa were confirmed by UV-Vis spectrophotometer, XRD, FTIR, SEM, TEM and AFM. The function of green gold nanomaterials extracted from A. cepa was tested on silkworm physiology. We have used UV for judgment of the nature of particles and spectrum peak wavelength showed an absorption peak at 535 nm and indicated the wavelength of the surface plasmon resonance in gold nanoparticles (Au NPs). In blank solutions no such absorption peak was observed at 535 nm. Moreover, the gold (Au) XRD spectrum is supposed to and does demonstrate (111), (200), (220), and (311) peaks in the assortment of superimpose on the background. The process includes the (002) trace graphite peaks, where the (111) peak appears to be exceptionally sharp and strong which helps to propose that it is gold in nature. The FTIR shows that the examined particles are gold in nature. In SEM where electrons interact with atoms in the sample, producing various signals that can be detected and that hold information about the sample's surface topography and composition. The electron beam in SEM is generally scanned in a raster scan pattern, and therefore the beam's position is combined and detects the signal to produce an image. SEM can attain a resolution better than 1 nanometer size. The transmission electron microscope helps to accelerate the electrons as a source of elucidation. The AFM measurement is made in three dimensions process and thus it may be measured as horizontal to X-Y plane. Therefore, decree (magnification) measured at Z–direction, which is normally higher than X-Y. The said repulsive force is major one in AFM. Thus the tip and sample may considered to be the specific force in AFM which may measured at Z–direction. The effect of green gold nanoparticles on mulberry silkworm (Bombyx mori L) can exaggerated the silkworm physiological function. Larvae at 50, 100, 200, and 300 ppm doses were studied right from 1st stage to 5th instar stage. Gold nano treatment resulted in significant alterations in the percentage of fibroin and sericin proteins in the 5th instar as compared to that of control. At a 300 ppm dose of green nano gold the percentage of fibroin was 78.07, while sericin decreased from 39.46 (control) to 21.92. It was observed that the green gold nanomaterials have the ability to not only alter the fibroin protein but also enhance the cocoon and silk traits. The aim of this study was to investigate the effect of extra foliation of mulberry leaves with G-GNPs extracted from A. cepa on larval duration, mature silk gland weight, pupal weight, cocoon weight, cocoon shell weight, fibroin and sericins contents, etc. Moreover, the enhanced production of fibroin will explore a new venture in bioengineering and also in biomedical field.     

Controlled nucleation and growth of surface-confined gold nanoparticles on a (3-aminopropyl)trimethoxysilane-modified glass slide: a strategy for SPR substrates

The thickness of the gold film and its morphology, including the surface roughness, are very important for getting a good, reproducible response in the SPR technique. Here, we report a novel alternative approach for preparing SPR-active substrates that is completely solution-based. Our strategy is based on self-assembly of the gold colloid monolayer on a (3-aminopropyl)trimethoxysilane-modified glass slide, followed by electroless gold plating. Using this method, the thickness of films can be easily controlled at the nanometer scale by setting the plating time in the same conditions. Surface roughness and morphology of gold films can be modified by both tuning the size of gold nanoparticles and agitation during the plating. Surface evolution of the Au film was followed in real time by UV-vis spectroscopy and in situ SPRS. To assess the surface roughness and electrochemical stability of the Au films, atomic force microscopy and cyclic voltammetry were used. In addition, the stability of the gold adhesion is demonstrated by three methods. The as-prepared Au films on substrates are reproducible and stable, which allows them to be used as electrodes for electrochemical experiments and as platforms for studying SAMs.     

Continuous laser irradiation under ambient conditions: A simple way for the space-selective growth of gold nanoparticles inside a silica monolith

Thanks to the potential and various applications of metal-dielectric nanocomposites, their syntheses constitute an interesting subject in material research. In this work, we demonstrate the achievement of gold nanocrystals growth through a visible and continuous laser irradiation. The in situ and direct space-selective generation of metallic nanoparticles is localized under the surface within transparent silica monoliths. For that purpose, the porous silica monoliths are prepared using a sol-gel route and post-doped with gold precursors before the irradiation. The presence of Au nanoparticles inside the irradiated areas was evidenced using absorption spectroscopy, X-ray diffraction analysis and transmission electron microscopy. The comparison between the results obtained after a laser irradiation and by a simple heat-treatment reveals that the local precipitation of gold nanoparticles by continuous photo-irradiation occurs following a photo-thermal activated mechanism.     

Immobilization of Au nanoparticles on Au electrode for hydrazine detection: Using thiolated single-stranded DNA as a linker

In this article, we report a method for effective immobilization of Au nanoparticles (AuNPs) on thiolated single-stranded DNA (thiol-ssDNA) modified Au electrode (AuE) surface via coordination interactions between the nitrogen atoms of DNA bases and AuNPs. It suggests that the resultant AuNP-immobilized AuE exhibits notable catalytic performance for hydrazine oxidation and the loading of AuNPs on the AuE surface and hence the effective catalytic area can be tuned by the immobilization time of thiol-ssDNA and adsorption time of AuNPs. This hydrazine sensor has a fast amperometric response time of less than 4 s. The linear range and detection limit are estimated to be from 0.1 mM to 100 mM (r = 0.998) and 0.56 μM at a signal-to-noise ratio of 3, respectively.