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Reduced graphene oxide/polyethylenimine based immunosensor for the selective and sensitive electrochemical detection of uropathogenic Escherichia coli

机译:还原型氧化石墨烯/聚乙烯亚胺基免疫传感器,用于选择性和灵敏地检测尿路致病性大肠杆菌

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Fast, reliable and selective detection of microorganisms is of uttermost importance in clinical analysis, but also in food and water quality monitoring. In this study, we report on the construction of an immunosensor for sensitive and selective electrochemical detection of uropathogenicEscherichia coli(E. coli) UTI89 bacteria in aqueous and serum samples. We took benefit of electrophoretic deposition (EPD) to prepare, in a simple, controllable and cost effective way, gold electrodes modified with thin active layers of reduced graphene oxide/polyethylenimine (rGO/PEI). While rGO exhibits high surface area and favourable electrochemical properties, the presence of abundant NH2groups on PEI offers a plethora of opportunities for the sensor’s surface functionalization. To achieve selectivity of detection, the electrode surface was covalently modified with anti-fimbrialE. coliantibodiesviaamide bond formation. To minimize non-specific adsorption, the immunosensor was additionally modified with pyrene-polyethyleneglycol (pyrene-PEG) moieties prior to antibody immobilization. The detection ofE. coliwas based on the restriction of electron transfer of a redox mediator, in our case potassium ferrocyanide, to the rGO/PEI modified electrical transducer due to the formation of an immune complex. The developed immunosensor displayed a sigmoidal shape with a linear range of 1 × 101–1 × 104 cfu mL−1(R2 = 0.995) according toi(μA) = −16.66–20.5 × log[E. coli] (cfu mL−1) and a detection limit of 10 cfu mL−1. Additionally, the sensor performed well both in aqueous, serum and urine media, which is essential for its potential use for clinical diagnosis of pathogenic diseases. Selectivity studies showed that the immunosensor was able to discriminate betweenE. coliUTI89 wild-type strain and UTI89Δfim,without fim operon.
机译:快速,可靠和选择性的微生物检测在临床分析以及食品和水质监测中至关重要。在这项研究中,我们报告了一种用于敏感和选择性电化学检测水性和血清样品中尿路致病性大肠杆菌UTI89细菌的免疫传感器的构建。我们利用电泳沉积(EPD)的优势,以一种简单,可控且具有成本效益的方式来制备金电极,该电极被还原的氧化石墨烯/聚乙烯亚胺(rGO / PEI)的薄活性层改性。尽管rGO具有较高的表面积和良好的电化学性能,但PEI上大量的NH2基团的存在为传感器的表面功能化提供了很多机会。为了实现检测的选择性,电极表面用anti-fimbrialE共价修饰。 coliantibodiesviaamide键形成。为了最小化非特异性吸附,在固定抗体之前,还用pyr-聚乙二醇(glyc-PEG)部分修饰了免疫传感器。 E的检测。大肠埃希菌的形成是基于由于形成免疫复合物而限制了氧化还原介体(在我们的情况下为亚铁氰化钾)向rGO / PEI修饰的电换能器的电子转移。根据[μA] displayed = −16.66–20.5×log [E],已开发的免疫传感器呈S形,线性范围为1×101–1×104 cfu mL-1(R2 = 0.995)。大肠埃希菌(cfu / mL-1)的检出限为10 / cfu / mL-1。此外,该传感器在水性,血清和尿液介质中均表现良好,这对于其潜在地用于病原性疾病的临床诊断至关重要。选择性研究表明免疫传感器能够区分E。没有fim操纵子的coliUTI89野生型菌株和UTI89Δfim。

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