Department of Chemistry, Selcuk University, Konya, Turkey.
Talanta. 2011 Dec 15;87:189-96. doi: 10.1016/j.talanta.2011.09.060. Epub 2011 Oct 1.
In this study, new xanthine biosensors, XO/Au/PVF/Pt and XO/Pt/PVF/Pt, based on electroless deposition of gold(Au) and platinum(Pt) nanoparticles on polyvinylferrocene(PVF) coated Pt electrode for detection of xanthine were presented. The amperometric responses of the enzyme electrodes were measured at the constant potential, which was due to the electrooxidation of enzymatically produced H(2)O(2). Compared with XO/PVF/Pt electrode, XO/Au/PVF/Pt and XO/Pt/PVF/Pt exhibited excellent electrocatalytic activity towards the oxidation of the analyte. Effect of Au and Pt nanoparticles was investigated by monitoring the response currents at the different deposition times and the different concentrations of KAuCl(4) and PtBr(2). Under the optimal conditions, the calibration curves of XO/Au/PVF/Pt and XO/Pt/PVF/Pt were obtained over the range of 2.5 × 10(-3) to 0.56 mM and 2.0 × 10(-3) to 0.66 mM, respectively. The detection limits were 7.5 × 10(-4)mM for XO/Au/PVF/Pt and 6.0 × 10(-4)mM for XO/Pt/PVF/Pt. The effects of interferents, the operational and the storage stabilities of the biosensors and the applicabilities of the proposed biosensors to the drug samples analysis were also evaluated.
在这项研究中,我们提出了两种基于无电镀法在聚二茂铁乙烯(PVF)修饰的铂电极上沉积金(Au)和铂(Pt)纳米粒子的新型黄嘌呤生物传感器,XO/Au/PVF/Pt 和 XO/Pt/PVF/Pt,用于检测黄嘌呤。在恒电位下测量酶电极的安培响应,这是由于酶促产生的 H(2)O(2)的电化学氧化。与 XO/PVF/Pt 电极相比,XO/Au/PVF/Pt 和 XO/Pt/PVF/Pt 对分析物的氧化表现出优异的电催化活性。通过监测不同沉积时间和不同浓度的 KAuCl(4)和 PtBr(2)下的响应电流来研究 Au 和 Pt 纳米粒子的影响。在最佳条件下,获得了 XO/Au/PVF/Pt 和 XO/Pt/PVF/Pt 的校准曲线,范围分别为 2.5 × 10(-3) 至 0.56 mM 和 2.0 × 10(-3) 至 0.66 mM。检测限分别为 XO/Au/PVF/Pt 为 7.5 × 10(-4)mM 和 XO/Pt/PVF/Pt 为 6.0 × 10(-4)mM。还评估了生物传感器的干扰物影响、操作和存储稳定性以及所提出的生物传感器在药物样品分析中的适用性。