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分析結果准确、操作迅速及使用小量檢品与试剂是审查与批准药品檢定方法的基本要求。評判与确定药物及制剂的質量是药物分析的任务。苏联国家药典規定了药物及制剂的質量标准以檢查質量並测定其含量。現在第八版苏联国家药典規定的方法基本上是符合上述基本要求的。如所共知,我們药典采用的方法需取用大量試品进行分析,耗用较多时間,等等。立刻改变药典的分析方法是非常困难的,而且也不可能。但我們必須尽快地赶上現代科学要求的水平。翻閱新版的外国药典可以看出,由于提出了較高的要求,某些外国药典也已試圖採用新的分析方式与方法,如第二版捷克斯洛伐克药
Accurate analysis results, rapid operation and the use of small quantities of test articles and reagents are the basic requirements for reviewing and approving drug test methods. Judging and determining the quality of drugs and preparations is the task of drug analysis. The Soviet Union Pharmacopoeia sets forth the quality standards for medicines and preparations to check the quality and measure its content. Now the method prescribed in the Eighth National Soviet Pharmacopoeia basically meets the above basic requirements. As we all know, the methods we use in Pharmacopoeia need to use a large number of samples for analysis, consume more time, and so on. It is very difficult and impossible to change the method of analysis of Pharmacopoeia at once. But we must catch up with the requirements of modern science as soon as possible. Reading the new edition of the Foreign Pharmacopoeia shows that some foreign pharmacopoeia have also tried to adopt new analytical methods and methods due to the higher requirements such as the second edition of Czechoslovak Medicine