摘要
目的:建立榼藤子药材的质量标准,为该药材质量控制提供依据。方法:以榼藤子中主要活性成分榼藤子苷、榼藤子酰胺A-O-β-D-吡喃葡萄糖苷为指标,分别采用TLC和HPLC进行定性鉴别和含量测定研究;参照《中国药典》2010年版附录相关方法,对榼藤子药材的水分、灰分及醇溶性浸出物进行测定。结果:TLC鉴别分离良好,斑点清晰。HPLC含量测定方法学结果表明榼藤子苷在0.014~2.747 g·L-1具有良好的线性关系,r=0.999 6(n=9),平均回收率为101.06%,RSD 0.90%(n=6);榼藤子酰胺A-O-β-D-吡喃葡萄糖苷在0.002~0.452 g·L-1具有良好的线性关系,r=0.999 7(n=9),平均回收率为101.52%,RSD 1.09%(n=6);21批样品含榼藤子苷质量分数为5.12%~9.24%,榼藤子酰胺A-β-D-吡喃葡萄糖苷的质量分数为0.55%~2.17%。醇溶性浸出物为30.9%~45.2%,水分为6.6%~8.6%,总灰分为2.4%~2.9%。结论:建立的方法可用于榼藤子药材的质量控制。
Objective: To establish the quality standard of Entadae Semen, and provide scientific basis for its quality control. Method: TIE and HPIE were used for qualitative identification and quantitative analysis of phaseoloidin and entadamide A-O-β-D-glucopyranoside in Entadae Semen. The test of water content, ash and ethanol-soluble extractives of Entadae Semen was carried out according to the methods re- corded in appendix of Chinese Pharmacopeia(2010 edition). Result: The TLC was well separated with clear spots. The linear range of phase- oloidin was between 0. 014 to 2. 747 g · L^-1 (r =0. 999 6, n =9) withan average recovery rate of 101.06% (RSD 0. 90%, n =6) ; the linear range of entadamide A-O-β-D-glucopyranoside was between O. 1302 to 0. 452 g · L^-1 ( r = 0. 999 7, n = 9) withan average recovery rate of 101.52% (RSD 1. 09%, n =6). The content of phaseeloidin in sample is between 5. 12% to 9. 24%, entadamide A-O-β-D-glucopyranoside is between 0. 55% to 2. 17%, alcohol-soluble extracts is between 30. 9% to 45. 2%, water is between 6. 6% to 8. 6%, and total ash is between 2. 4% to 2. 9%. Conclusion:The established standard is acceptable for quality control of Entadae Semen.
出处
《中国中药杂志》
CAS
CSCD
北大核心
2015年第10期1860-1864,共5页
China Journal of Chinese Materia Medica
基金
2015版中国药典科研项目