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Flow Injection Chemiluminescence Determination of Puerarin in Pharmaceutical Preparations Using Eosin Y-Fenton System

机译:曙红Y-Fenton体系流动注射化学发光法测定药物制剂中的葛根素

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摘要

A novel chemiluminescence (CL) system was established for the determination of puerarin in pharmaceutical preparations. It was shown that a strong CL signal was observed when Eosin Y reacted with the hydroxyl radicals which were generated from Fenton reagent in acidic medium. The CL intensity was decreased significantly when puerarin was added to the reaction system and partially scavenged the hydroxyl radicals in the solution. The extent of decrease in the CL intensity had a good stoichiometrical relationship with puerarin concentration. Based on this, a new method for the determination of puerarin using a flow injection chemiluminescence technique was developed. The experimental parameters that affected the CL intensity were optimized. Under the optimal conditions, the linear range for puerarin concentration was 8.0×10?8?2.0×10?6 mol/L (R=0.9982) with a detection limit of 7.5×10?9 mol/L (S/N=3) and the relative standard deviation was 1.7% for 4.0×10?7 mol/L puerarin (n=11). The proposed method was applied to the determination of puerarin in a puerarin injection with satisfactory results.
机译:建立了一种新的化学发光(CL)系统,用于测定药物制剂中的葛根素。结果表明,当曙红Y与Fenton试剂在酸性介质中产生的羟基自由基反应时,观察到了强烈的CL信号。当葛根素加入反应体系并部分清除溶液中的羟基自由基时,CL强度显着降低。 CL强度降低的程度与葛根素浓度具有良好的化学计量关系。在此基础上,开发了一种利用流动注射化学发光技术测定葛根素的新方法。优化了影响CL强度的实验参数。在最佳条件下,葛根素浓度的线性范围为8.0×10 ?8 ?2.0×10 ?6 mol / L(R = 0.9982),检出限为葛根素4.0×10 ?7 mol / L的相对标准偏差为7.5×10 ?9 mol / L(S / N = 3)(n = 11)。该方法用于葛根素注射液中葛根素的测定,结果令人满意。

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