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作 者:陈金兴[1] 赵毛香[1] 陈土荣[1] 袁伟彬[1]
机构地区:[1]广州中医药大学附属骨伤科医院药学部,广东广州510240
出 处:《系统医学》2017年第1期4-6,共3页Systems Medicine
基 金:2015年中医药强省专项基金医院中药制剂建设项目(粤中医办函[2015]102号)
摘 要:目的该文对2014年生产的验方温通膏所有批号进行年度产品质量回顾分析。方法考察验方温通膏的生产工艺是否稳定,以保证工艺流程顺利稳定、质控标准的可行性,以及中药材、辅料、半成品、制剂成品现有质量标准的可控性、及时发现不良的趋势。结果验方验方温通膏按现有的制备工艺流程及控制标准生产的制剂符合法定的质控标准。但是还存在不足,可在原工艺上从浸膏提取所需的乙醇浓度、提取时间和提取次数更好地从药材中提取出有效成分。结论为验方温通膏制剂制剂及工艺流程过程进行改善确定方向。Objective In order to study the production processstability of Wen Tong Hydrogels,the annual product quality of Wen Tong Hydrogels were reviewed and analysed. Methods The data would be analysed to ensure the smooth and stable process and the feasibility of quality control standards. The controllability of the existing standards which test Chineseherbal medicines,Accessories,semi-finished products and finished product.Adverse trends will be detected timely. Results The moulding technics were feassible and in accordance with the quality standards of wen tong hydrogels in traditional Chinese medicine. But there is not enough available on the original process extracts the required alcohol concentration,time and extraction times better extraction of active ingredients from herbs. Conclusion The formulation and process to improve the direction of the process will be determined.
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