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capsule
相关语句
  胶囊
    SIMULTANEOUS SPECTROPHOTOMETRIC DETERMINATION OF L-TRYPTOPHAN AND TRAZODONE HYDROCHLORIDE IN CAPSULE
    分光光度法同时测定胶囊中L-色氨酸及氯哌三唑酮的含量
短句来源
    Determination of“Suxiao Shang Feng”Capsule and Caffeine and Sodium Benzoate Injection by A_2~s Method
    A_2~s 法测定速效伤风胶囊和安钠加注射液的含量
短句来源
    Treatment of essential hypertension with slow release nicardipine capsule in 62 patients
    尼卡地平缓释胶囊治疗原发性高血压62例
短句来源
    Therapy of angina pectoris with Di-ao-xin-xue-kang capsule in 713 patients
    地奥心血康胶囊治疗心绞痛713例
短句来源
    Determining the Content and Release Rate of Dextromethorphan Hydrobromide from Sustained Capsule with UV
    紫外分光光度法测定氢溴酸右美沙芬缓释胶囊的含量及溶出度
短句来源
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  胶囊剂
    Quality control of Liuwei Muxiang capsule
    六味木香胶囊剂质量控制
短句来源
    Study on pharmacokinetic and bioavailability of roxithromycin capsule and granule
    罗红霉素胶囊剂和颗粒剂药代动力学和相对生物利用度研究
短句来源
    The Rough Estimation of the Methods of Producing Capsule
    胶囊剂生产方法浅析
短句来源
    Clinical pharmacokinetics and relative bioavailability of roxithromycin capsule
    罗红霉素胶囊剂的临床药物动力学及相对生物利用度
短句来源
    The clinical efficacy and safety evaluation of flucloxacillin capsule
    氟氯西林胶囊剂口服的疗效及安全性临床评价
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  “capsule”译为未确定词的双语例句
    Determination of vitamin E in the capsule by HPLC
    高效液相色谱法测定维生素E胶丸含量
短句来源
    After filling the micro capsule powder of enteric-characteristic PLC into the stomach,antiplatelet aggregation average suppression rate is 86.9%±1.4% in the dog.
    犬胃灌肠溶性PLC微囊粉后,抗血小板聚集的平均抑制率为86.9%±1.4%。
短句来源
    The relative bioavailability of omeprazole capsule was (105.00±30.08)%.
    ml-1。 受试制剂对参比制剂的相对生物利用度为(105.00±30.08)%。
短句来源
    Objective To study the pharmacokinetics and bioequivalence of two fluconazole capsule formulations in 20 healthy volunteers who received a single oral dose of floconazle(200mg).
    目的研究氟康唑在人体中药代动力学和生物等效性。 方法20名健康志愿者随机交叉口服氟康唑两种制剂(参比制剂与受试制剂)各200mg,采用HPLC法测定血药浓度。
短句来源
    Results: The average recovery was 116.35mg/capsule.
    结果:用HPLC测定平均每粒含量为116.35 mg。
短句来源
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  capsule
Prolongation of Azospirillum cultivation to five days introduced new glucose-containing polysaccharide components in the capsule.
      
The basic sources of vibroaccelerations acting upon the frames of devices are determined in the capsule zone, where technological processes of producing new materials take place.
      
In the frequency band of 1-500 Hz the vibroaccelerations are shown to be generated by the operation of Fotonspacecraft units and a drive of capsule translation during the technological process.
      
On the capsule frame they reach the values of (1-3) × 10-3g.
      
In this case, the vehicle is a composite construction consisting of two rigid bodies, a return capsule and a stabilizing block, which is put in rotation.
      
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The injection of microencapsulat-ed compound megestrol acetate is awhite or almost white sterilized sus-pension which consists of megestrolacetate and estradiol valerate. Thediameters of the majority of micro-capsules range from 50-80μm. The injection has been used forthe treatment of 434 volunteers for5351 periods. Each volunteer was in-jected intramuscularly 2 ml once amonth. It showed a clinical appraisalthat the contraceptive effect of theinjection proved satisfactory, withan effeciency of 99.12% and...

The injection of microencapsulat-ed compound megestrol acetate is awhite or almost white sterilized sus-pension which consists of megestrolacetate and estradiol valerate. Thediameters of the majority of micro-capsules range from 50-80μm. The injection has been used forthe treatment of 434 volunteers for5351 periods. Each volunteer was in-jected intramuscularly 2 ml once amonth. It showed a clinical appraisalthat the contraceptive effect of theinjection proved satisfactory, withan effeciency of 99.12% and that theeffect was operative. The suitability of using gelatin-acacia as the encapsulating materialwas confirmed. Megestrol acetate and estradiolvalerate were tested to find a properratio to be used in the formula withwhich the contraceptive effect of thecore material was proved satisfactory. The injection was prepared as fol-lows: megestrol acetate and estradiolvalerate were encapsulated in gelatin-acacia by complex coacervationmethod, and acetic acid was used toadjust pH to 4.0-4.1. Then the micro-capsules were hardened by theaddition of formaldehyde, and themicroencapsulated products filtratedand washed to get a suspension whichwas then filled and sealed inampoules and sterilized to give thefinal products. A suitable suspending agent ofthe injection was selected for increas-ing stability. After two years ofstorage the contraceptive effect, mi-croencapsule shape, and the contentsof the injection all remainedunchanged.

