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sodium diclofenac
相关语句
  双氯芬酸钠
     LC-MS Identification of Related Substances in Sodium Diclofenac Lozenges
     LC-MS确定双氯芬酸钠含片中的有关物质
短句来源
     Aceclofenac was synthesized in 82% overall yield from sodium diclofenac and t-butyl chloroacetate viaesterification and hydrolysis.
     双氯芬酸钠与氯乙酸叔丁酯经酯化、水解反应制得非甾体抗炎药醋氯芬酸,收率82%。
短句来源
     Objective:A method was described for the identification of related substances in sodium diclofenac loz- enges with LC-MS.
     目的:报道了双氯芬酸钠含片中有关物质的 LC-MS 的鉴定方法。
短句来源
     Research and Preparation of Sodium Diclofenac Liniment
     双氯芬酸钠搽剂的研制
短句来源
     Studies on the Quantitative Determination of Sodium Diclofenac by HPLC
     高效液相色谱法测定双氯芬酸钠栓含量的研究
短句来源
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  酸钠
     Inflammation Influence and Antinflammation Therapeutic Effect of Sodium Diclofenac on Experimental Acute Myocardial Ischemia of Rabbits
     炎症对急性缺血性心脏病的影响及其双氯酚酸钠抗炎治疗的实验研究
短句来源
  “sodium diclofenac”译为未确定词的双语例句
     Detemination of Sodium Diclofenac Suppository by Ultravioet Spectrophotometry
     紫外分光光度法测定双氯灭痛栓剂的含量
短句来源
     STUDIES ON IN-VITRO PERCUTANEOUSPENETRATION OF SODIUM DICLOFENAC PIGMENT
     双氯灭痛药膜体外透皮速率的实验研究
短句来源
     While in that of ultraviolet spectrophotometry, chloroform was used for resolving the suppositories and phosphate buffer solution for extracting sodium diclofenac. The wavelength of determination was (276±1) nm.
     UV法采用氯仿溶解药栓 ,pH 7.8磷酸盐缓冲液萃取的方法 ,检测波长 ( 2 76± 1)nm。
短句来源
     VE: Chitosan and sodium tripolyphosphate were used as Complex matrix material for preparing pellets loading sodium diclofenac and its properties were studied.
     目的:开发应用新辅料甲壳胺与三聚磷酸钠发生聚合反应,生成聚电解质复合物,作为骨架材料制备双氟灭痛微丸。
短句来源
     The preparation process, effective factors and the optimal condition for the pellets loading sodium diclofenac were studied.
     考察双氯灭痛微丸的制备工艺,影响因素。
短句来源
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  sodium diclofenac
The 1:1 weight ratio of neocel to flo-starch was more suitable for designing the microdispersed sodium diclofenac enteric-coated tablets.
      
The weight ratio of neocel to flo-starch plays an important role in controlling the release of sodium diclofenac from enteric tablets.
      
The release rates of sodium diclofenac from the spray-dried powder, the mixed powder before tableting, and the tablets were determined in 0.1 N HC1 solution, pH 6.8, phosphate buffer solution, distilled water, and pH-changed medium.
      
Sodium diclofenac enteric-coated microcapsules were prepared by a spray-drying technique with Eudragit L 30D as enteric-coating material.
      
Tablet Formulation Study of Spray-Dried Sodium Diclofenac Enteric-Coated Microcapsules
      
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In this paper the ~(1 3)C NMR researches of N-2, 6-dichlorophenyl-N-phenylamine-2′-aceticacid and N-2, 6-dichloropheny1-N-phenylamine-2′-acetie ac id sodium (diclofenac sodium)[X=H, Na]hlave beenmade.The ~(1 3)C-H coupled proton offresonanee decoupled and proton complete decoupledNMR spectra for two compounds are obtained at the FX-60Q PFTNMR spectrometer(the magnetic field insensity being 14093G, the observation frequency being 15.04MHz).with the aid of the techniques of proton offresonance...

