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Inkjet-printed electrochemically reduced graphene oxide microelectrode as a platform for HT-2 mycotoxin immunoenzymatic biosensing
Biosensors and Bioelectronics ( IF 10.7 ) Pub Date : 2020-02-21 , DOI: 10.1016/j.bios.2020.112109
Jiri Kudr , Lei Zhao , Emily P. Nguyen , Henri Arola , Tarja K. Nevanen , Vojtech Adam , Ondrej Zitka , Arben Merkoçi

The design and application of an inkjet-printed electrochemically reduced graphene oxide microelectrode for HT-2 mycotoxin immunoenzymatic biosensing is reported. A water-based graphene oxide ink was first formulated and single-drop line working microelectrodes were inkjet-printed onto poly(ethylene 2,6-naphthalate) substrates, with dimensions of 78 μm in width and 30 nm in height after solvent evaporation. The printed graphene oxide microelectrodes were electrochemically reduced and characterized by Raman and X-ray photoelectron spectroscopy spectroscopies in addition to microscopies. Through optimization of the electrochemical reduction parameters, differential pulse voltammetry were performed to examine the sensing of 1-naphthol (1-N), where it was revealed that reduction times had significant effects on electrode performance. The developed microelectrodes were then used as an immunoenzymatic biosensor for the detection of HT-2 mycotoxin based on carbodiimide linking of the microelectrode surface and HT-2 toxin antigen binding fragment of antibody (anti-HT2 (10) Fab). The HT-2 toxin and anti-HT2 (10) Fab reaction was reported by anti-HT2 immune complex single-chain variable fragment of antibody fused with alkaline phosphatase (anti-IC-HT2 scFv-ALP) which is able to produce an electroactive reporter – 1-N. The biosensor showed detection limits of 1.6 ng ∙ mL−1 and a linear dynamic range of 6.3 – 100.0 ng ∙ mL−1 within a 5 min incubation with 1-naphthyl phosphate (1-NP) substrate.



中文翻译:

喷墨印刷的电化学还原氧化石墨烯微电极作为HT-2霉菌毒素免疫酶生物传感的平台

报道了喷墨印刷的电化学还原的氧化石墨烯微电极用于HT-2真菌毒素免疫酶生物传感的设计和应用。首先配制一种水性氧化石墨烯墨水,并将单滴线工作型微电极喷墨印刷到聚(2,6-萘二甲酸乙二醇酯)基底上,溶剂蒸发后的宽度为78μm,高度为30 nm。电化学还原印刷的氧化石墨烯微电极,并通过显微技术和拉曼光谱和X射线光电子能谱技术对其进行表征。通过优化电化学还原参数,执行差分脉冲伏安法检查1-萘酚(1-N)的感测,结果表明还原时间对电极性能有重大影响。然后将开发的微电极用作免疫酶生物传感器,基于微电极表面的碳二亚胺与抗体(抗HT2(10)Fab)的HT-2毒素抗原结合片段的连接来检测HT-2霉菌毒素。通过与碱性磷酸酶融合的抗体的抗HT2免疫复合物单链可变片段报道了HT-2毒素和抗HT2(10)Fab反应,该抗体能够产生电活性记者– 1-N。生物传感器的检测限为1.6 ng∙mL 通过与碱性磷酸酶融合的抗体的抗HT2免疫复合物单链可变片段报道了HT-2毒素和抗HT2(10)Fab反应,该抗体能够产生电活性记者– 1-N。生物传感器的检测限为1.6 ng∙mL 通过与碱性磷酸酶融合的抗体的抗HT2免疫复合物单链可变片段报道了HT-2毒素和抗HT2(10)Fab反应,该抗体能够产生电活性记者– 1-N。生物传感器的检测限为1.6 ng∙mL-1和磷酸1萘酯(1-NP)底物孵育5分钟后的线性动态范围为6.3 – 100.0 ng∙mL -1

更新日期:2020-02-23
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