本文报导复方甲地孕酮微囊注射液的处方与工艺,经动物实验和临床试用证明;甲地孕酮与戊酸雌二醇配伍为囊心物,用明胶和阿拉伯胶作囊材,以复凝聚法包囊,羧甲基纤维素钠作助悬剂,硫柳汞作抑菌剂,能达到降低主药剂量,减少付作用,延长避孕效果的目的。稳定性考查结果,该制剂贮存二年,其囊形与疗效基本不变。

Two sustained-release dosage forms, the enteric-coated granules in gelatin capsules and the tablets compresred from enteric-coated granules, were prepared for a long-acting effect of the prodrug—clorprenalinpamoate. In vitro, rates of dissoution were combined with the duration of antiasthmatic activity to obtain an in vitro minimum dissolving concentration (in vitro clinical effect correlation) and consequently a compa rison was made between the sustained release effect of the two dosage forms. The tablets...

Two sustained-release dosage forms, the enteric-coated granules in gelatin capsules and the tablets compresred from enteric-coated granules, were prepared for a long-acting effect of the prodrug—clorprenalinpamoate. In vitro, rates of dissoution were combined with the duration of antiasthmatic activity to obtain an in vitro minimum dissolving concentration (in vitro clinical effect correlation) and consequently a compa rison was made between the sustained release effect of the two dosage forms. The tablets made from enteric-coated granules proved to be an ideal sustained-release dosage form. It provided a release for as long as 10 hours in vitro. The tablets were shown through clinical tests, as expected to have insignificant side-effects and to prolong the antiasthmatic activity to above 12 hours.

为了进一步解决喘通的前体药物——双羟荼酸喘通在体内的长效作用,制成了肠溶颗粒装入硬胶囊,及将肠溶颗粒压成片剂两种剂型。用体外溶出试验与临床平喘时间相结合得出体外溶出最低浓度,并以此比较两种制剂的缓释效果。肠溶颗粒压成片剂为比较理想的长效喘通制剂。它能较恒定地缓释药物,体外溶出最低浓度达10小时以上。并试用于临床,初步取得了予期的副作用小、平喘时间达12小时的良好效果。

The bioavailability and basic pharmaeokinetio data of three different dosage forms of sodium phenytoin (DPH-Na), namely, capsule, conventional compressed tablet and sugar coated tablet were studied in eight volunteers by using 3H-DPH radioimmunoassay kit as analytical technique. In comparing the bioavailability parameters (Cm, tm, AUG) from the three dosage forms computed by microcomputer, there was no significant differeroe shown except that the AUO from the conventional form (42.79μg.h/ml) was somewhat...

The bioavailability and basic pharmaeokinetio data of three different dosage forms of sodium phenytoin (DPH-Na), namely, capsule, conventional compressed tablet and sugar coated tablet were studied in eight volunteers by using 3H-DPH radioimmunoassay kit as analytical technique. In comparing the bioavailability parameters (Cm, tm, AUG) from the three dosage forms computed by microcomputer, there was no significant differeroe shown except that the AUO from the conventional form (42.79μg.h/ml) was somewhat larger than those from the other two (36.74, 36.40 respectively). These results indicated that the three different dosage forms are bioequivalent in effect and can be chosen according to one's preference for clinical use. The conventional tablet is the simplest form in its manufacturing process.The mean biological half-life obtained from the present study was found to be 9.6±1.3 hrs, which is very close to that reported by Japanese authors (9.1-11.2), while those reported for Caucasians and Negroes were much longer, being 18.5 and 26.5 hrs respectively. The short half-life datum found in our series may be of some help in designing a rational dosage re.gimen of phenytoin adapted for Chinese.

用~3H-苯妥英(~3H-DPH)放射免疫药盒为分析手段,研究了8个志愿者对DPH-Na的三种不同制剂——胶囊剂(A)、普通压制片(B)和糖衣片(C)的生物利用度及基本药物动力学参数。比较了经微处理机计算的生物利用度参数(C_m、t_m、AUC),未发现有显著差异;故认为所研究的三种制剂是生物等效性的,其中以B的生产过程最为简单,在临床上可互相替换使用。由本实验所得我国人体内DPH-Na的生物半衰期为9.6±1.3h,与:日本人的9.1~11.2h十分接近,而在白种人与黑种人中则要长得多,分别为18.5及26.5h;这对合理制定符合我国人的DPH给药方案是有所裨益的。

 
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