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作 者:王培 许保海 孙逸轩 刘长利[2] WANG Pei;XU Baohai;SUN Yixuan;LIU Changli(Department of Chinese Pharmacy,Beijing Jishuitan Hospital,Capital Medical University,Beijing 100035,China;College of Traditional Chinese Medicine,Capital Medical University,Beijing 100069,China)
机构地区:[1]首都医科大学附属北京积水潭医院中药房,北京100035 [2]首都医科大学中医药学院,北京100069
出 处:《现代药物与临床》2024年第8期2001-2005,共5页Drugs & Clinic
基 金:北京市中医药管理局第三批中药骨干人才培养项目(京中医科字[2022]59号)。
摘 要:目的建立UPLC法测定小柴胡颗粒中柴胡皂苷b_(1)、b_(2)。方法使用Acquity UPLC BHE C_(18)色谱柱(100 mm×2.1mm,1.7μm);流动相:水–乙腈,梯度洗脱;检测波长:254 nm;体积流量:0.3 mL/min;柱温:30℃;进样量3μL。结果柴胡皂苷b1、b2线性范围分别为0.006~0.374 mg、0.003~0.214 mg,平均回收率分别为98.97%、99.35%,RSD值分别为1.82%、1.16%。结论所建立方法准确、稳定,重现性好,可用于小柴胡颗粒的质量控制和评价。Objective To develop an UPLC method for determination the saikosaponin b_(1) and saikosaponin b_(2) in Xiaochaihu Granules.Methods The analysis was applied on Acquity UPLC BHE C_(18) column(100 mm×2.1 mm,1.7μm).The mobile phase consisted of water and acetonitrile with gradient elution.The detection wavelength was set at 254 nm,flow rate was 0.3 mL/min,column temperature was 30℃,and volume of injection was 3μL.Results Saikosaponin b_(1) and saikosaponin b_(2) showed good linear relationships of 0.006—0.374 mg and 0.003—0.214 mg,whose average recoveries were 98.97%and 99.35%with RSD values of 1.82%and 1.16%.Conclusion The established method is accurate,stable,and has good reproducibility,and can be used for quality control and evaluation for Xiaochaihu Granules.
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