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tablets
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    DETERMINATION OF INDIRUBIN IN TABLETS BY DUAL WAVELENGTH SPECTROPHOTOMETRY
    双波长分光光度法测定靛玉红中靛玉红的含量
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    DETERMINATION OF FAT-SOLUBLE COMPONENTS OF SALVIA MILTIORRHIZA IN COMPOUND SALVIA MILTIORRHIZA TABLETS BY HPLC
    HPLC测定复方丹参中丹参三种脂溶性成分的含量
短句来源
    Study on Quality Standards of Xiao erxiaoshi Tablets
    小儿消食质量标准的研究
短句来源
    Pharmacological Study on Xiaoerzhixie Tablets
    小儿止泻的药理研究
短句来源
    Determination of Ginsenosides in Xintaisu Tablets by Colorimetry
    比色法测定心肽素中人参总甙的含量
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  片剂
    COLORIMETRIC DETERMINATION OF MENADIONE SODIUM BISULFITE IN TABLETS
    亚硫酸氢钠甲萘醌片剂含量测定
短句来源
    Determination of Effective Compounds Hypericin and Hyperoside in Hypericum perforatum Tablets by RP-HPLC
    RP-HPLC法测定贯叶连翘片剂中有效成分金丝桃素和金丝桃苷的含量
短句来源
    Pharmacodynamic study of Xinqin Tablets on allergic rhinitis
    辛芩片剂治疗过敏性鼻炎的主要药效学研究
短句来源
    Determination of the contents of salidroside in the compound tablets of Rhodiola by RP-HPLC
    RP-HPLC法测定复方红景天片剂中红景天苷的含量
短句来源
    Study on HPLC-fingerprint of Flavonol in Ginkgo leaves tablets
    银杏叶片剂中银杏黄酮的HPLC指纹图谱研究
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  “tablets”译为未确定词的双语例句
    ORTHOGONAL DESIGN-SIMPLEX METHOD AND ITS APPLICATION TO THE ANALYSIS OF COMPOUND ANTIHYPERTENSIVE TABLETS
    正交设计—单纯形组合优化方法及其在复方降压片分析中的应用
短句来源
    Assay of the Content of the polysaccharide of Spirulina Nutritive Tablets
    螺旋藻营养片多糖含量的测定
短句来源
    Conclusion The method is fast,simple and can be used for quality control of Qiangli Naoqingsu tablets.
    结论方法可靠,操作简便,适用于该制剂的质量控制。
短句来源
    Results:Icariine showed a good linear relationship at the range of 0.1622~0.8112μg(r=0.9995); The average recovery of Icariine was 97.2%(RSD=1.8%,n=5),in the tablets.
    结果:淫羊藿苷进样量在0.1622-0.8112μg之间呈良好的线性关系(r=0.9995),平均加样回收率为97.2%(RSD=1.8%,n=5)。
短句来源
    Results:The main pharmacokinetics parameters of xuesaitong tablets were that tmax was(56.7±5.2) min,Cmax was(15.49±3.14) ng/μL,t1/2 was(55.66±13.64) min,and AUC(0→4h) was(1543.93±157.07) ng·min/μl.
    结果:达峰时间(tmax),峰浓度(Cmax),半衰期(t1/2)和曲线下面积(AUC)(0→4h)分别为56.7±5.2min,15.49±3.14ng/μl,55.66±13.64min和1543.93±157.07ng·min·μl-1。
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  tablets
Analytical results for two batches of compound ibuprofen tablets by the SEKI-based FI-CE approach were in good agreement with that obtained by a conventional high performance liquid chromatographic method.
      
Sulfanilamides were determined in Pharmaceuticals (tablets, ointments, and drops) and biological fluids (protein hydrolyzates, urine, blood serum, and whole blood).
      
The proposed method has been successfully applied for the determination of DPH, LD and MD in injections and tablets of pharmaceutical preparations.
      
Sulfanilamides were determined in medicinal forms (tablets, ointments, and drops) and biological fluids (protein hydrolyzate, blood plasma, and whole blood).
      
Finally, this method was used in the analysis of the vitamin C content of different pharmaceutical preparations, such as multivitamin tablets and syrups, vitamin-C tablets and powders, and effervescent tablets.
      
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Commonly used alkaloidal salts may be titrated accurately with acetous HClO_4 in non-aquous media in semi-micro scale using crystal violet as visual indi- cator.The method gave results compared favorably with those obtained by usual method in the respect of its simplicity,rapidity and reproducibility. A modified method was suggested to facilitate the extraction of alkaloidal salts as such from tablets by means of water,aqueous alcohol or other strong polar solvents.

