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作 者:郑盈莹 吴燕红 袁铭铭 许妍 ZHENG Yingying;WU Yanhong;YUAN Mingming;XU Yan(Jiangxi Institute for Drug Control,NMPA Key Laboratory of Quality Evaluation of Traditional Chinese Patent Medicine,Jiangxi Province Engineering Research Center of Drug and Medical Device Center,Nanchang 330029,China)
机构地区:[1]江西省药品检验检测研究院,国家药品监督管理局中成药质量评价重点实验室,江西省药品与医疗器械质量工程技术研究中心,南昌330029
出 处:《药品评价》2020年第15期34-36,共3页Drug Evaluation
摘 要:目的:考察消炎镇痛膏不同生产工艺的质量。方法:分别测定热压法和溶剂法生产的消炎镇痛膏挥发性成分的含量和黏附力,使用统计学软件SPSS 22.0处理实验数据。结果:热压法和溶剂法生产的消炎镇痛膏特征理化指标均有统计学意义。结论:溶剂法和热压法生产的消炎镇痛膏各有优缺点,两种生产工艺均需要进一步改进。Objective:Investigate the quality of xiaoyanzhentong plaster made by different production processes.Methods:Determine content of volatile components and adhesion of xiaoyanzhentong plaster made by hot-pressing method and solvent method,process,analyse corresponding data by SPSS 22.0.Results:The differences between physial and cemical indexes of xiaoyanzhentong plaster made by hot-pressing method and solvent method are stastistical significant.Conclusion:Xiaoyanzhentong plaster made by hot-pressing method and solvent method have its own advantages and disadvantages,both of the production processes should be further improved.
分 类 号:R917[医药卫生—药物分析学]
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