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pharmacodynamic effect
相关语句
  药理作用
     MINERALOGICAL INTERPRETATION OF PHARMACODYNAMIC EFFECT OF MONTMORILLONITE WITH An Axial Length of 1.8nm
     纳米级的轴长1.8nm蒙脱石药理作用的矿物学解释
短句来源
     Objective:To study the therapeutic mechanism and pharmacodynamic effect of Tiaowei pill.
     目的 :研究调胃丸的治疗机制及药理作用
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     AIM:To explore the pharmacodynamic effect of bikang wine so as to provide experimental evidence for clinical application.
     目的:探讨痹康酒药理作用,为临床应用提供实验依据。
短句来源
     Objective To explore the pharmacodynamic effect of Kechuanning capsule provides the experimental evidence for clinical application.
     目的 探讨咳喘宁胶囊药理作用 ,为临床应用提供实验依据。
短句来源
     Preliminary Pharmacodynamic Effect Study of Three Nettles' Decoction
     三种活麻水煎液药理作用探索
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  “pharmacodynamic effect”译为未确定词的双语例句
     Study on pharmacodynamic effect of Gangnianling Capsule (更年灵胶囊)
     更年灵胶囊主要药效学研究
短句来源
     CONCLUSION: 50 g/L propofol has the pharmacodynamic effect similar to that of 10 g/L propofol, but the former can delay the occurrence of serum lipid metabolism.
     结论:50g/L异丙酚与10g/L异丙酚的药效相似,但能延缓脂代谢紊乱的发生时间.
短句来源
     Objective To study the pharmacodynamic effect of nanoemulsion-encapsulated tumor specific antigen protein vaccine on mice bearing B16-MAGE-1 tumor cells and to determine the effective dose and median effective dose corresponding to the 30% and 50% tumor suppressive rate.
     目的观察肿瘤基因工程纳米疫苗对荷B16-MAGE-1肿瘤小鼠的疗效,并确定肿瘤抑制率分别为30%和50%的有效剂量和半数有效量(ED50)。
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     OBJECTIVE To explore into the pharmacodynamic effect of rhinitis spray on rat models with allergic rhinitis.
     目的探讨中药鼻炎喷雾剂对变应性鼻炎模型大鼠的药效作用。
短句来源
     A Study on Pharmacodynamic Effect of Tiaowei Pill
     调胃丸药理作用的实验研究
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  相似匹配句对
     Pharmacodynamic Research on Analgesic Effect of Kebitong Capsule
     克痹痛胶囊剂的止痛药效动力学研究
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     Pharmacokinetic-pharmacodynamic modeling of hypertensive effect of metoprolol
     美多洛尔药动学药效学结合模型的研究
短句来源
     Zeeman Effect
     塞曼效应
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     The effect of temperature on the
     乙醇过量时会削弱空化效应,使聚合反应
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  pharmacodynamic effect
A prolonged pharmacodynamic effect influences further clinical studies as well as our thinking about adverse drug effects.
      
The purpose of this study was to test the hypothesis that numerical descriptors of powder flow properties predict aerosol dispersion and pharmacodynamic effect.
      
To investigate the influence of complexation between bupivacaine and hydroxypropyl-β-cyclodextrin (HP-β-CD) on the systemic absorption and on the pharmacodynamic effect of bupivacaine following epidural administration in a rabbit model.
      
The application and validation of this approach are demonstrated using the pharmacodynamic effect of alfentanil, a short-acting narcotic analgesic agent, in New Zealand White rabbits.
      
The pharmacodynamic effect of the model drug bupranolol in vivo was investigated over a 10-hr time period.
      
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This experiment was designed to estimate the pharmacodynamic effects of a sustained release vitamin A injection in mice.One hundred eighty mice fed by the ration deficient vitamin A were devided into two series (ip and im).Each series was devided into five groups:group 1,NS;group 2,vitamin A emulsion 0.05mg/10g;group 3-5,sustained release vitamin A 0.025,0.05,0.1 mg/10g.The liver and serum vitamin A concentrations were analyzed by the reverse phase high performance liquid chromatography (Backman 344M)....