1.作者对常用的生物碱类药物及其注射剂片剂,试用半微量非水溶液滴定法进行测定其含量.所得结果与药典方法测得者均能相近.2.非水溶液滴定法极简捷,结果准确.可能代替药典中若干药物的法定含量测定方法,但须注意杂质影响.3.用水或醇自片剂中半微量法滤出有效成分,直接滴定,方法简便,可得满意结果.

Since 1954 in authors' laboratory, various digitalis preparations, including digitalis leaves, tablets and tinctures and digitoxin and its injections, were assayed by both guineapig method and pigeon (lethal dose) method, using standardized digitalis powder as reference standard. It was found that results of digitalis leaf preparations obtained by guinea pig method and those by pigeon method were reasonably agreeable; while the results of digitoxin preparations obtained by guinea pig method were always...

Since 1954 in authors' laboratory, various digitalis preparations, including digitalis leaves, tablets and tinctures and digitoxin and its injections, were assayed by both guineapig method and pigeon (lethal dose) method, using standardized digitalis powder as reference standard. It was found that results of digitalis leaf preparations obtained by guinea pig method and those by pigeon method were reasonably agreeable; while the results of digitoxin preparations obtained by guinea pig method were always significantly lower than those obtained by pigeon method. In this paper, these facts were again shown, when 6 digitalis leaf preparations and 7 commercial digitoxin preparations were investigated. In digitoxin preparations, the potency estimated by pigeon method could be 2.36 times greater than that estimated by guinea pig method. The authors ascribed the difference to the inadequate standard preparation employed in the assay, as digitalis purpurea consisting of chiefly purpurea glycosides A and B being different in the mode of action to digitoxin (commercial) which was chiefly degraded product of purpurea glycoside A. They concluded that in bioassay of digitoxin against a digitalis standard, a suitable authorised method should be strictly followed; and the 4 methods employing different kinds of animals recommended by British Pharmacopeia 1953 and quoted by Bristish Pharmacopeia Codex 1954 for digitoxin would make confusions.

1、本文用豚鼠法和鸽法比較了6种国产洋地黄粉、2种国产洋地黄毒甙和5种进口洋地黄毒甙的生物效价,用洋地黄粉作标准品。 2、洋地黄粉用两种方法測定的結果比較接近。洋地黄毒甙相差达一倍,鸽法的結果较高,此种較大的差异,显然是与样品和标准品在成分上的不同有关。 3、本文指出英国副藥典(1954)对洋地黃毒甙的检驗,叫种方法并列,并以洋地黄叶粉为标准品是有問題的。作者考虑到如果用一定純度的洋地黄毒甙作为生物检定的标准品时,各法可以并用,否則应按一种規定的方法进行。本室張淑坤、赵秀文、周海鈞三位同志曾参与本文一部分实驗工作。

This work was undertaken to invgate the application of nonaqueous titration to the determination of tablets of anti-malarial drugs, with the view of finding out a simple, rapid and accurate method of analysis. Eleven kinds of tablets have been determined and the results as compared with those by the official methods are satisfactory. With the elimination of tedious extractions and evaporation of the solvent, a method is proposed as follows: Dissolve the finely pulverized and accurately weighed sample...

This work was undertaken to invgate the application of nonaqueous titration to the determination of tablets of anti-malarial drugs, with the view of finding out a simple, rapid and accurate method of analysis. Eleven kinds of tablets have been determined and the results as compared with those by the official methods are satisfactory. With the elimination of tedious extractions and evaporation of the solvent, a method is proposed as follows: Dissolve the finely pulverized and accurately weighed sample of about 0.5 milliequivalent weight of 1N HCl, in a 100ml Erlenmeyer flask and digest on a water bath for 10 min. After cooling, the solution, made alkaline with 3ml of 6N NaOH, is cooled under tap water and extracted with 30ml of chloroform with vigorous shaking for 10 min. Add 1 gm of tragacanth powder, shake for 2 min. till the solution becomes clear (if it remains turbid, add one more gm of tragacanth powder and shake) and filter through absorbent cotton. Titrate 20 ml of the clear filtrate with acetous perchloric acid, using 1 drop of crystal violet solution as indicator, to the end point which is blue for colorless sample or green without red tint for yellow-colored sample. A blank is run.

本文报告了一个簡單快速而准确的非水溶液滴定法测定抗瘧药物片剂,用以测定十一种抗瘧药物片剂,所得的結果与药典方法符合。

 
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