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排序方式: 共有160条查询结果,搜索用时 11 毫秒
81.
A method that allows direct identification and quantitative determination of dipropylene glycol (DPG) using 13C NMR spectroscopy was developed. The quantitative procedure was checked and validated with commercially available DPG, controlled with two DPG-added essential oils, and then applied to commercial “Extraits de parfum” (perfume extracts). 相似文献
82.
Philip D. P. Taylor Danuta Barałkiewicz Ricardo Bettencourt da Silva Darinka Brodnjak Vončina Ewa Bulska Maria Filomena Camoes Ryszard Dobrowolski Marc Elskens Ivo Leito Nineta H. Majcen Petko Mandjukov Josephine McCourt Jérôme Randon Paavo Perämäki 《Analytical and bioanalytical chemistry》2015,407(23):6899-6907
83.
McGrath DM Naish JH O'Connor JP Hutchinson CE Waterton JC Taylor CJ Parker GJ 《Magnetic resonance imaging》2008,26(2):221-227
The objective was to measure the effect of 100% oxygen inhalation on T1 relaxation times in skeletal muscle. Healthy volunteers were scanned using three different MRI protocols while breathing medical air and 100% oxygen. Measurements of T1 were made from regions of interest (ROIs) within various skeletal muscle groups. Dynamic data of subjects breathing a sequence of air-oxygen-air allowed the calculation of characteristic wash-in and -out times for dissolved oxygen in muscle. Contrary to previous findings, a statistically significant decrease in T1 in skeletal muscle was observed due to oxygen inhalation. We report approximate baseline characteristic values for the response of skeletal muscle to oxygen inhalation. This measurement may provide new biomarkers for evaluation of oxygen delivery and consumption in normal and diseased skeletal muscle. 相似文献
84.
Cummins HK Jones C Furze A Soffe NF Mosca M Peach JM Jones JA 《Physical review letters》2002,88(18):187901
Here we describe a nuclear magnetic resonance (NMR) experiment that uses a three qubit NMR device to implement the one-to-two approximate quantum cloning network of Buzek et al. [Phys. Rev. A 56, 3446 (1997)]. As expected the experimental results indicate that the network clones all input states with similar fidelities, but as a result of decoherence and incoherent evolution arising from B(1) inhomogeneity the total fidelity achieved does not exceed the measurement bound. 相似文献
85.
Chandler BD Coté AP Cramb DT Hill JM Shimizu GK 《Chemical communications (Cambridge, England)》2002,(17):1900-1901
A luminescent mixed-metal coordination network with sponge-like sorption features is formed by stepwise assembly. 相似文献
86.
Kim H Kumari P Laughlin M Hilbert MJ Indelicato SR Lim J Lin CC Nomeir AA 《Journal of chromatography. A》2003,987(1-2):243-248
Posaconazole (SCH 56592) is a novel broad spectrum triazole antifungal agent that is currently in phase III clinical trials for the treatment of systemic fungal infections. This study was initiated to determine if orally administered posaconazole to humans would result in the formation of active metabolite(s). Plasma samples from a multiple-rising dose study in healthy volunteers were analyzed by validated HPLC and microbiological methods. The HPLC analysis involved extraction with a mixture of organic solvent (methylene chloride-hexane) followed by separation on a C18 column and quantification by UV absorbance at 262 nm. The microbiological assay was performed utilizing an agar diffusion method using Candida pseudorropicalis ATCC 46764 as the test organism. Potency was determined by comparing the growth inhibition zones produced by the test sample to those produced by standard concentrations prepared in plasma. Individual and mean plasma concentration-time profiles were similar for both HPLC and microbiological assays. The area under the plasma concentration-time curves of the microbiological and HPLC results were similar with a mean (RSD) ratio of 105.5% 15.3%), indicating that there was no relevant biologically active metabolite of posaconazole in human plasma. 相似文献
87.
