Chen Liang, Yin Ye, Yi Hongwei, Xu Qiang, Chen Ting
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210093, PR China.
J Pharm Biomed Anal. 2007 Apr 11;43(5):1715-20. doi: 10.1016/j.jpba.2007.01.007. Epub 2007 Jan 12.
A high-performance liquid chromatographic (HPLC) method was developed for the simultaneous determination of five flavonoids, taxifolin, neoastilbin, astilbin, neoisoastilbin and isoastilbin, contained in rhizoma smilacis glabrae. The optimal conditions of separation and detection were achieved on a Lichrospher C18 column (250 mm x 4.6 mm, 5 microm), with a gradient elution program, detected at 291 nm. The correlation coefficients of all the calibration curves showed good linearity (r>0.999) within test ranges. The relative deviation of this method was less than 3% for intra- and inter-day assays, and the average recoveries (n=3) were between 96.2 and 103.1%. The extraction process was also optimized as 2 h immersion and 30 min sonication in 60% ethanol. Eight samples of rhizoma smilacis glabrae from different locations in China were analyzed. The results indicate that the assay is reproducible and precise and could be readily utilized for the quality control of rhizoma smilacis glabrae.
建立了一种高效液相色谱(HPLC)法,用于同时测定光叶菝葜根茎中所含的5种黄酮类化合物,即 taxifolin、新橙皮苷、橙皮苷、新异橙皮苷和异橙皮苷。在Lichrospher C18柱(250 mm×4.6 mm,5μm)上,采用梯度洗脱程序,于291 nm波长处检测,实现了分离和检测的最佳条件。所有校准曲线的相关系数在测试范围内均呈现良好的线性关系(r>0.999)。该方法日内和日间测定的相对偏差均小于3%,平均回收率(n = 3)在96.2%至103.1%之间。提取工艺也进行了优化,采用60%乙醇浸泡2小时并超声处理30分钟。对来自中国不同产地的8份光叶菝葜根茎样品进行了分析。结果表明,该测定方法具有可重复性和准确性,可方便地用于光叶菝葜的质量控制。