Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:6.2.1.1 (ACS)
 78,556 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In this study, we demonstrate the unique application of X-ray absorption spectroscopy (XAS) as a fundamental characterization tool to help in designing and controlling the architecture of Pd-Au bimetallic nanoparticles within a water-in-oil microemulsion system of water/sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/n-heptane. Structural insights obtained from the in situ XAS measurements recorded at each step during the formation process revealed that Pd-Au bimetallic clusters with various Pd-Au atomic stackings are formed by properly performing hydrazine reduction and redox transmetalation reactions sequentially within water-in-oil microemulsions. A structural model is provided to explain reasonably each reaction step and to give detailed insight into the nucleation and growth mechanism of Pd-Au bimetallic clusters. The combination of in situ XAS analysis at both the Pd K-edge and the Au L(III)-edge and UV-vis absorption spectral features confirms that the formation of Pd-Au bimetallic clusters follows a (Pd(nuclei)-Au(stack))-Pd(surf) stacking. This result further implies that the thickness of Au(stack) and Pd(surf) layers may be modulated by varying the dosage of the Au precursor and hydrazine, respectively. In addition, a bimetallic (Pd-Au)(alloy) nanocluster with a (Pd(nuclei)-Au(stack))-(Pd-Au(alloy))(surf) stacking was also designed and synthesized in order to check the feasibility of Pd(surf) layer modification. The result reveals that the Pd(surf) layer of the stacked (Pd(nuclei)-Au)(stack) bimetallic clusters can be successfully modified to form a (Au-Pd alloy)(surf) layer by a co-reduction of Pd and Au ions by hydrazine. Further, we demonstrate the alloying extent or atomic distribution of Pd and Au in Pd-Au bimetallic nanoparticles from the derived XAS structural parameters. The complete XAS-based methodology, demonstrated here on the Pd-Au bimetallic system, can easily be extended to design and control the alloying extent or atomic distribution, atomic stacking, and electronic structure to construct many other types of bimetallic systems for interesting applications.
ACS Nano 2007 Sep
PMID:Architecture of Pd-Au bimetallic nanoparticles in sodium bis(2-ethylhexyl)sulfosuccinate reverse micelles as investigated by X-ray absorption spectroscopy. 1920 27

Designing water-soluble peptides that camouflage their polarity to cross an anhydrous phase may significantly impact drug delivery. We engineered neutrally charged peptides endowed with a conformational switch that enables them to solubilize in both water and lipid. These peptides are capable of translocating without resorting to active internalization mechanisms. Lipid solubility is induced by a quadrupolar arrangement. Our passive translocation motif possesses the highest efficiency and is derived from cellular prions.
ACS Nano 2008 Jan
PMID:Bottom-up engineering of peptide cell translocators based on environmentally modulated quadrupole switches. 1920 48

The preorganized bis(polypseudorotaxane) (approximately 20 nm long) formed by the multiple metallo-bridged poly(beta-cyclodextrin)s has been successfully converted to the lengthened bis(molecular tube) (approximately 200 nm long) through the intermolecular joining of approximately 10 discrete bis(polypseudorotaxane) units and the subsequent removal of the polymer templates. The obtained bis(molecular tube), which is quite soluble in water, dimethylformamide, and dimethyl sulfoxide, has been comprehensively characterized by NMR, gel permeation chromatography, static light scattering, X-ray powder diffraction, thermogravimetric analysis, scanning electron microscopy, transmission electron microscopy, and scanning tunneling microscopy. Further investigations demonstrate that this bis(molecular tube) can capture C(60) through interaction with its many pi-electron-rich biquinolino groups.
ACS Nano 2008 Mar
PMID:Construction of a long cyclodextrin-based bis(molecular tube) from bis(polypseudorotaxane) and its capture of C60. 1920 82

The photoluminescence (PL) of 2D monolayers of CdSe/CdS/ZnS semiconductor nanocrystals (NCs) deposited on gold substrates and incorporated into electrochemical cells has been studied. By combining simultaneous cyclic voltammetry and confocal microscopy it is demonstrated that when a positive potential is applied to the film in an acetonitrile electrolyte, the PL is irreversibly quenched. This is irrespective of whether the samples are under an inert atmosphere or exposed to air or water vapor. When a negative potential is applied under nitrogen, quenching is also observed; however, it is reversible. Conversely when a negative potential is applied to the NC films in aerated acetonitrile, the PL intensity increases. The enhancement of the PL is stable for at least 180 s while the potential is held at -1.0 V (vs Ag quasi-reference electrode). When the potential is removed the PL intensity returns to the starting value. These results clearly indicate that photobrightening and charge carrier injection are coupled processes. On the basis of these data, we propose a simple kinetic model that explains the origins of photobrightening.
ACS Nano 2008 Apr
PMID:The effects of electron and hole injection on the photoluminescence of CdSe/CdS/ZnS nanocrystal monolayers. 1920 97

