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作 者:朱星宇[1] 赵根华 高倩倩[1] 王恒[1] 刘玲[1] 陈志鹏[1] 吴丽[1] 李伟东[1] ZHU Xing-yu ZHAO Gen-hua GAO Qian-qian WANG Heng CHEN Zhi-peng WU Li LI Wei-dong(Department of Pharmacy, Nanjing University of Chinese Medicine, Jiangsu Key Laboratory of Chinese Medicine Processing, Nanfing 210023, China)
机构地区:[1]南京中医药大学药学院江苏省中药炮制重点实验室,南京210023
出 处:《中国实验方剂学杂志》2017年第15期85-91,共7页Chinese Journal of Experimental Traditional Medical Formulae
基 金:浙江省重中之重一级学科--中药学学科科研开放基金资助项目;江苏省高校自然科学基金重点项目(11KJA360001);江苏省高校"青蓝工程"资助项目(2014)
摘 要:目的:为了提高补骨脂饮片的质量标准,解决部分对照品稀缺问题,建立以补骨脂对照提取物为对照的补骨脂饮片中7种成分含量测定的方法。方法:采用高效液相色谱法。Thermo-endcapped C18色谱柱(4.6 mm×250 mm,5μm),流动相水-乙腈-甲醇梯度洗脱,柱温30℃,检测波长254 nm,进样量10μL。自制了补骨脂对照提取物并标定了其中补骨脂素、异补骨脂素、补骨脂甲素、补骨脂定、补骨脂乙素、补骨脂二氢黄酮甲醚、补骨脂酚7种成分的含量,并用补骨脂对照提取物为对照测定了12批补骨脂饮片中7种成分的含量,与对照品测定法的试验结果进行比较。结果:补骨脂饮片中补骨脂素、异补骨脂素、补骨脂甲素、补骨脂定、补骨脂乙素、补骨脂二氢黄酮甲醚、补骨脂酚7种成分均能达到基线分离、线性关系良好,平均回收率分别为97.4%,98.8%,99.6%,102%,99.6%,98.0%,103%,RSD均≤2.8%。该方法的精密度、稳定性、重复性良好,并且测定结果与对照品测定法所得结果无显著性差异,2种测定方法所得数据的RSD<3%。结论:补骨脂对照提取物法可用于补骨脂饮片中7种成分的含量测定,能有效地对补骨脂饮片进行质量控制。Objective:To improve the quality standard of Psoraleae Fructus,solve the problem of lacking relevant reference substance,and establish a content determination method for 7 compounds in Psoraleae Fructus decoration piece based on the standard reference extract.Method:HPLC was performed on Thermo-C18 endcapped column(4.6 mm×250 mm,5 μm),with water-methanol-acetonitrile system as the mobile phase for gradient elution.The column temperature was 30 ℃;the injection volume was 10 μL,and the detection wavelength was set at 254 nm.Self-prepared reference extracts of Psoraleae Fructus was used for determining the contents of psorale,isopsorale,psoralidin,corylifolinin,bavachinin and bakuchiol;then the contents of the 7 components in 12 batches of Psoraleae Fructus decoration piece were determined and compared with the experimental results obtained with the reference substance determination method.Result:The seven markers including psorale,isopsorale,psoralidin,corylifolinin,bavachinin and bakuchiol,reached baseline separation and showed good linearity.Their average recovery rate was 97.4%,98.8%,99.6%,102%,99.6%,98.0%,103% and RSDs of seven compounds were all no more than 2.8%.The reference extraction determination method showed high precision,stability and reproducibility,and there was no significant difference with the results of reference substance determination method.Conclusion:The reference extraction determination method was simple,and can be used for the contents determination of 7 compounds in Psoraleae Fructus decoration piece.
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