This experiment was designed to estimate the pharmacodynamic effects of a sustained release vitamin A injection in mice.One hundred eighty mice fed by the ration deficient vitamin A were devided into two series (ip and im).Each series was devided into five groups:group 1,NS;group 2,vitamin A emulsion 0.05mg/10g;group 3-5,sustained release vitamin A 0.025,0.05,0.1 mg/10g.The liver and serum vitamin A concentrations were analyzed by the reverse phase high performance liquid chromatography (Backman 344M). The results showed that the vitamin A deficiency model was brought on in the mice fed by the ration deficientin vitamin A and the sustained release vitamin A injection,ip or im,could prevent the decrease of serum vitamin A concentration for these animals.

本实验目的在于定量观察,当饲料中缺乏维生素 A 时,长效维生素 A 注射液对小鼠肝脏和血清维生素 A 含量的影响。结果表明,喂以缺乏维生素 A 的饲料,可在20天内造成小鼠体内维生素 A 的缺乏;1次性腹腔或肌肉注射长效维生素 A,可通过缓慢的吸收作用,预防小鼠因维生素 A 营养缺乏引起的血清维生素 A 浓度的降低,但对肝脏维生素 A 的含量无影响。

The pharmacokinetics and pharmacodynamics of famotidine were investigated in 10 healthy male volunteers after single intravenous administration of 20 mg. The blood drug levels were determined by a high performance liquid chromatography. The 1gC of famotidine in plasma vs time curve were found to be twcncompartment open model in healthy volunteers. The terminal half-life averaged 3.16h; the total distribution volume 99.40L; the total plasma clearance 392.12ml/min; the area under the plasma concentration curve...

The pharmacokinetics and pharmacodynamics of famotidine were investigated in 10 healthy male volunteers after single intravenous administration of 20 mg. The blood drug levels were determined by a high performance liquid chromatography. The 1gC of famotidine in plasma vs time curve were found to be twcncompartment open model in healthy volunteers. The terminal half-life averaged 3.16h; the total distribution volume 99.40L; the total plasma clearance 392.12ml/min; the area under the plasma concentration curve 1057.45 h·ng/ml. A mathematic equation describing the whole course of blood drug levels in relation to inhibitory effects on intragastric acid output is as follows: E= 100·C2.60/(C2.60+14.712.60). The constant 14.71 is EC50 (ng/ml), the blood drug concentration producing 50% of maximal pharmacological effects. Prediction of pharmacodynamic effects from blood drug level and vice versa becomes possible by using the mathematic equation.

作者建立了测定法莫替丁血药浓度的高效液相色谱方法,并对正常志愿者静脉注射法莫替丁的药物动力学和药效学进行了研究。结果表明,药物动力学符合开放性二室模型,终端消除半减期3.16h;表观分布容积99.40L;总体清除率392.12ml/min;药时曲线下面积1057.45h ng/ml;胃液pH值、分泌量和胃酸分泌量等药效学指标测定表明,单剂量静脉注射法莫替丁20mg,体内有效作用时间可持续8~9h。以Hill作图法描述了血药浓度与药效学(胃酸抑制率)的关系,推导出描述血药浓度与药效的数学关系式为E=100·C~(2.60)/(C~(2.60)+14.71~(2.60)),用此数学模型可由血药浓度预测药效,或由药效预测血药浓度。

To apply acetylcholine sensor studied by Wang Houxing to determination of acetylcholine activity in Injectio braintonic from brain proves that acetylcholine is high level of 900 mmol. This furnishes convining proof for elucidating pharmacodynamic effect.

用自制的乙酰胆碱传感器检测本室研制的脑健脑注射液,证明其乙酰胆碱活性约高达900mmol.为阐明其药效作用提供了有力的佐证.

 
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