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 language | English |
---|---|
Article number | 1724 |
Journal | Scientific reports |
Volume | 12 |
Issue number | 1 |
DOIs | |
Publication status | Published - 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