Ghaedamini Hamidreza, Kim Dong-Shik
Department of Chemical Engineering, University of Toledo, Toledo, OH 43606, USA.
Department of Chemical Engineering, University of Toledo, Toledo, OH 43606, USA.
Bioelectrochemistry. 2025 Feb;161:108823. doi: 10.1016/j.bioelechem.2024.108823. Epub 2024 Sep 21.
This study presents the development of a novel non-enzymatic electrochemical biosensor for the real-time detection of hydrogen peroxide (HO) based on a composite of cerium metal-organic frameworks (Ce-MOFs), hemin, and graphene oxide (GO). The Ce-MOFs served as an efficient matrix for hemin encapsulation, while GO enhanced the conductivity of the composite. Characterization techniques including scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, UV-vis spectroscopy, and thermogravimetric analysis (TGA) confirmed the successful integration of hemin into the Ce-MOFs. The Ce-MOFs@hemin/GO-modified sensor demonstrated sensitive HO detection due to the exceptional electrocatalytic activity of Ce-MOFs@hemin and the high conductivity of GO. This biosensor exhibited a linear response to HO concentrations from 0.05 to 10 mM with a limit of detection (LOD) of 9.3 μM. The capability of the biosensor to detect HO released from human prostate carcinoma cells was demonstrated, highlighting its potential for real-time monitoring of cellular oxidative stress in complex biological environments. To further assess its practical applicability, the sensor was tested in human serum samples, yielding promising results with recovery values ranging from 94.50 % to 103.29 %. In addition, the sensor showed excellent selectivity against common interfering compounds due to the outstanding peroxidase-like activity of the composite.
本研究展示了一种基于铈金属有机框架(Ce-MOFs)、血红素和氧化石墨烯(GO)复合材料的新型非酶电化学生物传感器的开发,用于实时检测过氧化氢(HO)。Ce-MOFs作为血红素封装的有效基质,而GO提高了复合材料的导电性。包括扫描电子显微镜(SEM)、X射线衍射(XRD)、傅里叶变换红外(FTIR)光谱、紫外可见光谱和热重分析(TGA)在内的表征技术证实了血红素成功整合到Ce-MOFs中。Ce-MOFs@血红素/GO修饰的传感器由于Ce-MOFs@血红素的优异电催化活性和GO的高导电性而表现出对HO的灵敏检测。该生物传感器对HO浓度在0.05至10 mM范围内呈现线性响应,检测限(LOD)为9.3 μM。证明了该生物传感器检测人前列腺癌细胞释放的HO的能力,突出了其在复杂生物环境中实时监测细胞氧化应激的潜力。为了进一步评估其实际适用性,该传感器在人血清样本中进行了测试,回收率在94.50%至103.29%之间,结果令人满意。此外,由于复合材料具有出色的过氧化物酶样活性,该传感器对常见干扰化合物表现出优异的选择性。