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作 者:郭爱枝[1] 何益峰[1] 王吉慧[1] 孙培文[1]
出 处:《中医药导报》2013年第8期82-84,共3页Guiding Journal of Traditional Chinese Medicine and Pharmacy
摘 要:目的:建立丹路口服液质量标准。方法:采用TLC法对丹路口服液中丹参、当归、川芎、红花进行定性鉴别;以HPLC法对其赤芍中的芍药苷进行含量测定。色谱柱:Symmetry C18柱(200 mm×4.6 mm,5μm);流动相:乙腈-1‰磷酸水溶液(19∶81);流速:1.0 mL.min-1;检测波长:230 nm;柱温:30℃。结果:在TLC色谱中检出丹参、当归、川芎、红花;芍药苷进样量在6.14-61.40μg mL-1范围内线性关系良好,r=0.9998;平均加样回收率101.0%,RSD%为2.5%。结论:所建立的方法简便可行,重现性好,为丹路口服液质量控制提供了方法。Objective: To establish a quality standard for Danlu Oral Liquid.Methods: Salvia mihiorrhiza Bge,Angelica sinensis(Oliv) Diels,Ligustici Chuanxiong Hort,Carthamus tinctorius L were indentified by TLC.HPLC was applied to determine the Paeoniflorin;The separation was performed on a Symmetry of C18 column(200 mm×4.6 nnn,5 μm);The mobile phase was consisted of acetonitrile and water(1‰ phosphoric acid)(19∶81);The detection wavelength was 230 nm;Flow rate was 1.0 mL.min-1;Column temperature was 30 ℃.Results: Salvia miltiorrhiza Bge,Angelica sinensis(Oliv) Diels,Ligusticum chuanxiong Hort,Carthamus tinctorius L could be detected by TLC.Paeoniflorin showed a good linear relationship at 6.14-61.40 μg.mL-1,r=0.9998;The average recovery of the added index was 101.0%,and RSD% was 2.5%.Conclusion: The method is simple,feasible and reproducible.The established quality standard can be used for the quality control of this medicine.
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