HPLC同时测定清热定眩合剂中3种成分的含量  被引量:3

Simultaneous Determination of Three Components in Qingre Dingxuan Mixture by HPLC

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作  者:许红玮[1] 刘轲[1] 张怀亮[1] 

机构地区:[1]河南中医学院第一附属医院,郑州450000

出  处:《中国实验方剂学杂志》2015年第7期72-74,共3页Chinese Journal of Experimental Traditional Medical Formulae

基  金:河南省科技攻关计划项目(082102310080)

摘  要:目的:建立HPLC同时测定清热定眩合剂中黄芩苷、新橙皮苷及丹酚酸B含量的方法。方法:采用Waters SunfireTMC18色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-0.1%磷酸(21∶79),流速l.0 mL·min^-1,柱温30℃,检测波长280nm。结果:黄芩苷、新橙皮苷及丹酚酸B的线性范围分别为0.08-0.79(r=0.999 9),0.07-0.75(r=0.999 9),0.04-0.19μg(r=0.999 8);平均回收率分别为96.5%,96.9%,97.4%。结论:建立的HPLC方法简便,结果准确、可靠、重复性好,可用于清热定眩合剂的质量控制。Objective: To establish an HPLC method for simultaneous determination of baicalin; neohesperidin; salvianolic acid B in Qingre Dingxuan Mixture. Method: The chromatographic method was carried out on an Waters SunfireTM C18 (4.6 mm×250 mm,5μm) with acetonitrile-0. 1% phosphoricaeid solution as the mobile phase by gradient elution. The flow rate was 1 mL·min^-1. The detection was set at the wavelength of 280 nm. The column temperature was at 30 ℃. Result: The linear ranges of baicalin ; neohesperidin ; salvianolie acid B were0.08-0.79 μg (r=0.9999) , 0.07-0.75 μg (r =0.999 9) , 0.04-0. 19 μg (r =0. 999 8) respectively.The average recoeries were 96.5% , 96.9% , 97.4% respectively. Conclusion: The method is simple, accurate and reproducible.

关 键 词:高效液相色谱法 清热定眩合剂 黄芩苷 新橙皮苷 丹酚酸B 

分 类 号:R284.1[医药卫生—中药学]

 

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