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使用 PdAu-PPy 修饰的碳纤维纸电极电化学传感维生素 B 缺乏标志物甲基丙二酸。

Electrochemical sensing of vitamin B deficiency marker methylmalonic acid using PdAu-PPy tailored carbon fiber paper electrode.

机构信息

Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bengaluru, 560029, India.

Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bengaluru, 560029, India.

出版信息

Talanta. 2020 Sep 1;217:121028. doi: 10.1016/j.talanta.2020.121028. Epub 2020 Apr 14.

Abstract

Vitamin B is very important for human metabolism and its deficiency can cause anemia and the production of large red blood cells. An increased concentration of methylmalonic acid (MMA) is detected much before the transformation of blood cells, which thereby is an early indicator for mild or serious Vitamin B deficiency. A simple electrochemical sensor based on Palladium-Gold (PdAu) was developed by electrodeposition of PdAu nanoparticles on Polypyrrole (PPy) modified carbon fiber paper (CFP) electrode. The modified electrodes were characterized by High resolution transmission electron microscopy (HRTEM), Field emission scanning electron microscopy (FESEM) with energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electroanalytical techniques. Differential Pulse Voltammetric (DPV) studies have established that under optimum conditions, the developed sensor exhibits a broad linear dynamic range (4.01 pM - 52.5 nM) with a very low detection limit (1.32 pM). The proposed method was effectively applied in the non-enzymatic determination of MMA at an ultralow level in human blood serum and urine samples. The method displayed high selectivity toward MMA in the presence of other interfering substances.

摘要

维生素 B 对人类新陈代谢非常重要,其缺乏会导致贫血和大红细胞的产生。甲基丙二酸(MMA)的浓度升高在血细胞转化之前就被检测到,因此它是轻度或严重维生素 B 缺乏的早期指标。通过在聚吡咯(PPy)修饰的碳纤维纸(CFP)电极上电沉积钯金(PdAu)纳米粒子,开发了一种基于钯金的简单电化学传感器。通过高分辨率透射电子显微镜(HRTEM)、场发射扫描电子显微镜(FESEM)与能量色散 X 射线光谱(EDS)、X 射线衍射(XRD)、X 射线光电子能谱(XPS)和电化学技术对修饰电极进行了表征。差分脉冲伏安法(DPV)研究表明,在最佳条件下,所开发的传感器在 4.01 pM - 52.5 nM 的宽线性动态范围内表现出非常低的检测限(1.32 pM)。该方法在人血清和尿液样本中超低水平的 MMA 非酶测定中得到了有效应用。该方法在存在其他干扰物质的情况下对 MMA 表现出高选择性。

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