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  • Author or Editor: X. Gao x
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Summary

Dauricine has a variety of pharmacological properties including anti-inflammatory, anti-arrhythmic, and antihypertensive effects as well as reversing multidrug resistance (MDR) of cancer cells. While its therapeutic application is increasing, its bioavailability of different administration routes has not been studied. In the present study, we developed and validated a liquid chromatography/electrospray ionization mass spectrometry method (LC-MS/MS). Using this method, we quantified dauricine in rat plasma after administration via intravenous (i.v.) injection, per oral (p.o.), and intraperitoneal injection (i.p.). Our results indicated that this method detected plasma dauricine with a good linearity in the range of 1.95–1000.00 ng/mL (r = 0.9997). The extraction method showed an average intra- and inter-day recovery of 98.21–104.35% and 98.0–103.58%, respectively. Dauricine showed a fast absorption and widespread distribution after administration in all three tested routes. After intravenous administration (2.5, 5.0, 10.0 mg/kg), the pharmacokinetics of dauricine exhibited a first-order kinetics. In addition, dauricine showed a slow elimination with a long half-life (t 1/2z) and double peaks phenomenon following p.o. and i.p. administration. Furthermore, using area under the plasma concentration-time curve (AUC), we calculated absolute bioavailability, which was over twofold higher when administered via i.p. than via p.o. administration. The newly obtained information from our study will provide important reference for dauricine dose and administration route in designing dauricine therapy for applicable diseases.

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Abstract  

We have developed a thermogravimetric system (TG system) for condensable gas adsorption by modifying a standard thermogravimetric analyzer Cahn TG 2121 and performed isotherm measurements of water vapor adsorption on Fuji Davison type RD silica gel and ethanol vapor adsorption on Maxsorp II activated carbon. For the water vapor-silica gel data, our results compare favorably with the data reported by the manufacturer and those obtained from a volumetric method. This confirms the reliability of our TG system for adsorbents which do not swell significantly. In addition, our isotherm data also provide useful design information for the development of adsorption chillers.

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Youzimai is a widespread wheat landrace and has been used extensively in breeding programs in China. In order to assess the genetic variation between and within Youzimai accessions, samples of 31 landrace accessions of wheat, all called ‘Youzimai’, were collected from 6 geographic regions in China and evaluated using morphological traits, seedling resistance to powdery mildew, gliadin and microsatellite markers. Typical differences among accessions were observed in morphological characteristics. Forty-five (58.4%) of 77 assayed SSR markers showed polymorphism over the entire collection and total 226 alleles were identified with an average of 5.02 alleles per locus. SSR data indicated that the accessions from Hebei province were the most diverse, as evidenced by greatest number of region-specific alleles and highest diversity index. These accessions, therefore, probably experienced the most substantial morphological and molecular evolution as a result of various natural and anthropomorphic influences. On the other hand, differentiation in gliadin phenotypes was found among seeds within 80.6% of total accessions and average 61.5% of entire collections showed heterogeneous and comprised resistant plants in reaction to powdery mildew, suggesting the presence of a wide diversity within the wheat landrace. By developing an intimate knowledge of the available wheat genotypes, appropriate selections can be made for commercial application in order to conserve and exploit the diversity of the wheat landraces.

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Abstract  

Both calorimetric determination of displacement adsorption enthalpies ΔH and measurement of adsorbed amounts of lysozyme (Lyz) denatured by 1.8 mol L−1 guanidine hydrochloride (GuHCl) on a moderately hydrophobic packings at 298 K, pH 7.0 and various salt concentrations were carried out. Based on the thermodynamics of stoichiometric displacement theory (SDT) the fractions of thermodynamic functions, which related to four subprocesses of denatured protein refolding on the surface, were calculated and thermodynamic analysis that which one of the subprocesses plays major role for contribution to the thermodynamic fractions was made in detail. The moderately hydrophobic surface can provide denatured Lyz energy and make it gain more conformation with surface coverage or salt concentration increment. The displacement adsorptions of denatured Lyz onto PEG-600 surface are exothermic, more structure-ordered and enthalpy driven processes.

