TY - JOUR
T1 - Synthesis and assessment of copper-based nanoparticles as a surface coating agent for antiviral properties against SARS-CoV-2
AU - Purniawan, Agung
AU - Lusida, Maria Inge
AU - Pujiyanto, Royan Wafi
AU - Nastri, Aldise Mareta
AU - Permanasari, Adita Ayu
AU - Harsono, Alfonsus Adrian Hadikusumo
AU - Oktavia, Nur Hafidzah
AU - Wicaksono, Sigit Tri
AU - Dewantari, Jezzy Renova
AU - Prasetya, Rima Ratnanggana
AU - Rahardjo, Krisnoadi
AU - Nishimura, Mitsuhiro
AU - Mori, Yasuko
AU - Shimizu, Kazufumi
N1 - Funding Information:
We sincerely thank the Ministry of Research, Technology and Higher Education of Indonesia for their advice to carry out this study in Indonesia. We would also like to thank Firas Farisi Alkaff for his contribution to analyzing the data and Yohko Koshi Shimizu for her advice in preparing the manuscript.
Funding Information:
This research was partly supported by the Japan Agency for Medical Research and Development (AMED), Japan Program for Infectious Diseases Research and Infrastructure (Global Research Infrastructure) under Grant Number JP 21wm0125009. The funder had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - To halt the pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), governments around the world have imposed policies, such as lockdowns, mandatory mask wearing, and social distancing. The application of disinfecting materials in shared public facilities can be an additional measure to control the spread of the virus. Copper is a prominent material with antibacterial and antiviral effects. In this study, we synthesized copper nanoparticles (CuNPs) as a surface coating agent and assessed their antiviral activity against SARS-CoV-2. CuNPs with a mean size of 254 nm in diameter were synthesized from copper sulfate as a source and were predominantly composed of copper oxide. The synthesized CuNPs were mixed with resin-based paint (CuNP/paint) and sprayed on the surface of stainless steel remnants. SARS-CoV-2 lost 97.8% infectivity on the CuNP/paint-coated surface after 30 min of exposure and more than 99.995% infectivity after 1 h of exposure. The inactivation rate was approximately 36-fold faster than that on the paint alone-coated and uncoated surfaces. The CuNP/paint-coated surface showed powerful inactivation of SARS-CoV-2 infectivity, although further study is needed to elucidate the inactivation mechanisms. Applications of CuNP/paint coatings to public or hospital facilities and other commonly touched areas are expected to be beneficial.
AB - To halt the pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), governments around the world have imposed policies, such as lockdowns, mandatory mask wearing, and social distancing. The application of disinfecting materials in shared public facilities can be an additional measure to control the spread of the virus. Copper is a prominent material with antibacterial and antiviral effects. In this study, we synthesized copper nanoparticles (CuNPs) as a surface coating agent and assessed their antiviral activity against SARS-CoV-2. CuNPs with a mean size of 254 nm in diameter were synthesized from copper sulfate as a source and were predominantly composed of copper oxide. The synthesized CuNPs were mixed with resin-based paint (CuNP/paint) and sprayed on the surface of stainless steel remnants. SARS-CoV-2 lost 97.8% infectivity on the CuNP/paint-coated surface after 30 min of exposure and more than 99.995% infectivity after 1 h of exposure. The inactivation rate was approximately 36-fold faster than that on the paint alone-coated and uncoated surfaces. The CuNP/paint-coated surface showed powerful inactivation of SARS-CoV-2 infectivity, although further study is needed to elucidate the inactivation mechanisms. Applications of CuNP/paint coatings to public or hospital facilities and other commonly touched areas are expected to be beneficial.
UR - http://www.scopus.com/inward/record.url?scp=85126834129&partnerID=8YFLogxK
U2 - 10.1038/s41598-022-08766-0
DO - 10.1038/s41598-022-08766-0
M3 - Article
C2 - 35318357
AN - SCOPUS:85126834129
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 4835
ER -