Czechowicz JA Wilhelm AK Spalding MD Larson AM Engel LK Alberg DG 《The Journal of organic chemistry》2007,72(10):3689-3693
Trypanothione reductase (TR) catalyzes the NADPH-dependent reduction of trypanothione disulfide (1). TR plays a central role in the trypanosomatid parasite's defense against oxidative stress and has emerged as a promising target for antitrypanosomal drugs. We describe the synthesis and activity of dethiotrypanothione and analogues (2-4) as inhibitors of Trypanosoma cruzi TR. The syntheses of these macrocycles feature ring-closing olefin metathesis (RCM) reactions catalyzed by ruthenium catalyst 17. Derivative 4 is our most potent inhibitor with a Ki=16 microM. 相似文献
88.
We describe a novel technique for improving the sensitivity of analytical instruments based on the measurement of fluorescent intensity. Independent measurement of the Rayleigh scattered intensity component by means of a second photodetector leads to normalized data, which are independent of various experimental parameters. Incorporation of this technique into a fully automated capillary waveguide biosensor improved the instrument sensitivity by a factor of three. The technique enables quantification, as well as detection, of the hybridized target molecules. 相似文献
89.
Cicciarelli BA Elia JA Hatton TA Smith KA 《Langmuir : the ACS journal of surfaces and colloids》2007,23(16):8323-8330
The response of a nonionic photoresponsive surfactant system to changes in temperature is reported. This surfactant contains the light-sensitive azobenzene group, and when exposed to light, a solution of this surfactant contains a mixture of the cis and trans photoisomers of this group. The temperature of the surfactant solution has a strong impact on the time needed for the surfactant to diffuse and adsorb to a freshly formed interface. At surfactant concentrations that give rise to trans aggregates but not to cis aggregates, the transport of cis and of trans isomers to the surface of a pendant bubble have quite different temperature dependencies, owing largely to the difference in their aggregation states in bulk solution. Diffusion and adsorption of the cis isomer are described reasonably well by a simple diffusion model that accounts for the effect of temperature on the diffusion coefficient. The trans isomer, which was primarily bound in aggregates during these measurements, exhibits a stronger dependence of this adsorption time scale on the temperature of the solution. This temperature dependence of trans diffusion and adsorption is quantitatively consistent between samples containing only the trans isomer and samples containing a mixture of isomers. Fluorescence studies were done to determine the effect of temperature on the cmc of the surfactant. The critical concentration associated with the formation of cis-dominant aggregates increases modestly with increasing temperature. The cmc of the trans isomer also increases with increasing temperature, most significantly when the temperature exceeds about 35 degrees C. These trans cmc temperature-dependence data were incorporated into diffusion models that account for the potential roles of aggregates in the adsorption process. The observed temperature dependency of the trans adsorption time scale is consistent with a model that includes the effect of temperature on both the diffusivity and the supply of monomer via its effect on the cmc. Specifically, the results suggest that the dissolution of trans-dominant aggregates is important to the trans adsorption process. Further fluorescence studies were performed in which surfactant solutions containing aggregates were diluted rapidly, and the rate of dissolution of these aggregates was inferred from fluorescence decay. Aggregate breakup in colder trans samples is slower than in warmer samples, but these dissolution time scales are significantly shorter than those associated with the adsorption process. This is consistent with the assumption that aggregation kinetics do not contribute to the observed adsorption kinetics. 相似文献
90.
The perfect penicillin? Inhibition of a bacterial DD-peptidase by peptidoglycan-mimetic beta-lactams
6-(Glycyl-l-alpha-aminopimelyl)-aminopenicillanic acid and 7-(glycyl-l-alpha-aminopimelyl)-aminocephalosporanic acid have been synthesized as Streptomyces sp. peptidoglycan-mimetic beta-lactams. These compounds inactivate the Streptomyces R61 DD-peptidase with rate constants of 1.5 x 107 s-1 M-1 and 5.6 x 105 s-1 M-1, respectively. The former compound is thus the most effective beta-lactam inhibitor of a DD-peptidase yet described. The analogous d-alanyl-d-alanine peptide has previously been shown to react with this enzyme with comparable efficiency, kcat/Km = 8.7 x 106 s-1 M-1. These results show that, in this case at least, incorporation of a peptidoglycan-mimetic side chain into a beta-lactam greatly enhances its activity as a DD-peptidase inhibitor. This result has interesting implications for beta-lactam design. 相似文献