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Abstract  

A complex of neodymium perchloric acid coordinated with L-glutamic acid and imidazole, [Nd(Glu)(H2O)5(Im)3](ClO4)6·2H2O was synthesized and characterized by IR and elements analysis for the first time. The thermodynamic properties of the complex were studied with an automatic adiabatic calorimeter and differential scanning calorimetry (DSC). Glass transition and phase transition were discovered at 221.83 and 245.45 K, respectively. The glass transition was interpreted as a freezing-in phenomenon of the reorientational motion of ClO4 ions and the phase transition was attributed to the orientational order/disorder process of ClO4 ions. The heat capacities of the complex were measured with the automatic adiabatic calorimeter and the thermodynamic functions [H T-H 298.15] and [S T-S 298.15] were derived in the temperature range from 80 to 390 K with temperature interval of 5 K. Thermal decomposition behavior of the complex in nitrogen atmosphere was studied by thermogravimetric (TG) analysis and differential scanning calorimetry (DSC).

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Abstract  

The molar heat capacity C p,m of 1,2-cyclohexane dicarboxylic anhydride was measured in the temperature range from T=80 to 390 K with a small sample automated adiabatic calorimeter. The melting point T m, the molar enthalpy Δfus H m and the entropy Δfus S m of fusion for the compound were determined to be 303.80 K, 14.71 kJ mol−1 and 48.43 J K−1 mol−1, respectively. The thermodynamic functions [H T-H 273.15] and [S T-S 273.15] were derived in the temperature range from T=80 to 385 K with temperature interval of 5 K. The thermal stability of the compound was investigated by differential scanning calorimeter (DSC) and thermogravimetry (TG), when the process of the mass-loss was due to the evaporation, instead of its thermal decomposition.

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Abstract  

The radiation effect of γ-ray on polyether-urethane foam was studied. The gas products from irradiated samples were analyzed quantitatively and qualitatively by gas chromatography, the thermal property and radical intensity were determined by differential thermal gravimetry and electron spin resonance. The dynamic mechanical property, compression and tensile properties were analyzed. Positron annihilation lifetime of irradiated samples was also measured at room temperature in vacuum. The results show that the general mechanical properties of ETPU sample irradiated by γ-rays at a dose of 8.0·105 Gy is excellent, but there are considerable gas products and a great deal of radicals created, which indicates that the sample has been damaged by radiation. Relatively, the thermal stability of the sample remained fine.

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Abstract

A complex of Erbium perchloric acid coordinated with l-aspartic acid and imidazole, Er2(Asp)2(Im)8(ClO4)6·10H2O was synthesized for the first time. It was characterized by IR and elements analysis. The heat capacity and thermodynamic properties of the complex were studied with an adiabatic calorimeter (AC) from 80 to 390 K and differential scanning calorimetry (DSC) from 100 to 300 K. Glass transition and phase transition were discovered at 220.45 and 246.15 K, respectively. The glass transition was interpreted as a freezing-in phenomenon of the reorientational motion of ClO4− ions and the phase transition was attributed to the orientational order/disorder process of ClO4− ions. The thermodynamic functions [H T H 298.15] and [S T S 298.15] were derived in the temperature range from 80 to 390 K with temperature interval of 5 K. Thermal decomposition behavior of the complex in nitrogen atmosphere was studied by thermogravimetric (TG) analysis and differential scanning calorimetry (DSC).

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Abstract  

Carburization and coke deposition of unsupported and carbon-supported Fe, Mo and Fe−Mo catalysts in syngas have been studied using thermogravimetry. Compositions of the carbides formed are evaluated on the basis of the amount of metals in the catalysts and amount of carbon deposited during carburization. It is shown that carburization temperature and the nature of the carbides formed (Fe5C2 and Fe2C for iron and Mo2C for molybdenum) depend on the metals but are influenced by the support and metal loading. Coke deposition on these catalysts takes place as soon as carburization is complete.

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Abstract  

The catalytic performance of unsupported and carbon-supported Fe, Mo and Fe−Mo catalysts for Fischer-Tropsch synthesis is greatly influenced by the final reduction states of the catalysts. In this investigation, the reduction process of the catalysts by H2 was studied by using TG-DTG. The reduction process depends not only on the reducibility of metals but also on the nature of the support. Methanation of the support occurred as soon as the supported metals were completely reduced for the carbon-supported catalysts. For these, the reduction temperature should by carefully selected so that the metal oxides are reduced as completely as possible, whilst the methanation of the support must be avoided to obtain optimum reduced catalysts.

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