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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 >Ultrasensitive electrochemical biosensor based on reduced graphene oxide-tetraethylene pentamine-BMIMPF6 hybrids for the detection of alpha 2,6-sialylated glycans in human serum
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Ultrasensitive electrochemical biosensor based on reduced graphene oxide-tetraethylene pentamine-BMIMPF6 hybrids for the detection of alpha 2,6-sialylated glycans in human serum

机译:基于还原性氧化石墨烯-四亚乙基五胺-BMIMPF6杂化物的超灵敏电化学生物传感器,用于检测人血清中的α2,6-唾液酸化聚糖

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摘要

In this paper, a simple, ultrasensitive and label-free electrochemical alpha 2,6-sialylated glycans biosensor based on reduced graphene oxide-tetraethylene pentamine-1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) hybrids was developed. Due to the abundance of amino groups from reduced graphene oxide-tetraethylene pentamine (rGO-TEPA) and the electrostatic interaction of BMIMPF6, bimetallic gold platinum alloy nanoparticles (AuPtNPs) were densely adsorbed onto the surface of the nanocomposite, providing a large surface area available for the immobilization of Sambucus nigra agglutinin (SNA). AuPtNPs have excellent conductivity and catalytic activity, which can promote electron transfer between the electrolyte solution and the surface of electrode and can enhance the sensitivity of biosensor. SNA, which specifically binds alpha 2,6-sialylated glycans, was covalently immobilized on AuPtNPs for specific detection of alpha 2,6-sialylated glycans in human serum. Under optimal experimental conditions, amperometric response changes were used to detect alpha 2,6-sialylated glycans with a broad linear range of 10 fg mL(-1)-1 mu g mL(-1) and a low detection limit of 3 fg mL(-1) (S/N=3). When applied to spiked serum samples, the recovery of the developed biosensor ranged from 100.8% to 101.4%, suggesting that the electrochemical biosensor would be suitable for the practical detection of alpha 2,6-sialylated glycans. (C) 2015 Elsevier B.V. All rights reserved.
机译:在本文中,基于还原的氧化石墨烯-四亚乙基五胺-1-丁基-3-甲基咪唑六氟磷酸盐(BMIMPF6)杂种,开发了一种简单,超灵敏,无标签的电化学α2,6-唾液酸化聚糖生物传感器。由于还原的氧化石墨烯-四亚乙基五胺(rGO-TEPA)中存在的大量氨基和BMIMPF6的静电相互作用,双金属金铂合金纳米颗粒(AuPtNPs)紧密吸附在纳米复合材料的表面上,从而提供了较大的表面积用于固定黑色接骨木凝集素(SNA)。 AuPtNPs具有优异的电导率和催化活性,可促进电解质溶液与电极表面之间的电子转移,并增强生物传感器的灵敏度。将特异性结合α2,6-唾液酸化聚糖的SNA共价固定在AuPtNP上,用于特异性检测人血清中的α2,6-唾液酸化聚糖。在最佳实验条件下,使用安培响应变化来检测线性范围为10 fg mL(-1)-1μg mL(-1)且检测限为3 fg mL低的α2,6-唾液酸化聚糖(-1)(S / N = 3)。当应用于加标血清样品时,开发的生物传感器的回收率为100.8%至101.4%,这表明该电化学生物传感器将适用于实际检测α2,6-唾液酸化聚糖。 (C)2015 Elsevier B.V.保留所有权利。

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