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_____________________________________________________________ Results and Discussion<br />

Figure 3.29. Nyquist plots with typical Rct values obtained by comparing the potentialassisted<br />

immobilization method with immobilization performed by simple incubation or<br />

supported by applying a constant potential. MCH passivation was done by incubation for<br />

19 h at 37 °C.<br />

Besides the ability of the potential-assisted immobilization method to tremendously accelerate<br />

the immobilization kinetics and to achieve much higher DNA coverages in a shorter time as<br />

compared to the incubation method or applications of constant potentials, a high reproducibility<br />

of the surface modification needs to be attained. Figure 3.30 presents average Rct values<br />

obtained with the potential-assisted immobilization method using different pulse profiles. In all<br />

cases Rct values are obtained with a standard deviation below 5 %, showing that the developed<br />

immobilization protocol leads to a highly reproducible surface modification. Thus, the<br />

envisaged ssDNA surface coverage can be pre-selected by choosing the number of applied<br />

potential pulse cycles.<br />

Looking at the results presented in this chapter it can be concluded that understanding the<br />

behavior of ssDNA in front of the electrode surface affected by the surrounding electrolyte and<br />

the polarization of the electrode is essential for the development of highly reproducible DNAmodified<br />

surfaces. The developed potential pulse-assisted immobilization strategy leads to<br />

high-quality DNA-modified surfaces helping by this to overcome difficulties in DNA sensor<br />

3.3 Importance of controlling the surface 65

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