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植酸诱导的 3D 石墨烯泡沫:用于细胞释放超氧阴离子电化学检测的有效酶模拟催化剂。

3D graphene-based foam induced by phytic acid: An effective enzyme-mimic catalyst for electrochemical detection of cell-released superoxide anion.

机构信息

Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.

Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.

出版信息

Biosens Bioelectron. 2019 Jan 1;123:101-107. doi: 10.1016/j.bios.2018.06.043. Epub 2018 Jun 25.

Abstract

Here we present a new method to fabricate enzyme-mimic metal-free catalysts for electrochemical detection of superoxide anion (O) by introducing phosphate groups into graphene-based foam. Through a template-free hydrothermal process, graphene oxide (GO) was treated with different amount of phytic acid (PA) to obtain 3D porous graphene-based foam (PAGF). Characterizations demonstrate that phosphate groups were successfully modified on the surface and inter layer structure of PAGF materials and the defects and disorder degree of PAGF could be controlled by adjusting the addition of PA precursors. Meanwhile, the synthesized PAGF was successfully immobilized on screen printed carbon electrodes (SPCEs) and employed in O detection. With PA treated on graphene structure, the resulted PAGF/SPCEs exhibit distinct characteristic redox peaks, showing enzyme-mimic catalytic activity toward O dismutation. Also, the amount of modified phosphate groups has caused a considerable variety on the performance of PAGF-based electrodes. Apart from high sensitivity, wide liner range, low detection limit, good selectivity and long-term stability, our sensors also present satisfying performance in the real-time monitoring of drug-induced O released from Hela cells. The reliability of the biological measurement was further demonstrated via electron paramagnetic resonance (EPR) to characterize the released O from stimulated cells by using 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPOL) to trap the transient O. The above results indicate that our established sensors hold potential application in the real-time detection of O in biological samples.

摘要

在这里,我们提出了一种新的方法,通过在基于石墨烯的泡沫中引入磷酸盐基团来制备用于超氧阴离子 (O) 电化学检测的酶模拟无金属催化剂。通过无模板水热过程,用不同量的植酸 (PA) 处理氧化石墨烯 (GO),以获得 3D 多孔基于石墨烯的泡沫 (PAGF)。表征结果表明,磷酸盐基团成功地修饰在 PAGF 材料的表面和层间结构上,并且可以通过调节 PA 前体的添加来控制 PAGF 的缺陷和无序程度。同时,合成的 PAGF 成功地固定在丝网印刷碳电极 (SPCE) 上,并用于 O 检测。通过在石墨烯结构上处理 PA,所得的 PAGF/SPCE 表现出明显的特征氧化还原峰,显示出对 O 歧化的酶模拟催化活性。此外,修饰的磷酸盐基团的数量对基于 PAGF 的电极的性能产生了相当大的影响。除了高灵敏度、宽线性范围、低检测限、良好的选择性和长期稳定性外,我们的传感器还在实时监测 HeLa 细胞中药物诱导的 O 释放方面表现出令人满意的性能。通过电子顺磁共振 (EPR) 进一步证明了生物测量的可靠性,以使用 2,2,6,6-四甲基哌啶-1-氧基 (TEMPOL) 来捕获瞬态 O 来表征刺激细胞中释放的 O。上述结果表明,我们建立的传感器在生物样品中 O 的实时检测方面具有潜在的应用前景。

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