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oral capsule
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  “oral capsule”译为未确定词的双语例句
     The relative-bioavailbility between equipotent oral capsule and water solution in man is 106. 9%.
     胶囊剂对水剂的相对生物利用度为106.9%.
短句来源
     Methods 75 patients with chronic liver diseases were given oral capsule of Ursofalk, 250mg thrice daily.
     方法75例慢性肝病患者日服优思弗胶囊,每次250mg,每日3次。
短句来源
     self-making microcapsule releasing time reach 32h in rabbit's brain organize environment, selling TMZ oral capsule release time as 20hr in rabbit(7) The toxic experiment of the big glue tumour cell of mouse's brain of C6
     自制TMZ微胶囊在兔脑组织环境下释放时间达到32h,市售TMZ
短句来源
     METHODS: When homatropine or tropicamide as a mydriatic were applied,twenty four patients ( 29 eyes ) with iridocyclitis following implantation of IOL were treated with oral capsule xueshuantong and lingxue qingre xiegantang . There was a follow up between 3 months and 12 months.
     方法:对24例(29只眼)人工晶状体植入术后虹膜睫状体炎患者,在后马托品或托品酰胺滴眼散瞳的情况下,用口服血栓通胶囊和凉血清热泻肝汤加减进行了治疗和为期3个月~12个月的随访观察。
短句来源
     Methods: The raw material of DMSA in the oral capsule was purified with a twostep method, then the drug was tested through intravenous injection in the animal experiments.
     方法:采用两步纯化法提纯口服胶囊中DMSA粗品,供动物实验中静脉注射用。
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  相似匹配句对
     the controlled group (oral placebo capsule) as well.
     试验组与开放组口服抗骨松胶囊3粒,每日3次;
短句来源
     Human Relative Bioavailability After Oral Ondansetron Capsule
     口服恩丹西酮胶囊的人体相对生物利用度
短句来源
     Oral Hygiene
     口腔卫生
短句来源
     On Oral Confession
     论口供
短句来源
     . and Ranjianduoji capsule.
     1、本草考证与文献考查
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  oral capsule
Independently absorbed components of a product, e.g., waxed pellets for an oral capsule, are administered separately and their plasma level-time profiles determined.
      
Equal doses of veralipride have been given to 12 healthy volunteers by three different administrations-intravenous infusion, oral solution, and oral capsule-in a randomized cross-over design.
      
When parthenolide was administered at doses up to 4 mg as a daily oral capsule in the feverfew preparation, there was not detectable concentration in the plasma.
      
At the time of study initiation, it was anticipated that vinorelbine would be developed as an oral capsule.
      
The pharmacokinetics of a new 10 mg sublingual tablet formulation of temazepam and those of a currently marketed 10 mg oral capsule formulation were evaluated in a group of ten healthy volunteers.
      
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This paper present plasma concentration the determination of with high pressure chromatography.Pharmacokinetic studies indicate that metoprolol is two compartment open models in man after oral ad-ministration of metoprolol. The kinetics of eliminition is one-order Kinetics. The parameters as follows.Ka=1. 474 h,VC=11. 89 L/kg, VB=15. 42 L/kg, t_1/2α=0. 573 h, t_2/2β=3. 563 h. The relative-bioavailbility between equipotent oral capsule and water solution in man is 106. 9%. Pharmacodynam-ic studies indicate...

This paper present plasma concentration the determination of with high pressure chromatography.Pharmacokinetic studies indicate that metoprolol is two compartment open models in man after oral ad-ministration of metoprolol. The kinetics of eliminition is one-order Kinetics. The parameters as follows.Ka=1. 474 h,VC=11. 89 L/kg, VB=15. 42 L/kg, t_1/2α=0. 573 h, t_2/2β=3. 563 h. The relative-bioavailbility between equipotent oral capsule and water solution in man is 106. 9%. Pharmacodynam-ic studies indicate that the inhibition of over-speed heart rate caused by physical exercises is associatedwith dose and declines linearly with time. The logarithm of the plasma concentration and the pharma-cological effect are parallel. Metoprolol remarkably inhibites systolic blood pressure after exercises. Thiseffect is associated with dose,and thc effect declines linearly with time. The resting blood pressure is in-significantly affected by the administration of metoprolol. It has no effect on the diastolic blood pres-sure. The effect of the dose of 1. 46mg/kg on Q--TC and STI is not significant.

用反相高效液相色谱法测定口服美多心安后药动学研究,结果表明:美多心安在人体为开放二房室模型,一级消除动力学,Ka=1.47h,t1/2α=0.57,t1/2β=3.56,VC=11.89L/kg,VB=15.42L/kg.胶囊剂对水剂的相对生物利用度为106.9%.药效学研究结果表明:美多心安抑制运动引起的心率过速与剂量相关,且随时间呈线性下降.血药浓度与药效平行,药效随时间为零级动力学消除.美多心安对运动后血压抑制明显,且与剂量有关;随时间延长药效减弱;对静止血压抑制作用弱,对舒张压无作用.用1.46mg/kg剂量对Q-TC和STI无明显影响.

