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   oral preparation 的翻译结果: 查询用时:0.182秒
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oral preparation
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  口服制剂
     It is indicates that the concentrated capsule of 1, 25-dihydroxyvitamin D3 oral preparation would be in favor of absorption and utilization.
     这提示1,25二羟基维生素D3口服制剂的浓缩剂型,将有利于其吸收利用。
短句来源
     Experimental Study on the Safer of Borneolum Syntheticum in Oral Preparation
     冰片口服制剂安全性的实验研究
短句来源
     Of the top 20 drugs on the list of DDDs,the ratio of oral preparation to injections was 2∶1,75% were >1 and 25% were <1 in order ratio,suggesting those anti-infectives that with low cost,safety and efficacy assumed a predominant place,and the clinical medication was rational on the whole.
     在DDDs排序前20位中,口服制剂占2/3,注射制剂占1/3; 排序比>1的占75%,<1者,占25%,表明安全有效、价格低廉的抗感染药物占主导地位,临床用药基本合理。
短句来源
     The analysis of related substance for cefradine and its oral preparation by HPLC
     头孢拉定口服制剂有关物质的HPLC法分析
短句来源
     AIM: To study the effect of honeysuckle flower compound oral preparation characterized as anti-inflammation, pain-killing, anti-bacterium, detoxication, enlarging blood vessels, anti-platelet aggregation and anti-thrombosis in rats with acute myocardial ischemia induced by isoprenaline.
     目的:探讨具有抗炎、镇痛、抑菌、解毒、扩张血管、抑制血小板聚集及抗血栓功效的纯中药金银花复方口服制剂对异丙肾上腺素诱发小鼠急性心肌缺血的影响。
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  “oral preparation”译为未确定词的双语例句
     Results Pharmacokinetic parameters of sodium ozagrel oral preparation in 12 voluteers were obtained as follows: t_ max was (0.42±0.12) h,C_ max was (3.10±1.06) mg·L -1 ,AUC_ 0-t was (3.50±0.91) mg·h·L -1 ,t_ 1/2β was (0.72±0.26) h.
     结果奥扎格雷钠口服液的药代动力学参数tmax为(0.42±0.12)h、Cmax为(3.10±1.06)mg·L-1、AUC0-t为(3.50±0.91)mg·h·L-1,t1/2β为(0.72±0.26)h。
短句来源
     1. Selection of new oral preparation of pyronaridine phosphate.
     本课题主要研究内容包括:1、磷酸咯萘啶口服新剂型的选择;
短句来源
     Study of the quality control methods on tripterygium oral preparation
     雷公藤口服液质量控制方法的研究
短句来源
     METHODS:The cyclosporine A blood concentration of rabbits was determined by FPIA following the dose of 25 mg·kg -1 cyclosporine suppository per rectum ( n=4 ) and oral preparation per os(po) (n=4),their pharmacokinetic parameters and the relative bioavailability were calculated and analyzed statistically.
     方法 :利用荧光偏振免疫分析仪测定家兔直肠给予环孢素A栓剂 2 5mg·kg-1(n =4)与口服环孢素A口服液 2 5mg·kg-1(n =4)后血药浓度 ,计算两者的药物动力学参数和相对生物利用度 ,并进行统计学分析。
短句来源
     Rats in control group were fed with normal diet. Hyperlipidemia and insulin resistance rat models were established by feeding high- lipid food and rat models were further divided into CoA protective agent group [1100mg/(kg·d)]and CoA oral preparation group [800U/(kg·d)and2000U/(kg·d)].
     其中1组饲以普通饲料作为正常对照组,另3组饲以高脂饮食制 备高脂血症及胰岛素抵抗模型,高脂饮食造成高血脂后每天经口分别给予辅酶A保护剂1100mg/(kg·d)、辅酶A口服剂 800或2000U/(kg·d)。
短句来源
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  相似匹配句对
     Preparation of Xiaoerqingfei oral solution
     小儿清肺口服液的制备工艺研究
短句来源
     Preparation of Cuiru Oral Liquid
     催乳口服液的研制
短句来源
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  oral preparation
With the oral preparation, within this dose range and at this schedule, nafazatrom has no antitumor or other biologic activity.
      
UFT, an oral preparation of tegafur and uracil at a molar ratio of 1:4, was reported to have higher antitumor effects than tegafur alone for patients with breast cancer.
      
Two separate parameters of chewing were studied on the same chewing gum bolus after 10 strokes of oral preparation, color mixing, and bolus shaping.
      
Penicillin is still the treatment of choice and an oral preparation given twice daily for 10 days is equally effective.
      
Iron should preferably be prescribed as an oral preparation.
      
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The anion of potassium antimony tartrate was found to be capable of combining with a weakly basic anion exchange resin and a resin antimony tartrate was thus prepared. When the resin antimony tartrate was eluted with artificial gastric juice or with arti- ficial intestinal juice, the effluates were found to contain 4.7% and 29.1% of the total antimony respectively, indicating that resin antimony tartrate may be used as an enteric preparation. In the absorption experiments resin antimony tartrate appeared to...

