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机构地区:[1]川北医学院基础医学院化学教研室,四川南充637000 [2]夹江水工机械厂电器分厂,四川乐山614000
出 处:《川北医学院学报》2007年第5期425-427,共3页Journal of North Sichuan Medical College
基 金:四川省教育厅青年科学基金(No:2003B013);川北医学院基金(No:理06-15)
摘 要:目的通过实验,以期建立一种测定穿琥宁的新方法。方法在pH4.4的酸性溶液中,取适量对照品溶液和甲基蓝溶液混合,以二次蒸馏水稀释,放置一段时间后在荧光光度计上以λem=λex方式进行同步扫描。结果甲基蓝和穿琥宁能够迅速反应生成离子缔合物,导致共振瑞利散射(RRS)光谱的改变,产生比较特征的新的RRS光谱,最大峰值在650.0nm,并且在2.0-14.0×10-5mol/L范围内,RRS强度和穿琥宁的浓度成正比。结论我们建立了测定穿琥宁的共振瑞利散射法。该法灵敏度较高,检测限达到2.65×10-5mg/L,用于检测某些穿琥宁样品中穿琥宁的含量,结果较满意。Objective We wish to find a method to determine PDS in medicine.Methods In pH 4.4 HAc-NaAc butter solution,we mixed patassium dehydroandrographolide succinate(PDS),water and Methyl blue(MB) with proper properation.After a while,we put it in Hitachi F-2500 and determined the resonance Rayleigh scattering(RRS) spectra.Results MB reacts rapidly with PDS to form complexes,which resulted in great enhancement of RRS and a new RRS spectrum.The maximum RRS peak was near 650.0nm.RRS intensity is proportional to the concentration of PDS in the range of 2.0-14.0×10-5mol/L.Conclusion We found a method to determine PDS based on our experiments.The method has high sensitivity and the detect limit(3σ) for PDS is 2.65×10^-5mg/L.The method has been used for the determination of total amounts of PDS in samples with satisfactory results.
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