首页|高效液相色谱法同时测定柴葛解酒颗粒中6种有效成分的含量

高效液相色谱法同时测定柴葛解酒颗粒中6种有效成分的含量

扫码查看
目的 建立高效液相色谱(HPLC)法同时测定柴葛解酒颗粒中6种有效成分(葛根素、二氢杨梅素、鸢尾苷、葛花苷、槲皮素、柴胡皂苷A)的含量,为其质量标准的完善提供参考.方法 采用Agilent 5 HC-C18色谱柱(4.6 mm×250 mm,5μm);以0.2% 磷酸水(A)-乙腈(B)为流动相,梯度洗脱;流速:1.0 mL·min-1;柱温:30℃;检测波长:210 nm;进样量:10μL.结果 在上述色谱条件下,柴葛解酒颗粒中葛根素、二氢杨梅素、鸢尾苷、葛花苷、槲皮素、柴胡皂苷A可实现较好的分离,其线性范围分别为21.16~677.00μg·mL-1(r=1.0000)、11.16~357.00μg·mL-1(r=0.9997)、19.28~617.00μg·mL-1(r=0.9999)、10.38~332.00μg·mL-1(r=0.9999)、15.38~492.00μg·mL-1(r=0.9998)、15.50~496.00μg·mL-1(r=0.9996),各成分均有良好的线性关系;平均加样回收率在98.43%~101.35% 之间,RSD均小于3%.结论 所建立的方法能同时测定柴葛解酒颗粒中葛根素、二氢杨梅素、鸢尾苷、葛花苷、槲皮素、柴胡皂苷A的含量.该方法准确、重复性好、可操作性强,可为柴葛解酒颗粒的质量评价与控制提供依据.
Simultaneous Determination of Six Active Components in Chaige Hangover-alleviating Granules by HPLC
Objective HPLC method was established to simultaneously determine the content of six active components including puerarin,dihydromyricetin,tectoridin,kakkalide,quercetin,and saikosaponin A in Chaige Hangover-alleviating Granules (CAG),and to provide a reference for the improvement of its quality standard. Methods The separation was performed on an Agilent 5HC-C18 column (4.6 mm × 250 mm,5 μm)with 0.2% phosphoric acid in water (A)-acetonitrile (B) as the mobile phase in a gradient elution at a flow rate of 1.0 mL·min-1. The column temperature was 30 ℃,the detection wavelength was 210 nm,and the injection volume was 10 μL. Results A good separation of puerarin,dihydromyricetin,tectoridin,kakkalide,quercetin,and saikosaponin A in CAG could be achieved under the above chromatographic conditions,with the linear ranges of 21.16~677.00 μg·mL-1(r=1.0000),11.16~357.00 μg·mL-1(r=0.9997),19.28~617.00 μg·mL-1(r=0.9999),10.38~332.00 μg·mL-1(r=0.9999),15.38~492.00 μg·mL-1 (r=0.9998),and 15.50~496.00 μg·mL-1 (r=0.9996)respectively,showing a good linear correlation. The average recoveries ranged from 98.43%~101.35%,and the RSDs were all less than 3%. Conclusion The method can simultaneously determine the content of puerarin,dihydromyricetin,tectoridin,kakkalide,quercetin,and saikosaponin A in the CAG. Moreover,the established method is accurate,reproducible and operable,which provides the basis for the quality evaluation and control of CAG.

Chaige Hangover-alleviating Granules(CAG)HPLCquality standardcontent determination

赵飞雨、陈颖、张荣珍、毕梦非、高慧慧、杨秀秀、汪荣斌、张艳华、王存琴

展开 >

皖南医学院药学院,安徽芜湖 241002

芜湖市中医医院急诊内科,安徽芜湖 241002

安徽中医药高等专科学校中药资源研究所,安徽芜湖 241002

柴葛解酒颗粒 高效液相色谱法 质量标准 含量测定

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(12)