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改性分形氧化铁磁性纳米结构:一种新型的高性能氧化还原蛋白固定化、直接电化学和生物电化学应用平台。

Modified fractal iron oxide magnetic nanostructure: A novel and high performance platform for redox protein immobilization, direct electrochemistry and bioelectrocatalysis application.

机构信息

Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Biopharmaceutics and Pharmacokinetics Division, Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 14155-6451, Iran.

出版信息

Biosens Bioelectron. 2016 Nov 15;85:814-821. doi: 10.1016/j.bios.2016.05.097. Epub 2016 Jun 3.

DOI:10.1016/j.bios.2016.05.097
PMID:27290665
Abstract

A novel biosensing platform based on fractal-pattern of iron oxides magnetic nanostructures (FIOMNs) and mixed hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for the magnetic immobilization of hemoglobin (Hb) at a screen printed carbon electrode (SPCE). The FIOMNs was successfully synthesized through hydrothermal approach and characterized by atomic force microscopy (AFM), scanning electron microscopy (SEM) and X-ray diffraction (XRD). In order to provide guidelines for the mixed hemi/ad-micelle formation, zeta-potential isotherms were investigated. The construction steps of the biosensor were evaluated by electrochemical impedance spectroscopy, cyclic voltammetry and Fourier transform infrared spectroscopy. Direct electron transfer of Hb incorporated into the biocomposite film was realized with a pair of quasi-reversible redox peak at the formal potential of -0.355V vs. Ag/AgCl attributing to heme Fe(III)/Fe(II) redox couple. The results suggested that synergistic functions regarding to the hyper-branched and multidirectional structure of FIOMNs and the dual interaction ability of mixed hemi/ad-micelle array of SDS molecules not only induce an effective electron transfer between the Hb and the underlying electrode (high heterogeneous electron transfer rate constant of 2.08s(-1)) but also provide powerful and special microenvironment for the adsorption of the redox proteins. Furthermore, the biosensor displayed an excellent performance to the electrocatalytic reduction of H2O2 with a detection limit of 0.48µM and Michaelis-Menten constant (Km) value of 44.2µM. The fabricated biosensor represented the features of sensitivity, disposable design, low sample volume, rapid and simple preparation step, and acceptable anti-interferences, which offer great perspectives for the screen-determination of H2O2 in real samples.

摘要

基于氧化铁磁性纳米结构(FIOMNs)分形图案和混合的半胶束/混合胶束的新型生物传感平台被设计用于血红蛋白(Hb)在丝网印刷碳电极(SPCE)上的磁性固定。FIOMNs 通过水热法成功合成,并通过原子力显微镜(AFM)、扫描电子显微镜(SEM)和 X 射线衍射(XRD)进行了表征。为了提供混合的半胶束/混合胶束形成的指导原则,研究了 zeta 电位等电点。通过电化学阻抗谱、循环伏安法和傅里叶变换红外光谱评估了生物传感器的构建步骤。嵌入生物复合材料薄膜中的 Hb 的直接电子转移在形式电位为-0.355V 相对于 Ag/AgCl 时实现了一对准可逆氧化还原峰,归因于血红素 Fe(III)/Fe(II)氧化还原对。结果表明,FIOMNs 的超支化和多方向结构以及 SDS 分子混合的半胶束/混合胶束阵列的双重相互作用能力的协同功能不仅在 Hb 和基础电极之间诱导了有效的电子转移(高的异质电子转移速率常数为 2.08s(-1)),而且为氧化还原蛋白的吸附提供了强大和特殊的微环境。此外,该生物传感器对 H2O2 的电催化还原表现出优异的性能,检测限为 0.48µM,米氏常数(Km)值为 44.2µM。所制备的生物传感器具有灵敏度高、一次性设计、样品体积小、快速简单的制备步骤和可接受的抗干扰能力等特点,为实际样品中 H2O2 的筛选测定提供了广阔的前景。

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