loxoprofen sodium tablets 洛索洛芬钠片(5)   洛索洛芬钠片      Determination and Dissolution of Loxoprofen Sodium Tablets      洛索洛芬钠片的含量及体外溶出度测定 短句来源      Determination of loxoprofen sodium tablets by UV spectrophtometry      紫外分光光度法测定洛索洛芬钠片的含量 短句来源      Objective: To establish an UV spectrophotometry method to determine the contents of loxoprofen sodium tablets.      目的:建立用紫外分光光度法测定洛索洛芬钠片含量的方法。 短句来源      Dissolution of Loxoprofen Sodium Tablets and Evaluation of in vitro-in vivo Correlation      洛索洛芬钠片溶出度测定及体内外相关性评价 短句来源      An UV method for determination of dissolution of loxoprofen sodium tablets was established according to ChP dissolution methodⅡ. The pharmacokinetics of loxoprofen sodium tablets in human was determined by HPLC.      参照中国药典2005年版溶出度试验第二法,建立了UV法测定洛索洛芬钠片体外溶出度的试验方法,并用HPLC法测定洛索洛芬钠片的人体药物动力学,进行了体内外相关性的评价。 短句来源   “loxoprofen sodium tablets”译为未确定词的双语例句      Conclusion: The method is accurate, rapid and simple for the quality control of loxoprofen sodium tablets.      结论:本方法准确、快速、简便,可用于洛索洛芬钠片的质量控制。 短句来源      Clinical observation: The 60 Rheumatoid arthritis patients that belongs to the damp-heat type divided into 2 groups randomly as follows: Experimental group(Re Bi Granule p.o 2g t.i.d ), comparative group(Loxoprofen Sodium Tablets, p.o 60mg t.i.d ).      试验组口服热痹颗粒,每次2.0克,一日3次; 对照组口服乐松(洛索洛芬钠),每次60mg,一日3次。 短句来源      METHODSAll 80 patients from the HuBei Provincial TCM Hospital conforming to the diagnostic standard, were randomly divided into two groups: therapeutic group of TongBi 2 (GroupA, n=40) and comparative group of Loxoprofen Sodium Tablets(GroupB, n=40), with MTX for both groups as basic treatment.      所选80例患者均来自湖北省中医院风湿科门诊及病房，均符合类风湿关节炎的诊断及中医辨证属痹证，寒湿阻络证标准。 将患者随机分为两组：治疗组(A组)，对照组(B组)各40例。 短句来源   相似匹配句对      Study of synthetic process of loxoprofen sodium      非甾体抗炎药洛索洛芬钠的合成工艺研究 短句来源      Determination and Dissolution of Loxoprofen Sodium Tablets      洛索洛芬钠片的含量及体外溶出度测定 短句来源      AIM To study the bioequivalence of loxoprofen sodium tablet.      目的　研究洛索洛芬钠片的人体生物等效性。 短句来源      Determination of loxoprofen sodium tablets by UV spectrophtometry      紫外分光光度法测定洛索洛芬钠片的含量 短句来源      Studies on Loxoprofen Sodium Sustained Release Tablets      洛索洛芬钠缓释片的研究 短句来源 查询“loxoprofen sodium tablets”译词为用户自定义的双语例句     我想查看译文中含有：的双语例句 为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法，我们为您准备了出自英文原文的大量英语例句，供您参考。          Objective: To establish an UV spectrophotometry method to determine the contents of loxoprofen sodium tablets. Methods: The water was used as solvent. The detection wavelength was set at 223nm. Results: The calibration curve was linear in the range from 4.016 to 16.064μg/mL, r=0.9997. The average recovery was 98.81% and the RSD was 1.29%(n=5). Conclusion: The method is accurate, rapid and simple for the quality control of loxoprofen sodium tablets.             目的:建立用紫外分光光度法测定洛索洛芬钠片含量的方法。方法:以水为溶剂,测定波长为223nm。结果:检测线性范围为4.01616.064μg/mL,r=0.9997。平均回收率为98.81％,RSD=1.19％。结论:本方法准确、快速、简便,可用于洛索洛芬钠片的质量控制。 文摘来源          An UV method for determination of dissolution of loxoprofen sodium tablets was established according to ChP dissolution methodⅡ.The pharmacokinetics of loxoprofen sodium tablets in human was determined by HPLC.The results showed that the relationship between dissolution in vitro and absorption in vivo was correlated,indicating the method for the dissolution test of loxoprofen sodium tablets was feasible.             参照中国药典2005年版溶出度试验第二法,建立了UV法测定洛索洛芬钠片体外溶出度的试验方法,并用HPLC法测定洛索洛芬钠片的人体药物动力学,进行了体内外相关性的评价。结果表明洛索洛芬钠片体内外相关性良好,提示体外溶山度试验方法合理。 文摘来源       相关查询: loxoprofen sodium (sodium sodium sodium nitrate faropenem sodium sodium valproic sodium triphosphate sodium monofluorophosphate sodium glutamine sodium hyaluronate sodium curve pentachlorophenol sodium  对查询结果不满意

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