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1)  similarity factors (f2)
相似因子f2
2)  f2 factor
f2因子
1.
Methods:The dissolution profiles of model drug were drawn through detecting samples by UV method,f2 factor was employed to evaluate the similarity of dissolution profiles of different formulations in order to optimize the formulation.
方法:以紫外分光光度法对格列齐特推拉式渗透泵的体外释放度曲线进行测定,应用f2因子法为手段,对不同处方中药物释放曲线的相似性进行评价,对处方进行优化。
2.
The dissolution curves were comparerd with f2 factor.
方法采用紫外分光光度法测定3厂家吲达帕胺片的含量和在2种不同介质中的溶出度,利用f2因子法比较溶出曲线。
3)  nuclear factor ery throid 2
核因子F2
4)  similarity factor
相似因子
1.
Studies on the influencing factors on compound metformin-glipizide bilayer sustained-release tablets using the similarity factor;
采用相似因子法评价不同因素对复方二甲双胍格列吡嗪双层缓释片体外释放的影响
2.
The release conditions in vitro were investigated by a similarity factor method.
方法:以PEO,HPMC,NaCl和柠檬酸组成片芯,以醋酸纤维素为包衣材料制备FMT单层渗透泵片,并对片芯组成优化;用相似因子法考察了体外释放条件。
3.
The influences of the film on release in vitro were investigated by use of similarity factor method.
方法以丙烯酸树脂水分散体EudragitRS30D为包衣材料制备奥昔布宁渗透泵片,采用相似因子法考察包衣方面因素对体外释药的影响,并与同类进口片进行比较。
5)  Similar factor
相似因子
1.
In order to realize the reliability assessment,prior information from multiple sources such as test data in different environment and test data of similar product should be well used by environmental factor and similar factor.
在此过程中,为合理融合各来源的验前信息,提出了环境因子和相似因子的概念及其估计方法。
6)  similarity factor method
相似因子法
1.
The experiment data were analyzed by similarity factor method and Regter Peppas .
方法:转篮法,用紫外分光光度法检测,描绘其三维释放图像,将释放数据用相似因子法、Peppas方程进行分析。
2.
The accumul ation release percentage of tramadol hydrochloride sustained-release tablets un der the different pH conditions was determined by ultraviolet spectrophotometry at λ=270nm, then the release characteristics were explored by similarity factor method, Zero grade model, First grade mod.
方法 转篮法,用紫外分光光度法检测,描绘其三维释放图像,对释放数据分别用相似因子法分析,以零级,一级,Higuchi,Peppas方程进行拟合。
3.
Also the media were selected,then the release equations were established,which were compared to an imported preparation with similarity factor method.
方法 湿法制粒压制双层片 ,HPLC检测释放度 ,并对释放介质进行筛选 ,建立了释药方程 ,采用相似因子法与国外制剂进行比较。
补充资料:Ⅷ因子缺乏病


Ⅷ因子缺乏病
factor Ⅷ deficiency

  即“血友病A”。见“血友病A”。
  
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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