Cargando…

Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli

Early detection of pathogens requires methods that are fast, selective, sensitive and affordable. We report the development of a biosensor with high sensitivity and selectivity based on the low-cost preparation of organosiloxane (OSX) polymers imprinted with E. coli-GFP (green fluorescent protein)....

Descripción completa

Detalles Bibliográficos
Autores principales: Dulay, Maria T., Zaman, Naina, Jaramillo, David, Mody, Alison C, Zare, Richard N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743956/
https://www.ncbi.nlm.nih.gov/pubmed/33381537
http://dx.doi.org/10.3390/c4020029
_version_ 1783624336278552576
author Dulay, Maria T.
Zaman, Naina
Jaramillo, David
Mody, Alison C
Zare, Richard N
author_facet Dulay, Maria T.
Zaman, Naina
Jaramillo, David
Mody, Alison C
Zare, Richard N
author_sort Dulay, Maria T.
collection PubMed
description Early detection of pathogens requires methods that are fast, selective, sensitive and affordable. We report the development of a biosensor with high sensitivity and selectivity based on the low-cost preparation of organosiloxane (OSX) polymers imprinted with E. coli-GFP (green fluorescent protein). OSX polymers with high optical transparency, no cracking, and no shrinkage were prepared by varying several parameters of the sol–gel reaction. The unique shape and chemical fingerprint of the targeted inactivated E. coli-GFP were imprinted into bulk polymers by replication imprinting where the polymer solution was dropcast onto a bacteria template that produced a replica of the bacterial shape and chemistry on the polymer surface upon removal of the template. Capture performances were studied under non-laminar flow conditions with samples containing inactivated E. coli-GFP and compared to inactivated S. typhimurium-GFP. Capture selectivity ratios are dependent on the type of alkoxysilanes used, the H(2)O:silane molar ratio, and the polymerization temperature. The bacteria concentration in suspension ranged from ~6 × 10(5) to 1.6 × 10(9) cells/mL. E. coli-imprinted OSX polymers with polyethylene glycol (PEG) differentiated between the targeted bacterium E. coli, and non-targeted bacteria S. typhimurium and native E. coli-GFP, achieving selectivity ratios up to 4.5 times higher than polydimethylsiloxane (PDMS) and OSX polymers without PEG.
format Online
Article
Text
id pubmed-7743956
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI AG
record_format MEDLINE/PubMed
spelling pubmed-77439562020-12-28 Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli Dulay, Maria T. Zaman, Naina Jaramillo, David Mody, Alison C Zare, Richard N C (Basel) Article Early detection of pathogens requires methods that are fast, selective, sensitive and affordable. We report the development of a biosensor with high sensitivity and selectivity based on the low-cost preparation of organosiloxane (OSX) polymers imprinted with E. coli-GFP (green fluorescent protein). OSX polymers with high optical transparency, no cracking, and no shrinkage were prepared by varying several parameters of the sol–gel reaction. The unique shape and chemical fingerprint of the targeted inactivated E. coli-GFP were imprinted into bulk polymers by replication imprinting where the polymer solution was dropcast onto a bacteria template that produced a replica of the bacterial shape and chemistry on the polymer surface upon removal of the template. Capture performances were studied under non-laminar flow conditions with samples containing inactivated E. coli-GFP and compared to inactivated S. typhimurium-GFP. Capture selectivity ratios are dependent on the type of alkoxysilanes used, the H(2)O:silane molar ratio, and the polymerization temperature. The bacteria concentration in suspension ranged from ~6 × 10(5) to 1.6 × 10(9) cells/mL. E. coli-imprinted OSX polymers with polyethylene glycol (PEG) differentiated between the targeted bacterium E. coli, and non-targeted bacteria S. typhimurium and native E. coli-GFP, achieving selectivity ratios up to 4.5 times higher than polydimethylsiloxane (PDMS) and OSX polymers without PEG. MDPI AG 2018-05-14 /pmc/articles/PMC7743956/ /pubmed/33381537 http://dx.doi.org/10.3390/c4020029 Text en © 2018 by the authors http://creativecommons.org/licenses/by/4.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dulay, Maria T.
Zaman, Naina
Jaramillo, David
Mody, Alison C
Zare, Richard N
Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title_full Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title_fullStr Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title_full_unstemmed Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title_short Pathogen-Imprinted Organosiloxane Polymers as Selective Biosensors for the Detection of Targeted E. coli
title_sort pathogen-imprinted organosiloxane polymers as selective biosensors for the detection of targeted e. coli
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743956/
https://www.ncbi.nlm.nih.gov/pubmed/33381537
http://dx.doi.org/10.3390/c4020029
work_keys_str_mv AT dulaymariat pathogenimprintedorganosiloxanepolymersasselectivebiosensorsforthedetectionoftargetedecoli
AT zamannaina pathogenimprintedorganosiloxanepolymersasselectivebiosensorsforthedetectionoftargetedecoli
AT jaramillodavid pathogenimprintedorganosiloxanepolymersasselectivebiosensorsforthedetectionoftargetedecoli
AT modyalisonc pathogenimprintedorganosiloxanepolymersasselectivebiosensorsforthedetectionoftargetedecoli
AT zarerichardn pathogenimprintedorganosiloxanepolymersasselectivebiosensorsforthedetectionoftargetedecoli