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   制备药物 的翻译结果: 查询用时:0.146秒
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制备药物
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  preparation of drug
     Preparation of Drug Microparticles and Drug-Carrier Coprecipitates by Gas Antisolvent Technology
     GAS技术制备药物微粒和药物载体复合粒子
短句来源
     USING LYOPfflLIZATION TO THE PREPARATION OF DRUG PAPER DISKS FOR ANTIMICROBIAL SUSCEPTIBILITY TEST
     冷冻干燥法制备药物敏感性试验试纸
短句来源
     Experimental Investigation on Preparation of Drug Micro-particles by Supercritical Assisted Atomization
     超临界辅助雾化过程制备药物微粒实验研究
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  “制备药物”译为未确定词的双语例句
     1.Preparation of pharmacologic serum: Twenty male Wistar rats, divided into normal control group and traditional Chinese drug group.
     1、药物血清的制备:雄性wistar大鼠20只,设立正常对照组和中药组各10只,采用3天灌胃法,末次灌胃后2小时,心脏取血,制备药物血清。
短句来源
     Application of Supercritical Fluids Technology in Drugs Delivery System Preparation
     超临界流体技术在制备药物输送系统中的应用
短句来源
     Mix PAA and PVP to their physical mixture and prepare the PAA/PVP interpolymer complexes by solvent evaporation method. The naproxen tablets were prepared with PAA,PVP,PAA/PVP mixture and PAA/PVP complexes respectively and also prepared by solid dispersion technique with PAA and PVP.
     将PVP和PAA简单混合制备物理混合物,通过旋转蒸发法制备PAA/PVP复合物,分别以PVP、PAA均聚物、物理混合物、复合物为载体制备药物(以萘普生为模型药物)片剂,采用固体分散技术制备以PAA、PVP为载体的萘普生片.
短句来源
     Sustained-release pellets were prepared by taking 4% Eurdrugit RS100, 10%PEG-400, 20%DEP, The loading formulation was optimized by orthogonal experiment and the accumulation release amount of 2hr,6hr and 10 hr as the evaluation target.
     在制备药物树脂缓释微丸时,采用正交设计试验,以2、6、10小时的药物释放度作为评价指标,优化得到最佳包衣液处方:4%RS100,10%PEG400,20%DEP; 以400r/min速度包衣,得缓释微丸。
短句来源
     In particular, optically active C 3- and C 4-synthetic units are quite important intermediates for the preparation of pharmaceuticals and fine chemicals.
     尤其是光学活性C3 和C4 有机合成单元对制备药物和精细化学产品是非常重要的中间体 .
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  相似匹配句对
     Preparation of berberine-selective electrode
     黄连素药物电极的制备
短句来源
     Fabrication and Characterization of Drug Coating on the Stent
     支架表面药物涂层制备和表征
短句来源
     THE PREPARATION OF ZEIN
     玉米醇溶蛋白的制备
短句来源
     Preparation of 2,3-Butanedione(AC 2)
     丁二酮的制备
短句来源
     Drug Patches
     药物贴片
短句来源
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  preparation of drug
Acid-initiated polymerization of ∈-caprolactone under microwave irradiation and its application in the preparation of drug contr
      
In particular, they have been widely used for the preparation of drug-delivery systems.
      
Application of Supercritical Carbon Dioxide for the Preparation of Drug-Cyclodextrin Inclusion Compounds
      
Mechanochemical preparation of drug carrier solid dispersions
      
Thus, the present method enables us a new method of one-step preparation of drug-excipient nanocomposites to eliminate tedious problems associated with nanoparticles handling.
      
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This paper presents the current situation of Edible Fungi estate and application of depths-layer-culture in the feild of Edible Fungi by four aspects: (1) Obtanning high protein hypha; (2) Pharmacy; (3) A way to exploit and use wild Edible Fungi; (4) Making Liquid fungi seeds. It has been advanced that theoricai basis for the application of this technology by the principle of depths-layer-technology. Facing the existing problems of this technology, we advanced a number of relevant countermea-sures.

本文介绍我国食用菌产业现状和深层培养技术在食用菌产业中四个方面的应用;获得高白蛋菌丝;制备药物;开发利用野生菌途径之一;液体菌种制备。运用深层培养技术原理提出这一技术应用广泛的理论依据。针对深层培养技术存在的问题提出相应对策。

In this paper, three ferrocene quaternary ammonium salts are introdued as ion-associate electroactive material for Subglycyrrhelinic Acid and Ibuprofen selcctive electrodes. The Glycyrrhelinic Acid electrode exhibits Nernstian response with a slope 45mV/deeade(13℃) over the concentrations 10~(-6)mol/L~10~(-2)mol/L in the pH ranges from 7.6 to 10. 6. The detection limit is down to 6. 3× 10(-7)mol/L. Using direct potentiometric method to determine Subglycyrrhelinic acid the rate of recovery is from 98. 5to 101.8%....

