乙胺甲酰氟尿嘧啶对进展期胃癌细胞免疫功能的影响

采用间接免疫荧光法检测２１例进展期胃癌患者应用低剂量乙胺甲酰氮尿嘧啶（ＨＣＦＵ）诱导前后的Ｔ淋巴细胞亚对。结果发现：与正常对照组相比，进展期胃癌患者ＣＤ３、ＣＤ４细胞明显减少，ＣＤ３细胞增加，ＣＤ４／ＣＤ８比值显著下降。而在ＨＣＦＵ诱导后ＣＤ３、ＣＤ４细胞增加．ＣＤ６细胞减少，ＣＤ４／ＣＤ９比值升高。提示低剂量ＨＣＦＵ可改善进展期胃癌患者的细胞免疫抑制状态。

DHDECMP-TBP/煤油萃取模拟高放废液中的裂片元素工艺研究

实验测定了22%DHDECMP 42%TBP OK从模拟高放废液中萃取Zr、Mo、Cs等裂片元素的分配比,并在微型离心萃取器(转鼓10mm)串联台架上进行了从模拟高放废液中萃取裂片元素的工艺研究。采用6级萃取,2级洗涤,6级反萃,流比AF∶AX∶AS=1∶1.5∶0.5,BF∶BX=1∶1,实验考察了裂片元素的各级浓度分布。对Zr、Mo的净化系数DF分别为3.2、18;对Rb、Cs、Sr、Ba,DF>103。

Electrodeposition of iridium from composite ionic liquid

In order to study the electrodeposition process of iridium in composite ionic liquid, the effects of N, N-dimethylacetamide（DMAC） on the viscosity, conductivity and electrochemical stability of composite ionic liquid BMIC-BMIBF4, as well as the electrochemical behavior of Ir Cl3 in this system were studied. Iridium（Ir） coatings were deposited at different constant potentials and characterized by SEM and XRD. The results show that the addition of DMAC can evidently decrease the viscosity of the composite system, increase conductivity and improve electrochemical stability of the composite system. Cyclic voltammograms of a Au electrode illustrate that the process controlled by diffusion rate is irreversible with the average charge transfer coefficient of 0.170 and average diffusion coefficient of 1.096×10-6 cm^2/s. In addition, SEM image shows that Ir film deposited at the reduction peak potential is dense and even, while XRD pattern shows that Ir deposit is polycrystalline structure.

Solid-Liquid Equilibrium of Terephthalic Acid in Several Solvents

Terephthalic acid(PTA) is practically one of the main materials of polyester. Its corresponding solid-liquid equilibrium data will provide essential support for industry design and further theoretical studies. In this work,solid-liquid equilibriums of terephthalic acid in four solvents, N,N-dimethylformamide, N,N-dimethylacetamide,dimethylsulphoxide and N-methyl-2-ketopyrrolidene, were determined in the temperature range from 293.15 K to 364.6 K by dynamic method. All these data were regressed by λh model, Wilson model and NRTL model, average absolute relative deviations of which are 1.25%, 15.02% and 7.22% respectively. It indicates that λh model is mostsuitable for description of the solid-liquid equilibrium containing PTA.

Decay Dynamics of N, N-Dimethylthioacetamide in S3（ππ＊） State

The decay dynamics of N, N-dimethylthioacetamide after excitation to the S3（ππ＊） state was studied by using the resonance Raman spectroscopy and complete active space self- consistent field method calculations. The UV-absorption and vibrational spectra were as- signed. The A-band resonance Raman spectra were obtained in acetonitrile, methanol and water with the laser excitation wavelengths in resonance with the first intense absorption band to probe the Franck-Condon region structural dynamics. The CASSCF calculations were carried out to determine the excitation energies and optimized structures of the lower- lying singlet states and conical intersection point. The A-band structural dynamics and the corresponding decay mechanism were obtained by the analysis of the resonance Raman in- tensity pattern and the CASSCF calculated structural parameters. The major decay channel of S3,FC （ππ＊）→S3（ππ＊）/S1 （nπ＊）→S1（nπ＊） is proposed.

