Zhao Shulin, Niu Tianxing, Song Yaru, Liu Yi-Ming
College of Chemistry and Chemical Engineering, Guangxi Normal University, Guilin, P. R. China.
Electrophoresis. 2009 Mar;30(6):1059-65. doi: 10.1002/elps.200800283.
Introducing gold nanoparticles (AuNPs) to the running buffer further improved the sensitivity of luminol-H(2)O(2) chemiluminescence (CL) detection for CE. This has led to the development of sensitive CE-CL assays of biomedically interesting compounds. Epinephrine and norfloxacin were taken as the model analytes. Epinephrine inhibited light emission from the AuNP-catalyzed CL while norfloxacin enhanced it. The CE-CL assays had detection limits of 6.9x10(-9) M for epinephrine and 7.3x10(-9) M for norfloxacin. It was noted that in the absence of AuNPs no CE-CL analytical signal was produced by epinephrine at 4.0x10(-5) M or norfloxacin at 1.5x10(-3) M under similar experimental conditions. Fluorescence spectroscopic measurements showed that although the fluorescence excitation/emission maxima remained the same, the fluorescence lifetime of luminol increased significantly in the presence of AuNPs (tau(2) increased from 8.49+/-0.12 to 9.18+/-0.047 ns in a two-exponential fit), indicating that the excited states of luminol molecules were stabilized through the interaction between luminol molecules and AuNPs. Finally, quantitation of epinephrine and norfloxacin in biological samples such as human urine by using the present AuNP-enhanced CE-CL method was demonstrated.
在运行缓冲液中引入金纳米颗粒(AuNPs)进一步提高了毛细管电泳(CE)中鲁米诺 - H₂O₂化学发光(CL)检测的灵敏度。这促使了对具有生物医学意义的化合物进行灵敏的CE - CL分析方法的开发。以肾上腺素和诺氟沙星作为模型分析物。肾上腺素抑制AuNP催化的CL发光,而诺氟沙星增强其发光。CE - CL分析方法对肾上腺素的检测限为6.9×10⁻⁹ M,对诺氟沙星的检测限为7.3×10⁻⁹ M。值得注意的是,在类似实验条件下,在没有AuNPs的情况下,4.0×10⁻⁵ M 的肾上腺素或1.5×10⁻³ M 的诺氟沙星均未产生CE - CL分析信号。荧光光谱测量表明,尽管荧光激发/发射最大值保持不变,但在AuNPs存在下,鲁米诺的荧光寿命显著增加(在双指数拟合中,τ₂从8.49±0.12增加到9.18±0.047 ns),这表明鲁米诺分子的激发态通过鲁米诺分子与AuNPs之间的相互作用而稳定。最后,展示了使用当前的AuNP增强CE - CL方法对人尿等生物样品中的肾上腺素和诺氟沙星进行定量分析。