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用于电化学DNA杂交检测的石墨烯-PAMAM树枝状大分子-金纳米颗粒复合材料

Graphene-PAMAM dendrimer-gold nanoparticle composite for electrochemical DNA hybridization detection.

作者信息

Jayakumar Kumarasamy, Rajesh Rajendiran, Dharuman Venkataraman, Venkatesan Rangarajan

机构信息

Molecular Electronics Lab, Department of Bioelectronics and Biosensors, Alagappa University, Karaikudi, India.

出版信息

Methods Mol Biol. 2013;1039:201-19. doi: 10.1007/978-1-62703-535-4_17.

Abstract

Graphene oxide is chemically functionalized using planar structured first generation polyamidoamine dendrimer (G1PAMAM) to form graphene core GG1PAMAM. The monolayer of GG1PAMAM is anchored on the 3-mercapto propionic acid monolayer pre-immobilized onto a gold transducer. The GG1PAMAM is decorated using gold nanoparticles for the covalent attachment of single-stranded DNA through simple gold-thiol chemistry. The single- and double-stranded DNAs are discriminated electrochemically in the presence of redox probe K3[Fe(CN)6]. Double-stranded-specific intercalator methylene blue is used to enhance the lower detection limit. The use of linear and planar G1PAMAM along with the graphene core has enhanced the detection limit 100 times higher than the G1PAMAM with the conventional ethylene core. This chapter presents the details of GG1PAMAM preparation and application to DNA sensing by electrochemical methods.

摘要

使用平面结构的第一代聚酰胺-胺树枝状大分子(G1PAMAM)对氧化石墨烯进行化学功能化,以形成石墨烯核心GG1PAMAM。GG1PAMAM的单层固定在预先固定在金传感器上的3-巯基丙酸单层上。使用金纳米颗粒对GG1PAMAM进行修饰,以便通过简单的金-硫醇化学方法实现单链DNA的共价连接。在氧化还原探针K3[Fe(CN)6]存在的情况下,通过电化学方法区分单链和双链DNA。使用双链特异性嵌入剂亚甲蓝来提高检测下限。线性和平面对称的G1PAMAM与石墨烯核心的结合使检测限比具有传统乙烯核心的G1PAMAM提高了100倍。本章详细介绍了GG1PAMAM的制备及其在电化学DNA传感中的应用。

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