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   重酒石酸 的翻译结果: 查询用时:0.177秒
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重酒石酸
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  mesotartaric acid
     Methods:40 Balb/c mice from 6 to 7 week age were infected inhanasally with respiratory syncytial virus(RSV). The experimental mice were treated with DPM 50 mg·kg-1·d-1 and control mice with mesotartaric acid 100 μl orally for three days.
     方法:40只6~7周龄Balb/c小鼠经鼻感染呼吸道合胞病毒(RSV)成为RSV肺炎,治疗组用潘生丁50mg·kg-1·d-1,对照组用重酒石酸100μl,均灌胃3天。
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  “重酒石酸”译为未确定词的双语例句
     Epinephrin indicated a good linear relationship (r=0.9987,n=5) in the range of 6.43~108.37 ng and the rate of sample recovery was 85.1%±4.60%.
     重酒石酸肾上腺素在6.43~108.37ng范围内,线性关系良好(r=0.9987,n=5),回收率85.1%±4.60%;
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     Results Norepinephrin showed a good linear relationship (r=0.9993,n=5) in the range of 8.61~101.76 ng and the rate of sample recovery was 94.9%±2.97%.
     结果重酒石酸去甲肾上腺素在8.61~101.76ng范围内,线性关系良好(r=0.9993,n=5),回收率94.9%±2.97%;
短句来源
     Experimental group(E,n = 9), Noradrenaline Bitartrate 3.1μmol/kg(0.53mg/kg) was injected intraperitoneally and 24 hours later isolated hearts were stored in 4 ℃for 3 hours with HTK,and then isolated hearts were perfused for 2 hours with Krebs-Henseleit(K-H) solutions by Langendorff model.
     实验组(E,n=9)腹腔注射重酒石酸去甲肾上腺素(溶于生理盐水中)3.1μmol/kg(0.53mg/kg),腹腔注射24h后取离体心脏,处理方法同C组。
短句来源
     ②The rats in the noradrenaline bitartrate group were injected with 3.1 μmol/kg noradrenaline bitartrate0.53 mg/kg intraperitoneally. The isolated heart was taken at 24 hours after injection by the same method as in the normal saline group.
     ②重酒石酸去甲肾上腺素组:腹腔注射重酒石酸去甲肾上腺素3.1μmol/kg(0.53mg/kg),24h后取体外心脏,方法同生理盐水组。
短句来源
     Results The sensitivity of CBL-TRFIA was 0.01μg/L,and the recovery rate was 99.7%. RSD of CBL-TRFIA was 3.9%.
     结果该方法的灵敏度为0.01μg/L,测量范围为0.01~25μg/L,平均回收率为99.7%,RSD3.9%,与盐酸异丙肾上腺素的交叉反应率为0.01%,与沙丁胺醇、盐酸肾上腺素、重酒石酸去甲肾上腺素无交叉反应。
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  相似匹配句对
     Metaraminoli Bitartratis
     酒石酸间羟胺
短句来源
     INVESTIGATION OF SYNTHESIS OF CHOLINE BITARTRATE
     酒石酸胆碱的合成研究
短句来源
     CHAPTER 5 MARINE SEDIMENTATION Section 4 Heavy Mineral
     矿物
短句来源
     making full use of conditions and connecting across;
     条件。
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     Synthesis of (+)-diethyl Tartrate
     L-酒石酸二乙酯的合成
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In this paper a new experimental method of evaluation of K_D is reported. The equation is derived from the occupation theory of drug-recesptor interaction using mathematical method. Through the experiments of rat's deferent duct specimens in vitro, treated with noradrenaline bitartrate, it is demonstrated that this new method is superior to the method of cummulative dose-response curve in simplicity, reprodu-cibility, and accuracy. In addition the K_D thus obtained is also in accordance with that of the latter....

In this paper a new experimental method of evaluation of K_D is reported. The equation is derived from the occupation theory of drug-recesptor interaction using mathematical method. Through the experiments of rat's deferent duct specimens in vitro, treated with noradrenaline bitartrate, it is demonstrated that this new method is superior to the method of cummulative dose-response curve in simplicity, reprodu-cibility, and accuracy. In addition the K_D thus obtained is also in accordance with that of the latter.

