Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1038/s41598-022-11902-5 http://hdl.handle.net/11449/241847 |
Resumo: | In the current COVID-19 pandemic, the next generation of innovative materials with enhanced anti-SARS-CoV-2 activity is urgently needed to prevent the spread of this virus within the community. Herein, we report the synthesis of chitosan/α-Ag2WO4 composites synthetized by femtosecond laser irradiation. The antimicrobial activity against Escherichia coli, Methicilin-susceptible Staphylococcus aureus (MSSA), and Candida albicans was determined by estimating the minimum inhibitory concentration (MIC) and minimal bactericidal/fungicidal concentration (MBC/MFC). To assess the biocompatibility of chitosan/α-Ag2WO4 composites in a range involving MIC and MBC/MFC on keratinocytes cells (NOK-si), an alamarBlue™ assay and an MTT assay were carried out. The SARS-CoV-2 virucidal effects was analyzed in Vero E6 cells through viral titer quantified in cell culture supernatant by PFU/mL assay. Our results showed a very similar antimicrobial activity of chitosan/α-Ag2WO4 3.3 and 6.6, with the last one demonstrating a slightly better action against MSSA. The chitosan/α-Ag2WO4 9.9 showed a wide range of antimicrobial activity (0.49–31.25 µg/mL). The cytotoxicity outcomes by alamarBlue™ revealed that the concentrations of interest (MIC and MBC/MFC) were considered non-cytotoxic to all composites after 72 h of exposure. The Chitosan/α-Ag2WO4 (CS6.6/α-Ag2WO4) composite reduced the SARS-CoV-2 viral titer quantification up to 80% of the controls. Then, our results suggest that these composites are highly efficient materials to kill bacteria (Escherichia coli, Methicillin-susceptible Staphylococcus aureus, and the yeast strain Candida albicans), in addition to inactivating SARS-CoV-2 by contact, through ROS production. |
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Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiationIn the current COVID-19 pandemic, the next generation of innovative materials with enhanced anti-SARS-CoV-2 activity is urgently needed to prevent the spread of this virus within the community. Herein, we report the synthesis of chitosan/α-Ag2WO4 composites synthetized by femtosecond laser irradiation. The antimicrobial activity against Escherichia coli, Methicilin-susceptible Staphylococcus aureus (MSSA), and Candida albicans was determined by estimating the minimum inhibitory concentration (MIC) and minimal bactericidal/fungicidal concentration (MBC/MFC). To assess the biocompatibility of chitosan/α-Ag2WO4 composites in a range involving MIC and MBC/MFC on keratinocytes cells (NOK-si), an alamarBlue™ assay and an MTT assay were carried out. The SARS-CoV-2 virucidal effects was analyzed in Vero E6 cells through viral titer quantified in cell culture supernatant by PFU/mL assay. Our results showed a very similar antimicrobial activity of chitosan/α-Ag2WO4 3.3 and 6.6, with the last one demonstrating a slightly better action against MSSA. The chitosan/α-Ag2WO4 9.9 showed a wide range of antimicrobial activity (0.49–31.25 µg/mL). The cytotoxicity outcomes by alamarBlue™ revealed that the concentrations of interest (MIC and MBC/MFC) were considered non-cytotoxic to all composites after 72 h of exposure. The Chitosan/α-Ag2WO4 (CS6.6/α-Ag2WO4) composite reduced the SARS-CoV-2 viral titer quantification up to 80% of the controls. Then, our results suggest that these composites are highly efficient materials to kill bacteria (Escherichia coli, Methicillin-susceptible Staphylococcus aureus, and the yeast strain Candida albicans), in addition to inactivating SARS-CoV-2 by contact, through ROS production.CDMF LIEC Department of Chemistry Federal University of São Carlos (UFSCar), P.O. Box 676, SPDepartment of Physical and Analytical Chemistry University Jaume I (UJI)Department of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), 1680 Humaitá Street, SPFaculty of Engineering of Guaratinguetá São Paulo State University (UNESP), SPLaboratory of Viral Morphology and Morphogenesis Oswaldo Cruz Institute, Fiocruz, Avenida BrasilLaboratory of Respiratory Viruses and Measles Oswaldo Cruz Institute, Fiocruz, Avenida BrasilGROC UJI Institute of New Imaging Technologies Universitat Jaume I, Avda. Sos Baynat snMaterials Science and Additive Manufacturing University of Wuppertal, Gaußstr. 20Department of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP), 1680 Humaitá Street, SPFaculty of Engineering of Guaratinguetá São Paulo State University (UNESP), SPUniversidade Federal de São Carlos (UFSCar)University Jaume I (UJI)Universidade Estadual Paulista (UNESP)Oswaldo Cruz InstituteUniversitat Jaume IUniversity of WuppertalPereira, Paula Fabiana Santosde Paula e Silva, Ana Carolina Alves [UNESP]da Silva Pimentel, Bruna Natália Alves [UNESP]Pinatti, Ivo Mateus [UNESP]Simões, Alexandre Zirpoli [UNESP]Vergani, Carlos Eduardo [UNESP]Barreto-Vieira, Débora Ferreirada Silva, Marcos Alexandre NunesMiranda, Milene DiasMonteiro, Maria Eduarda SantosTucci, AmandaDoñate-Buendía, CarlosMínguez-Vega, GladysAndrés, JuanLongo, Elson2023-03-02T00:30:32Z2023-03-02T00:30:32Z2022-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1038/s41598-022-11902-5Scientific Reports, v. 12, n. 1, 2022.2045-2322http://hdl.handle.net/11449/24184710.1038/s41598-022-11902-52-s2.0-85130162995Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengScientific Reportsinfo:eu-repo/semantics/openAccess2024-09-27T14:56:27Zoai:repositorio.unesp.br:11449/241847Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:56:27Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
