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作 者:陈方剑[1] 宋洪杰[1] 高鸿彬[1] 王志君[1] 陆松伟[1] 袁文琳[1]
机构地区:[1]第二军医大学长海医院药学部,上海200433
出 处:《药学服务与研究》2013年第4期285-287,共3页Pharmaceutical Care and Research
基 金:上海市卫生局中药新药及院内制剂研发项目(2011ZJ028)
摘 要:目的:采用紫外-可见分光光度法测定感冒安颗粒中总酚酸的含量,并优化超声提取感冒安颗粒中总酚酸的工艺条件。方法:以没食子酸为对照品,在760nm处用紫外-可见分光光度法测定总酚酸的含量。考察甲醇浓度、甲醇用量和超声提取时间3个因素对感冒安颗粒中总酚酸提取率的影响,用L9(34)正交设计确定最佳超声提取条件。结果:感冒安颗粒中总酚酸的最佳提取工艺为用35ml 50%甲醇超声提取30min。没食子酸浓度在10~60μg/ml范围内与吸光度呈良好线性关系(r=0.999 8)。用紫外-可见分光光度法测定感冒安颗粒中总酚酸含量的加样回收率为(100.72±2.53)%(n=9),精密度、重复性和稳定性良好。结论:该方法简便易行,稳定性好,对提高感冒安颗粒的质量控制标准具有参考意义。Objective: To determine the content of total phenolic acid in Ganmao' an granules by ultraviolet-visible (UV-VIS) spectrophotometry and to optimize the ultrasonic extraction technology of total phenolic acid from Ganmao' an granules. Methods: The content of total phenolic acid was determined at 760 nm by UV-VIS spectropbotometry. Gallic acid was used as the control. Ultrasonic extraction technology was optimized by L9 (34) orthogonal design, with methanol concentration, methanol volume and extraction time as 3 influential factors. Results: The optimal extraction technology of total phenolic acid from Ganmao'an granules was using 35 ml 50% methanol as solvent and ultrasonic extraction for 30 min. The concentration of gallic acid displayed good linearity within the range of 10-60μg/ml(r=0. 999 8). The recovery of total phenolic acid determined by UV-VIS spectrophotometry was (100.72±2. 53) % (n = 9), with good precision, reproducibility and stability. Conclusion: The method is simple,stable and useful for enhancing the quality control standards of Ganmao'an granules.
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