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991.
I. W. Ellms S. I. Hauser L. W. Winkler H. Pecker V. Froboese A. T. Stuart F. Malméjac J. Tillmans O. Heublein H. Noll J. M. Kolthoff H. Klut Dietl L. Dede E. Hauser E. M. Chamot D. S. Pratt A. E. Johnson H. Silvester W. Vaubel G. Denigès E. H. Miller S. Rothenfusser M. Bornand L. Rosenthaler V. Jahn A. Dané L. v. Liebermann D. Acel E. B. Phelps H. L. Shoub Escaich H. Berger G. D. Elsdon N. Evers H. W. Brubaker F. W. Bruckmiller 《Analytical and bioanalytical chemistry》1922,61(4-5):196-205
992.
This article deals with the solution properties of poly(vinylpyrrolidone) (PVP) in salt and surfactant environment. The cloud point (CP) of PVP has been found to be induced by the salts NaCl, KCl, KBr, Na2SO4, MgSO4, and Na3PO4. On the basis of CP values for a salt at different [PVP], the energetics of the clouding process have been estimated. The effect of the surfactant, sodium dodecyl sulfate (SDS), on the salt-induced CP has also been studied, and reduction in CP at low [SDS] and increase in CP at high [SDS] have been observed. The water vapor adsorption of PVP has been determined by isopiestic method. The results display a BET Type III isotherm whose analysis has helped to obtain the monolayer capacity of PVP and formation of multilayer on it. The solvation of PVP in a solution of water and a water-isopropanol mixture has been determined by conductometry from which contribution of the individual components were estimated. The interaction of PVP with SDS in solution led to formation of a complex entity, which has been studied also by conductometry adopting a binding-equilibrium scheme. SDS has been found to undergo two types of binding as monomers in the pre- critical aggregation concentration (CAC) range and as small clusters in the post CAC region. The stoichiometries of binding and binding constant were evaluated. 相似文献
993.
Cao YG Zhang M Yu D Shao JP Chen YC Liu XQ 《Analytical and bioanalytical chemistry》2008,391(3):1063-1071
An advanced quantification method was developed with solid-phase extraction (SPE) and mass spectrometry (MS) determination
for nafamostat, an unstable and highly polar drug, in human plasma. For unstable drugs with an ester group, the main analytical
challenge is how to avoid the ester hydrolysis, and strong acid or alkaline conditions should be excluded during sample preparation.
Considering that, we developed a relatively mild method with SPE for sample preparation without strong acid and alkaline treatment,
which was optimized with different pHs and salt concentrations in phosphate-buffered saline treatment. The results indicated
that pH 5 gave the most efficient extraction and 0.1 M salt concentration enhanced the extraction the most, with a minor effect
on MS monitoring. The extraction method effectively avoided drug hydrolysis and achieved good drug enrichment over 82.2%.
The linear range of quantification was 1.25–160 ng mL−1. The stability of the drug in sample treatment was fully validated according to the sample processing procedure, including
the stability in fresh blood, mobile phase, plasma and acidic methanol, and the results indicated that the drug remained stable
during the whole sample preparation. Compared with a previous isotope-labeling method, more accurate and specific quantification
of plasma concentration was achieved with liquid chromatography–electrospray ionization MS determination. With use of our
method, nafamostat mesilate pharmacokinetics in 30 Chinese healthy volunteers was investigated with three doses via intravenous-drip
infusion. The pharmacokinetic parameters were also estimated and compared with those of Japanese volunteers (slightly lower
plasma concentration and longer terminal elimination half-life for Chinese volunteers). The difference in the pharmacokinetics
may be ascribed to the quantification method, because previous isotope labeling may have overestimated the parent drug. 相似文献
994.
Dan Jin Zhao‐Fu Dai De‐Chun Zhang 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(2):o50-o52
In the title compound, C15H16NO+·C24H20B−, the pyridinium ring of the cation makes a dihedral angle of 4.3 (2)° with the benzene ring. Each is rotated in the same direction with respect to the central C—CH=CH—C linkage, by 10.0 (2) and 7.8 (2)°, respectively. The anions have a slightly distorted tetrahedral geometry. The most interesting feature of the structure is that the anions form a honeycomb‐like hexagonal structure down the b axis through C—H...π interactions. The hexagon is constructed from six BPh4− anions. The cations interact in a head‐to‐tail fashion along [010], forming chains, and pack antiparallel inside the above honeycomb‐like structure through C—H...π interactions. 相似文献
995.
