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首页> 外文期刊>Nanoscale >Tailoring pore structures with optimal mesopores to remarkably promote DNA adsorption guiding the growth of active Mn-3(PO4)(2) toward sensitive superoxide biomimetic enzyme sensors
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Tailoring pore structures with optimal mesopores to remarkably promote DNA adsorption guiding the growth of active Mn-3(PO4)(2) toward sensitive superoxide biomimetic enzyme sensors

机译:裁剪与最优间隙孔孔隙结构显著促进DNA吸附指导增长的活跃Mn-3 (PO4)(2)敏感过氧化物酶仿生传感器

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The great challenge in preparing a biomimetic enzyme sensor is to have sensitivity and selectivity equal to or better than its corresponding biological sensor. Porous electrodes possess a large surface area and are often used to greatly improve the sensor sensitivity. However, how to tailor the pore structure, especially the pore size distribution to further improve the sensitivity and selectivity of a biomimetic sensor, has not been investigated yet. The superoxide anion (O-2(-)) plays essential roles in various biological processes and is of importance in clinical diagnosis and life science research. It is generally detected by the superoxide dismutase enzyme. Herein, we delicately tailor the pore structure of carbon nanofibers (CNFs) by pyrolysis to obtain an optimal mesopore structure for strong adsorption of DNA, followed by guiding the growth of Mn-3(PO4)(2) as a biomimetic enzyme toward highly sensitive detection of O-2(-). The Mn-3(PO4)(2)-DNA/CNF sensor achieves the best sensitivity among the reported O-2(-) sensors while possessing good selectivity. The enhancement mechanism is also investigated, indicating that the mesopore ratio of CNFs plays an essential role in the high sensitivity and selectivity due to their strong adsorption of DNA for guiding the growth of a large amount of uniform sensing components, Mn-3(PO4)(2), toward high sensitivity and selectivity. The biomimetic sensor was further used to in situ monitor O-2(-) released from human keratinocyte cells and human malignant melanoma cells under drug stimulation, showing high sensitivity to real-time quantitative detection of O-2(-). This work provides a highly sensitive in situ real-time biomimetic O-2(-) sensor for applications in biological research and diagnosis, while shedding light on the enhancement mechanism of the pore structure, especially the pore size distribution of a porous electrode for high performance sensing processes.
机译:准备一个仿生的巨大的挑战酶传感器灵敏度和选择性等于或比它更好相应的生物传感器。电极具有大的表面积和常用于大大提高传感器敏感度。结构,特别是孔隙大小分布为了进一步提高灵敏度和选择性的仿生传感器,没有然而调查。在各种生物中扮演至关重要的角色流程和临床重要性诊断和生命科学研究。一般检测超氧化物歧化酶酶。纳米碳纤维的结构(cnf)热解获得一个最优的中孔结构强劲吸附DNA,紧随其后的是指导的增长Mn-3 (PO4)作为仿生酶(2)对高度敏感检测0 2(-)。Mn-3 (PO4) (2) dna / CNF传感器达到最好的敏感性报道中0 2(-)传感器同时具有良好的选择性。增强机理也进行调查,表明cnf扮演的中孔率在高灵敏度和不可或缺的作用由于其强大的吸附选择性的DNA指导大量的增长统一的传感组件,Mn-3 (PO4)(2),方向高灵敏度和选择性。传感器被进一步用于原位监测0 2 (-)从人类细胞角化细胞和释放恶性黑色素瘤细胞在药物的刺激下,实时显示高灵敏度定量检测0 2(-)。提供了一个高度敏感的原位实时仿生0 2(-)传感器的应用生物研究和诊断,而脱落孔隙的增强机制结构,特别是孔隙大小分布多孔电极的高性能感应过程。

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