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81.
α_1-抗胰蛋白酶的制备及其防治急性肺损伤的疗效 总被引:1,自引:0,他引:1
《中国生物制品学杂志》2004,17(1)
目的 以FIV 1为原料 ,制备较高纯度α1 AT制剂 ,用该制剂干预急性肺损伤动物模型作疗效考核。方法 FIV 1抽提液经PEG沉淀 ,离子交换 ,病毒灭活、超滤、除菌、分装 ,冻干制备α1 AT制剂。用急性肺损伤动物模型 ,比较静脉注射与雾化吸入α1 AT的治疗效果。结果 3批制剂纯度 >70 % ,无菌、热原、安全试验均符合生物制品规程要求。静脉注射或雾化吸入 ,可降低由内毒素诱发急性肺损伤程度。结论 α1 AT制备工艺适合大规模生产。在防治急性肺损伤时有一定效果 相似文献
82.
Matthias Berger Manfred P. Schnelder 《Journal of the American Oil Chemists' Society》1992,69(10):961-965
Regioisomerically pure 1(3)-rac-monoacylglycerols are conveniently prepared in high yields (>75%) and in multigram quantities by enzymatic esterification
of glycerol in the presence of various lipases(Chromobacterium viscosum, Rhizopus delemar, Rhizomucor miehei) with a variety of different acyl donors, such as free fatty acids, fatty acid alkyl esters, vinyl esters and triacylglycerols,
as well as natural fats and oils. All reactions are carried out in aprotic organic solvents with low water content, namelyn-hexane, diethyl ether, tBuOMe or mixtures of these solvents. Essential for the success of these transformations were the
following two factors. First, the creation of an artificial interphase between the solvent-immiscible hydrophilic glycerol
and the hydrophobic reaction medium by its adsorption onto a solid support. Second, a facile system for the separation of
the desired monoacylglycerol from the reaction mixture, coupled with the continuous recycling of acyl donor and undesirable
by-products. 相似文献
83.
以北京市妫水河为研究区,基于2011年9月25日和2012年9月30日的两期叶绿素a浓度实测数据和准同步的环境一号卫星(HJ-1A)多光谱数据,分别构建一元线性和多元支持向量机模型(SVMM),通过决定系数R2和平均相对误差对模型的精度进行检验,用模型进行水体叶绿素a浓度的反演,并分析其时空分布特征。研究表明:在样本数较少的情况下,SVM具有很强的非线性映射能力,能够取得较好的预测结果,更适用于反演叶绿素a浓度。时间分布上,研究区叶绿素a浓度呈增加趋势,均值上升了6.86 μg/L;空间分布上,深水区叶绿素a浓度值低于浅水区,上游高于下游。国产HJ-1A CCD2多光谱数据以其4 d的时间分辨率,在水质动态变化监测方面具有优势。 相似文献
84.
A fast and simple 1H NMR spectroscopic method was developed for the concentration measurement of aromatic, olefinic and aliphatic fractions in gasoline samples. Simultaneously, individual components such as benzene, methyl tert-butyl ether and several dienes could be determined. The method relies on only a few, well-established assumptions about the molecular compositions and is therefore applicable to a broad range of gasolines. It is well suited for laboratories with high sample throughput since measurement time is short and all concentrations are determined within one NMR experiment. The method was applied to commercial gasolines and samples used in European round robin tests. Comparisons of NMR and round robin test results showed excellent agreement. 相似文献
85.
86.
对二聚炔醇化合物DMH的合成、分子结构及缓蚀作用机理进行了论述。因DMH化合物具有独特的分子结构,形成了稳定的络合体系及基团的屏蔽效应,增加了缓蚀被膜厚度及缓蚀体系的化学稳定性,实验证实DMH是酸性介质中的高效缓蚀剂。 相似文献
87.
88.
本文对生产高纯度丁烯-1的Alphabntol工艺进行了技术经济评价,认为该工艺条件简单、反应条件温和,而且投资少,所以很适合事在发展中国家应用。 相似文献
89.
Martel Zeldin Eric Granger Wilmer K. Fife 《Journal of Inorganic and Organometallic Polymers》1993,3(2):141-154
New silane monomers with the pendant 4-(3-pyridine)butyl group have been synthesized by hydrosilation of 3-(3-butenyl)pyridine with Me
n
Si(OEt)3-n
H (n=0, 1) using a platinum catalyst. Only -addition products were observed. The products were characterized by elemental analysis, infrared,1H- and13C-NMR spectroscopy, and gas chromatography-mass spectrometry. Hydrolysis-polycondensation of the difunctional monomer with a basic catalyst, Me4NOH, gave a mixture of cyclic oligomers, principally cyclic tetramer, and linear homopolymer. Under similar reaction conditions, the trifunctional monomer gave crosslinked material which was soluble in common organic solvents. The linear homopolymer and crosslinked polymer were trimethylsilyl end-blocked with hexamethyldisilazane. The cyclic and end-blocked polymers were characterized by elemental analysis and spectroscopic methods. Molecular weights of the polymers were obtained by end-group analysis using1H-NMR spectral data, size exclusion chromatography, and direct insertion-probe mass spectrometry. The cyclic, linear, and crosslinked materials were N-oxidized withm-chloroperoxybenzoic acid and characterized by spectroscopic methods. The polymeric N-oxide derivatives were shown to be effective transacylation catalysts in the synthesis of mixed carboxylic acid anhydrides in immiscible solvents (H2O/CH2Cl2) under phase-transfer conditions. The implications of the results on the mechanism of catalysis are discussed. 相似文献
90.
Santosh D. Wanjale 《Polymer》2006,47(18):6414-6421
Poly(1-butene)/MWCNT nanocomposites were prepared by simple melt processing technique. Crystallization, crystal-to-crystal phase transformation and spherulitic morphology were studied using differential scanning calorimetry (DSC), wide angle X-ray diffraction (WAXD) and optical microscopy (OM). The non-isothermal crystallization exhibited higher values of Zt derived from Avrami theory and lower values of F(T) obtained from Avrami-Ozawa analysis, while the isothermal crystallization revealed a significant increase in crystallization temperatures and lower crystallization half times compared to pristine PB. The observed changes in the crystallization kinetics were ascribed to the enhanced nucleation of PB in the presence of MWCNT. The nucleating activity calculated from the non-isothermal crystallization data revealed that the MWCNTs provide an active surface for the nucleation of PB. The optical micrographs exhibited significantly smaller crystallites with disordered morphology for the nanocomposites compared to the well defined spherulitic morphology for pristine PB. The rate of phase transformation from kinetically favored tetragonal to thermodynamically stable hexagonal form was noticeably enhanced as evidenced by the reduction in the half time for phase transformation from 58 h to 25 h for PB reinforced with 7% MWCNT. 相似文献