摘要
目的:优选防己黄芪颗粒的真空带式干燥工艺条件。方法:采用HPLC测定粉防己碱、防己诺林碱及黄芪甲苷含量。以干燥物含水量、粉防己碱和防己诺林碱的总含量、黄芪甲苷含量的综合评分为指标,通过正交试验考察干燥温度、履带速度、进料速度对防己黄芪颗粒真空带式干燥工艺的影响。结果:最佳真空带式干燥工艺条件为3个干燥区的温度依次为80,85,80℃,履带速度20 cm·min-1,进料速度12 L·h-1;含水量4.58%,粉防己碱和防己诺林碱总提取量11.97 mg·g-1,黄芪甲苷提取量0.54 mg·g-1。结论:优选的干燥工艺具有干燥速率高、产品质量好等优点,符合GMP要求,为防己黄芪颗粒的工业化生产提供实验依据。
Objective: To optimize vacuum-belt drying process of Fangji Huangqi granules. Method: HPLC was adopted to determine contents of tetrandrine,fangchinoline and astragaloside.With moisture content,total content of tetrandrine and fangchinoline,content of astragaloside as comprehensive evaluating indexes,orthogonal test was used to optimize vacuum-belt drying process of Fangji Huangqi granules with drying temperature,charging rate and belt speed as factors. Result: Optimal vacuum-belt drying process parameters were as follows:temperature of three heated regions at 80,85,80℃,belt speed of 20 cm·min-1,feeding rate of 12 L·h-1,moisture content 4.58%,total content of tetrandrine and fangchinoline 11.97 mg·g-1,content of astragaloside 0.54 mg·g-1. Conclusion: Optimized vacuum-belt drying technology had advantages of high drying rate,good product quality and so on.This study could provide a reasonable basis for industrial production of Fangji Huangqi granules in line with the GMP requirements.
出处
《中国实验方剂学杂志》
CAS
北大核心
2013年第24期10-12,共3页
Chinese Journal of Experimental Traditional Medical Formulae
基金
国家"重大新药创制"科技重大专项(2011ZX09201-201-10)