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101.
This study examined the pharmacokinetic disposition, oral absorption and hepatic extraction of itraconazole and its active metabolite, hydroxyitraconazole, in rats. After i.v. injection, serum itraconazole concentrations decreased biexponentially, with an average terminal elimination half-life, volume of distribution and systemic clearance of 4.9 h, 6.0 l/kg and 14.2 ml/min/kg, respectively. When given orally, its absorption was low, with a mean absolute bioavailability of 16.6%. The metabolite to parent drug area under the curve (AUC) ratio was higher after oral administration compared with i.v. injection (mean ratio, 2.7 vs. 0.9). The hepatic drug extraction ratio determined after femoral and portal vein administration averaged 18.5%. When hydroxyitraconazole was injected i.v., the elimination half-life, volume of distribution and systemic clearance of itraconazole averaged 10.0 h, 2.4 l/kg and 3.4 ml/min/kg, respectively. The fraction of the systemically available itraconazole that was metabolized to hydroxyitraconazole was 21.0% and 76.0% after i.v. and oral administration, respectively. In summary, this study is the first reporting the hepatic extraction of itraconazole and the i.v. disposition characteristics of hydroxyitraconazole in rats. Itraconazole is a drug with a low hepatic extraction ratio and its systemic clearance appears to be largely accounted for by hepatic metabolism. 相似文献
102.
Al-Rashid ZF Johnson WL Hsung RP Wei Y Yao PY Liu R Zhao K 《The Journal of organic chemistry》2008,73(22):8780-8784
A de novo preparation of alpha-keto-imides via ynamide oxidation is described. With a number of alkyne oxidation conditions screened, a highly efficient RuO2-NaIO4 mediated oxidation and a DMDO oxidation have been identified to tolerate a wide range of ynamide types. In addition to accessing a wide variety of alpha-keto-imides, the RuO2-NaIO4 protocol provides a novel entry to the vicinal tricarbonyl motif via oxidation of push-pull ynamides, and imido acylsilanes from silyl-substituted ynamides. Chemoselective oxidation of ynamides containing olefins can be achieved by using DMDO, while the RuO2-NaIO4 protocol is not effective. These studies provide further support for the synthetic utility of ynamides. 相似文献
103.
Baik JM Shon Y Lee SJ Jeong YH Kang TW Lee JL 《Journal of the American Chemical Society》2008,130(41):13522-13523
We report the room-temperature ferromagnetism in transition metals (Co, Ni)-doped 8-hydroxy-quinoline aluminum (Alq3) by thermal coevaporation of high purity metal and Alq3 powders. For 5% Co-doped Alq3, a maximum magnetization of approximately 0.33 microB/Co at 10 K was obtained and ferromagnetic behavior was observed up to 300 K. The Co atoms interact chemically with O atoms and provide electrons to Alq3, forming new states acting as electron trap sites. From this, it is suggested that ferromagnetism may be associated with the strong chemical interaction of Co atoms and Alq3 molecules. 相似文献
104.
105.
Hydrophobic bacteria, like colloidal solids, can spontaneously adsorb onto fluid-fluid interfaces and modify their mechanical properties. In this study, two strains of bacteria--Acinetobacter venetianus RAG-1 and Rhodococcus erythropolis 20S-E1-c--were prepared in their stationary (i.e. non-dividing) phase in the absence of biosurfactants; the cells were then used as emulsifiers to stabilize n-hexadecane droplets in aqueous environments. Using the micropipette technique, colloidal stability of the bacteria-coated droplets was examined through direct-contact experiments. Both types of bacteria were seen to function as effective stabilizers, although the Acinetobacter venetianus RAG-1 film provided stronger resistance to droplet-droplet coalescence. In addition to creating steric barriers, the adsorbed bacteria also interacted with one another at the interface, giving rise to higher order rheological properties. A technique of directly probing the mechanical properties of the emulsion drop surfaces (i.e. the adsorbed films) on the micrometre-scale revealed that (a) the films behaved as purely elastic sheets, and (b) with a reduction in cell concentration in the aqueous phase, less oil was emulsified, but the elastic moduli of the adsorbed films remained unchanged (suggesting an "all or none" adsorption process). These results are in contrast to a previous macroscopic (i.e. millimetre-scale) study, which showed that the absorbed films were viscoelastic, with the apparent elastic moduli depending strongly on cell concentration. The rheological properties of these bacteria-adsorbed interfaces appeared therefore to be length scale-dependent. 相似文献
106.
The Ag nanoprisms with controlled arrangements show distinct optical, crystallographic, and surface-enhanced Raman scattering properties depending on their orientation in the assemblies, demonstrating that the controlled assembly of anisotropic nanostructures can be utilized as a powerful tool for studying their physicochemical properties and for the creation of new classes of functional materials. 相似文献
107.
