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HPLC法测定辽源七厘复方中药控释微丸中龙血素B的含量

Content Determination of Loureirin B in Liaoyuan Qili Compound TCM Controlled-release Pellets by HPLC
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摘要 目的:改良测定辽源七厘复方中药控释微丸中龙血素B含量的方法。方法:采用高效液相色谱法。色谱柱为KromasilC18(250mm×4.6mm,5μm),流动相为甲醇.1%冰醋酸溶液(梯度洗脱),流速为1.0ml/min,检测波长为206nm。结果:龙血素B的质量浓度在0.40-20.00μg/ml范围内与峰面积积分值呈良好线性关系(r=0.9995);精密度、稳定性、重复性试验的RSD〈2%;平均加样回收率为100.50%,RSD=1.90%(n=6)。结论:该改良方法操作简便、分离效果好、灵敏度高、重复性好,可用于辽源七厘复方中药控释微丸的质量控制。 OBJECTIVE : To improve the method for content determination of loureirin B in Liaoyuan qili compound TCM controlled-release pellets. METHODS: HPLC method was adopted. The determination was carded out on Kromasil C18 (250 mm×4.6mm,5μm) column with mobile phase consisted of methanol-1% glacial acetic acid (gradient elution) at a flow rate of 1.0 ml/min. The detection wavelength was set at 206 nm. RESULTS: The linear range of loureirin B was 0.40-20.00 μg/ml(r=0.999 5), respectively. RSDs of precision, stability and reproducibility tests were all lower than 2%. The average recoveries was 100.50% (RSD=1.90%, n=6). CONCLUSIONS: The improved method is simple, well-separated, sensitive and reproducible, and can be used for the quality control of Liaoyuan qili controlled-release pellets.
出处 《中国药房》 CAS CSCD 2014年第31期2929-2930,共2页 China Pharmacy
基金 重庆市卫生局中医药科研计划立项(No.2011-2-171)
关键词 辽源七厘复方中药控释微丸 龙血素B 高效液相色谱法 含量测定 Liaoyuan qili controlled-release pellets Loureirin B HPLC Content determination
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