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作 者:李玉灵[1] 赵铁[1] 徐英宏[1] 阮国虎[1] 菅凌燕[1]
机构地区:[1]中国医科大学附属盛京医院药剂科,辽宁沈阳110003
出 处:《沈阳药科大学学报》2007年第10期623-626,共4页Journal of Shenyang Pharmaceutical University
基 金:辽宁省自然科学基金资助项目(20042189)
摘 要:目的建立同时测定赤丹丸中黄芩苷、丹参酮ⅡA含量的方法。方法采用RP-HPLC法。使用Agilent Zorbax Extend C18柱(4.6 mm×250 mm,5μm),以甲醇-水(磷酸调pH=3)-乙腈(体积比30∶50∶20~55∶15∶30)为流动相进行梯度洗脱,流速为1.0 mL.min-1,检测波长为270 nm,柱温为25℃。结果黄芩苷质量浓度在15.80~126.40 mg.L-1内与峰面积呈良好的线性关系,r=0.9999(n=5),平均加样回收率为99.0%,RSD为1.28%;丹参酮ⅡA质量浓度在5.04~80.56 mg.L-1内与峰面积呈良好的线性关系,r=0.999 2(n=5),平均加样回收率为98.3%,RSD为1.12%。结论RP-HPLC法简便、灵敏度高,重复性好,可用于赤丹丸的质量控制。Objective To establish an RP-HPLC method for simultaneous determination of the contents of baicalin and tanshinone Ⅱ A in Chidan ( traditional Chinese medicines) pills. Methods The column of Agilent Zorbax Extend C18(4.6 mm × 250 mm, 5 μm) was used, the mobile phase was consisted of methanol, water adjusted to pH 3 with phosphoric acid and acetonitrile, gradient elution was performed; the detection wavelength was set at 270 nm and the column temperature was 25 ℃. Results The linear range of baicalin and tanshinone Ⅱ A were 15.80 - 126.40 mg· L^- 1 and 5.04 - 80.56 mg· L^- 1 respectively. The average recoveries of baicalin and tanshinone Ⅱ A were 99.0 % with RSD of 1.28 %, 98.3 % with RSD of 1.12 % ( n = 5), respectively. Conclusions The method is simple, sensitive and good reproducibility. It can be used for quality control of Chidan pills.
分 类 号:R917[医药卫生—药物分析学]
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