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Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization

[Image: see text] While chemical vapor deposition of diamond films is currently cost prohibitive for biosensor construction, in this paper, we show that sonication-assisted nanostructuring of biosensing electrodes with nanodiamonds (NDs) allows harnessing the hydrolytic stability of the diamond biof...

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Autores principales: Zhang, Wenli, Patel, Kush, Schexnider, Andrew, Banu, Shirin, Radadia, Adarsh D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004312/
https://www.ncbi.nlm.nih.gov/pubmed/24397797
http://dx.doi.org/10.1021/nn405240g
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author Zhang, Wenli
Patel, Kush
Schexnider, Andrew
Banu, Shirin
Radadia, Adarsh D.
author_facet Zhang, Wenli
Patel, Kush
Schexnider, Andrew
Banu, Shirin
Radadia, Adarsh D.
author_sort Zhang, Wenli
collection PubMed
description [Image: see text] While chemical vapor deposition of diamond films is currently cost prohibitive for biosensor construction, in this paper, we show that sonication-assisted nanostructuring of biosensing electrodes with nanodiamonds (NDs) allows harnessing the hydrolytic stability of the diamond biofunctionalization chemistry for real-time continuous sensing, while improving the detector sensitivity and stability. We find that the higher surface coverages were important for improved bacterial capture and can be achieved through proper choice of solvent, ND concentration, and seeding time. A mixture of methanol and dimethyl sulfoxide provides the highest surface coverage (33.6 ± 3.4%) for the NDs with positive zeta-potential, compared to dilutions of dimethyl sulfoxide with acetone, ethanol, isopropyl alcohol, or water. Through impedance spectroscopy of ND-seeded interdigitated electrodes (IDEs), we found that the ND seeds serve as electrically conductive islands only a few nanometers apart. Also we show that the seeded NDs are amply hydrogenated to be decorated with antibodies using the UV-alkene chemistry, and higher bacterial captures can be obtained compared to our previously reported work with diamond films. When sensing bacteria from 10(6) cfu/mL E. coliO157:H7, the resistance to charge transfer at the IDEs decreased by ∼38.8%, which is nearly 1.5 times better than that reported previously using redox probes. Further in the case of 10(8) cfu/mL E. coliO157:H7, the charge transfer resistance changed by ∼46%, which is similar to the magnitude of improvement reported using magnetic nanoparticle-based sample enrichment prior to impedance detection. Thus ND seeding allows impedance biosensing in low conductivity solutions with competitive sensitivity.
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spelling pubmed-40043122015-01-07 Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization Zhang, Wenli Patel, Kush Schexnider, Andrew Banu, Shirin Radadia, Adarsh D. ACS Nano [Image: see text] While chemical vapor deposition of diamond films is currently cost prohibitive for biosensor construction, in this paper, we show that sonication-assisted nanostructuring of biosensing electrodes with nanodiamonds (NDs) allows harnessing the hydrolytic stability of the diamond biofunctionalization chemistry for real-time continuous sensing, while improving the detector sensitivity and stability. We find that the higher surface coverages were important for improved bacterial capture and can be achieved through proper choice of solvent, ND concentration, and seeding time. A mixture of methanol and dimethyl sulfoxide provides the highest surface coverage (33.6 ± 3.4%) for the NDs with positive zeta-potential, compared to dilutions of dimethyl sulfoxide with acetone, ethanol, isopropyl alcohol, or water. Through impedance spectroscopy of ND-seeded interdigitated electrodes (IDEs), we found that the ND seeds serve as electrically conductive islands only a few nanometers apart. Also we show that the seeded NDs are amply hydrogenated to be decorated with antibodies using the UV-alkene chemistry, and higher bacterial captures can be obtained compared to our previously reported work with diamond films. When sensing bacteria from 10(6) cfu/mL E. coliO157:H7, the resistance to charge transfer at the IDEs decreased by ∼38.8%, which is nearly 1.5 times better than that reported previously using redox probes. Further in the case of 10(8) cfu/mL E. coliO157:H7, the charge transfer resistance changed by ∼46%, which is similar to the magnitude of improvement reported using magnetic nanoparticle-based sample enrichment prior to impedance detection. Thus ND seeding allows impedance biosensing in low conductivity solutions with competitive sensitivity. American Chemical Society 2014-01-07 2014-02-25 /pmc/articles/PMC4004312/ /pubmed/24397797 http://dx.doi.org/10.1021/nn405240g Text en Copyright © 2014 American Chemical Society
spellingShingle Zhang, Wenli
Patel, Kush
Schexnider, Andrew
Banu, Shirin
Radadia, Adarsh D.
Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title_full Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title_fullStr Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title_full_unstemmed Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title_short Nanostructuring of Biosensing Electrodes with Nanodiamonds for Antibody Immobilization
title_sort nanostructuring of biosensing electrodes with nanodiamonds for antibody immobilization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004312/
https://www.ncbi.nlm.nih.gov/pubmed/24397797
http://dx.doi.org/10.1021/nn405240g
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AT banushirin nanostructuringofbiosensingelectrodeswithnanodiamondsforantibodyimmobilization
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