Browse
Submit Data
Databases
API
Help

Dataset Information

25 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Colloidal synthesis of gold semishells.

ABSTRACT: This work describes a novel and scalable colloid chemistry strategy to fabricate gold semishells based on the selective growth of gold on Janus silica particles (500 nm in diameter) partly functionalized with amino groups. The modulation of the geometry of the Janus silica particles allows us to tune the final morphology of the gold semishells. This method also provides a route to fabricating hollow gold semishells through etching of the silica cores with hydrofluoric acid. The optical properties were characterized by visible near-infrared (vis-NIR) spectroscopy and compared with simulations performed using the boundary element method (BEM). These revealed that the main optical features are located beyond the NIR region because of the large core size.

SUBMITTER: Rodriguez-Fernandez D

PROVIDER: S-EPMC3922459 | biostudies-literature | 2012 Apr

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Colloidal synthesis of gold semishells.

Rodríguez-Fernández Denis D Pérez-Juste Jorge J Pastoriza-Santos Isabel I Liz-Marzán Luis M LM

ChemistryOpen 20120313 2

This work describes a novel and scalable colloid chemistry strategy to fabricate gold semishells based on the selective growth of gold on Janus silica particles (500 nm in diameter) partly functionalized with amino groups. The modulation of the geometry of the Janus silica particles allows us to tune the final morphology of the gold semishells. This method also provides a route to fabricating hollow gold semishells through etching of the silica cores with hydrofluoric acid. The optical propertie ...[more]

PMID: 24551496

Similar Datasets

Robust Colloidal Synthesis of Palladium-Gold Alloy Nanoparticles for Hydrogen Sensing.

Project description:Metal nanoparticles are currently used in a variety of applications, ranging from life sciences to nanoelectronic devices to gas sensors. In particular, the use of palladium nanoparticles is gaining increasing attention due to their ability to catalyze the rapid dissociation of hydrogen, which leads to an excellent response in hydrogen-sensing applications. However, current palladium-nanoparticle-based sensors are hindered by the presence of hysteresis upon hydride formation and decomposition, as this hysteresis limits sensor accuracy. Here, we present a robust colloidal synthesis for palladium-gold alloy nanoparticles and demonstrate their hysteresis-free response when used for hydrogen detection. The obtained colloidal particles, synthesized in an aqueous, room-temperature environment, can be tailored to a variety of applications through changing the size, ratio of metals, and surface stabilization. In particular, the variation of the viscosity of the mixture during synthesis resulted in a highly tunable size distribution and contributed to a significant improvement in size dispersity compared to the state-of-the-art methods.

| S-EPMC8485326 | biostudies-literature

Purposefully Designed Surfactants for Facile and Controllable Gold Colloidal Nanocrystal Synthesis.

Project description:Three new cationic surfactants-N-cetyl-bis(2-dimethylaminoethyl)ether bromide (CBDEB), N-dodecyl-bis(2-dimethylaminoethyl)ether bromide (DBDEB), and N-hexyl-bis(2-dimethylaminoethyl)ether bromide (HBDEB)-have been designed herein using a simple and tailorable synthesis route. CBDEB and DBDEB, the 16- and 12-carbon chain surfactants, demonstrate facile, rapid, and controllable aqueous syntheses of gold nanoparticles (AuNPs) as dual-action reducing and capping agents. The synthesis strategy, using only surfactant and HAuCl4 salt, and 4 min of heating at 80 °C, results in spherical AuNPs (average diameters of 13.4 ± 3.8 nm for CBDEB and 12.0 ± 3.8 nm for DBDEB). Microwave irradiation was also investigated as a heating method and produces AuNPs in as little as 30 s. Control over the size and shape of AuNPs was proven to be feasible (toward populations of Euclidean shapes) by appropriately tuning reaction parameters, such as the molar ratio of surfactant to Au3+, temperature, incorporation of a time delay before heating, or shape control agents, such as Cu2+. Frustratingly, the cytotoxicity of CBDEB is similar to that of cetyltrimethylammonium bromide (CTAB), a popular 16-carbon chain cationic surfactant. Notably, while the shorter HBDEB (6-carbon chain) does not produce AuNPs under the applied conditions, it does appear to improve cell viability upon cytotoxicity evaluation and may be favorable as a new biological surfactant.

| S-EPMC10633875 | biostudies-literature

Bioinspired Synthesis of Mesoporous Gold-silica Hybrid Microspheres as Recyclable Colloidal SERS Substrates.

