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基于中空CoNi-LDH@肌酐印迹聚甲基丙烯酸(i-PMA)复合材料的高性能一次性肌酐电化学传感器。

High-performance disposable electrochemical sensors for creatinine derived from hollow CoNi-LDH@Creatinine-imprinted Poly(methacrylic acid) (i-PMA) composites.

作者信息

Faheem Muhammad, Saddique Zohaib, Akhter Toheed, Wang Kun, Qian Jing, Gu Wuyan, Afzal Adeel, Long Lingliang

机构信息

School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, Jiangsu, 212013, PR China.

Sensors and Diagnostic Lab, School of Chemistry, University of the Punjab, Quaid-i-Azam Campus, Lahore, 54590, Pakistan.

出版信息

Anal Chim Acta. 2025 Apr 8;1346:343768. doi: 10.1016/j.aca.2025.343768. Epub 2025 Feb 3.

Abstract

BACKGROUND

Layered double hydroxides (LDHs), featuring a 2D layered structure, are an emerging class of inorganic porous materials for electrochemical biosensors. Presently, they are primarily utilized in the electrochemical detection of oxygen-containing biomolecules. However, there are currently no reported LDH sensors, particularly CoNi-LDH ones, designed for the electrochemical detection of creatinine (Cre), a widely studied nitrogen-containing biomolecule. Here, to realize electrochemical detection of creatinine, a unique hollow CoNi-LDH/creatinine imprinted polymethacrylic acid (H-LDH@i-PMA) composite is developed through a pioneering combination of a hollow CoNi-LDH (H-LDH) structure and the molecular imprinting polymer (MIP) coating technique.

RESULTS

The materials are comprehensively characterized using FT-IR, PXRD, XPS, TEM, CV, and EIS. Disposable Au-screen printed electrodes are fabricated with both H-LDH and H-LDH@i-PMA, and the sensing of Cre is subsequently investigated via cyclic voltammetry and differential pulse voltammetry methods. The H-LDH@i-PMA sensor exhibits superior porosity, a larger electroactive area, and enhanced electron-transfer kinetics in comparison to H-LDH sensor. The H-LDH@i-PMA sensor achieves a wide detection range of 0-1000 nM, accompanied by a low detection limit of 236 pM, and five-times more sensitivity for Cre than non-imprinted H-LDH sensor. Futhermore, it demonstrates robust selectivity against interferents such as ascorbic acid, uric acid, guanine, and glutamine. When tested with real salivary samples, it exhibits a recovery rate of 99.0 ± 1.80 %, and maintains excellent reusability over a period of four weeks.

SIGNIFICANCE

These exceptional results are due to superior electroactive area, tailor-made recognition sites, and greater electron-transfer kinetics of H-LDH@i-PMA as compared to the non-imprinted LDH sensor. This is the first reported use of an LDH-based sensor for the detection of Cre, providing valuable insights into developing high-performance electrochemical sensors for various biomolecules.

摘要

背景

层状双氢氧化物(LDHs)具有二维层状结构,是一类新兴的用于电化学生物传感器的无机多孔材料。目前,它们主要用于含氧化生物分子的电化学检测。然而,目前尚无报道用于电化学检测肌酐(Cre)的LDH传感器,特别是CoNi-LDH传感器,肌酐是一种经过广泛研究的含氮生物分子。在此,为实现肌酐的电化学检测,通过将中空CoNi-LDH(H-LDH)结构与分子印迹聚合物(MIP)涂层技术开创性地结合,开发出一种独特的中空CoNi-LDH/肌酐印迹聚甲基丙烯酸(H-LDH@i-PMA)复合材料。

结果

使用傅里叶变换红外光谱(FT-IR)、粉末X射线衍射(PXRD)、X射线光电子能谱(XPS)、透射电子显微镜(TEM)、循环伏安法(CV)和电化学阻抗谱(EIS)对材料进行了全面表征。用H-LDH和H-LDH@i-PMA制备了一次性金丝网印刷电极,随后通过循环伏安法和差分脉冲伏安法研究了对Cre的传感性能。与H-LDH传感器相比,H-LDH@i-PMA传感器具有更高的孔隙率、更大的电活性面积和增强的电子转移动力学。H-LDH@i-PMA传感器实现了0-1000 nM的宽检测范围,检测限低至236 pM,对Cre的灵敏度是非印迹H-LDH传感器的五倍。此外,它对诸如抗坏血酸、尿酸、鸟嘌呤和谷氨酰胺等干扰物表现出强大的选择性。在用真实唾液样本进行测试时,其回收率为99.0±1.80%,并在四周内保持优异的可重复使用性。

意义

这些优异的结果归因于与非印迹LDH传感器相比,H-LDH@i-PMA具有更高的电活性面积、量身定制的识别位点和更大的电子转移动力学。这是首次报道使用基于LDH的传感器检测Cre,为开发用于各种生物分子的高性能电化学生物传感器提供了有价值的见解。

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