摘要
采用正交试验法,以投料药材的干粉得率和干粉的总蒽醌含量为考核指标,对肝毒净颗粒剂所采用的“提取—浓缩—喷雾干燥”工艺与药材煎煮时间,煎煮次数,加水量,欲干燥药物清膏的相对密度,喷雾干燥器进风温度及出风温度等主要工艺因素的相关性进行研究,为优选该制剂的生产工艺提供依据。
By using orthogonal tests, the ratio of dry powder obtained from crude drugs and the total anthrquinone content of powder as criteria, the correlation among the “Extract-concentrate-spray drier” technology for Gandujing granule and the main technological factors such as time and frequency of decoction,volume of water, relative density of extract, the in_temperature and out_temperature of spray drier, etc. was studied. It provided a scientific basis for the optimal production technology of the preparation.
出处
《中药新药与临床药理》
CAS
CSCD
1997年第4期234-236,共3页
Traditional Chinese Drug Research and Clinical Pharmacology
关键词
肝毒净颗粒
中药
正交试验
工艺
提取
喷雾干燥
@Gandujing Granule
pharmaceutical technology
@orthogonal experiment