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

Seunghwan Yoo, Sun Woo Yoon, Woo Nam Jung, Moon Hyun Chung, Hyunjun Kim, Hagkeun Jeong, Kyung Hwa Yoo

Research output: Contribution to journalArticlepeer-review

Abstract

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 (TCID50) 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 TCID50 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.

Original languageEnglish
Article number1724
JournalScientific reports
Volume12
Issue number1
DOIs
Publication statusPublished - 2022 Dec

Bibliographical note

Funding Information:
This research was supported by the framework of the Research and Development Program of the Korea Institute of Energy Research (C1-2467) and the Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program (KGM5182113). For the inactivation test of SARS-CoV-2, the pathogen resources (NCCP43326) for this study were provided by the National Culture Collection for Pathogens.

Funding Information:
This research was supported by the framework of the Research and Development Program of the Korea Institute of Energy Research (C1-2467) and the Korea Research Institute of Bioscience and Biotechnology (KRIBB) Research Initiative Program (KGM5182113). For the inactivation test of SARS-CoV-2, the pathogen resources (NCCP43326) for this study were provided by the National Culture Collection for Pathogens.

Publisher Copyright:
© 2022, The Author(s).

All Science Journal Classification (ASJC) codes

  • General

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