药剂学 填空（Fill in the blanks）.docVIP

药剂学 填空（Fill in the blanks） Fill in the blanks 1.GLP: Specification for quality control of clinical research on drugs, GCP: drug clinical trial management specification 2. pharmacopoeia is a national code that records the standards and specifications of drugs. It is organized, edited and published by the State Pharmacopoeia Commission, and promulgated and executed by the government. It is legally binding. 3. Simple Syrup is a near saturated solution of sucrose, with a concentration of 85% (g/ml) or 64.7% (g/g), widely used in oral liquid preparations as a flavor modifying agent and a suspending agent. Preparation method: hot melt method, cold dissolution method and mixed method. Simple Syrup common thermosol prepared by mixing method; medicinal syrup, such as Codeine Phosphate Syrup. The settlement of 4. particle stationary particles natural sedimentation, sedimentation velocity obeys the Stokes law, according to the law, the speed of settlement can take two measures: one is to reduce the delay of particle particle radius (R); the two is to increase the viscosity of the suspension (ETA), can be added to the suspending agent. 5.: the stability of emulsion layer, flocculation, phase transfer, merging and breaking, rancidity 6. wet granulation production process: raw materials - crushing, screening - weighing - mixing - making soft wood - making wet particles - dry - whole, a mixed - tabletting. Process for the preparation of 7. solid preparation: drug - Crush - sieving mixing granulation tabletting (or drug - crushing sieving - mixing (powder) - granulation (granules) - tablets (tablets); granules and powder and capsules can do.) 8. powder preparation process: material - crushing - Screening - mixing (adding excipients) - - dose - quality inspection - Packaging - powder. 9. the preparation process of granule: mixing raw and auxiliary medicine, making soft material (principle: hand holding into groups, light pressing or dispersing) - making wet particles - drying granul