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机构地区:[1]南京中医药大学江阴附属医院,江阴市214400
出 处:《中国药房》2011年第48期4594-4596,共3页China Pharmacy
摘 要:目的:建立同时测定双黄连片中黄芩苷、绿原酸、连翘苷、连翘酯苷含量的方法。方法:采用高效液相色谱法。色谱柱为Hedera ODS 2柱,流动相为甲醇-0.2%磷酸溶液,采用梯度洗脱,流速为1.0mL.min-1,检测波长为324、280nm,进样量为10μL,柱温为30℃。结果:黄芩苷、绿原酸、连翘苷、连翘酯苷检测浓度分别在28.525~342.3μg.mL-1(r=0.9999)、4.56~54.72μg.mL-1(r=0.9995)、1.55~18.6μg.mL-1(r=0.9994)、1.81~21.72μg.mL-1(r=0.9996)范围内与峰面积积分值线性关系良好;4种成分平均加样回收率分别为98.12%、96.99%、103.16%、100.14%(n=6),均符合含量测定要求。结论:本法简单易行,可用于双黄连片的质量控制。To establish a method for simultaneously determination of baicalin, chlorogenic acid, forsythin and forsythoside A in Shuanghuanglian tablets. METHODS: HPLC method was carried out on a Hedera ODS 2 column with mobile phase consisted of methanol-0.2 % phosphoric acid solution (gradient elution) at the flow rate of 1.0 mL. rain ~. The detection wave- length was 324 nm and 280 nm. Injection volume was 10μL and column temperature was 30 ℃.RESULTS: The linear ranges of baicalin, chlorogenic acid, forsythin, Forsythosid A were in the range of 28.525~342.3 μg.mL^-1(r=0.999 9), 4.5654.72 pg.mL-l(r=0.999 5), 1.55~18.6 lag.mL 1(r=0.999 4), 1.81~21.72 p.g.mL^-1(r=0.999 6), respectively. The average recoveries of four active ingredients were 98.12%, 96.99%, 103.16%, 100.14%, respectively (n=6). CONCLUSION: The method is sim- ple, feasible and very suitable for the quality control of Shuanghuanglian tablets.
分 类 号:R917[医药卫生—药物分析学]
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