title |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
spellingShingle |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation Pereira, Paula Fabiana Santos |
title_short |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
title_full |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
title_fullStr |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
title_full_unstemmed |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
title_sort |
Inactivation of SARS-CoV-2 by a chitosan/α-Ag2WO4 composite generated by femtosecond laser irradiation |
author |
Pereira, Paula Fabiana Santos |
author_facet |
Pereira, Paula Fabiana Santos de Paula e Silva, Ana Carolina Alves [UNESP] da Silva Pimentel, Bruna Natália Alves [UNESP] Pinatti, Ivo Mateus [UNESP] Simões, Alexandre Zirpoli [UNESP] Vergani, Carlos Eduardo [UNESP] Barreto-Vieira, Débora Ferreira da Silva, Marcos Alexandre Nunes Miranda, Milene Dias Monteiro, Maria Eduarda Santos Tucci, Amanda Doñate-Buendía, Carlos Mínguez-Vega, Gladys Andrés, Juan Longo, Elson |
author_role |
author |
author2 |
de Paula e Silva, Ana Carolina Alves [UNESP] da Silva Pimentel, Bruna Natália Alves [UNESP] Pinatti, Ivo Mateus [UNESP] Simões, Alexandre Zirpoli [UNESP] Vergani, Carlos Eduardo [UNESP] Barreto-Vieira, Débora Ferreira da Silva, Marcos Alexandre Nunes Miranda, Milene Dias Monteiro, Maria Eduarda Santos Tucci, Amanda Doñate-Buendía, Carlos Mínguez-Vega, Gladys Andrés, Juan Longo, Elson |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Carlos (UFSCar) University Jaume I (UJI) Universidade Estadual Paulista (UNESP) Oswaldo Cruz Institute Universitat Jaume I University of Wuppertal |
dc.contributor.author.fl_str_mv |
Pereira, Paula Fabiana Santos de Paula e Silva, Ana Carolina Alves [UNESP] da Silva Pimentel, Bruna Natália Alves [UNESP] Pinatti, Ivo Mateus [UNESP] Simões, Alexandre Zirpoli [UNESP] Vergani, Carlos Eduardo [UNESP] Barreto-Vieira, Débora Ferreira da Silva, Marcos Alexandre Nunes Miranda, Milene Dias Monteiro, Maria Eduarda Santos Tucci, Amanda Doñate-Buendía, Carlos Mínguez-Vega, Gladys Andrés, Juan Longo, Elson |
description |
In the current COVID-19 pandemic, the next generation of innovative materials with enhanced anti-SARS-CoV-2 activity is urgently needed to prevent the spread of this virus within the community. Herein, we report the synthesis of chitosan/α-Ag2WO4 composites synthetized by femtosecond laser irradiation. The antimicrobial activity against Escherichia coli, Methicilin-susceptible Staphylococcus aureus (MSSA), and Candida albicans was determined by estimating the minimum inhibitory concentration (MIC) and minimal bactericidal/fungicidal concentration (MBC/MFC). To assess the biocompatibility of chitosan/α-Ag2WO4 composites in a range involving MIC and MBC/MFC on keratinocytes cells (NOK-si), an alamarBlue™ assay and an MTT assay were carried out. The SARS-CoV-2 virucidal effects was analyzed in Vero E6 cells through viral titer quantified in cell culture supernatant by PFU/mL assay. Our results showed a very similar antimicrobial activity of chitosan/α-Ag2WO4 3.3 and 6.6, with the last one demonstrating a slightly better action against MSSA. The chitosan/α-Ag2WO4 9.9 showed a wide range of antimicrobial activity (0.49–31.25 µg/mL). The cytotoxicity outcomes by alamarBlue™ revealed that the concentrations of interest (MIC and MBC/MFC) were considered non-cytotoxic to all composites after 72 h of exposure. The Chitosan/α-Ag2WO4 (CS6.6/α-Ag2WO4) composite reduced the SARS-CoV-2 viral titer quantification up to 80% of the controls. Then, our results suggest that these composites are highly efficient materials to kill bacteria (Escherichia coli, Methicillin-susceptible Staphylococcus aureus, and the yeast strain Candida albicans), in addition to inactivating SARS-CoV-2 by contact, through ROS production. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-12-01 2023-03-02T00:30:32Z 2023-03-02T00:30:32Z |
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/10.1038/s41598-022-11902-5 Scientific Reports, v. 12, n. 1, 2022. 2045-2322 http://hdl.handle.net/11449/241847 10.1038/s41598-022-11902-5 2-s2.0-85130162995 |
url |
http://dx.doi.org/10.1038/s41598-022-11902-5 http://hdl.handle.net/11449/241847 |
identifier_str_mv |
Scientific Reports, v. 12, n. 1, 2022. 2045-2322 10.1038/s41598-022-11902-5 2-s2.0-85130162995 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Scientific Reports |
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 |
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Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
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