Protective effect of low dose of melatonin against cholestatic oxidative stress after common bile duct ligation in rats

AIM: To investigate the role of oxidative injury and the effect of exogenous melatonin administration on liver damage induced by bile duct ligation (BDL), and second, to evaluate the role of nitric oxide (NO), a free oxygen radical, in oxidative injury. METHODS: Thirty-two Sprague-Dawley rats were assigned to four groups: sham operation (SO), BDL, BDL+melatonin, and BDL+vehicle. Cholestasis was achieved by double ligature of the common bile duct. Melatonin was injected intraperitoneally 500 μg/(kg·d) for 8 d. Hepatic oxidative stress markers were evaluated by changes in the amount of lipid peroxides, measured as malondialdehyde (MDA), and reduced GSH. Total nitrite (NOx) concentrations were determined in hepatic homogenates. Histopathological examination was performed using a histological scoring system. RESULTS: The histopathological changes including portal inflammation, necrosis,apoptosis, focal inflammation and fibrosis were severe in the BDL and BDL+vehicle groups. There were numerous large areas of coagulation necrosis. Histological Activity Index scores of these groups were significantly higher than that of the SO group. Treatment with melatonin reduced these alterations significantly. The degree of necro-inflammation and fibrosis showed significant difference between the BDL and BDL+melatonin groups. BDL was accompanied by a significant increase in MDA and NOx, and a significant decrease in GSH levels. Mean±SE values of MDA, GSH and NOx levels of SO group were 147.47±6.69, 0.88±0.33 μmol/g and 180.70±6.58 nm/g, respectively. The values of BDL group were 200.14±21.30, 0.65±0.02 μmol/g, and 400.46±48.89 nm/g, respectively, whereas the values of BDL+melatonin group were 115.93±6.8,0.74±0.02 μmol/g, and 290.38±32.32 nm/g, respectively. Melatonin treatment was associated with a significant recovery of MDA, GSH and NOx levels. CONCLUSION: We have concluded that oxidative stress is associated with the pathogenesis of cholestatic liver damage and NO contributes to oxidative damage. Melatonin, even at low dose, is an efficient agent in reducing negative parameters of cholestasis.

Pharmacokinetics and acetylation of sulfamethoxazole in turbot Scophthalmus maximus after intravascular administration

The pharmacokinetic profi les and sulfamethoxazole(SMX) acetylation process in turbot reared at 18°C were investigated. Either SMX(parent drug) or its acetylized metabolite, N4-acetylsulfamethoxazole(Ac SMX), was administered intravascularly to turbot at a dosage of 50 mg/kg BW. Serum concentrations of the parent drug and its metabolite were both measured by HPLC, and the changes in concentration over time were analyzed in two- and non-compartment models because SMX treatment produced multiple peaks. The results demonstrated that the elimination half-life of the parent drugs, SMX and Ac SMX, were 159.2 and 5.9 h, respectively. The apparent volume of distribution was 0.2 and 0.8 L/kg, and the clearance was 0.038 and 0.222 L/(h·kg), for SMX and Ac SMX, respectively. SMX acetylation in turbot was 2.8%, and the deacetylation of Ac SMX was 0.2%. These fi ndings may be useful in optimizing SMX dosage regimens in turbot aquaculture.

MODIFICATION OF X-5 RESIN AND ADSORPTION PROPERTY OF THE MODIFIED RESINS

Three polymeric adsorbents with hydrogen bonding acceptors, methylamine, N-methyl-acetamide and aminotri(hydroxymethyl)methane modified resins are synthesized from chloromethylated X-5 resin. Adsorption isotherms of phenol and theophylline onto the three modified resins and the original X-5 resin from aqueous solution are measured. The results show that adsorption of compounds with hydrogen bonding donor onto methylamine and N-methylacetamide modified resins is enhanced as compared with that onto X-5 resin, and adsorption mechanism between the adsorbents and the adsorbates is mainly based on hydrogen bonding and hydrophobic interaction. While adsorption of compounds with hydrogen bonding donor onto aminotri(hydroxymethyl)methane modified resin is lowered as compared with that onto X-5 resin, and adsorption mechanism between the adsorbent and the adsorbates is mainly based on hydrophobic interaction.