The patterning of biologically active materials has been accomplished by the use of imprint lithography of functional photopolymer resins to create controlled nanoscale patterns of a cross-linked photopolymer containing embedded initiator groups. Functionalized polymer brushes consisting of polystyrene and poly(N,N-dimethylacrylamide) were grown from these patterned layers by nitroxide-mediated polymerization. Chain-end functionalization of the brush layer was accomplished by nitroxide radical exchange during the polymerization. Accordingly, brush layers terminated by pyrene and biotin functional groups were obtained by exchange with the appropriate alkoxyamines. The presence of pyrene functionality at the chain ends of the brushes was confirmed by fluorescent emission measurements. Fluorescently labeled streptavidin protein was selectively attached with high selectivity to the patterned biotinylated brush layer through biotin-streptavidin interactions. The functionalized polymer grafted surfaces and nanopatterns have been successfully characterized using a fluorescence spectrophotometer, AFM, SEM, confocal microscopy, and water contact angle measurements.
ACS Nano 2008 Apr
PMID:Chain-end functionalized nanopatterned polymer brushes grown via in situ nitroxide free radical exchange. 1920 3

Organic-coated superparamagnetic iron oxide nanoparticles (OC-SPIONs) were synthesized and characterized by transmission electron microscopy and X-ray photoelectron spectroscopy. OC-SPIONs were transferred from organic media into water using poly(amidoamine) dendrimers modified with 6-TAMRA fluorescent dye and folic acid molecules. The saturation magnetization of the resulting dendrimer-coated SPIONs (DC-SPIONs) was determined, using a superconducting quantum interference device, to be 60 emu/g Fe versus 90 emu/g Fe for bulk magnetite. Selective targeting of the DC-SPIONs to KB cancer cells in vitro was demonstrated and quantified using two distinct and complementary imaging modalities: UV-visible and X-ray fluorescence; confocal microscopy confirmed internalization. The results were consistent between the uptake distribution quantified by flow cytometry using 6-TAMRA UV-visible fluorescence intensity and the cellular iron content determined using X-ray fluorescence microscopy.
ACS Nano 2008 Apr
PMID:Synthesis, characterization, and in vitro testing of superparamagnetic iron oxide nanoparticles targeted using folic Acid-conjugated dendrimers. 1920 10

Using a novel hydrogen peroxide heating method, we synthesized milky white, water-soluble polyhydroxylated fullerenes (fullerenols) with 36-40 hydroxyl groups (estimated average) along with 8-9 secondary bound water molecules. The fullerenols exhibited high water solubility up to 58.9 mg/mL in a neutral (pH = 7) condition. Dynamic light scattering analysis showed a high dispersion property, to give a narrow particle size distribution within 0.7-2.0 nm.
ACS Nano 2008 Feb
PMID:Facile synthesis of highly water-soluble fullerenes more than half-covered by hydroxyl groups. 1920 34

Contamination of the environment with mercury has been an important concern throughout the world for decades. Exposure to high Hg levels can be harmful to the brain, heart, kidneys, lungs, and immune system of humans of all ages. Driven by the need to detect trace amounts of mercury in environmental samples, here we present a miniaturized, inexpensive, and battery-operated ultrasensitive gold nanoparticle-based nanomaterial surface energy transfer probe for screening mercury levels in contaminated soil, water, and fish which has excellent sensitivity (2 ppt) and selectivity for Hg(II) over competing analytes, with the largest fluorescence enhancement to date for sensing Hg(II) in environmental samples (1100-fold). The sensitivity of our probe to detect mercury level in soil, water, and fish is about 2-3 orders of magnitude higher than the EPA standard limit. We demonstrate that our probe is suitable to screen the amount of mercury in different fish, shellfish, and water samples from various commercial sources.
ACS Nano 2007 Oct
PMID:Gold nanoparticle-based miniaturized nanomaterial surface energy transfer probe for rapid and ultrasensitive detection of mercury in soil, water, and fish. 1920 51

This report describes a simple method for preparing encoded microspheres for use in multiplexed biological detection. In this method, hydrophobic trioctylphosphine oxide (TOPO)-capped CdSe@ZnS quantum dots (QDs) are assembled on polyamine-coated microspheres in chloroform and encapsulated in an outer shell of silica nanoparticles functionalized with a specific recognition surface. Because TOPO-capped QDs are assembled instead of their water-soluble equivalents, the microspheres are highly luminescent. The amount of QDs assembled depends only on the surface area of the substrate, and therefore, the photoluminescence intensity increased uniformly in proportion to the number of QD layers assembled. The outer shell of silica nanoparticles confers stability on the assembled QDs but has no effect on their photoluminescence because it is transparent to excitatory and emitted light. It was activated with aminosilane and functionalized with a recognition surface of protein antigens using disulfide exchange chemistry. Magnetic beads furnished with spectral codes of up to three colors of QDs matched to specific recognition surfaces were used as multianalyte sensors for serum proteins.
ACS Nano 2007 Dec
PMID:A simple method for preparing spectrally encoded magnetic beads for multiplexed detection. 1920 70

Nanostructured metal (Fe, Co, Mn, Cr, Mo) oxides were fabricated under microwave irradiation conditions in pure water without using any reducing or capping reagent. The metal oxides self-assembled into octahedra, spheres, triangular rods, pine, and hexagonal snowflake-like three-dimensional morphologies. Pine-structured nano-iron oxides were studied as a novel support for various catalytic organic transformations.
ACS Nano 2009 Mar 24
PMID:Self-assembly of metal oxides into three-dimensional nanostructures: synthesis and application in catalysis. 1920 27


<< Previous 1 2 3 4 5 6 7 8 9 10 Next >>