A low molecular weight hydrogel which exhibits electroosmotic flow is described, and its use for separation and biocatalytic applications that require passage of a solvent stream through the gel is demonstrated. 相似文献
996.
A novel nanostructure of a PtAu catalyst, alloyed PtAu nanodendrites, has been synthesized via a reproducible single-step hydrothermal co-reduction of Pt and Au inorganic precursors and shows exceptionally high catalytic activity towards the electrooxidation of formic acid. 相似文献
997.
Zhao D Cheng WD Zhang H Hang SP Fang M 《Dalton transactions (Cambridge, England : 2003)》2008,(28):3709-3714
The structural, optical, and electronic properties of two rare-earth molybdenum borate compounds, LnMoBO(6) (Ln = La, Ce), have been investigated by means of single-crystal X-ray diffraction, elemental analyses, and spectral measurements, as well as calculations of energy band structures, density of states, and optical response functions by the density functional method. The title compounds, which crystallize in monoclinic space group P2(1)/c, possess a similar network of interconnected [Ce(2)(MoO(4))(2)](2+) chains and [BO(2)](-) wavy chains. Novel 1D molybdenum oxide chains are contained in their three-dimensional (3D) networks. The calculated results of crystal energy band structure by the density functional theory (DFT) method show that the solid-state compound LaMoBO(6) is a semiconductor with indirect band gaps. 相似文献
998.
Determination of trace chlorine dioxide based on the plasmon resonance scattering of silver nanoparticles 总被引:1,自引:0,他引:1
A plasmon resonance scattering (PRS) method for chlorine dioxide is reported based on the oxidization of silver nanoparticles (NPs) by it, in pH 9.1 ammonia-ammonium nitrate buffer solutions. Silver NPs exhibit strong PRS signals at 470nm, and can be oxidized by ClO(2), which results in PRS quenching at 470nm. It was found that the PRS quenching intensity is proportional to the concentration of chlorine dioxide over the range of 0.0011-0.185microg/mL, with a detection limit (3sigma) of 0.00050microg/mL and the correlation coefficient of 0.9995. The method is simple, rapid and cost effective. It was applied to the determination of chlorine dioxide in drinking water, with satisfactory results. 相似文献
999.
Electrochemical pesticide sensitivity test using acetylcholinesterase biosensor based on colloidal gold nanoparticle modified sol-gel interface 总被引:2,自引:0,他引:2
Based on the change in electrochemical behavior of enzymatic activity induced by pesticide, a novel electrochemical method for investigation of pesticide sensitivity using acetylcholinesterase (AChE) biosensor was developed. The sol-gel-derived silicate network assembling gold nanoparticles (AuNPs-SiSG) provided a biocompatible microenvironment around the enzyme molecule to stabilize its biological activity and prevented them from leaking out of the interface. The composite was characterized using atomic force microscopy and proved to be chemically clean, porous and homogeneous. AuNPs promoted a conductive pathway for electron transfer and improved electrochemical reactions at a lower potential. Typical pesticides such as monocrotophos, methyl parathion and carbaryl were selected for pesticide sensitivity tests. Due to the inhibitions of pesticides, the electrochemical responses of substrate on AChE-sensors decreased greatly. The inhibition curves showed good correspondence with the results by UV spectrophotometry assay. The proposed electrochemical pesticide sensitivity test exhibited high sensitivity, desirable accuracy, low cost and simplified procedures. This method could be developed as a conventional method to select efficient enzyme inhibitors and investigate toxic compounds against to enzyme. 相似文献
1000.
Functionalization of pentacene at the 6- and 13-positions affords versatile building blocks for oligomer and polymer formation. Di- and trimeric materials are synthesized using unsymmetrical building block 18, while symmetrical diol monomer 17 allows for the synthesis of polymers. The materials reported herein are soluble in common organic solvents and air-stable. UV-vis and fluorescence spectroscopic properties have been investigated. Solid-state X-ray crystallography of building blocks 17 and 19 shows that these derivatives can π-stack with significant acene face-to-face interactions with spacing of less than 3.5 Å. 相似文献