摘要
目的:建立雷公藤口服液中雷公藤甲素、总二萜内酯以及总生物碱的含量测定方法,为质量控制提供依据。方法:采用高效液相色谱(HPLC)法,Eclipse XDB-C18色谱柱(150 mm×4.6 mm,5μm),以乙腈-水为流动相进行梯度洗脱,流速1.0 ml·min^(-1),柱温40℃,检测波长218 nm,测定雷公藤口服液中雷公藤甲素的含量。采用紫外可见分光光度法,分别以雷公藤甲素、雷公藤次碱为对照,测定雷公藤总二萜内酯、总生物碱的含量。结果:雷公藤甲素、总二萜内酯(以雷公藤甲素计)和总生物碱(以雷公藤次碱计)的线性关系良好(r≥0.999 8),平均加样回收率分别为91.96%、90.73%、99.18%,RSD均小于3%。结论:本研究所建立的方法稳定可靠,重复性良好,可用于雷公藤口服液的质量控制。
Objective: To establish a method for the content determination of triptolide, total diterpenoids and total alkaloids in Leigongteng oral solution to provide basis for the quality control. Methods: An HPLC analysis was used to detect the content of triptol- ide, which was carried out on an Eclipse XDB-C18column ( 150mm×4.6mm,5μm) with the mobile phase consisting of aeetonitrile- water with gradient elntion. The flow rate was maintained at 1.0 ml. min -1, the column temperature was kept at 40℃ and the detec- tion wavelength was set at 218 nm. Using triptolide and wilforine as the contrast, the total diterpenoids and total alkaloids were deter- mined by UV-Vis speetrophotometry. Results : There were good linear relationship in the determination of triptolide, total diterpenoids (eaculated as triptolide) and total alkaloids (caculated as wilforine) (r ≥0. 999 8 ), the average recovery were 91.96%, 90.56%, 99.18%, and the RSD were less than 3%. Conclusion: The method is with good reproducibility and stability, which can be used for the quality control of Leigongteng oral solution.
出处
《中国药师》
CAS
2016年第10期1986-1989,共4页
China Pharmacist