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作 者:陈方剑 赵娟娟 叶侃倜 孙煜昕 刘继勇[2,5] 杨骏 CHEN Fangjian;ZHAO Juanjuan;YE Kanti;SUN Yuxin;LIU Jiyong;YANG Jun(Department of Pharmacy,Geriatric Nursing Hospital of Huangpu District,Shanghai 200010,China;School of Pharmacy,Shandong University of Traditional Chinese Medicine,Pharmacy Department,Jinan 250399,China;Department of Pharmacy,Xiangshan Hospital of Traditional Chinese Medicine,Shanghai 200020,China;Department of Pharmacy,Yuyuan Sub-district Community Health Service Center of Huangpu District,Shanghai 200010,China;Department of Pharmacy,Fudan University Affiliated Cancer Hospital,Shanghai 200032,China)
机构地区:[1]黄浦区老年护理医院药剂科,上海200010 [2]山东中医药大学药学院,山东济南250399 [3]上海市黄浦区香山中医医院药剂科,上海200020 [4]黄浦区豫园街道社区卫生服务中心药剂科,上海200010 [5]复旦大学附属肿瘤医院药剂科,上海200032
出 处:《药学实践与服务》2025年第2期82-86,91,共6页Journal of Pharmaceutical Practice and Service
基 金:上海市2022年度“科技创新行动计划”生物医药科技支撑专项项目(22S21903600)。
摘 要:目的优化血通胶囊提取工艺,建立质量控制方法。方法采用乙醇回流法,通过正交试验考察不同因素对二苯乙烯苷、芦荟大黄素、浸膏得率的影响;采用HPLC法同时测定血通胶囊5种蒽醌类成分含量。结果最佳提取工艺为加10倍乙醇,乙醇浓度70%,提取3次,每次1 h;5种成分在一定浓度范围内与峰面积具有良好的线性关系,相关系数r均>0.9997;平均加样回收率在93.66%~96.85%之间,RSD范围在1.48%~1.66%。3批血通胶囊中5种成分的含量测定结果分别为(0.632~0.641)、(0.660~0.681)、(1.968~1.991)、(2.547~2.580)、(1.076~1.101)mg/g。结论该方法准确、重复性好、可行性高,对血通胶囊生产和质量控制标准提高具有参考意义。Objective To optimize the extraction process of Xuetong capsules and establish its quality control method.Methods The extraction process was optimized by orthogonal experiment using ethanol reflux method to investigate the effects of different factors on diphenylstilbene,aloin and extraction yield.The content of 5 anthraquinone compounds in Xuetong capsule was determined by HPLC.Results The optimal extraction process was to add 10 times ethanol,with an ethanol concentration of 70%,and extract 3 times,each time for 1 h;5 components had a good linear relationship with peak area within a certain concentration range,r>0.9997;The range of sample recovery rate was 93.66%-96.85%,RSD range of 1.48%-1.66%.The content determination results of the 5 components in three batches of Xuetong capsules were(0.632-0.641),(0.660-0.681),(1.968-1.991),(2.547-2.580),and(1.076-1.101)mg/g.Conclusion The method was accurate,reproducible,and highly feasible,which could be references for producing and improving the quality control standards of Xuetong capsules.
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