Project description:Noble metal nanostructures have been intensively investigated as active substrates for surface-enhanced Raman spectroscopy (SERS) from visible to near-IR wavelengths. However, metal nanoparticle-based SERS analysis in solutions is very challenging due to uncontrollable and irreproducible colloid aggregation. Here we report the templated synthesis of porous gold-silica hybrid microspheres and their application as reusable colloidal SERS substrates. Mesoporous polymer microspheres are synthesized and used as templates for the synthesis of non-aggregated gold nanoparticles, followed by polydopamine-mediated silicification to fabricate mesoporous gold-silica hybrid microspheres. The mesoporous hybrid particles detect crystal violet in the order of 10-8 M and provide the structural durability of the immobilized gold nanoparticles, allowing them to be recycled for repeated SERS analyses for analytes in a solution with the similar sensitivity. This work suggests that the mesoporous gold-silica hybrid microspheres are attractive SERS substrates in terms of reusability, sensitivity, and stability.

| S-EPMC5676677 | biostudies-literature

Gold nanoparticle shape dependence of colloidal stability domains.

Project description:Controlling the spatial arrangement of plasmonic nanoparticles is of particular interest to utilize inter-particle plasmonic coupling, which allows changing their optical properties. For bottom-up approaches, colloidal nanoparticles are interesting building blocks to generate more complex structures via controlled self-assembly using the destabilization of colloidal particles. For plasmonic noble metal nanoparticles, cationic surfactants, such as CTAB, are widely used in synthesis, both as shaping and stabilizing agents. In such a context, understanding and predicting the colloidal stability of a system solely composed of AuNPs and CTAB is fundamentally crucial. Here, we tried to rationalize the particle behavior by reporting the stability diagrams of colloidal gold nanostructures taking into account parameters such as the size, shape, and CTAB/AuNP concentration. We found that the overall stability was dependent on the shape of the nanoparticles, with the presence of sharp tips being the source of instability. For all morphologies evaluated here, a metastable area was systematically observed, in which the system aggregated in a controlled way while maintaining the colloidal stability. Combining different strategies with the help of transmission electron microscopy, the behavior of the system in the different zones of the diagrams was addressed. Finally, by controlling the experimental conditions with the previously obtained diagrams, we were able to obtain linear structures with a rather good control over the number of particles participating in the assembly while maintaining good colloidal stability.

| S-EPMC10044300 | biostudies-literature

pH-Driven Reversible Assembly and Disassembly of Colloidal Gold Nanoparticles.

Project description:Owing to the localized surface plasmon resonance (LSPR), dynamic manipulation of optical properties through the structure evolution of plasmonic nanoparticles has been intensively studied for practical applications. This paper describes a novel method for direct reversible self-assembly and dis-assembly of Au nanoparticles (AuNPs) in water driven by pH stimuli. Using 3-aminopropyltriethoxysilane (APTES) as the capping ligand and pH-responsive agent, the APTES hydrolyzes rapidly in response to acid and then condenses into silicon. On the contrary, the condensed silicon can be broken down into silicate by base, which subsequently deprotonates the APTES on AuNPs. By controlling condensation and decomposition of APTES, the plasmonic coupling among adjacent AuNPs could be reversible tuned to display the plasmonic color switching. This study provides a facile and distinctive strategy to regulate the reversible self-assembly of AuNPs, and it also offers a new avenue for other plasmonic nanoparticles to adjust plasmonic properties via reversible self-assembly.

| S-EPMC8116534 | biostudies-literature

Rubin H. Flocks and colloidal gold treatments for prostate cancer.

Project description:In the early 1950s, Rubin H. Flocks of the University of Iowa began to treat prostate cancer patients with colloidal gold (Au(198)) therapy, evolving his technique over nearly 25 years in 1515 patients. We reviewed the long-term outcomes of Flocks' prostate cancer patients as compared to those patients treated by other methods at the University of Iowa before Flocks' chairmanship. We reviewed archived patient records, Flocks' published data, and long-term survival data from the Iowa Tumor Registry to determine short- and long-term outcomes of Flocks' work with colloidal gold. We also reviewed the literature of Flocks' time to compare his outcomes against those of his contemporaries. The use of colloidal gold, either as primary or adjunctive therapy, provided short- and long-term survival benefit for the majority of Flocks' patients as compared to historical treatment options (p < 0.001). Flocks' use of colloidal gold for the treatment of locally advanced prostate cancer offered short- and long-term survival benefits compared to other contemporary treatments.

| S-EPMC3201627 | biostudies-other

SERS substrates formed by gold nanorods deposited on colloidal silica films.

Project description:We describe a new approach to the fabrication of surface-enhanced Raman scattering (SERS) substrates using gold nanorod (GNR) nanopowders to prepare concentrated GNR sols, followed by their deposition on an opal-like photonic crystal (OPC) film formed on a silicon wafer. For comparative experiments, we also prepared GNR assemblies on plain silicon wafers. GNR-OPC substrates combine the increased specific surface, owing to the multilayer silicon nanosphere structure, and various spatial GNR configurations, including those with possible plasmonic hot spots. We demonstrate here the existence of the optimal OPC thickness and GNR deposition density for the maximal SERS effect. All other things being equal, the analytical integral SERS enhancement of the GNR-OPC substrates is higher than that of the thick, randomly oriented GNR assemblies on plain silicon wafers. Several ways to further optimize the strategy suggested are discussed.

| S-EPMC3664605 | biostudies-literature

Nematic Order, Plasmonic Switching and Self-Patterning of Colloidal Gold Bipyramids.

