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基于氮掺杂石墨烯量子点的电化学发光适体传感器用于检测凝血酶。

Electrochemiluminescent aptasensor for thrombin using nitrogen-doped graphene quantum dots.

机构信息

State Key Laboratory of Fine Chemicals, Dalian University of Technology, No. 2, Linggong Road, Ganjingzi District, Dalian, 116023, China.

Key Laboratory of Xinjiang Endemic Phytomedicine Resources, Ministry of Education, School of Pharmacy, Shihezi University, Shihezi, 832000, China.

出版信息

Mikrochim Acta. 2018 Aug 24;185(9):430. doi: 10.1007/s00604-018-2942-z.

Abstract

An electrochemiluminescent (ECL) aptamer based method is described for the determination of thrombin. Three-dimensional nitrogen-doped graphene oxide (3D-NGO) was placed on a glassy carbon electrode (GCE) to provide an electrode surface that displays excellent electrical conductivity and acts as a strong emitter of ECL. The modified electrode was further coated with chitosan via electrodeposition. Finally, the amino-modified aptamer was immobilized on the modified GCE. The interaction between thrombin and aptamer results in a decrease in ECL. The assay has a linear response in the 1 fM to 1 nM thrombin concentration range and a 0.25 fM lower detection limit (at an S/N ratio of 3). The method was applied to the determination of thrombin in spiked human plasma samples, and recoveries ranged between 94 and 105% (with RSDs of <3.6%). The calibration plot was recorded at potential and wavelength of fluorescence emission (wavelength: 445 nm; potential: 0 to -2 V). Graphical abstract A bare glassy carbon electrode (GCE) does not display electrochemiluminescence (ECL). If, however, nitrogen-doped graphene quantum dots, chitosan, and three-dimensional nitrogen-doped graphene oxide (NGQD-chitosan/3D-NGO) are electrodeposited on the GCE, strong ECL can be observed. The ECL intensity decreased after aptamer and bovine serum albumin (BSA) were dropped onto the electrode (curve a). However, the ECL further decreases after addition of thrombin (TB; curve b).

摘要

一种基于电化学发光(ECL)适体的方法被用来测定凝血酶。将三维氮掺杂石墨烯氧化物(3D-NGO)置于玻碳电极(GCE)上,提供一个具有优异导电性的电极表面,并作为 ECL 的强发射器。通过电沉积进一步在修饰电极上涂覆壳聚糖。最后,将氨基修饰的适体固定在修饰的 GCE 上。凝血酶与适体的相互作用导致 ECL 降低。该测定法在 1 fM 至 1 nM 凝血酶浓度范围内呈线性响应,检测下限为 0.25 fM(信噪比为 3)。该方法被应用于测定加标人血浆样品中的凝血酶,回收率在 94%至 105%之间(相对标准偏差小于 3.6%)。校准曲线是在荧光发射的电位和波长(波长:445 nm;电位:0 至-2 V)下记录的。

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