Highly sensitive label free electrochemical detection of VGEF165 tumor marker based on "signal off" and "signal on" strategies using an anti-VEGF165 aptamer immobilized BSA-gold nanoclusters/ionic liquid/glassy carbon electrode

被引:86
|
作者
Shamsipur, Mojtaba [1 ]
Farzin, Leila [2 ]
Tabrizi, Mahmoud Amouzadeh [1 ]
Molaabasi, Fatemeh [3 ]
机构
[1] Razi Univ, Dept Chem, Kermanshah, Iran
[2] Univ Tehran, Sch Chem, Dept Analyt Chem, Coll Sci, Tehran, Iran
[3] Tarbiat Modares Univ, Dept Chem, Tehran, Iran
来源
关键词
Electrochemical aptasensor; VEGF(165); BSA-nananoclusters; Differential pulse voltammetry; Impedimetry; ENDOTHELIAL GROWTH-FACTOR; APTASENSOR; DNA; NANOPARTICLES; VEGF; NANOCOMPOSITE; RECEPTORS; BIOSENSOR; BIOMARKER; SENSOR;
D O I
10.1016/j.bios.2015.06.079
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, a label free electrochemical aptasensor for the detection of ultra-traces of vascular endothelial growth factor (VEGF(165)) based on "signal off" and "signal on" mechanisms of response was developed. The BSA-gold nanoclusters/ionic liquid (BSA-AuNCs/IL) was used as a suitable nanocomposite platform for immobilization of the aptamer on a glassy carbon electrode. In "signal off" mechanism, the interaction of VEGF(165) with its anti-VEGF(165) aptamers, resulted in desorption of methylene blue (MB) probe from aptamer and its release into solution. Consequently, the decrease in current intensity of the differential pulse voltammogram of adsorbed MB was monitored and found to be linearly proportional with increasing concentration of VEGF(165) in sample solution in the range of 1-120 pM with a limit of detection of 0.32 pM. While, in "signal on" mechanism, the interaction of immobilized anti-VEGF(165) aptamers on the electrode surface with VEGF(165), led to more mass-transfer limiting of the [Fe(CN)(6)](3-/4-) probe to the electrode surface. Therefore, the charge transfer resistance (R-ct) of the probe was increased linearly with increasing concentration of VEGF(165) in the range of 2.5-250 pM with a limit of detection of 0.48 pM. The experimental results demonstrated that both of these mechanisms are suitable for determination of low levels of the VEGF(165) tumor marker in serum samples. (C) 2015 Elsevier B.V. All rights reserved.
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页码:369 / 375
页数:7
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