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首页> 外文期刊>Analytical and bioanalytical chemistry >Non-enzymatic monitoring of hydrogen peroxide using novel nanosensor based on CoFe2O4@CdSeQD magnetic nanocomposite and rifampicin mediator
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Non-enzymatic monitoring of hydrogen peroxide using novel nanosensor based on CoFe2O4@CdSeQD magnetic nanocomposite and rifampicin mediator

机译:基于COFE2O4的新型纳米传感器的非酶促监测过氧化氢的CDSEQD磁性纳米复合材料和利福平介质

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摘要

In this work, a novel strategy was introduced to develop a non-enzymatic hydrogen peroxide (H2O2) sensor based on rifampicin (RIF) electrodeposited on a polyvinylpyrrolidone (PVP)-capped CdSe quantum dot (CdSeQD), CoFe2O4 magnetic nanoparticle-modified glassy carbon electrode (CoFe2O4@CdSeQDs/RIF/GCE). CoFe2O4@CdSeQD magnetic nanocomposite (CoFe2O4@CdSeQD MNCs) was synthesized by a chemical co-precipitation method and characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). To prepare the non-enzymatic H2O2 sensor, firstly, the glassy carbon electrode surface was modified by dropping 10 mu L of 5 mg mL(-1) CoFe2O4@CdSeQD MNCs. Then, rifampicin was electrodeposited on the activated CoFe2O4@CdSeQDs/GCE by applying a potential of - 0.7 V for 400 s in pH 2.0 phosphate buffer containing 190 mu M of rifampicin. Cyclic voltammetry and electrochemical impedance spectroscopy was used to investigate the electrochemical behavior of this sensor and was used for the reduction of H2O2. Construction of the calibration plot for H2O2 was performed using an amperometric method (- 0.2 V vs. Ag/AgCl) at the modified electrode. Two linearity ranges were obtained from 7 to 145 mu M and 145 mu M to 1.43 mM with sensitivities of 143.01 mu A mM(-1) and 28.67 mu A mM(-1) for the first and second linearity ranges, respectively. The detection limit was obtained as 0.38 mu M (S/N = 3). Finally, the reliability of the nanosensor was confirmed with real sample analysis in different beverages such as juice and milk with satisfactory recovery results.
机译:在这项工作中,引入了一种新的策略,用于在聚乙烯吡咯烷酮(PVP)CdSeum Dot(CdseQD)上电沉积的利福平(RIF)基于利福平(RIF)的非酶促过氧化氢(H2O2)传感器,COFE2O4磁性纳米粒子改性玻璃碳电极(Cofe2O4 @ CDSeqds / RIF / GCE)。 Cofe2O4 @ Cdseqd磁性纳米复合材料(Cofe2O4 @ CdSeqd MNCs)通过化学共沉淀方法合成,并通过扫描电子显微镜(SEM),能量分散X射线光谱(EDX),傅里叶变换红外光谱(FTIR),和X射线衍射(XRD)。为了制备非酶促的H 2 O 2传感器,首先,通过滴加10μl5mgml(-1)cofe2O4 @ cdseqd mnc来改变玻璃碳电极表面。然后,通过在含有190μm的利福平的pH 2.0磷酸盐缓冲液中施加-0.7V的电位,在活化的COFE2O4 @ CDSeqds / GCE上电沉积利福平。使用循环伏安法和电化学阻抗光谱来研究该传感器的电化学行为并用于还原H2O2。使用改性电极的电流法( - 0.2V与Ag / AgCl)进行H 2 O 2的校准图的结构。从7至145μm和145μm至1.43mm获得两个线性范围,敏感性为143.01μmmm(-1)和28.67μmmm(-1),分别为第一和第二线性范围。获得检测极限为0.38μm(s / n = 3)。最后,在不同饮料(如果汁和牛奶)的实际样品分析中确认了纳米传感器的可靠性,饮用令人满意的恢复结果。

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