Pharmacokinetics on injection of sodium naproxen in experimental rabbits was studied in comparison with its capsules.The results indicated that T_(max) of the injection (1.32±0.25 h) was shorter than that of the capsules (4.66±1.36 h);C_(max) of the injection (3.27.45±2.66μg/ml) was higher than that of the capsules (168.13±27.91μg/ml);Ka and Ke of the injection (5.54±1.770 10~(-1)h~(-1),1.066±0.245 10~(-1)h~(-1)) were larger than that of the capsules (4.000±1.973 10~(-1)h~(-1),5.040±1.435...

Pharmacokinetics on injection of sodium naproxen in experimental rabbits was studied in comparison with its capsules.The results indicated that T_(max) of the injection (1.32±0.25 h) was shorter than that of the capsules (4.66±1.36 h);C_(max) of the injection (3.27.45±2.66μg/ml) was higher than that of the capsules (168.13±27.91μg/ml);Ka and Ke of the injection (5.54±1.770 10~(-1)h~(-1),1.066±0.245 10~(-1)h~(-1)) were larger than that of the capsules (4.000±1.973 10~(-1)h~(-1),5.040±1.435 10~(-2)h~(-1)).The bioavailability of the injec- tion was 115.45% with neference to the capsules.These results demonstrated that absorption and excretion of injection were faster than that of the capsules,absotption ex- tent of injection was higher than oral capsules.

以萘普生钠胶囊剂作对照,研究了萘普生的注射液在家兔体内的药代动力学.结果表明萘普生钠注射液的 T_(max)(1.32±0.25h)较胶囊剂(4.66±1.36h)短:C_(max)(327.45±26.66μg/ml)较胶囊剂(168.13±27.91μg/ml)高;而 Ka 和 Ke(5.540±1.770 10~(-1)h~(-1),1.066±0.24510~(-11)h~(-1))均较胶囊剂(4.000±1.973 10~(-1)h~(-1).5.040±1.435 10~(-2)h~(-1))大.以胶囊剂作参比制剂,注射液的相对生物利用度为115.4%.说明萘普生钠注射液肌注给药比胶囊剂口服吸收快,排泄也快,吸收程度高.

A low molecular weight heparin (LMWH) was prepared from low anticoagulant activity heparin (LAAH),a side product accompanying commercial heparin, by depolymerization with nitrous acid. With pH value and content of nitrous acid fixed,the molecular weight of LMWH showed an inverse change between reaction temperature and time.The physical and chemical parameters, anticoagulant activity and anti-FXa activity of the product were determined. The LMWH with molecular weight 5300d possessed the strongest antithrombotic...

A low molecular weight heparin (LMWH) was prepared from low anticoagulant activity heparin (LAAH),a side product accompanying commercial heparin, by depolymerization with nitrous acid. With pH value and content of nitrous acid fixed,the molecular weight of LMWH showed an inverse change between reaction temperature and time.The physical and chemical parameters, anticoagulant activity and anti-FXa activity of the product were determined. The LMWH with molecular weight 5300d possessed the strongest antithrombotic activity evaluated by the thrombus model in common carotid artery of rats.The LMWH could significantly inhibit agar-induced paw edema in rats and cotton-ball-induced inflammatory granulation tissue hyperplasia in mice.With anti-FXa activity as index,the pharmacokinetics of LMWH was studied in rabbits after a single iv injection, which showed that the biological half-life of LMWH was almost three times as long as that of heparin, the systematic clearance of LMWH was slower,the AUC and V of LMWH were bigger. With the effect on experimental thrombus formation as the pharmacodynamics index, the formulation and effects of LMWH oral capsules composed of oleic acid and bovine bile salt upon rabbit hemorheology and thrombus formation were studied.

以生产肝素的副产品──低抗凝活性肝素为原料,采用亚硝酸控制解聚法制得低分子肝素(LMWH);在固定pH值和亚硝酸用量的条件下,探明LMWH分子量与反应温度和时间呈反变。测定了产物的理化常数,抗凝效价和抗FXa活性。以大鼠颈动脉血栓模型研究证明分子量为5300d的产物具有较强的抗栓活性;此外对琼脂所致大鼠足跖肿胀、棉球所致小鼠炎症性肉芽肿组织增生都具有显著抑制作用。以抗FXa活性为检测指标,研究了家兔一次静脉注射的药物动力学,结果显示LMWH的生物半衰期t(1/2)约为肝素的3倍,全身清除率Cls比肝素小,血药-时曲线下面积AUC和表观分布容积V比肝素大。以对家兔实验性血栓形成的影响为药效学指标,确定了LMWH口服胶囊的配方组成及其对家兔血液流变学及实验性血栓形成的影响。

 
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