A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles

Detalhes bibliográficos
Autor(a) principal: Basso, Caroline R. [UNESP]
Data de Publicação: 2020
Outros Autores: Cruz, Taís F. [UNESP], Silva, Bruna L. [UNESP], Pedrosa, Valber A. [UNESP], Araújo, João P. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/ma13051087
http://hdl.handle.net/11449/200165
Resumo: The aim of the current study is to introduce a methodology aimed at producing a biosensor that uses gold nanoparticles (AuNPs) to detect porcine circovirus 2 (PCV-2). This biosensor was based on AuNPs, which were modified with self-assembled monolayers (SAMs) and antibodies. The AuNPs' surface and virus modification process applied to enable antibody binding was accompanied by localized surface plasmon resonance (LSPR), surface plasmon resonance (SPR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). Virus quantification was possible by the light absorption difference in the spectrum at concentrations of 105, 106, 107, 108, and 109 DNA copies/mL PCV-2 in relation to quantitative PCR (qPCR), with an R2 value >0.98. The visualization of colorimetric changes in the different PCV-2 concentrations was possible without the use of equipment. The biosensor production methodology presented reproducibility and specificity, as well as easy synthesis and low cost. An enhanced version of it may be used in the future to replace traditional tests such as PCR.
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spelling A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticlesBiosensorGold nanoparticlesPorcine circovirus 2The aim of the current study is to introduce a methodology aimed at producing a biosensor that uses gold nanoparticles (AuNPs) to detect porcine circovirus 2 (PCV-2). This biosensor was based on AuNPs, which were modified with self-assembled monolayers (SAMs) and antibodies. The AuNPs' surface and virus modification process applied to enable antibody binding was accompanied by localized surface plasmon resonance (LSPR), surface plasmon resonance (SPR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). Virus quantification was possible by the light absorption difference in the spectrum at concentrations of 105, 106, 107, 108, and 109 DNA copies/mL PCV-2 in relation to quantitative PCR (qPCR), with an R2 value >0.98. The visualization of colorimetric changes in the different PCV-2 concentrations was possible without the use of equipment. The biosensor production methodology presented reproducibility and specificity, as well as easy synthesis and low cost. An enhanced version of it may be used in the future to replace traditional tests such as PCR.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Institute of Biotechnology UNESPDepartment of Microbiology and Immunology Institute of Bioscience UNESPDepartment of Chemistry and Biochemistry Institute of Bioscience UNESPInstitute of Biotechnology UNESPDepartment of Microbiology and Immunology Institute of Bioscience UNESPDepartment of Chemistry and Biochemistry Institute of Bioscience UNESPCNPq: 157877/2018-3Universidade Estadual Paulista (Unesp)Basso, Caroline R. [UNESP]Cruz, Taís F. [UNESP]Silva, Bruna L. [UNESP]Pedrosa, Valber A. [UNESP]Araújo, João P. [UNESP]2020-12-12T01:59:25Z2020-12-12T01:59:25Z2020-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/ma13051087Materials, v. 13, n. 5, 2020.1996-1944http://hdl.handle.net/11449/20016510.3390/ma130510872-s2.0-85081648567Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMaterialsinfo:eu-repo/semantics/openAccess2021-10-23T12:24:12Zoai:repositorio.unesp.br:11449/200165Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T20:22:49.739837Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
title A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
spellingShingle A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
Basso, Caroline R. [UNESP]
Biosensor
Gold nanoparticles
Porcine circovirus 2
title_short A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
title_full A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
title_fullStr A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
title_full_unstemmed A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
title_sort A methodology for porcine circovirus 2 (PCV-2) quantification based on gold nanoparticles
author Basso, Caroline R. [UNESP]
author_facet Basso, Caroline R. [UNESP]
Cruz, Taís F. [UNESP]
Silva, Bruna L. [UNESP]
Pedrosa, Valber A. [UNESP]
Araújo, João P. [UNESP]
author_role author
author2 Cruz, Taís F. [UNESP]
Silva, Bruna L. [UNESP]
Pedrosa, Valber A. [UNESP]
Araújo, João P. [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Basso, Caroline R. [UNESP]
Cruz, Taís F. [UNESP]
Silva, Bruna L. [UNESP]
Pedrosa, Valber A. [UNESP]
Araújo, João P. [UNESP]
dc.subject.por.fl_str_mv Biosensor
Gold nanoparticles
Porcine circovirus 2
topic Biosensor
Gold nanoparticles
Porcine circovirus 2
description The aim of the current study is to introduce a methodology aimed at producing a biosensor that uses gold nanoparticles (AuNPs) to detect porcine circovirus 2 (PCV-2). This biosensor was based on AuNPs, which were modified with self-assembled monolayers (SAMs) and antibodies. The AuNPs' surface and virus modification process applied to enable antibody binding was accompanied by localized surface plasmon resonance (LSPR), surface plasmon resonance (SPR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). Virus quantification was possible by the light absorption difference in the spectrum at concentrations of 105, 106, 107, 108, and 109 DNA copies/mL PCV-2 in relation to quantitative PCR (qPCR), with an R2 value >0.98. The visualization of colorimetric changes in the different PCV-2 concentrations was possible without the use of equipment. The biosensor production methodology presented reproducibility and specificity, as well as easy synthesis and low cost. An enhanced version of it may be used in the future to replace traditional tests such as PCR.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T01:59:25Z
2020-12-12T01:59:25Z
2020-03-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/ma13051087
Materials, v. 13, n. 5, 2020.
1996-1944
http://hdl.handle.net/11449/200165
10.3390/ma13051087
2-s2.0-85081648567
url http://dx.doi.org/10.3390/ma13051087
http://hdl.handle.net/11449/200165
identifier_str_mv Materials, v. 13, n. 5, 2020.
1996-1944
10.3390/ma13051087
2-s2.0-85081648567
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Materials
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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