Cargando…

Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane

This study introduces localized surface plasmon resonance (L-SPR) mediated heating filter membrane (HFM) for inactivating universal viral particles by using the photothermal effect of plasmonic metal nanoparticles (NPs). Plasmonic metal NPs were coated onto filter membrane via a conventional spray-c...

Descripción completa

Detalles Bibliográficos
Autores principales: Yoo, Seunghwan, Yoon, Sun-Woo, Jung, Woo-Nam, Chung, Moon Hyun, Kim, Hyunjun, Jeong, Hagkeun, Yoo, Kyung-Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810778/
https://www.ncbi.nlm.nih.gov/pubmed/35110635
http://dx.doi.org/10.1038/s41598-022-05738-2
_version_ 1784644299893243904
author Yoo, Seunghwan
Yoon, Sun-Woo
Jung, Woo-Nam
Chung, Moon Hyun
Kim, Hyunjun
Jeong, Hagkeun
Yoo, Kyung-Hwa
author_facet Yoo, Seunghwan
Yoon, Sun-Woo
Jung, Woo-Nam
Chung, Moon Hyun
Kim, Hyunjun
Jeong, Hagkeun
Yoo, Kyung-Hwa
author_sort Yoo, Seunghwan
collection PubMed
description This study introduces localized surface plasmon resonance (L-SPR) mediated heating filter membrane (HFM) for inactivating universal viral particles by using the photothermal effect of plasmonic metal nanoparticles (NPs). Plasmonic metal NPs were coated onto filter membrane via a conventional spray-coating method. The surface temperature of the HFM could be controlled to approximately 40–60 °C at room temperature, owing to the photothermal effect of the gold (Au) NPs coated on them, under irradiation by visible light-emitting diodes. Due to the photothermal effect of the HFMs, the virus titer of H1Npdm09 was reduced by > 99.9%, the full inactivation time being < 10 min, confirming the 50% tissue culture infective dose (TCID(50)) assay. Crystal violet staining showed that the infectious samples with photothermal inactivation lost their infectivity against Mardin-Darby Canine Kidney cells. Moreover, photothermal inactivation could also be applied to reduce the infectivity of SARS-CoV-2, showing reduction rate of 99%. We used quantitative reverse transcription polymerase chain reaction (qRT-PCR) techniques to confirm the existence of viral genes on the surface of the HFM. The results of the TCID(50) assay, crystal violet staining method, and qRT-PCR showed that the effective and immediate reduction in viral infectivity possibly originated from the denaturation or deformation of membrane proteins and components. This study provides a new, simple, and effective method to inactivate viral infectivity, leading to its potential application in various fields of indoor air quality control and medical science.
format Online
Article
Text
id pubmed-8810778
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-88107782022-02-03 Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane Yoo, Seunghwan Yoon, Sun-Woo Jung, Woo-Nam Chung, Moon Hyun Kim, Hyunjun Jeong, Hagkeun Yoo, Kyung-Hwa Sci Rep Article This study introduces localized surface plasmon resonance (L-SPR) mediated heating filter membrane (HFM) for inactivating universal viral particles by using the photothermal effect of plasmonic metal nanoparticles (NPs). Plasmonic metal NPs were coated onto filter membrane via a conventional spray-coating method. The surface temperature of the HFM could be controlled to approximately 40–60 °C at room temperature, owing to the photothermal effect of the gold (Au) NPs coated on them, under irradiation by visible light-emitting diodes. Due to the photothermal effect of the HFMs, the virus titer of H1Npdm09 was reduced by > 99.9%, the full inactivation time being < 10 min, confirming the 50% tissue culture infective dose (TCID(50)) assay. Crystal violet staining showed that the infectious samples with photothermal inactivation lost their infectivity against Mardin-Darby Canine Kidney cells. Moreover, photothermal inactivation could also be applied to reduce the infectivity of SARS-CoV-2, showing reduction rate of 99%. We used quantitative reverse transcription polymerase chain reaction (qRT-PCR) techniques to confirm the existence of viral genes on the surface of the HFM. The results of the TCID(50) assay, crystal violet staining method, and qRT-PCR showed that the effective and immediate reduction in viral infectivity possibly originated from the denaturation or deformation of membrane proteins and components. This study provides a new, simple, and effective method to inactivate viral infectivity, leading to its potential application in various fields of indoor air quality control and medical science. Nature Publishing Group UK 2022-02-02 /pmc/articles/PMC8810778/ /pubmed/35110635 http://dx.doi.org/10.1038/s41598-022-05738-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yoo, Seunghwan
Yoon, Sun-Woo
Jung, Woo-Nam
Chung, Moon Hyun
Kim, Hyunjun
Jeong, Hagkeun
Yoo, Kyung-Hwa
Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title_full Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title_fullStr Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title_full_unstemmed Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title_short Photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
title_sort photothermal inactivation of universal viral particles by localized surface plasmon resonance mediated heating filter membrane
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810778/
https://www.ncbi.nlm.nih.gov/pubmed/35110635
http://dx.doi.org/10.1038/s41598-022-05738-2
work_keys_str_mv AT yooseunghwan photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT yoonsunwoo photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT jungwoonam photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT chungmoonhyun photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT kimhyunjun photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT jeonghagkeun photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane
AT yookyunghwa photothermalinactivationofuniversalviralparticlesbylocalizedsurfaceplasmonresonancemediatedheatingfiltermembrane