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tablets
相关语句
  片剂
    EXPERIMENTAL STUDY ON PRODUCTIVE CAPACITY OF TRAY DRYER FOR TABLETS
    片剂生产中厢式干燥器生产能力的实验研究
短句来源
    SPECTROFLUOROMETRIC DETERMINATION OF ATENOLOL IN TABLETS
    荧光分光光度法测定片剂中氨酰心安
短句来源
    BUOYANT SUSTAINED RELEASE TABLETS OF VITAMIN B_6
    维生素B_6胃漂浮片剂的研制
短句来源
    METHODS: With selection of compositions and design of structure, donut-shape multi-layer tablets fabricated by 3DP were evaluated through the routine tablet analysis, structure analysis and dissolution tests in vitro.
    方法:通过对片剂局部组成及结构进行选择与设计,利用三维打印技术制备了豆腐果苷馅饼型多层控释片,并对所制备的片剂进行常规分析、结构分析及体外释药试验。
短句来源
    Application of Acid dye Colorimetry in Quality Control of Cyclovirobuxine D and Its Tablets
    酸性染料比色法在黄杨宁及其片剂质量控制中的应用
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  “tablets”译为未确定词的双语例句
    Performances and Applications of Drug Selective Electrode Ⅰ.Determination of Benzydazine Hydrochloride in Raw Drug arid Tablets
    药物选择性电极的性能及应用 盐酸炎痛静原料及制剂的测定
短句来源
    STUDY OF COPOLYMER OF STYRENE-2-VINYLPYRIDINE IN COATING OF OXYTETRACYCLINE TABLETS
    苯乙烯-2-乙烯吡啶共聚物在土霉素薄膜包衣中的研究
短句来源
    Study on Quality Standards of Compound Rabdosia Rubescens Buccal Tablets
    复方冬凌草含片的质量标准研究
短句来源
    Objective To develop zidovudine tablets and to study its quality-control method.
    目的制备齐多夫定片并探讨其质量控制方法。
短句来源
    RESULTS When the filler was composed of mannitol and MCC at the ratio of 1:2, the MCC was 102QD, the disintegrants was PPVP with the dosage of 10% and the glidants was AEROSIL200, paracetamol orally disintegrating tablets could be prepared by direct compression.
    结果填充剂用甘露醇:微晶纤维素=1:2,微晶纤维素选用ISP102QD,崩解剂用10%交联聚乙烯吡咯烷酮,助流剂用进口AEROSIL200能满足直接压片要求。
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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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Microencapsulated nithiocyamine (4-nitro-4' -isothiocyanatodiphenyla-mine) tablets are made of nithiocyamine microcapsules. When an oraldose (6-7mg/kg 1 day) of it was given to patients with schistosomiasis,high antischistosomal activity was observed. These tablets have theadvantages of high stability, no coacervation of the micropowder ofnithiocyamine, precision of dosage and convenience of administration. Cellulose acetate phthalate was selected as an appropriate coatingmaterial which is chemically...

Microencapsulated nithiocyamine (4-nitro-4' -isothiocyanatodiphenyla-mine) tablets are made of nithiocyamine microcapsules. When an oraldose (6-7mg/kg 1 day) of it was given to patients with schistosomiasis,high antischistosomal activity was observed. These tablets have theadvantages of high stability, no coacervation of the micropowder ofnithiocyamine, precision of dosage and convenience of administration. Cellulose acetate phthalate was selected as an appropriate coatingmaterial which is chemically compatible and nonreactive with the corematerial. The microencapsulated nithiocyamine tablets were prepared as follows:micropowder of nithiocyamine was encapsulated in cellulose acetatephthalate by simple coacervation, using sodium sulfate as the coacerva-ting agent. Then the miocrocapsules were hardened with 2% aqueousacetic acid. The microencapsulated products were filtrated and washed,granulated, and finally compressed into tablets. After two years of storage, the content and bioavailability of thetablets remained unchanged. The tablets had been used for the treatment of 992 patients withschistosomiasis and the therapeutic effects were satisfactory. The assay methods of the microencapsulated nithiocyamine tabletsare discussed.

