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951.
952.
Chang‐xi Wang Jia‐li Li Xue‐ding Wang Long‐shan Liu Xiao Chen Min Huang 《Biomedical chromatography : BMC》2010,24(4):399-405
A liquid chromatography/tandem mass spectrometry (LC‐MS/MS) method was developed and validated for determining tacrolimus (FK506) in rat tissues to study the effect of Schisandra sphenanthera extract on FK506 tissue distribution. After a liquid–liquid extraction with ethyl acetate, FK506 and ascomycin (IS) were subjected to LC‐MS/MS analysis using positive electrospray ionization under multiple reactions monitoring mode. Chromatographic separation of FK506 and ascomycin was achieved on a Hypersil BDS C18 column with a mobile phase consisting of methanol‐water (containing 2 mM ammonium acetate, 95 : 5, v/v). The intra‐ and inter‐batch precision of the method were less than 8.8 and 9.8%, respectively. The intra‐ and inter‐batch accuracies ranged from 97.5 to 104.0%. The lowest limit of quantification for FK506 was 0.5 ng/mL. The method was applied to a FK506 tissue distribution study with or without a dose of Wuzhi (WZ) tablet. Most of the FK506 tissue concentrations were slightly increased after a concomitant WZ tablet dose, but the whole blood concentration of FK506 was dramatically increased 3‐fold after a concomitant WZ tablet dose. These results indicated that the LC‐MS/MS method was rapid and sensitive enough to quantify FK506 in different rat tissues, and strict drug monitoring is recommended when co‐administering WZ tablet in clinical use. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
953.
954.
A micrometer-sized nanostructured, magnetic, ball-like Fe x O y -CeO2 composite was synthesized through an ethylene-glycol mediated process. The synthesized samples were characterized by scanning electron microscopy combined with energydisperse X-ray analysis, transmission electron microscopy and X-ray powder diffraction. In the synthesis system, polyethylene glycol (PEG) and urea were found to play significant roles in the formation of the micrometer-sized spherical architecture of the precursor. The details of morphology and particle size could be changed with the initial concentration of Fe(NO3)3·9H2O and Ce(NO3)3·6H2O as the reactants. The magnetic Fe x O y -CeO2 composite with a similar morphology was readily obtained by calcination from the precursor. The characterization of transmission electron microscopy showed the calcined ball-like architecture was a highly porous structure consisting of many nanoparticles. Because of the micrometer-sized nanostructure and the multi-components as well as the magnetism, the as-obtained Fe x O y -CeO2 composite showed better activity and potentially easy recovery for the harmless degradation of hexachlorobenzene (HCB). 相似文献
955.
956.
A formal synthesis of semiaquilegin A is achieved starting from readily available oridonin in 19 linear steps. The absolute configuration of the natural product has been established. A variety of useful analogues were prepared through this synthetic route. 相似文献
957.
Jia‐Jian Wang Hua‐Ming Zeng Zhi‐Gang She Cheng‐Du Miao Kui Hong Yu‐Cheng Gu Lan Liu Yong‐Cheng Lin 《Helvetica chimica acta》2011,94(10):1875-1880
Two new meroterpenes, ‘acetoxydehydroaustin B’ ( 1 ) and ‘1,2‐dihydro‐acetoxydehydroaustin B’ ( 2 ) were isolated in the form of a mixed crystal from the mangrove endophytic fungus Aspergillus sp. 085241B. Their structures and absolute configurations were determined by extensive analysis of their spectra and X‐ray diffraction data. In a preliminary bioassay, the mixed crystal did not exhibit activities against cancer cell lines of MDA‐MB‐435, SKBR3, HepG2, HEP3B, PC‐3, and A549, as well as against α‐glucosidase and tyrosinase. 相似文献
958.
Conjugatedpolymerswithlargethird-orderopticalnonlinearityhavebeedfocusedfortheirpromisingpotentialsforadvancedmaterialsapplications'.Recently,investigationsoftransitionmetalwithorganicligandsystemshavebeengreatlyintensifiedduetothedelectronsincorporatedintheconjugatedsystem,whichareexpectedtoellhancethehyperpolarizability.Phenylacetyleneandthemetalphenylacetylidesplayimportantrolesinformationofuniquecoordinatedc-lusters',butitseamsthatthestudyofmetalphenylacetylides,particularlyofthesilverphen… 相似文献
959.
Novel lanthanide coordination compounds with ciprofloxacin (CPFX), including eleven complexes Ln(CPFX)2Cl(H2O), (Ln=Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb; n = 7, 8, 9) and crystalline [Ce(CPFX)2 (H2O)4] Cl (H2O)3.25 (C2H5‐OH)0.25, were synthesized. The crystal is of triclinic space group Pi with a= 1.3865(2) nm, b = 1.3899(3) nm, c = 1.6505(2) nm, a = 92.73(1)°, β= 114.39(1)°, γ=115.55 (1)°, Z = 2 and R = 0.0449. FT‐IR, electronic spectroscopy and X‐ray diffraction were employed to show that the lanthanide ion, which displays an eight‐coordinate structure, is chelated by 3‐carboxyl and 4‐keto oxygen donors of CPFX and two six‐membered chelate rings are formed. Test of in vitro antibacterial activity against E. coli, P. aeruginosa and S. aureus indicated that the in vitro antibacterial activity of the ligand can be improved by complexation with Ce(III). 相似文献
960.
The contribution of solvation energy to guiding molecular recognition for six rigid protein‐peptide systems bad been evaluated by the variation in the number of the identified native‐like configurations and in the driving force of specific interaction resulting from the addition of the explicit solvation term in the force field function. The AMBER force field energy and the total energy including the force field energy and the WZS solvation energy were calculated for sampled configurations. The results obtained by the calculations of both force field and total energies were compared with each other. It suggests that the contribution of solvation energy is important to guiding the specific recognition of the systems in which the ligands possess larger hydrophobic or aromatic residues while the protein receptors provide the active surfaces with hydrophobic property. 相似文献