Project description:Dispersing inorganic colloidal nanoparticles within nematic liquid crystals provides a versatile platform both for forming new soft matter phases and for predefining physical behavior through mesoscale molecular-colloidal self-organization. However, owing to formation of particle-induced singular defects and complex elasticity-mediated interactions, this approach has been implemented mainly just for colloidal nanorods and nanoplatelets, limiting its potential technological utility. Here, orientationally ordered nematic colloidal dispersions are reported of pentagonal gold bipyramids that exhibit narrow but controlled polarization-dependent surface plasmon resonance spectra and facile electric switching. Bipyramids tend to orient with their C5 rotation symmetry axes along the nematic director, exhibiting spatially homogeneous density within aligned samples. Topological solitons, like heliknotons, allow for spatial reorganization of these nanoparticles according to elastic free energy density within their micrometer-scale structures. With the nanoparticle orientations slaved to the nematic director and being switched by low voltages ≈1 V within a fraction of a second, these plasmonic composite materials are of interest for technological uses like color filters and plasmonic polarizers, as well as may lead to the development of unusual nematic phases, like pentatic liquid crystals.

| S-EPMC8596134 | biostudies-literature

Laser-Induced Plasmonic Nanobubbles and Microbubbles in Gold Nanorod Colloidal Solution.

Project description:In this work, we studied the initiated plasmonic nanobubbles and the follow-up microbubble in gold nanorod (GNR) colloidal solution induced by a pulsed laser. Owing to the surface plasmon resonance (SPR)-enhanced photothermal effect of GNR, several nanobubbles are initiated at the beginning of illumination and then to trigger the optical breakdown of water at the focal spot of a laser beam. Consequently, microbubble generation is facilitated; the threshold of pulsed laser energy is significantly reduced for the generation of microbubbles in water with the aid of GNRs. We used a probing He-Ne laser with a photodetector and an ultrasonic transducer to measure and investigate the dynamic formations of nanobubbles and the follow-up microbubble in GNR colloids. Two wavelengths (700 nm and 980 nm) of pulsed laser beams are used to irradiate two kinds of dilute GNR colloids with different longitudinal SPRs (718 nm and 966 nm). By characterizing the optical and photoacoustic signals, three types of microbubbles are identified: a single microbubble, a coalesced microbubble of multiple microbubbles, and a splitting microbubble. The former is caused by a single breakdown, whereas the latter two are caused by discrete and series-connected multiple breakdowns, respectively. We found that the thresholds of pulsed energy to induce different types of microbubbles are reduced as the concentration of GNRs increases, particularly when the wavelength of the laser is in the near-infrared (NIR) region and close to the SPR of GNRs. This advantage of a dilute GNR colloid facilitating the laser-induced microbubble in the NIR range of the bio-optical window could make biomedical applications available. Our study may provide an insight into the relationship between plasmonic nanobubbles and the triggered microbubbles.

| S-EPMC9000872 | biostudies-literature

Preparation of colloidal gold immunochromatographic strip for detection of Paragonimiasis skrjabini.

Project description:BackgroundParagonimiasis is a food-borne trematodiasis, a serious public health issue and a neglected tropical disease. Paragonimus skrjabini is a unique species found in China. Unlike paragonimiasis westermani, it is nearly impossible to make a definitive diagnosis for paragonimiasis skrjabini by finding eggs in sputum or feces. Immunodiagnosis is the best choice to detect paragonimiasis skrjabini. There is an urgent need to develop a novel, rapid and simple immunoassay for large-scale screening patients in endemic areas.Methodology/principal findingsTo develop a rapid, simple immunodiagnostic assay for paragonimiasis, rabbit anti-human IgG was conjugated to colloidal gold particles and used to detect antibodies in the sera of paragonimiasis patients. The synthesis and identification of colloidal gold particles and antibody-colloidal gold conjugates were performed. The size of colloidal gold particles was examined using a transmission electron microscope (TEM). The average diameter of colloidal gold particles was 17.46 nm with a range of 14.32-21.80 nm according to the TEM images. The formation of antibody-colloidal gold conjugates was monitored by UV/Vis spectroscopy. Excretory-secretory (ES) antigen of Paragonimus skrjabini was coated on nitrocellulose membrane as the capture line. Recombinant Staphylococcus protein A was used to prepare the control line. This rapid gold immunochromatographic strip was assembled in regular sequence through different accessories sticked on PVC board. The relative sensitivity and specificity of the strip was 94.4% (51/54) and 94.1% (32/34) respectively using ELISA as the standard method. Its stability and reproducibility were quite excellent after storage of the strip at 4°C for 6 months.Conclusions/significanceImmunochromatographic strip prepared in this study can be used in a rapid one-step immunochromatographic assay, which is instantaneous and convenient.

| S-EPMC3958401 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data