本文报告了硝硫氰胺微粉单凝聚成囊的处方与工艺和微囊片剂的处方与工艺。经动物试验和临床试用证明:用邻苯二甲酸醋酸纤维素作囊材,以单凝聚包囊,既不降低硝硫氰胺微粉的疗效,且可减轻其付作用。经稳定性考查,该片剂贮存二年以上其含量与生物疗效基本不变。

Elastase is a new and effectiveremedy made from pig pancrease forthe treatment of lipemia and coronaryheart disease, but it is obtained withdifficulty. Therefore, a study of thepreparation of Elastase and its tab-lets was achieved. This paper presents the techno-logical processes of making Elastase,the method for the determination ofthe activity of Elastase, the techni-que of tableting and coating oftablets, and the testing of thestability of Elastase tablets at varioustemperatures. Elastase is prepared...

Elastase is a new and effectiveremedy made from pig pancrease forthe treatment of lipemia and coronaryheart disease, but it is obtained withdifficulty. Therefore, a study of thepreparation of Elastase and its tab-lets was achieved. This paper presents the techno-logical processes of making Elastase,the method for the determination ofthe activity of Elastase, the techni-que of tableting and coating oftablets, and the testing of thestability of Elastase tablets at varioustemperatures. Elastase is prepared by the fol-lowing method: Pig pancreatin, madefrom pig pancrease, is extracted withpH 4.7 buffer solution. To the extractadd ammonium suflate and crudeElastase is salted out as precipitate.The precipitate is dissolved in pH7.0phosphate buffer solution and allowedto stand for 20-22 hours at 20℃.Then, it is salted out as precipitatewith ammonium sulfate. The preci-pitate is purified by crystallisationfrom pH7.0 buffer solution in refri-gerator. After separation and drying,active Elastase is obtained, having abiological activity of 25 units permg. The testing results of the stabi-lity of Elastase demonstrate thatElastase tablets are preserved best at0-5℃, and it may be preserved below30℃. These processes have been adop-ted for the production of Elastaseand its tablets in this pharmaceuticalfactory.

本文介绍了我厂用猪胰酶制备弹性酶的工艺过程,测定弹性酶活力的方法,弹性酶片的压制和包衣,以及在不同的温度条件下弹性酶片的稳定性。

Clenbuterol(NAB-365)is one of the aetive ingredients contained in CompoundTablet of Yuanhuatong,but it couldn't be determined owing to it's microamount andinterference of Ynanhuatong(total flavones crude extract obtained from Flos Genkwa).A suitable method for determination of μg amount of clenbuterol contained in thecompound tablets is desoribed by a six-point orthogonal functions spectrophotometryto eliminate the interference of yuanhuatong.The proposed method involves an addition of a certain amount...

Clenbuterol(NAB-365)is one of the aetive ingredients contained in CompoundTablet of Yuanhuatong,but it couldn't be determined owing to it's microamount andinterference of Ynanhuatong(total flavones crude extract obtained from Flos Genkwa).A suitable method for determination of μg amount of clenbuterol contained in thecompound tablets is desoribed by a six-point orthogonal functions spectrophotometryto eliminate the interference of yuanhuatong.The proposed method involves an addition of a certain amount of NAB-365 to thesample being tested,a suitable extraction and a subsequent spectrophotometric determina-tion with six wavelengths from 292~302 nm at 2 nm intervals,and a calculation ofthe quadratic polynomial regression coefficient,d_2.

复方芫花酮片中含有盐酸克喘素,由于量微和芫花酮的干扰,不能用一般的分光光度法测定含量。本文提出了在样品中追加一定量的盐酸克喘素,经适当提取分离,用六点正交函数——分光光度法,从292~302nm,波长间隔为2nm,求二次多项式回归系数 d2值,可以消除芫花酮的干扰,测定盐酸克喘素的含量。

 
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