In this paper, three ferrocene quaternary ammonium salts are introdued as ion-associate electroactive material for Subglycyrrhelinic Acid and Ibuprofen selcctive electrodes. The Glycyrrhelinic Acid electrode exhibits Nernstian response with a slope 45mV/deeade(13℃) over the concentrations 10~(-6)mol/L~10~(-2)mol/L in the pH ranges from 7.6 to 10. 6. The detection limit is down to 6. 3× 10(-7)mol/L. Using direct potentiometric method to determine Subglycyrrhelinic acid the rate of recovery is from 98. 5to 101.8%. The Ibuprofen electrode exhibits Nernstian response with a slope of 58mV/decade(15℃)over the concentration 10~(-8)mol/L~10~(-2)mol/L in the pH ranges from 6.8 to 10.0. The detection limit is down to 8. 5×10~(-7)mol/L. Using direct potentiometric method to determine Ibuprofen the rate of recovery is from 97.59% to 99.5%. The wide selectivity and good stability of the two electrodes show superior qualities.

本文选用了三种二茂铁季铵盐: C_2H_5F′c—CH_2—N(CH_2)_3I、C_5H(17)—F′c—CH_2(CH_3)3 为电极活性材料,邻苯二甲酸二丁酯、邻苯二甲酸二壬酯为增塑剂,制备了药物甘草次酸和布洛芬电极,其中以C_5H_(17)—F′c—CH_2N~+(CH_3)3I~-为活性材料,邻苯二甲酸二丁酯为增塑剂制备的甘草次酸电极和布洛芬电极性能较好,甘草次酸电极的线性响应范围为10(-5)mol/L~10(-2)mol/L,斜率为45mV(13℃),检测下限为6.3×10(-7)mol/L,pH范围为7.6~10.6,用直接电位法测定甘草次酸的回收率为98.5%~101.8%;布洛芬电极的线性响应范围为10(-5)mol/L~10(-2)mol/L,斜率为58mV(15℃),检测下限为8.5×10(-7)mol/L,pH范围为6.8~10.0,布洛芬的回收率为97.5%~99.5%。

In order to increase the chemotherapy index of adenine arabinoside monophosphate (ara-AMP), research on liver receptor-targeting drugs was carried out. The targeting carrier,lactosaminated human serum albumin(Ⅱ) was prepared by reductive amination of the protein with lactose in the presence of sodium cyanoborohydride. (Ⅱ) was then conjugated with araAMP. The molar incorportion ratio was obtained as HSA: Lactose: ara-AMP=1: 28: 15.The effect of pH on the reaction of lactosmination and the conjugating of (Ⅱ) with...

In order to increase the chemotherapy index of adenine arabinoside monophosphate (ara-AMP), research on liver receptor-targeting drugs was carried out. The targeting carrier,lactosaminated human serum albumin(Ⅱ) was prepared by reductive amination of the protein with lactose in the presence of sodium cyanoborohydride. (Ⅱ) was then conjugated with araAMP. The molar incorportion ratio was obtained as HSA: Lactose: ara-AMP=1: 28: 15.The effect of pH on the reaction of lactosmination and the conjugating of (Ⅱ) with ara-AMP was discussed. Preliminary evaluation revealed that both (Ⅱ) and (Ⅲ) could be selectively delivered to the liver with concentrations 4~8 times as those in the heart,blood,spleen,etc.

为了提高ara-AMP抗肝炎病毒作用的选择性,进行肝受体导向药物的研究。首先利用乳糖在氰基硼氢化钠作用下,与人血清白蛋白进行还原胺化反应,制备导向载体乳糖化白蛋白(Ⅱ);在碳二亚胺作用下,(Ⅱ)与ara-AMP缩合,制备药物载体偶合物(Ⅲ).每分子蛋白上连接28分子的半乳糖残基,15分子的药物。文中讨论了pH值对乳糖化反应及偶联反应的影响。初步评价结果表明,(Ⅱ)和(Ⅲ)在小鼠体内的分布具有较好的肝导向性,肝脏中偶合物的浓度可达心、血、脾等的4~8倍。

 
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