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81.
Determination of teicoplanin in human plasma and urine by affinity and reversed-phase high-performance liquid chromatography 总被引:2,自引:0,他引:2
E Riva N Ferry A Cometti G Cuisinaud G G Gallo J Sassard 《Journal of chromatography. A》1987,421(1):99-110
A sensitive, highly selective and simple high-performance liquid chromatographic method for the determination of teicoplanin, a novel glycopeptide antibiotic, composed of six components, in human plasma and urine is described. After an isolation step by affinity chromatography, the antibiotic substances were chromatographed on a Nucleosil C18 column with phosphate buffer-acetonitrile according to a gradient profile. All the components were detected by their UV absorption at 240 nm. The concentration of teicoplanin was determined by using the external standard procedure. This method was applied to the sum of the six major components as well as to each of them separately. The linearity of the method was checked between 0.5 and 50 micrograms/ml for plasma and between 2 and 50 micrograms/ml for urine. The limit of detection was 0.1 microgram/ml for both biological fluids. The coefficients of variation of the between-day assays did not exceed 8.6 and 8.9% in plasma and urine, respectively. The application of the method to a pharmacokinetic study of teicoplanin after a single intravenous therapeutic dose in a patient is reported. This rapid technique also appears to be suitable for drug monitoring. 相似文献
82.
The electron impact mass spectra of the 4-formyl-1, 3-dihydro-2H-imidazole-2-thione, its six 1-methyl(n-propyl, n-hexyl)-3-methyl(phenyl)-disubstptuted derivatives, and the 1,3-dihydro-1-phenyl-2H-imidazole-2-thiome are discussed. The fragmentation pattern is strongly influenced by the alkyl or phenyl N-substituents, as well as by the length of the alkyl chain. The odd-electron ions containing an N-phenyl substituent, but not a propyl or hexyl group, eject a hydrogen atom from the phenyl ring, while the presence of a long alkyl chain greatly enhances the loss of the sulphyhydryl radical and facilitates the expulsion of several alkenes, and alkyl and alkenyl radicals. 相似文献
83.
The thermal decompositions of azodicarbamide (AZDICA), 2,2′-azobisisobutyronitrile (AIBN), benzoyl peroxide (Bz2O2), dicumyl peroxide (DICUP) andα, α′-bis(t.-butylperoxy)-m/p-diisopropylbenzene (PEROXIMON F) in binary and ternary mixtures containing low density polyethylene (LDPE) have been studied by means of DSC alone. Binary mixtures including 2% by weight of Bz2O2 or DICUP develop a decomposition heat of 64.2 and 59.1 J/g mixture, respectively. These values are higher than those measured for the decomposition of the pure peroxides. In all the ternary mixtures studied, containing LDPE, a peroxide and an azoderivative, the absolute enthalpic values attributed to the peroxide are lower than those obtained from the LDPE-peroxide mixtures. The enthalpy changes observed have been interpreted on the basis of interactions of the peroxide radicals with the polymer support and with the azo derivative. 相似文献
84.
Zorica M. Bugar?i? Vera M. Divac Mariana P. Gavrilovi? 《Monatshefte für Chemie / Chemical Monthly》2007,40(9):985-988
An efficient protocol for the preparation of phenylselenoethers from unsaturated alcohols using phenylselenenyl halides at
room temperature was developed. The procedure employs phenylselenenyl chloride and bromide, some Δ 4- and Δ 5-alkenols and Ag2O, as an additive, to generate the tetrahydropyrans or tetrahydrofurans. This method permits the preparation of cyclic phenylselenoethers
in high yields and under extremely mild conditions. 相似文献
85.
Boneva MP Christov NC Danov KD Kralchevsky PA 《Physical chemistry chemical physics : PCCP》2007,9(48):6371-6384
Here, we investigate experimentally and theoretically the motion of spherical glass particles of radii 240-310 microm attached to a tetradecane-water interface. Pairs of particles, which are moving toward each other under the action of lateral capillary force, are observed by optical microscopy. The purpose is to check whether the particle electric charges influence the particle motion, and whether an electric-field-induced capillary attraction could be detected. The particles have been hydrophobized by using two different procedures, which allow one to prepare charged and uncharged particles. To quantify the hydrodynamic viscous effects, we developed a semiempirical quantitative approach, whose validity was verified by control experiments with uncharged particles. An appropriate trajectory function was defined, which should increase linearly with time if the particle motion is driven solely by the gravity-induced capillary force. The analysis of the experimental results evidences for the existence of an additional attraction between two like-charged particles at the oil-water interface. This attraction exceeds the direct electrostatic repulsion between the two particles and leads to a noticeable acceleration of their motion. 相似文献
86.
Silva NL Betancur GJ Vasquez MP Gomes Ede B Pereira N 《Applied biochemistry and biotechnology》2011,163(7):928-936
Current research indicates the ethanol fuel production from lignocellulosic materials, such as residual wood chips from the
cellulose industry, as new emerging technology. This work aimed at evaluating the ethanol production from hemicellulose of
eucalyptus chips by diluted acid pretreatment and the subsequent fermentation of the generated hydrolysate by a flocculating
strain of Pichia stipitis. The remaining solid fraction generated after pretreatment was subjected to enzymatic hydrolysis, which was carried out simultaneously
with glucose fermentation [saccharification and fermentation (SSF) process] using a strain of Saccharomyces cerevisiae. The acid pretreatment was evaluated using a central composite design for sulfuric acid concentration (1.0–4.0 v/v) and solid to liquid ratio (1:2–1:4, grams to milliliter) as independent variables. A maximum xylose concentration of 50 g/L
was obtained in the hemicellulosic hydrolysate. The fermentation of hemicellulosic hydrolysate and the SSF process were performed
in bioreactors and the final ethanol concentrations of 15.3 g/L and 28.7 g/L were obtained, respectively. 相似文献
87.
Mariana Antunes Vieira Bernhard Welz Adilson Jos Curtius 《Spectrochimica Acta Part B: Atomic Spectroscopy》2002,57(12):251-2067
A simple and reliable method for the determination of arsenic in sediment and in coal without sample digestion, based on hydride generation from slurry samples is proposed. After grinding the samples to a particle size of 50 μm, the sample powder was mixed with aqua regia and hydrofluoric acid in an ultrasonic bath for 30 min. After diluting the mixture with hydrochloric acid, the slurry was allowed to stand for 48 h, and an aliquot was used for hydride generation with sodium borohydride. More than 80% of the arsenic was leached to the aqueous phase under these conditions, except for one sediment sample with very high silica content. The generated arsine was collected in a graphite tube, treated with 0.5 mg of iridium as a permanent modifier, and the arsenic determination was carried out by electrothermal atomic absorption spectrometry. The same tube could be used for at least 160 cycles without any re-treatment. The greatest advantage of the method was that only a minimum of reagents and sample handling were required, reducing the risks of contamination and/or analyte loss. However, the addition calibration technique had to be used in order to obtain results within the 95% confidence level for 11 certified reference materials, 5 sediments, 5 coals and one coal fly ash. One certified sediment slurry was spiked with the analyte and the resulting addition calibration curve was used for the analysis of the certified sediments. Similarly, one certified coal was used to obtain the addition calibration curve for the coal and coal fly ash samples. The recoveries of the certified values, except for one sediment, were between 91 and 115%. The limits of detection in the samples were 0.54 and 0.7 μg g−1 for the coal and sediment samples, respectively, obtained for 1 ml of slurry containing 1 mg of sample. 相似文献
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