Cargando…
Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
In this article we describe a new class of high-density optical microarrays based on molecularly imprinted microsphere sensors that directly incorporate specific recognition capabilities to detect enrofloxacin (ENRO), an antibiotic widely used for both human and veterinary applications. This approac...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657405/ https://www.ncbi.nlm.nih.gov/pubmed/29142687 http://dx.doi.org/10.1039/c5sc00115c |
_version_ | 1783273839731408896 |
---|---|
author | Carrasco, Sergio Benito-Peña, Elena Walt, David R. Moreno-Bondi, María C. |
author_facet | Carrasco, Sergio Benito-Peña, Elena Walt, David R. Moreno-Bondi, María C. |
author_sort | Carrasco, Sergio |
collection | PubMed |
description | In this article we describe a new class of high-density optical microarrays based on molecularly imprinted microsphere sensors that directly incorporate specific recognition capabilities to detect enrofloxacin (ENRO), an antibiotic widely used for both human and veterinary applications. This approach involves the preparation of highly cross-linked polymer microspheres by thermal precipitation–polymerization in the presence and absence of the target analyte ENRO to generate either molecularly imprinted (MIP) or non-imprinted polymer (NIP) microspheres, respectively. Each polymer type of tailor-made microsphere is fluorescently encoded with either coumarin-30 or tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(ii) dichloride [Ru(dip)(3)]Cl(2) to enable the microspheres to be distinguished. The new MIP-based sensing platform utilizes an optical fiber bundle containing approximately 50 000 individual 3.1 μm diameter fibers that are chemically etched to create microwells in which MIP and NIP microspheres can be deposited and imaged using an epi-fluorescence microscope. The method enables multiplexed detection by independently addressing both types of beads through their separate light channels. The unique response to the presence of ENRO is manifested on the basis of a competitive immunoassay. A red-fluorescent dye-tagged ENRO, labeled with BODIPY® TR Cadaverine, competes with ENRO for specific binding sites. The developed immuno-like assay displayed a limit of detection (LOD) of 0.04 μM (10% binding inhibition) and a dynamic range of 0.29–21.54 μM (20–80% binding inhibition). The selectivity of the assay was evaluated by measuring the cross-reactivity of other fluoroquinolones (ciprofloxacin, norfloxacin, danofloxacin, and flumequine) and non-related antibiotics (penicillin G and doxycycline). This work demonstrates, for the first time, the applicability of MIPs, as an alternative to biomolecule receptors, for the development of multiplexed detection fiber-optic microarrays paving the way for a new generation of biomimetic sensors. |
format | Online Article Text |
id | pubmed-5657405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56574052017-11-15 Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis Carrasco, Sergio Benito-Peña, Elena Walt, David R. Moreno-Bondi, María C. Chem Sci Chemistry In this article we describe a new class of high-density optical microarrays based on molecularly imprinted microsphere sensors that directly incorporate specific recognition capabilities to detect enrofloxacin (ENRO), an antibiotic widely used for both human and veterinary applications. This approach involves the preparation of highly cross-linked polymer microspheres by thermal precipitation–polymerization in the presence and absence of the target analyte ENRO to generate either molecularly imprinted (MIP) or non-imprinted polymer (NIP) microspheres, respectively. Each polymer type of tailor-made microsphere is fluorescently encoded with either coumarin-30 or tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(ii) dichloride [Ru(dip)(3)]Cl(2) to enable the microspheres to be distinguished. The new MIP-based sensing platform utilizes an optical fiber bundle containing approximately 50 000 individual 3.1 μm diameter fibers that are chemically etched to create microwells in which MIP and NIP microspheres can be deposited and imaged using an epi-fluorescence microscope. The method enables multiplexed detection by independently addressing both types of beads through their separate light channels. The unique response to the presence of ENRO is manifested on the basis of a competitive immunoassay. A red-fluorescent dye-tagged ENRO, labeled with BODIPY® TR Cadaverine, competes with ENRO for specific binding sites. The developed immuno-like assay displayed a limit of detection (LOD) of 0.04 μM (10% binding inhibition) and a dynamic range of 0.29–21.54 μM (20–80% binding inhibition). The selectivity of the assay was evaluated by measuring the cross-reactivity of other fluoroquinolones (ciprofloxacin, norfloxacin, danofloxacin, and flumequine) and non-related antibiotics (penicillin G and doxycycline). This work demonstrates, for the first time, the applicability of MIPs, as an alternative to biomolecule receptors, for the development of multiplexed detection fiber-optic microarrays paving the way for a new generation of biomimetic sensors. Royal Society of Chemistry 2015-05-01 2015-03-25 /pmc/articles/PMC5657405/ /pubmed/29142687 http://dx.doi.org/10.1039/c5sc00115c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Carrasco, Sergio Benito-Peña, Elena Walt, David R. Moreno-Bondi, María C. Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis |
title | Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
|
title_full | Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
|
title_fullStr | Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
|
title_full_unstemmed | Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
|
title_short | Fiber-optic array using molecularly imprinted microspheres for antibiotic analysis
|
title_sort | fiber-optic array using molecularly imprinted microspheres for antibiotic analysis |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5657405/ https://www.ncbi.nlm.nih.gov/pubmed/29142687 http://dx.doi.org/10.1039/c5sc00115c |
work_keys_str_mv | AT carrascosergio fiberopticarrayusingmolecularlyimprintedmicrospheresforantibioticanalysis AT benitopenaelena fiberopticarrayusingmolecularlyimprintedmicrospheresforantibioticanalysis AT waltdavidr fiberopticarrayusingmolecularlyimprintedmicrospheresforantibioticanalysis AT morenobondimariac fiberopticarrayusingmolecularlyimprintedmicrospheresforantibioticanalysis |