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利用改良的辣根过氧化物酶基生物传感器测量水辐射分解产生的过氧化氢作为替代剂量测定方法。

Measuring hydrogen peroxide due to water radiolysis using a modified horseradish peroxidase based biosensor as an alternative dosimetry method.

机构信息

Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran; Department of Physiology and Biophysics, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Bioelectrochemistry. 2015 Aug;104:79-84. doi: 10.1016/j.bioelechem.2015.03.006. Epub 2015 Apr 8.

Abstract

H2O2 generated during water radiolysis was measured electrochemically as an alternative dosimetry method. A biosensor was fabricated by immobilising modified horseradish peroxidase (HRP) on a glassy carbon electrode (GCE) followed by evaluation of its analytical parameters. Anthraquinone 2-carboxylic acid was used to modify HRP. To assess sensor performance, phosphate buffer solutions were irradiated with 0.510 Gy of gamma ray emitted from (60)Co. The results showed that this sensor can detect low quantities of hydrogen peroxide in water radiolysis. Sensitivity, detection limit and linear range of the biosensor were 260 nA/Gy, 0.392 Gy and 0.5-5 Gy, respectively. Long term stability studies showed that sensor responses were stable for at least a month. The cathodic peak current, as biosensor response, subsequently decreased to 20% of its initial value.

摘要

水辐解过程中产生的 H2O2 可以通过电化学方法测量,作为替代剂量测定方法。通过将修饰辣根过氧化物酶(HRP)固定在玻碳电极(GCE)上来制备生物传感器,然后评估其分析参数。蒽醌-2-羧酸用于修饰 HRP。为了评估传感器的性能,用(60)Co 发射的 0.510 Gyγ射线辐照磷酸盐缓冲溶液。结果表明,该传感器可以检测水辐解过程中低浓度的过氧化氢。生物传感器的灵敏度、检测限和线性范围分别为 260 nA/Gy、0.392 Gy 和 0.5-5 Gy。长期稳定性研究表明,传感器的响应至少在一个月内保持稳定。作为生物传感器响应的阴极峰电流随后降低到初始值的 20%。

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