| نویسندگان | حسینعلی رفیعی پور,محسن بهپور,مهین کشاورز |
| نشریه | Journal of Nanostructures |
| شماره صفحات | 235 |
| شماره مجلد | 6 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2016-06-11 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | ISI ,ISC ,SID ,Inspec |
چکیده مقاله
Over the past years, DNA biosensors have been developed to analyze DNA
interaction and damage that have important applications in biotechnological
researches. The immobilization of DNA onto a substrate is one key step for
construction of DNA electrochemical biosensors. In this report, a direct
approach has been described for immobilization of single strand DNA
onto carboxylic acid-functionalized carbon nanotubes modified glassy
carbon electrode. To do this, we first modified the glassy carbon electrode
surface with MWCNT-COOH. The immersion of MWCNT-COOH/
GCE in ss-DNA probe solution, with different pH and ionic strength, was
followed by suitable interaction between amine group of ss-DNA bases and
carboxylic groups of MWCNT-COOH. This interaction leads to successful
ss-DNA immobilization on MWCNT-COOH that was confirmed by
cyclic voltammetry, electrochemical impedance spectroscopy and atomic
force microscopy. Immobilization of ss-DNA on the modified electrode
increased the charge transfer resistant but decreased the peak current of
redox probe ([Fe(CN)6]3-/4-). The result of cyclic voltammograms implicates
that enhancements in the DNA immobilization are possible by adroit choice
of low pH and high ionic strength. The standard free-energy of adsorption
(ΔG°ads) was calculated from electrochemical impedance spectroscopy data
(-47.75 kJ mol-1) and was confirmed covalent bond formation. atomic force
microscopy topographic images demonstrate increased surface roughness
after ss-DNA immobilization. Results offer a simple, rapid and low-cost
of DNA immobilization strategy can be opportunities to design of novel
nucleic acid biosensors.