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991.
A gas chromatographic method for monitoring diacetyl guanfubase A in plasma is described. The procedure involved a single solvent extraction of drug from rabbit plasma into ethyl acetate with guanfubase A as an internal standard. The extract was analyzed subsequently on a gas chromatograph equipped with a hydrogen flame ionization detector. The recovery was 86.43% +/- 6.90% (+/- SD); the RSD of within-day and between-day was 2.81%-5.26% and 5.22%-8.24%, respectively; the regression line was linear over the concentration range of 25-200 micrograms/mL, the limit of detection was 10 micrograms/mL. No endogeneous interference was found in chromatograms of the biological samples. This method was applied to the pharmacokinetic study of diacetyl guanfubase A in rabbits. 相似文献
992.
A new series of thiophene‐ and furan‐containing chromophores with a chiral prolinol donor and a sulfone acceptor has been synthesized. The UV‐vis absorptions, second‐order nonlinear optical properties, and X‐ray crystal structures are described. 相似文献
993.
A highly effective, economical, and environmentally friendly method using of CAN as oxidant and water as solvent for oxidative coupling of N,N-dialkylarylamines was reported. 相似文献
994.
995.
A sensitive stripping voltammetric procedure for quantifying rhodium is described. The complex of rhodium with chloride ions is adsorbed on the hanging mercury drop electrode, and the reduction current of the accumulated complex is measured during a negative-going scan. Cyclic voltammetry is used to characterize the interfacial and redox behaviors. The effect of pH, chloride concentration, accumulation potential and other variables is discussed. The detection limit is 1 x 10(-8)M ( approximately 1 ng/ml) with 5-min accumulation. A linear current-concentration relationship is observed up to 7 x 10(-7)M and the relative standard deviation (at the 2 x 10(-7)M level) is 3.0%. Possible interferences by co-existing metals are investigated. 相似文献
996.
997.
998.
A sensitive stripping voltammetric procedure for quantifying thorium is described. The chelate of thorium with the azo dye Mordant Blue 9 is adsorbed on the hanging mercury drop electrode, and the reduction current of the accumulated chelate is measured during a negative-going potential scan. Cyclic voltammetry is used to characterize the interfacial and redox behaviors. The effects of pH, dye concentration and accumulation potential are discussed. The detection limit is 4 × 10?10 M (4-min accumulation), a linear current-concentration relationship is observed up to 1.3 × 10?7 M, and the relative standard deviation (at the 6 × 10?8 M level) is 3.1%. Possible interferences by trace metals and organic surfactants are investigated. Simultaneous quantitation of thorium and nickel is illustrated. 相似文献
999.
Ming Guo Jue Wang Man Xiong Ronghui Wu Xuejuan Yang Jianzhong Zhou Minghui Li Jiajun Li 《大学化学》1986,35(12):237-246
In order to improve university laboratory teaching and practical education under the background of information technology, as well as overcome the difficulty for practical training, develop a virtual simulation experiment platform for rapid pyrolysis of natal materials and high-performance liquid chromatographic (HPLC) detection of its components. The experiment integrates the actual operation process of the plant to produce cleaved products by rapid pyrolysis of biomass with HPLC detection. The virtual experiment is divided into biomass sample pretreatment, rapid biomass pyrolysis, bio-oil extraction, and HPLC determination of complex components, making the biomass cleavage workshop "real" through simulation. This virtual simulation experiment fully integrates the utilization of biomass resources and basic chemistry courses (such as organic chemistry, instrumental analysis, chemical engineering principles, etc.), which are widely involved in agricultural and forestry majors with advantageous characteristics value. 相似文献
1000.
J. M. Wang R. Ballad P. Grimaldi W. Lei 《Journal of Radioanalytical and Nuclear Chemistry》1983,76(1):105-108
A manganese dioxide coprecipitation procedure is utilized to replace a time-consuming evaporation step for the extraction
of thorium, uranium and cerium from freshwater samples. The average recovery for 20-liter samples is greater than 95% for234Th and144Ce. The data indicate that the manganese dioxide coprecipitation process does not affect the recovery of thorium and uranium
during our routine analytical procedure. 相似文献