本文报道一种新的求K_D的实验方法(简称微分法)。本法公式是根据药物—受体相互作用的占领学说,用数学方法推导而的。只需用药物的两个不同浓度,做两根单收缩曲线。在同一大白鼠左侧离体输精管标本上,用该法先后求得重酒石酸去甲肾上腺素的两个K_D值,也用累积剂量一效应曲线法简称累积法求得两个;共17个标本,各求得17对K_D值。两方法先后四次实验所求得的K_D均值之间,除累积法第二次的均值分别与微分法先后两次均值相比,差别显著外,其余均不显著。经方差齐性检验,本法17对K_D值的变异,显著小于累积法。本法不仅操作、计算简便,重现性好,精密度高,而且求得的K_D值也与累积法相符。

In 0.1% adrenaline(AD) and 0.2% noradrenaline (NOAD) injec-lions deactivation of the main component by sulfonation increased with theincrease of the concentration of the antioxidant sodium metabisulfite and pH value; deactivation by mutarotation sped up with the increase of the concentra-tion of sodium metabisulfite and decrease of the pH value. The optimal formula-tion for 0.1% AD and 0.2% NOAD injections was 0.020% of Na_2S_2O_5,pH3.6~4.8, 0.025% of EDTA·2Na. Under these conditions the shelft life could beprolonged...

In 0.1% adrenaline(AD) and 0.2% noradrenaline (NOAD) injec-lions deactivation of the main component by sulfonation increased with theincrease of the concentration of the antioxidant sodium metabisulfite and pH value; deactivation by mutarotation sped up with the increase of the concentra-tion of sodium metabisulfite and decrease of the pH value. The optimal formula-tion for 0.1% AD and 0.2% NOAD injections was 0.020% of Na_2S_2O_5,pH3.6~4.8, 0.025% of EDTA·2Na. Under these conditions the shelft life could beprolonged to at least 4 years.

0.1%肾上腺素和0.2%重酒石酸去甲肾上腺素注射液在贮存过程中;主药磺化速度随pH值增加以及所含抗氧剂焦亚硫酸钠浓度增加而加快,变旋失活速度则随pH值变小及焦亚硫酸钠浓度增大而加快。最佳处方条件为:焦亚硫酸钠浓度0.02%,pH值3.60~4.80,EDTA二钠浓度0.025%。在此条件下贮存期可达4年以上。

The reaction between tartaric acid and choline has been investigated by means of chemical analysis. It has been found that the reaction in anhydrous ethanol is not simple neutralization. The mechanism is related to feeding order. When adding tartaric acid into choline solution, the soluble choline tartrate is formed first, then it reacts with extra tartaric acid to produce choline bitartrate precipitate. When adding choline into tartaric acid solution, a tartaric acid-choline bitartrate molecular complex is...

The reaction between tartaric acid and choline has been investigated by means of chemical analysis. It has been found that the reaction in anhydrous ethanol is not simple neutralization. The mechanism is related to feeding order. When adding tartaric acid into choline solution, the soluble choline tartrate is formed first, then it reacts with extra tartaric acid to produce choline bitartrate precipitate. When adding choline into tartaric acid solution, a tartaric acid-choline bitartrate molecular complex is formed as precipitate first in which the molecule ratio is 1:1. Then the complex reacts with extra choline to produce choline bitartrate. This kind of molecular complex has never been reported in literature. There is solid-solid-solution three phases equilibrium among tartaric acid, choline bitartrate and the molecular complex. The equilibrium constant is about 0.04.

用化学分析法研究酒石酸与胆碱的反应.发现在无水乙醇溶液中反应并非是简单的中和反应,其反应历程与加料次序有关.酒石酸加到胆碱中,则先生成可溶性酒石酸二胆碱盐,然后二盐与过量的酒石酸反应,生成重酒石酸胆碱沉淀.当胆碱加到酒石酸中去时,则先生成酒石酸与重酒石酸胆碱摩尔比为1:1的分子复合物沉淀,而后复合物再与胆碱反应生成重酒石酸胆碱沉淀.此种复合物未见诸于文献.复合物、重酒石酸胆碱盐与酒石酸溶液间存在着固、固、液三相平衡,平衡常数约为0.04.

 
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