In this paper the ~(1 3)C NMR researches of N-2, 6-dichlorophenyl-N-phenylamine-2′-aceticacid and N-2, 6-dichloropheny1-N-phenylamine-2′-acetie ac id sodium (diclofenac sodium)[X=H, Na]hlave beenmade.The ~(1 3)C-H coupled proton offresonanee decoupled and proton complete decoupledNMR spectra for two compounds are obtained at the FX-60Q PFTNMR spectrometer(the magnetic field insensity being 14093G, the observation frequency being 15.04MHz).with the aid of the techniques of proton offresonance decoupling, proton complete deeoupling,substituent electronegativity, induction effect, field effect, conjugated effect and thesubstituent chemistry shift additivity rules ete, the chemical shift and coupling constants~(1)_(C-H),~(2)_(C-C-H) of all peaks have been determined.The experimental results show that carbon-13 chemical shift and one-bondcoupling constant ~(1)J_(C-H), two-bond coupling constant ~(2)J_(C-C-H) have afixed law.Therefore, not only a forceful basis may be provided for distinguishing various structures ofthese compounds, but also carbon bonded states of unknown compounds can be deduced.

本文对N-2.6-二氯苯基-N-苯基胺-2’-乙酸和N-2.6-二氯苯基-N-苯基胺-2’乙酸钠(双氯灭痛)进行了~(13)C核磁共振的研究。本实验利用FX—60Q脉冲付里叶变换核磁共振波谱仪(磁场强度为14093高斯,观察频率为15.04MHz)测定了这两种化合物的非去偶谱质子完全去偶谱和偏共振谱。借助于偏共振技术、质子完全去偶谱、取代基电负性,诱导效应,共轭效应、场效应、取代基化学位移加和规则等确定了各峰的化学位移和一键、二键偶合常数。实验结果表明C~(13)化学位移和一键、二键偶合常数~1Jc-Ⅱ、~2Jc-c-Ⅱ都有一定的规律。因此.它们不仅对鉴别此类化合物的结构可提供有力的依据,而且还能推断未知化合物的碳键状态。

Sodium diclofenac(DS)pigment was prepared by using ethylcellulose and polyvinyl alcohol.The percutaneous penetration rate of DS through rat skin was measured in vitro by using modified Franz diffusion cell.The results showed that azone and propylene glycol increased the skin permeability of DS,and various polymers affected the release and percutaneous penetration rate of DS in the pigment.In comparison with the formulated vehicle without the polymer and the penetration enhancers.the percutaneous penetration...

Sodium diclofenac(DS)pigment was prepared by using ethylcellulose and polyvinyl alcohol.The percutaneous penetration rate of DS through rat skin was measured in vitro by using modified Franz diffusion cell.The results showed that azone and propylene glycol increased the skin permeability of DS,and various polymers affected the release and percutaneous penetration rate of DS in the pigment.In comparison with the formulated vehicle without the polymer and the penetration enhancers.the percutaneous penetration rate of DS from ethylcellulose were not increased, while the increasing magnitude in the percutaneous penetration rate from polyvinyl alcohol was very significant.

作者选择乙基纤维素、聚乙烯醇等高分子材料制成涂膜剂,用大鼠皮进行双氯灭痛药膜的体外透皮速率测定。结果表明,氮酮与丙二醇可以促进药物渗透。不同的高分子材料可影响药物的扩散与释放,从而影响其透皮速率。与无膜无促透剂处方相比,药物在乙基纤维素中的透皮速率没有增加,在聚乙烯醇膜中的透皮速率有显著增加。

Prescription, technique, quality standard, and stability of sodium diclofenac liniment were experimented. The results showed that the prescription accorded with the preparation demand, the technique and quality standard was feasible, and the stability of the agent was good.

对双氯芬酸钠搽剂的处方、工艺、质量标准、稳定性等内容进行了实验,结果表明符合搽剂要求,工艺、质量标准可行,药物稳定性好

 
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