摘要
目的:建立测定多叶越南槐药材中红车轴草苷及高丽槐素2个黄酮类成分含量的高效液相色谱法。方法:采用Agilent Eclipse XDB-C18色谱柱(4.6 mm×250 mm,5μm),柱温25℃,以乙腈-0.1%乙酸水溶液为流动相,梯度洗脱,流速1.0 m L·min^-1,检测波长310 nm,进样量10μL,外标法定量。结果:红车轴草苷进样量在0.025 1-2.51μg范围内与峰面积呈良好的线性关系(r=0.999 0),平均回收率为97.0%(RSD=1.5%);高丽槐素进样量在0.025 2-2.52μg范围内与峰面积呈良好的线性关系(r=0.999 0),平均回收率为101.3%(RSD=2.2%)。结论:建立的含量测定方法符合方法验证要求。
Objective: To establish an HPLC method to determine the content of two flavonoids( trifolirhizin and maackiain) in Sophora tonkinensis Gagnep. var. polyphylla S. Z. Huang et Z. C. Zhou. Methods: An Agilent Eclipse XDB-C18column( 4. 6 mm × 250 mm,5 μm) was adopted,and the mobile phase consisted of acetonitrile and0. 1% aqueous acetic acid with a gradient elution. The flow rate was 1. 0 m L·min^-1,the column temperature was25 ℃,the detection wavelength was 310 nm and the injection volume was 10 μL,the sample was quantified with external standard. Results: The calibration curve of trifolirhizin was in good linearity at 0. 025 1-2. 51 μg( r = 0. 999 0)and the average recovery was 97. 0% with RSD of 1. 5%. The calibration curve of maackiain was in good linearity at0. 025 2-2. 52 μg( r = 0. 999 0) and the average recovery was 101. 3% with RSD of 2. 2%. Conclusion: The method established in this paper conforms to the requirements of the methodology validation.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2015年第1期121-124,共4页
Chinese Journal of Pharmaceutical Analysis
基金
广西科学研究与技术开发计划项目(桂科攻11107009-3-4)
关键词
多叶越南槐
红车轴草苷
高丽槐素
高效液相色谱
黄酮成分测定
方法验证
Sophora tonkinensis Gagnep.var.polyphylla S.Z.Huang et Z.C.Zhou
trifolirhizin
maackiain
HPLC
flavonoid determination
method validation