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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Enhancing sensitivity and selectivity in a label-free colorimetric sensor for detection of iron(II) ions with luminescent molybdenum disulfide nanosheet-based peroxidase mimetics
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Enhancing sensitivity and selectivity in a label-free colorimetric sensor for detection of iron(II) ions with luminescent molybdenum disulfide nanosheet-based peroxidase mimetics

机译:利用基于二硫化钼纳米片的过氧化物酶模拟物提高用于检测铁离子的无标记比色传感器的灵敏度和选择性

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摘要

In the present study, we demonstrated that the luminescent molybdenum disulfide (MoS2) nanosheets, which were prepared hydrothermally by using sodium molybdate and thiourea as precursors, possessed peroxidase-like activity, and could catalyze the oxidation of peroxidase substrate o-phenylenediamine (OPD) in the presence of hydrogen peroxide (H2O2) to produce a yellow color reaction. Further addition of Fe2+ into the nanosheets led to peroxidase mimetics with greatly enhanced catalytic activity. The observation was exploited to develop a label-free colorimetric nanozyme sensor for detection of Fe2+. The fabricated MoS2/OPD/H2O2 sensor showed a wide linear range of 0.01-0.8 mu M with a detection limit of 7 nM. Moreover, it was found that the MoS2/OPD/H2O2 sensor displayed enhanced sensitivity and selectivity toward Fe2+ compared with the OPD/H2O2 sensor, suggesting that the MoS2 nanosheets could improve the performance of the Fe2+ sensor. An advanced chemometrics algorithm, multivariate curve resolution by alternating least squares (MCR-ALS), was further applied to interpret the origin of enhancing sensitivity and selectivity in the Fe2+ sensor with the MoS2 nanosheets. The time-dependent UV-vis spectral data of the studied systems were collected, and submitted to the MCR-ALS. The results showed that the increased sensitivity and selectivity of the MoS2/OPD/H2O2 sensor for Fe2+ detection likely arose from its large reaction rate constant. Finally, the proposed MoS2/OPD/H2O2 sensor was successfully applied for detection of Fe2+ in water samples. (C) 2016 Elsevier B.V. All rights reserved.
机译:在本研究中,我们证明了以钼酸钠和硫脲为前体水热制备的发光二硫化钼(MoS2)纳米片具有类似过氧化物酶的活性,并且可以催化过氧化物酶底物邻苯二胺(OPD)的氧化。在过氧化氢(H2O2)存在下产生黄色反应。将Fe 2+进一步添加到纳米片中导致过氧化物酶模拟物具有大大增强的催化活性。利用该观察结果开发了用于检测Fe2 +的无标记比色纳米酶传感器。制成的MoS2 / OPD / H2O2传感器显示0.01-0.8μM的宽线性范围,检测极限为7nM。此外,发现与OPD / H2O2传感器相比,MoS2 / OPD / H2O2传感器显示出更高的对Fe2 +的灵敏度和选择性,这表明MoS2纳米片可以改善Fe2 +传感器的性能。先进的化学计量学算法,即通过交替最小二乘进行的多变量曲线分辨率(MCR-ALS),进一步用于解释MoS2纳米片增强Fe2 +传感器中灵敏度和选择性的起源。收集了所研究系统随时间变化的紫外可见光谱数据,并将其提交给MCR-ALS。结果表明,MoS2 / OPD / H2O2传感器对Fe2 +的检测灵敏度和选择性都有所提高,这是由于其较大的反应速率常数所致。最终,所提出的MoS2 / OPD / H2O2传感器成功应用于水样中Fe2 +的检测。 (C)2016 Elsevier B.V.保留所有权利。

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