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71.
We present a new, simple, inexpensive, and highly precise approach to excited-state fluorescence-lifetime-based measurements. The detection system consists of a closed-loop optoelectronic arrangement containing a radio frequency resonance amplifier, a fluorescence excitation light source, a fiber-optic delay line, and a photodetector. The system exhibits auto-oscillations in the form of intensity modulation. The oscillation frequency varies with the modulation phase shift of the fluorescent light. This frequency is used as the detection parameter, which is advantageous because frequency may be measured easily, inexpensively, and with high precision. This technique is well suited for chemical or biosensor applications. 相似文献
72.
Introduction of a homochiral p-tolylsulfinyl group at an appropriate position in the alkene accelerates the thermal [5C + 2C] intramolecular cycloaddition to beta-silyloxy-gamma-pyrones and, most importantly, leads to excellent levels of diastereodifferentiation. The resulting adducts can be easily desulfinylated to give optically active 8-oxabicyclic[3.2.1]octane intermediates which by virtue of their rich functionalization might be susceptible to elaboration into enantiomerically pure natural products containing seven-membered carbocycles and tetrahydrofurans. 相似文献
73.
Alexandra Fidalgo Tessy M. Lopez Laura M. Ilharco 《Journal of Sol-Gel Science and Technology》2009,49(3):320-328
Wet sol–gel silica matrices produced under different hydrolysis conditions were used as delivery devices to the active principle
of an antiepileptic drug (phenytoin sodium), encapsulated during the condensation stage. Post-incorporation into dry silica
powder was an alternative loading procedure. It was proven by infrared spectroscopy that neither the silica network nor the
drug loose integrity by encapsulation. The kinetics of in vitro drug release was studied at 37 °C, to water and to artificial
cerebrospinal fluid (ACSF). Emphasis has been given to the release to ACSF under dynamic conditions (with fluid renovation,
emulating what occurs in the brain). Different delivery regimes were identified and correlated with the loading method and
the matrix structure. Matrices with lower total porosity and smaller average pore size proved to be better for a long term
release. Renovation of ACSF is relevant to assure a constant concentration of phenytoin in the vicinity of the device. 相似文献
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75.
C. Aguilar‐Lugo R. Le Lagadec Alexander D. Ryabov G. Cedillo Valverde S. Lopez Morales L. Alexandrova 《Journal of polymer science. Part A, Polymer chemistry》2009,47(15):3814-3828
Cationic substitutionally inert cyclometalated ruthenium (II) and osmium (II) complexes, ([Mt(o‐C6H4‐2‐py)(LL)2]PF6), where LL‐1,10‐phenanthroline (phen) or 2,2′‐bipyridine (bipy), were used for radical polymerization of styrene. Gradual modification of the complexes within the series allowed comparison of the catalytic activity and the redox properties. There was no correlation between the reducing powers of the complexes and their catalytic activities. The osmium compound of the lowest reduction potential was not active. All the ruthenium complexes catalyzed the polymerization of styrene in a controlled manner; but the level of control and the catalytic activity were different under the same polymerization conditions. [Ru(o‐C6H4‐2‐py)(phen)2]PF6 demonstrated the best catalytic performance though its redox potential was the highest. It catalyzed the “living” polymerization with a reasonable rate at a catalyst‐to‐initiator ratio of 0.1. 1 equiv. of Al(OiPr)3 accelerated the polymerization and improved the control, but higher amount of Al(OiPr)3 did not speed up the polymerization and moved the process into the uncontrollable regime. Under the most optimal conditions, the controlled polymerization occurs fast without any additive and the catalyst degradation. Added free ligands inhibited the polymerization suggesting that the catalytically active ruthenium intermediates are generated via the reversible dechelation of bidentate phen or bipy ligands. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3814–3828, 2009 相似文献
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78.
Y. Kudriavtsev A. Hernandez R. Asomoza S. Gallardo M. Lopez K. Moiseev 《Surface and interface analysis : SIA》2017,49(2):145-148
We have performed secondary ion mass spectrometry depth profiling analysis of III–V based hetero‐structures at different target temperatures and found that both the surface segregation and surface roughness caused by ion sputtering can be radically reduced if the sample temperature is lowered to ?150 °C. The depth profiling of ‘frozen’ samples can be a good alternative to sample rotation and oxygen flooding used for ultra‐low‐energy depth profiling of compound semiconductors. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
79.
Véronique Raverot Jonathan Lopez Catherine Grenot Henri Déchaud 《Analytica chimica acta》2010,658(1):87-9857
Testosterone (T) circulates in the blood tightly bound to sex hormone-binding globulin (SHBG) and weakly to albumin. Measuring protein unbound T (free) or non-SHBG-bound T rather than total T has been recommended for the evaluation of androgen disorders in humans. Ammonium sulfate precipitation has been widely used to separate [SHBG-T] complex from free and albumin-bound T. To achieve more specificity in this separation, we used monoclonal anti-SHBG antibody and developed a suitable and convenient immunoassay for measuring non-SHBG-bound T. Magnetic beads were covalently coupled to a monoclonal anti-SHBG antibody to capture [SHBG-T] complex from plasma samples. Magnetic separation was then performed to allow measurement of non-SHBG-bound T in the supernatant by direct radioimmunoassay. When 300 μL of plasma samples were incubated at room temperature with 10 μL of anti-SHBG beads, residual SHBG concentration was undetectable in the supernatant. The specificity of proteins retained on anti-SHBG beads was further demonstrated by peptide mass fingerprint on a MALDI-TOF analyzer. The non-specific adsorption of T on beads was low (5%), and dissociation of T from SHBG-T complex was less than 5% after 180 min of incubation. The plasma concentrations of non-SHBG-bound T using anti-SHBG beads were highly correlated to those obtained using ammonium sulfate precipitation. We conclude that SHBG immunocapture is a highly specific and useful tool for an experimental direct measurement of plasma non-SHBG-bound T. This methodology is also convenient and appropriate for routine and automated assay. 相似文献
80.
Katrin Hartl Karl J.J. Mayrhofer Marco Lopez Dan Goia Matthias Arenz 《Electrochemistry communications》2010,12(11):1487-1489
In the presented work, the evaluation of an unsupported AuPt core–shell catalyst for the oxygen reduction reaction is introduced. Applying only basic chemicals in an upscalable synthesis route, it is demonstrated that uniform, flat, and complete Pt layers around a spherical Au core are obtained. The electrocatalytic measurements show that the surface area specific activity of the AuPt core–shell catalyst towards the important oxygen reduction reaction equals the one of polycrystalline bulk Pt. To our knowledge, this is the first time that the unfavorable particle size effect of Pt nanoparticles could be by-passed for a nanoscale catalyst. 相似文献