Synthesis and characterization of 2-hydroxy-N-methyl-N-phenyl-acetamide

2-hydroxy N methyl N phenyl acetamide was synthesized by using N methylaniline, chloracetyl chloride, anhydrous sodium acetate and methanol through the acetylation, esterfication and ester interchange steps. The acetylation of N methylaniline with chloracetyl chloride, catalyzed by triethylamide with mole ratio n (C 6H 5NHCH 3)∶ n (ClCH 2C(O)Cl)∶ n (N(C 2H 5) 3)=1∶1.05∶1, the yield of 2 chloro N methyl N phenyl acetamide(Ⅰ) was 93.8%; Then the esterification of Ⅰ with anhydrous sodium acetate in the presence of phase transfer catalyst tetrabutyl ammonia bromide gave 97.3% yield of 2 acetoxyl N methyl N phenyl acetamide (Ⅱ); The ester interchange of with methanol catalyzed by potassium hydroxide gave 2 hydroxy N methyl N phenyl acetamide (Ⅲ) in 96.4% yield. And the total yield was 88.0%. IR and MS spectroscopy of products were analyzed and their characteristic peaks were assigned. Combining the results of elemental analysis, the molecular structure of Ⅰ, Ⅱ and Ⅲ was identified.

Study on Drying Process of 3Al_2O_3·2SiO_2 Mullite Gel

Monophasic mullite gel with composition 3Al2O3·2SiO2 was prepared by the sol-gel method using aluminium nitrate nonahydrate, aluminium-tri-isopropoxide, and tetraethylorthosili-cate as reagents. Gels with different drying control chemical additives(DCCAs) and polyvinylpyrrolidone(PVP) as spinning assistant were dried at several temperatures. The influences of temperature, DCCAs and PVP in the drying process were investigated. N,N-dimethylformamide(DMF) was the optimum DCCA at 70℃ in the drying process. PVP decreased the solvent volatilization speed and prevented gel crack to a certain extent. FTIR results revealed that free water, ethanol, and isopropanol were completely removed by the drying procedure.

A new luminescent metal-organic framework for selective sensing of nitroaromatic explosives

A microporous luminescent metal-organic framework [Zn4L2（H2O）2]＇（H2O）m（DMA）n （1） （H4L=5,5＇-（（1H-pyrazole-3,5-di- carbonyl）bis（azanediyl））diisophthalic acid, DMA=N,N-dimethylacetamide） was synthesized and characterized by infrared ra- diation （IR）, thermogravimetric analyses （TGA）, powder X-ray diffraction spectra （PXRD） and X-ray diffraction. Complex 1 has a three dimensional （3D） framework, which can be simplified as 5,5,5,5-c net with the Schlafi symbol of {43.64.83} {44.65.8 } {45.65 }2. This luminescent metal-organic framework （MOF） shows selectively sensitive to nitrobenzene and series of nitroaromatic explosives such as 4-nitrotoluene, 1,4-dinitrobenzene, 1,3-dinitrobenzene and 2,4-dinitrotoluene, and exhibits well recyclability. So complex 1 could be used to detect nitroaromatic explosives as a selective sensing material.

Preparation and Characterization of Polysulfonamide Statistical Copolymers from Three Aromatic Diamines

Various polysulfonamide （PSA） statistical copolymers were synthesized by polycondensation of three aromatic diamines and terephthaloyl chloride. The inherent viscosities of the resulting PSA copolymers range from 1.54 to 1.66 dL/g. The precipitated PSA copolymers with feed content of p-phenylene diamine （PPD） being less than 50% （mole fraction） can be redissolved in N-methyl-2-pryrrolidone （NMP） or N, N-dimethylacetamide （DMAc） with lithium chloride of WLiC1 ： 0.02. All of the PSA copolymers exhibit enhanced tensile strength in comparison with PSA and still maintain excellent thermal stability in either air or nitrogen atmosphere