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Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7

[Image: see text] Nonthermal plasma, a nondestructive, fast, and highly reproducible surface functionalization technique, was used to introduce desired functional groups onto the surface of carbon powder. The primary benefit is that it is highly scalable, with a high throughput, making it easily ada...

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Autores principales: Gangwar, Rahul, Ray, Debjyoti, Rao, Karri Trinadha, Khatun, Sajmina, Subrahmanyam, Challapalli, Rengan, Aravind Kumar, Vanjari, Siva Rama Krishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219096/
https://www.ncbi.nlm.nih.gov/pubmed/35755381
http://dx.doi.org/10.1021/acsomega.2c01802
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author Gangwar, Rahul
Ray, Debjyoti
Rao, Karri Trinadha
Khatun, Sajmina
Subrahmanyam, Challapalli
Rengan, Aravind Kumar
Vanjari, Siva Rama Krishna
author_facet Gangwar, Rahul
Ray, Debjyoti
Rao, Karri Trinadha
Khatun, Sajmina
Subrahmanyam, Challapalli
Rengan, Aravind Kumar
Vanjari, Siva Rama Krishna
author_sort Gangwar, Rahul
collection PubMed
description [Image: see text] Nonthermal plasma, a nondestructive, fast, and highly reproducible surface functionalization technique, was used to introduce desired functional groups onto the surface of carbon powder. The primary benefit is that it is highly scalable, with a high throughput, making it easily adaptable to bulk production. The plasma functionalized carbon powder was later used to create highly specific and low-cost electrochemical biosensors. The functional groups on the carbon surface were confirmed using NH(3)-temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) analysis. In addition, for biosensing applications, a novel, cost-effective, robust, and scalable electrochemical sensor platform comprising in-house-fabricated carbon paste electrodes and a miniaturized E-cell was developed. Biotin–Streptavidin was chosen as a model ligand–analyte combination to demonstrate its applicability toward biosensor application, and then, the specific identification of the target Escherchia coliO157:H7 was accomplished using an anti-E. coliO157:H7 antibody-modified electrode. The proposed biosensing platform detected E. coliO157:H7 in a broad linear range of (1 × 10(–1)–1 × 10(6)) CFU/mL, with a limit of detection (LOD) of 0.1 CFU/mL. In addition, the developed plasma functionalized carbon paste electrodes demonstrated high specificity for the target E. coliO157:H7 spiked in pond water, making them ideal for real-time bacterial detection.
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spelling pubmed-92190962022-06-24 Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7 Gangwar, Rahul Ray, Debjyoti Rao, Karri Trinadha Khatun, Sajmina Subrahmanyam, Challapalli Rengan, Aravind Kumar Vanjari, Siva Rama Krishna ACS Omega [Image: see text] Nonthermal plasma, a nondestructive, fast, and highly reproducible surface functionalization technique, was used to introduce desired functional groups onto the surface of carbon powder. The primary benefit is that it is highly scalable, with a high throughput, making it easily adaptable to bulk production. The plasma functionalized carbon powder was later used to create highly specific and low-cost electrochemical biosensors. The functional groups on the carbon surface were confirmed using NH(3)-temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) analysis. In addition, for biosensing applications, a novel, cost-effective, robust, and scalable electrochemical sensor platform comprising in-house-fabricated carbon paste electrodes and a miniaturized E-cell was developed. Biotin–Streptavidin was chosen as a model ligand–analyte combination to demonstrate its applicability toward biosensor application, and then, the specific identification of the target Escherchia coliO157:H7 was accomplished using an anti-E. coliO157:H7 antibody-modified electrode. The proposed biosensing platform detected E. coliO157:H7 in a broad linear range of (1 × 10(–1)–1 × 10(6)) CFU/mL, with a limit of detection (LOD) of 0.1 CFU/mL. In addition, the developed plasma functionalized carbon paste electrodes demonstrated high specificity for the target E. coliO157:H7 spiked in pond water, making them ideal for real-time bacterial detection. American Chemical Society 2022-06-06 /pmc/articles/PMC9219096/ /pubmed/35755381 http://dx.doi.org/10.1021/acsomega.2c01802 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Gangwar, Rahul
Ray, Debjyoti
Rao, Karri Trinadha
Khatun, Sajmina
Subrahmanyam, Challapalli
Rengan, Aravind Kumar
Vanjari, Siva Rama Krishna
Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title_full Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title_fullStr Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title_full_unstemmed Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title_short Plasma Functionalized Carbon Interfaces for Biosensor Application: Toward the Real-Time Detection of Escherichia coli O157:H7
title_sort plasma functionalized carbon interfaces for biosensor application: toward the real-time detection of escherichia coli o157:h7
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219096/
https://www.ncbi.nlm.nih.gov/pubmed/35755381
http://dx.doi.org/10.1021/acsomega.2c01802
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