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机构地区:[1]青海大学医学院药学系,青海西宁810001 [2]西北师范大学化学化工学院,甘肃兰州730070
出 处:《中国中药杂志》2010年第18期2399-2401,共3页China Journal of Chinese Materia Medica
摘 要:目的:利用铕离子掺杂普鲁士蓝(europium-doped prussian blue analogue,Eu-PB)化学修饰型复合汞膜电极(GC/Eu-PB/MFE)建立了黄芩苷的测定方法,并探讨了其电化学行为。方法:在BR(pH6.0)支持电解质中,采用差示脉冲伏安法(DPV)和循环伏安法(CV)。结果:GC/Eu-PB/MFE电极与传统玻碳汞膜电极(GC/MFE)相比,同浓度的黄芩苷在GC/Eu-PB/MFE上响应灵敏度高,重复性好。黄芩苷在该电极上表现较强的吸附行为,其还原峰电位为-1.22 V(vs SCE)。还原峰电流与黄芩苷浓度在8.0×10-9~1.0×10-6mol.L-1呈线性关系(r=0.999 2),检测下限为1.2×10?9mol.L-1(S/N=3)。不经预分离直接测定双黄连口服液中黄芩苷的含量,平均回收率为99.83%,平均RSD 2.3%(n=8)。结论:GC/Eu-PB/MFE用于双黄连口服液中黄芩苷含量的测定,检测限低、灵敏、可靠,可用于该制剂的质量控制。Objective: A novel Eu-PB composite mercury film electrode(GC/Eu-PB/MFE)based on chemical modfied was developed for the determination of baicalin and the investigation of its the electrochemical behavior.Method: Cyclic voltammetry and differential pulse voltammetry were used.Result: The adsorption characteristic of baicalin was observed in Britton-Robinson buffer solution(pH 6.0)at GC/Eu-PB/MFE.The reduction peak of baicalin was observed at-1.22 V(vs SCE)and peak current was linear to the baicalin from 8.0×10^-9 to 1.0×10^-6 mol·L^-1(r=0.999 2,n=8).The limit of detection was 1.2×10^-9 mol·L^-1(S/N=3).The average recovery was 99.83%,with RSD of 2.3 %(n=8).The baicalin in Shuanghuanglian oral can be directly determined without pretreatment.Conclusion: The GC/Eu-PB/MFE was used to determin ebaicalin in Shuanghuanglian oral with good repeatability and high sensitivity.The method can be used for the quality control of Chinese traditional medicines containing Scutellaria baicalensis.
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