TY - JOUR
T1 - A microfluidic-based electrochemical biochip for label-free diffusion-restricted DNA hybridization analysis
AU - Ben-Yoav, Hadar
AU - Dykstra, Peter H.
AU - Bentley, William E.
AU - Ghodssi, Reza
N1 - Funding Information:
The authors acknowledge the Robert W. Deutsch Foundation and National Science Foundation Emerging Frontiers in Research and Innovation (EFRI) for financial support. The authors also thank the Maryland Nanocenter and its Fablab for cleanroom facility support.
PY - 2012/10/1
Y1 - 2012/10/1
N2 - 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 3.8. nM, and cross-reactivity of 13% following 20. min 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.
AB - 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 3.8. nM, and cross-reactivity of 13% following 20. min 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.
KW - Biochip
KW - DNA hybridization biosensor
KW - Electrochemical impedance spectroscopy
KW - Label-free detection
KW - Microfluidics
KW - Restricted diffusion
UR - http://www.scopus.com/inward/record.url?scp=84864390665&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2012.05.009
DO - 10.1016/j.bios.2012.05.009
M3 - Article
C2 - 22651970
AN - SCOPUS:84864390665
SN - 0956-5663
VL - 38
SP - 114
EP - 120
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 1
ER -