摘要
目的:建立HPLC-DAD测定白花蛇舌草药材中2个蒽醌类成分2-甲基-3-甲氧基蒽醌(蒽醌Ⅰ)、2,3-二甲氧基-6-甲基蒽醌(蒽醌Ⅱ)含量的方法.方法:采用ZORBAX Extend-C18色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-0.5%磷酸溶液(48∶52),检测波长265 nm,流速1.0 mL·min^-1,柱温25℃.结果:蒽醌Ⅰ在0.998 ~ 9.98 μg(r=0.999 6)、蒽醌Ⅱ在0.675 ~6.75 μg(r =0.999 9)线性关系良好,平均加样回收率分别为99.87% (RSD 1.13%)和99.51% (RSD 0.69%).不同批次的白花蛇舌草药材中蒽醌Ⅰ和蒽醌Ⅱ成分含量差异较大,蒽醌Ⅰ和蒽醌Ⅱ的比例也无明显规律.结论:该方法简单、准确,适用于白花蛇舌草药材中2-甲基-3-甲氧基蒽醌和2,3-二甲氧基-6-甲基蒽醌的质量控制.
Objective:The aim of this study was to establish an HPLC-DAD method for the determination of 2-methy-3-methoxyanthraquinone,2,3-dimethoxy-6-methyanthraquinone in Hedyotidis Herba.Method:The assay was performed on a ZORBAX Extend-C18 column (4.6 mm × 250 mm,5 μm) eluted with acetonitrile-0.5% phosphate (48∶ 52).The detection wavelength was 265 nm,the flow rate was 1.0 mL ·min^-1,and the column temperature was set at 25 ℃.Result:The calibration curves were linear in the ranges of 0.998-9.98 μg (r =0.999 6) for anthraquinone Ⅰ and 0.675-6.75 μg (r =0.999 9) for anthraquinone Ⅱ.The average recoveries of anthraquinone Ⅰ and anthraquinone Ⅱ were 99.87% (RSD 1.13%) and 99.51% (RSD 0.69%),respectively.Conclusion:The method is simple and accurate for the quality control of 2-methy-3-methoxyanthraquinone and 2,3-dimethoxy-6-methyanthraquinone in Hedyotidis Herba.
出处
《中国实验方剂学杂志》
CAS
北大核心
2014年第20期54-56,共3页
Chinese Journal of Experimental Traditional Medical Formulae
基金
国家自然科学基金项目(81274052
81303206)
山东省自然科学基金项目(ZR2011HL043)
山东省优秀中青年科学家科研奖励基金项目(BS2013YY052)