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artemether tablets
相关语句
  蒿甲醚片
     Determination of Artemether in Compound Artemether Tablets by Quantitative TLC Scanning Technique
     薄层扫描法测定复方蒿甲醚片中蒿甲醚的含量
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  “artemether tablets”译为未确定词的双语例句
     DETERMINATION OF ARTEMETHER IN ARTEMETHER TABLETS BY HPLC
     高效液相色谱法测定蒿甲醚含量方法的研究
短句来源
     CONCLUSION The method can be used for the determination of Artemether in Artemether tablets.
     结论:本法可用于蒿甲醚片剂的含量测定。
短句来源
  相似匹配句对
     DETERMINATION OF ARTEMETHER IN ARTEMETHER TABLETS BY HPLC
     高效液相色谱法测定蒿甲醚含量方法的研究
短句来源
     CONCLUSION The method can be used for the determination of Artemether in Artemether tablets.
     结论:本法可用于蒿甲醚片剂的含量测定。
短句来源
     Aminoglutethimide Tablets
     治疗乳腺癌及皮质醇增多症特效药——氨鲁米特片
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     Sennoside Tablets
     美国药典(24版):番泻苷片
短句来源
     Preparation of artemether capsules
     蒿甲醚胶囊的制备
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52 cases of falciparun malaria were treated with artemether tablet, a new antimalarial formulation developed in Kunming Pharmaceutical Factory, at the dosage of 100 mg/d×5 (initial loaking dose was doubled) in chloroquine-resistant region. The clinical cure rate was 100%, the mean defervescence time was 32. 6±12. 8h and the parasitemia clearance time was 31.9±12. 7 h. At the same time, 39 cases of vivax malaria were treated with same method.The clinical cure rate was 100%, the mean defervescence time 27....

52 cases of falciparun malaria were treated with artemether tablet, a new antimalarial formulation developed in Kunming Pharmaceutical Factory, at the dosage of 100 mg/d×5 (initial loaking dose was doubled) in chloroquine-resistant region. The clinical cure rate was 100%, the mean defervescence time was 32. 6±12. 8h and the parasitemia clearance time was 31.9±12. 7 h. At the same time, 39 cases of vivax malaria were treated with same method.The clinical cure rate was 100%, the mean defervescence time 27. 9±15. 2 h and parasitemia clearance time 33.3±10. 4 h.The results showed that artemether tablet in the treatment of falciparum and vivax malaria had high efficacy, fasting-acting and less adverse effects as compared with artemether injection, and it may be used for treating chloroquine-resistant falciparum malaria.

以蒿甲醚国服片剂,总量600mg/d×5在抗氯喹恶性疟流行区治疗恶性疟,间日疟各52例和39例,临床治愈率均达100%,退热时间、疟原虫转阴时间及近期复燃率恶性疟分别为32.6±12.8h、31.9±12.7h和14.0%,间日疟分别为27.9±15.2h、33.3±10.4h和9.7%。结果显示,蒿甲醚片剂治疗恶性疟、间日疟具有与针剂同样高效、速效及不良反应少的优点.

This paper established a TLC scanning method to determin artemether in compound artemether tablets. The results showed that is a simple, rapid quantitative determination. The average recovery is 101.2%. RSD=2. 3%. n=5.

用薄层色谱法定量扫描技术测定复方蒿甲醚片中的蒿甲醚含量,处方中的本芴醇及杂质无干扰,方法简便、易行,24~28h测定结果稳定。平均回收率为101.2%,相对标准偏差为2.3%。

OBJECTIVE: To establish determination method of Artemether during release in vitro of delayed released Artemether tablet and to investigate its behavior in vitro. METHODS: Release medium was used as an acidic hydrolytic solvent and acid hydrolytic indirect UV spectrophotometer was used for determination of accumulate percent release rate in vitro and paddle method for release study in vitro. RESULTS: The best condition of acidic hydrolytic was selected and the determination method in vitro release...

OBJECTIVE: To establish determination method of Artemether during release in vitro of delayed released Artemether tablet and to investigate its behavior in vitro. METHODS: Release medium was used as an acidic hydrolytic solvent and acid hydrolytic indirect UV spectrophotometer was used for determination of accumulate percent release rate in vitro and paddle method for release study in vitro. RESULTS: The best condition of acidic hydrolytic was selected and the determination method in vitro release was defined; the accumulative released percentage from delayed release Artemether tablet was 25%, 60%, 85% respectively in 2 nd ,5 th ,10 th hour; ionic strengths greatly affected the release from delayed release Artemether tablet in investigated factors. CONCLUSION: The method was accurate, fast and applicable for release study in vitro with of many samples and jobs.$

目的:建立蒿甲醚缓释片体外释放的含量测定方法,并对其进行体外释放考察。方法:以释放介质作为酸消解溶剂,用酸消解间接紫外分光光度法测定片剂在释放过程中的累计百分释放度;浆法考察片剂的体外释放。结果:优选了最佳酸消解条件,并确定了片剂体外释放含量测定方法:蒿甲醚缓释片2h,5h,10h的体外累计百分释放度分别为25%,60%,85%;在诸多因素中离子强度是影响缓释片释放较灵敏的因素。结论:方法准确、快速、可行,适于体外释放实验样品量大的要求;体外实验表明蒿甲醚缓释片具有比普通片明显的缓释效果。

 
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