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作 者:杨明宇[1] 高婧 杜义龙[1] 李艳荣[1] 赵胜男[1] 潘海峰[1] YANG Mingyu;GAO Jing;DU Yilong;LI Yanrong;ZHAO Shengnan;PAN Haifeng(Key Laboratory of Study and Development of Traditional Chinese Medicine in Hebei Province,Chengde Medical University,Hebei Chengde 067000,China;Chengde Center for Food and Drug Control,Hebei Chengde 067000,China)
机构地区:[1]承德医学院河北省中药研究与开发重点实验室,河北承德067000 [2]承德市食品药品检验检测中心,河北承德067000
出 处:《中国药房》2016年第24期3404-3407,共4页China Pharmacy
基 金:河北省高等学校科学技术研究项目(No.ZD2015097);河北省高等学校科学研究计划项目(No.冀教科〔2015〕7号)
摘 要:目的:建立同时测定山楂叶中绿原酸、牡荆素葡萄糖苷、牡荆素鼠李糖苷、牡荆素、芦丁、金丝桃苷含量的方法。方法:采用高效液相色谱法,以牡荆素葡萄糖苷为基准峰,分别计算其与绿原酸、牡荆素鼠李糖苷、牡荆素、芦丁、金丝桃苷的相对校正因子(RCF),通过RCF计算山楂叶中上述5种成分的含量。色谱柱为AgilentZORBAXSBC18,流动相为0.1%甲酸-乙腈-四氢呋喃(梯度洗脱),流速为1.0ml/min,检测波长为350nm,柱温为30℃,进样量为10μl。结果:绿原酸、牡荆素葡萄糖苷、牡荆素鼠李糖苷、牡荆素、芦丁、金丝桃苷检测进样量线性范围分别为12.50~400.0μg(r=0.9998)、25.00~800.0μg(r=0.9999)、31.25~1000.0μg(r=0.9999)、6.470~260.0μg(r=0.9999)、2.50~80.0μg(r=0.9998)、9.375~300.0μg(r=0.9999);精密度、稳定性、重复性试验的RSD<2.0%;加样回收率分别为99.2%~103.9%(RSD=1.6%)、97.9%~100.8%(RSD=1.2%)、99.2%~100.8%(RSD=0.5%)、97.3%~101.3%(RSD=1.5%)、98.0%~103.0%(RSD=1.9%)、95.5%~101.5%(RSD=2.2%),n均为6。牡荆素葡萄糖苷与绿原酸、牡荆素鼠李糖苷、牡荆素、芦丁、金丝桃苷间的RCF分别为1.119、1.009、0.706、1.063、0.830。结论:该方法操作简便,精密度、稳定性、重复性好,可用于6种有效成分含量的同时测定。OBJECTIVE:To establish a method for the simultaneous determination of chlorogenic acid,vitexin glucoside,vitexinrhamnoside,vitexin,rutin and hyperoside in Crataegus pinnatifida. METHODS:With reference peak of vitexin glucoside,HPLC was conducted to calculate the relative correction factor(RCF)of chlorogenic acid,vitexin glucoside,vitexin rhamnoside,vitexin,rutin and hyperoside,then the contents of above-mentioned 5 components in C. pinnatifida were calculated. The columnwas Agilent ZORBAX SB C18 with mobile phase of 0.1% formic acid-acetonitrile-tetrahydrofuran(gradient elution)at a flow rateof 1.0 ml/min,the detection wavelength was 350 nm,column temperature was 30 ℃,and the injection volume was 10 μl. RESULTS:The linear range was 12.50-400.0 μg for chlorogenic acid(r=0.999 8),25.00-800.0 μg for vitexin glucoside(r=0.999 9),31.25-1 000.0 μg for vitexin rhamnoside(r=0.999 9),6.470-260.0 μg for vitexin(r=0.999 9),2.50-80.0 μg for rutin(r=0.999 8)and 9.375-300.0 μg for hyperoside(r=0.999 9);RSDs of precision,stability and reproducibility tests were lower than 2.0%;recoverieswere 99.2%-103.9%(RSD=1.6%,n=6),97.9%-100.8%(RSD=1.2%,n=6),99.2%-100.8%(RSD=0.5%,n=6),97.3%-101.3%(RSD=1.5%,n=6),98.0%-103.0%(RSD=1.9%,n=6)and 95.5%-101.5%(RSD=2.2%,n=6). RCFs of vitexinglucoside with chlorogenic acid,vitexin rhamnoside,vitexin,rutin and hyperoside were 1.119,1.009,0.706,1.063 and 0.830,respectively. CONCLUSIONS:The method is simple with good precision,stability and reproducibility,and it can be sued for thesimultaneous determination of 6 components in C. pinnatifida.
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