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作 者:黄丽霞[1] 贾晓斌[1] 陈彦[1] 赵呈雷[1] 封亮[1] 蔡垠[1]
机构地区:[1]江苏省中医药研究院
出 处:《中国药房》2008年第12期910-912,共3页China Pharmacy
基 金:江苏省自然科学基金资助项目(BK2006155);江苏省中医药领军人才项目(2006)
摘 要:目的:建立以高效液相色谱法测定夏枯草中熊果酸含量的方法,并检测不同产地夏枯草中熊果酸的含量。方法:色谱柱为ZorbaxSBC18(150mm×4.6mm,5μm),流动相为乙腈-磷酸盐缓冲液(pH7.6)=45∶55,检测波长为210nm,流速为1.0mL·min-1。结果:熊果酸进样量在0.1115~1.7840μg范围内与峰面积积分值呈良好的线性关系(r=0.9992);平均回收率为99.93%,RSD=0.77%(n=6)。不同产地夏枯草中熊果酸的含量在0.08%~0.18%之间。结论:不同产地夏枯草中熊果酸含量差异很大。本方法简便、准确、重现性好,可用于夏枯草的质量控制。OBJECTIVE: To establish an HPLC method for determination of the content of Ursolic acid in Spica Prunellae, and to determine the content of Ursolic acid in Spica Prunellae from different habitat. METHODS: Ursolic acid was sep- arated on Zorbax SB C18(150 mm×4.6 mm, 5 μm) with mobile phase consisted of acetonitrile- phosphate buffer (pH 7.6) = 45 : 55 at a flow rate of 1.0 mL· min^-1. The detective wavelength was set at 210 nm. RESULTS: The linear range of Ursolic acid was 0.111 5~1.784 0μg ( r =0.999 2). The average recovery rate of Ursolic acid was 99.93% (RSD = 0.77%, n = 6). The content of Ursolic acid in Spica Prunellae from different habitat ranged from 0.08% to 0.18%. CONCLUSION: The content of Ursolic acid in Spica Prunellae from different habitat varied greatly. This determination method is simple, accurate and reproducible, and suitable for the quality control of Spica Prunellae.
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