The controllable preparation of metal nanoclusters in high yield is an essential prerequisite for their fundamental research and extensive application. Here a synthetic approach termed “dual-level kinetic control” was developed to fabricate a family of new silver nanoclusters. The introduction of secondary ligands was first exploited to retard the reduction rate and accomplish the first-level kinetic control. And the cooling of the reaction was performed to further slow the reduction down and accomplish the second-level kinetic control. A family of atomically precise silver nanoclusters (including [Ag25(SR)18]−, [Ag34(SR)18(DPPP)3Cl4]2+, [Ag36(SR)26S4]2+, [Ag37(SR)25Cl1]+, and [Ag52(SR)28Cl4]2+) were controllably prepared and structurally determined. The developed “dual-level kinetic control” hopefully acts as a powerful synthetic tool to manufacture more nanoclusters with unprecedented compositions, structures, and properties.A dual-level kinetic control was exploited to fabricate a family of atomically precise silver nanoclusters. 相似文献
108.
In this study, a facultative bacterium that converts fumarate to succinate at a high yield was isolated. The yield of biocon
version was enhanced about 1.2 times by addition of glucose into culture medium at an initial concentration of 6 g/L. When
the initial cell density was high (2 g/L), the succinate produced at pH 7.0 for initial fumarate concentrations of 30, 50,
80, and 100 g/L were 29.3, 40.9, 63.6, and 82.5 g/L, respectively, showing an increase with the initial fumarate concentration.
The high yield of 96.8%/mole of fumarate in just 4 h was obtained at the initial fumarate concentration of 30 g/L. Comparing
these values to those obtained with low cell culture (0.2 g/L), we found that the amount of succinate produced was similar,
but the production rate in the high cell culture was about three times higher than was the case in the low cell culture. This
strain converted fumarate to succinate at a rate of 3.5 g/L·h under the sparge of CO2. 相似文献
109.
Kang Y Wu J Yin G Huang Z Liao X Yao Y Ouyang P Wang H Yang Q 《Langmuir : the ACS journal of surfaces and colloids》2008,24(14):7432-7441
In this study, paclitaxel loaded poly( L-lactic acid) (PTX-PLLA) microparticles were prepared using solution enhanced dispersion by supercritical CO2(SEDS) technique. This supercritical antisolvent technique offers the advantage of negligible organic solvent residua in the drug loaded microparticles. Scanning electron microscopy (SEM) showed that microparticles exhibited rather spherical shape and small particle size with narrow particle size distribution. X-ray diffraction (XRD) and differential scanning calorimeter (DSC) indicated that PTX was amorphously dispersed in the PLLA matrix. The drug loading and encapsulation efficiency of PTX-PLLA microparticles were 14.33% and 62.68%, respectively. In vitro cytotoxicity evaluation of PTX-PLLA microparticles against nonsmall-cell lung cancer A549 and ovarian cancer SKOV3 cell lines indicated that PTX-PLLA had superior antiproliferation activity against the A549 and SKOV3 cell lines, compared with free PTX formulations. The cellular internalization of fluorescent microparticles was evidenced by fluorescence microscope and further confirmed by transmission electron microscopy (TEM). This was attributed to the efficient intracellular accumulation of PTX via cell phagocytosis and sustained release of PTX from PLLA matrix. The anticancer activity of PTX-PLLA was associated with PTX-induced cell apoptosis such as nuclear aberrations, condensation of chromatin and swelling damage in mitochondria. The cell apoptosis index detected by flow cytometry was higher in PTX-PLLA group than in free PTX. The PTX-PLLA formulation, which was obtained through micronization of PTX and encapsulation of micronized PTX into PLLA simultaneously in the SEDS process, significantly potentiated the anticancer activity of PTX. 相似文献
110.
Veltman TR Stover AK Narducci Sarjeant A Ok KM Halasyamani PS Norquist AJ 《Inorganic chemistry》2006,45(14):5529-5537
A systematic investigation of the factors governing the reaction product composition, hydrogen bonding, and symmetry was conducted in the MoO3/3-aminoquinuclidine/H2O system. Composition space analysis was performed through 36 individual reactions under mild hydrothermal conditions using racemic 3-aminoquinuclidine. Single crystals of three new compounds, [C7H16N2][Mo3O10] x H2O, [C7H16N2]2[Mo8O26] x H2O, and [C7H16N2]2[Mo8O26] x 4 H2O, were grown. The relative phase stabilities for these products are dependent upon the reactant mole fractions in the initial reaction gel. This phase stability information was used to direct the synthesis of two new noncentrosymmetric compounds, using either (S)-(-)-3-aminoquinuclidine dihydrochloride or (R)-(+)-3-aminoquinuclidine dihydrochloride. [(R)-C7H16N2]2[Mo8O26] and [(S)-C7H16N2]2[Mo8O26] both crystallize in the noncentrosymmetric space group P2(1) (No. 4), which has the polar crystal class 2 (C2). The second-harmonic generation activities were measured on sieved powders. The structure-directing properties of the molybdate components in each compound were determined using bond valence sums. The structures of all five compounds were determined using single-crystal X-ray diffraction. 相似文献