A microfluidic-based electrochemical biochip for label-free diffusion-restricted DNA hybridization analysis
DNA hybridization detection in microfluidic devices can reduce sample volumes, processing times, and can be integrated with other measurements. However, as device footprints decrease and their complexity increase, the signal-to-noise ratio in these systems also decreases and the sensitivity is there...
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Veröffentlicht in: | Biosensors & bioelectronics 2012-10, Vol.38 (1), p.114-120 |
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Sprache: | eng |
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Zusammenfassung: | DNA hybridization detection in microfluidic devices can reduce sample volumes, processing times, and can be integrated with other measurements. However, as device footprints decrease and their complexity increase, the signal-to-noise ratio in these systems also decreases and the sensitivity is thereby compromised. Device miniaturization produces distinct properties and phenomena with greater influence at the micro-scale than at the macro-scale. Here, a diffusion-restriction model was applied to a miniaturized biochip nanovolume reactor to accurately characterize DNA hybridization events that contribute to shifts in both charge transfer resistance and diffusional resistance. These effects are shown to play a significant role in electrochemical impedance spectroscopy (EIS) analyses at these length scales. Our highly functional microfluidic biosensor enables the detection of ssDNA targets selectively, with a calculated detection limit of 3.8nM, and cross-reactivity of 13% following 20min incubation with the target. This new biosensing approach can be further modeled and tested elucidating diffusion behavior in miniaturized devices and improving the performance of biosensors.
► We fabricate a microfluidic lab-on-a-chip device. ► The device contains an array of individually addressable 25nL reaction chambers. ► We detect DNA hybridization with electrochemical impedance spectroscopy analysis. ► Restricted diffusion model is used for the first time to analyze DNA hybridization. ► We detect ssDNA targets selectively and with a calculated detection limit of 3.8nM. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2012.05.009 |