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clarity of solution
相关语句
  溶液澄清度
     Introduction of clarity of solution, color of solution, dissolution, particulate matter, test for bacterial endotoxin for antibiotics in the Chinese Pharmacopoeia 2005
     中国药典2005年版关于抗生素溶液澄清度、颜色、溶出度、异物、细菌内毒素等检查项目介绍
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  “clarity of solution”译为未确定词的双语例句
     The key technology of the development is how to remove the carbohydrate gum and pigment as well as raise the clarity of solution,so as to make all the indexes reach the pharmcopoeia standards.
     研制过程中的技术关键是如何去除糖胶、色素等杂质,提高溶液的澄清度,使各项指标达到药典标准。
短句来源
  相似匹配句对
     solution.
     溶液进行对照。
短句来源
     T's solution.
     T解集中不出现空集;
短句来源
     b) The solution of the inequality.
     (2)解不等式;
短句来源
     The range of the solution of S.D.
     D.
短句来源
     The film gained by painting the solution on the surface of glass has high clarity.
     将此溶胶涂至玻璃表面,所得涂膜透明度高。
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The medicinal potassium chloride developed using “high temperature salts”is another co product of preparation iodine from seaweed,which can solve not only the pollution of the high temperature salts,but also provide obvious economic benefit.The key technology of the development is how to remove the carbohydrate gum and pigment as well as raise the clarity of solution,so as to make all the indexes reach the pharmcopoeia standards.

利用“高温盐”废料研制成功药用氯化钾,是海藻制碘中的又一联产品。它不但解决了废料(高温盐)对环境的污染,而且还给企业带来了明显的经济效益。研制过程中的技术关键是如何去除糖胶、色素等杂质,提高溶液的澄清度,使各项指标达到药典标准。

Objective: To study the stabilities of cefuroxime sodium for injection. Methods: Using drug and polymer content,color and clarity of solution as the quality indexes,the stabilities of cefuroxime sodium for injection made by different raw materials from different suppliers were investigated by accelerated experiments and influencing - factor tests, including temperature, light and nitrogen. Results: The results showed that the drug content of sample A hardly changed and its clarity and color of solution...

Objective: To study the stabilities of cefuroxime sodium for injection. Methods: Using drug and polymer content,color and clarity of solution as the quality indexes,the stabilities of cefuroxime sodium for injection made by different raw materials from different suppliers were investigated by accelerated experiments and influencing - factor tests, including temperature, light and nitrogen. Results: The results showed that the drug content of sample A hardly changed and its clarity and color of solution were the best, the polymer contents had no apparent difference among three samples. Conclusion: The quality of cefuroxime sodium raw material has great influence on the stabilities of products.

目的:探讨注射用头孢呋辛钠的稳定性。方法:通过加速、温度、光照、充氮影响实验,以含量(%)、聚合物(%)、溶液的颜色和澄清度为指标,考察不同原料厂家注射用头孢呋辛钠的稳定性。结果:样品A的含量变化最小,其溶液的澄清度和颜色最好,3个样品的聚合物(%)则相差不大。结论:头孢呋辛钠原料质量是影响产品稳定性的主要因素。

The chapter introduces the test items related to antibiotics in the Chinese Pharmacopoeia 2005 which include clarity of solution, color of solution, dissolution, visible particles, particulate matter, test for bacterial endotoxin, etc. It focused to discuss the importance of each test item, the revisions and new admissions in appendix, changes in monographs and the problems that may occur in practice. The appendices for these items are more precise, complete and standardized, with rather extensive...

The chapter introduces the test items related to antibiotics in the Chinese Pharmacopoeia 2005 which include clarity of solution, color of solution, dissolution, visible particles, particulate matter, test for bacterial endotoxin, etc. It focused to discuss the importance of each test item, the revisions and new admissions in appendix, changes in monographs and the problems that may occur in practice. The appendices for these items are more precise, complete and standardized, with rather extensive revision in comparison with previous edition. Especially, it is the first time that test for visible particles is adopted by the Chinese Pharmacopoeia, and light scattering method for visible particles is firstly commenced by China and included in this edition.

对中国药典2005年版中与抗生素检验有关的部分检查项目:溶液澄清度和颜色、溶出度、可见异物、不溶性微粒和细菌内毒素检查法等进行介绍,其中对各项检查控制的意义、2005年版附录增修订情况、品种项下的变化及实际检验中应注意的问题进行重点分析与探讨。与中国药典2000年版相比,2005年版药典中各项检查的标准均有不同程度提高,对药品质量的控制更全面严格,尤其值得指出的是,可见异物检查法首次载入中国药典,其中光散射检查法是本版药典附录中收载的由我国首创的方法。

 
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