The anion of potassium antimony tartrate was found to be capable of combining with a weakly basic anion exchange resin and a resin antimony tartrate was thus prepared. When the resin antimony tartrate was eluted with artificial gastric juice or with arti- ficial intestinal juice, the effluates were found to contain 4.7% and 29.1% of the total antimony respectively, indicating that resin antimony tartrate may be used as an enteric preparation. In the absorption experiments resin antimony tartrate appeared to cause a steady re- lease of antimony over a relatively long period, as the peak of blood Sb level was reached during 9 to 24 hours after a single dose. When a course of treatment with resin antimony tartrate was given, blood antimony levels, determined before giving the next dose, were found to vary between 1 and 3.5μg Sb/10 ml. Therapeutic test with this preparation was conducted on 9 dogs. The average number of worms in the treated animals was reduced to 14% of that of the controls. During the experiments of absorption and experimental therapy emesis was observed 29 times, diarrhoea 21 times, and anorexia 154 times for a total of 224 doses of the preparation in 10 dogs. Thus with this new oral preparation the gastro-intestinal reac- tions were considerably reduced, but not completely abolished. From these results it is considered that resin antimony tartrate may serve as a new possibility for researches on the oral preparation of tartar emetic.

弱碱性阴离子交换树脂,能与吐酒石的阴离子结合,形成酒石酸锑树脂.口服时可减轻胃肠道反应,吸收缓慢而均匀.家犬一次给药后,血锑高峯约在9-24小时间,多次给药后基础血锑浓度可达1.0-3.5微克/10毫升全血.血吸虫病犬经用酒石酸锑树脂治疗二周后,减虫率达86%以上.

Bioavailability study and pharmacokinetic analysis on three dosage forms of riboflavin oral preparation, namely, conventional tablet (IA), hexavitamin pill coated with a gelatin shell (IB) and a sustained-release tablet (IC) were carried out in nine healthy human volunteers by using urinary excretion method. All the three dosage forms were administered in 16 mg single dose immediately after a light breakfast. A bioavailability reference standard was set up by administering a total amount of 16 mg conventional...

Bioavailability study and pharmacokinetic analysis on three dosage forms of riboflavin oral preparation, namely, conventional tablet (IA), hexavitamin pill coated with a gelatin shell (IB) and a sustained-release tablet (IC) were carried out in nine healthy human volunteers by using urinary excretion method. All the three dosage forms were administered in 16 mg single dose immediately after a light breakfast. A bioavailability reference standard was set up by administering a total amount of 16 mg conventional tablets (6 mg each) in 3 divided doses (IIA) immediately after each meal. The results of recovery rate of riboflavin from the urine showed that IIA gained the highest percentage, being 67.62%., while IA, IB and 10 were 62.09%, 61.7% and 47.12% respectively.The above results indicated that there was no difference in bioavailability (bioe-quivalent) between IIA and IA, and that the bioavailability of the fast-release dosage-forms is superior to the slow-release dosage forms.The results obtained from pharmacokinetio analysis showed that there were no distinct differences amoung IA, IB and IC in elimination rate constants, however, distinct differences existed in the absorption rate constants and time needed to reach the maximun concentration.

本文用尿排药法,将三种核黄素(R)制剂给9个志愿者顿服15mg后,研究其生物利用度,并作药物动力学分析。三种制剂为普通片(IA)、包有软明胶皮的六合维生素丸(IB)以及一种长效缓释片剂(IC)。另外,口服R片剂(IIA),5mg,日服三次,作为生物利用度的参比标准。尿中R的回收率以IIA为最高,达67.52%,IA、IB、IC分别为62.09、51.7和47.12%。从以上结果可见:①IIA与IA为生物等效性,这表明普遍使用的给药方案(5mg,日服三次)从生物利用度观点来看,可以简化为15mg日服一次,②释药迅速的制剂较缓释制剂(明胶包衣的丸剂、缓释片剂)为优。六合维生素丸中的核黄素,生物利用度较差。对IA、IB、IC的药物动力学分析,结果显示消除速度常数β无显著差异,但吸收速度常数K。及达峰时t_m均有显著差异。

In this experiment the urokinase is entrapped in egg lecithin liposomes. The hand-shaken and sonication liposomes are prepared. The liposomes have different encapsulation efficiency, but both can lysis fibrin clot in vitro. The liposomes are capsulized with microcapsule, the products are two oral preparation scontaining urokinase.

本文将尿激酶包容在由蛋黄卵磷脂制备的脂质体中。分别用手摇法和超声法制备脂质体,二者的包容效率不同,但体外实验证实都有溶解纤维蛋白凝块的作用。用微型胶囊进一步包容含尿激酶脂质体可制得二种口服尿激酶的制备物。

 
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