药物分析ⅰ教案（I plan for drug analysis）.docVIP

药物分析ⅰ教案（I plan for drug analysis） Drug analysis I lesson plan Course name Drug analysis I Teaching methods Theory Course Prelect object 2000 classes of students assigned to elective courses Hours taught 24 hours Date set January 2004 The content of the first class (2 hours) The first chapter is introduction 1. the nature and tasks of pharmaceutical analysis. Pharmaceutical analysis is the use of physical and chemical, physical and chemical methods of definite structure of synthetic medicine, natural medicine and its preparation method for the quality control of traditional Chinese medicine preparation, and biochemical drugs and preparation method for quality control of representative. It is a systematic discipline. 2. drug quality standard system and Pharmacopoeia introduction. The pharmacopoeia is a national code relating to drug standards. The Chinese Pharmacopoeia, the current quality standard system in China and the foreign pharmacopoeia in common use are introduced emphatically. 3. scientific management standards for the overall control of drug quality. Mainly about the role of GLP, GMP, GSP, GCP and the main content. 4. efficacy indicators for analytical methods for drug analysis. The commonly used analytical efficiency evaluation indexes were introduced, including precision, accuracy, detection limit, quantitative limit, selectivity, linearity, range, durability, and correlation with reference method. 5. combining the teaching and research examples of the Department of pharmaceutical analysis, the application of pharmaceutical analysis in drug research is enumerated. (quality standards research, quality control methods, etc.) The second chapter is the basic procedure of drug analysis (I) 1. basic procedures for drug analysis: Sampling - Identification - Inspection - Determination of content - writing test reports and original records. The content of the second class (2 hours) The second chapter is the basic procedure of drug analysis (II) 2. general identific