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Plasmacluster Technology Demonstrates Effectiveness in Reducing Airborne Novel Coronavirus (SARS-CoV-2)*1, a World First*2

In a world first, Sharp Corporation developed a device equipped with Plasmacluster technology, which exposed an airborne novel coronavirus (SARS-CoV-2) to Plasmacluster ions for approximately 30 seconds*3, and demonstrated that the virus infectious titer*4 was reduced more than 90%. This achievement was accomplished in collaboration with Professor Jiro Yasuda of the National Research Center for the Control and Prevention of Infectious Diseases/Institute of Tropical Medicine, Nagasaki University, Professor Asuka Nanbo (a Board member of the Japanese Society for Virology) of the same institution, and Professor Hironori Yoshiyama of the Department of Microbiology, Shimane University Faculty of Medicine (also a Board member of the Japanese Society for Virology), and in cooperation with Nagasaki University, an internationally respected authority on infectious disease research.

1

In December 2019,

an outbreak of “Coronavirus disease 2019 (COVID-19)” caused by a novel coronavirus (SARS-CoV-2) was reported, and by August 2020, more than 25 million people have been infected with SARS-CoV-2 and more than 840,000 individuals died of this infectious disease in a world*5. This outbreak represents an urgent problem facing society, and demands that immediate countermeasures be taken across a wide range of fields.

2

In 2004,

Sharp demonstrated the effectiveness of Plasmacluster technology against feline (cat) coronavirus, a member of the Coronaviridae family*6. In the following year, 2005, Sharp also demonstrated its effectiveness against the original SARS coronavirus*7 (SARS-CoV), which caused the outbreak (2002-2003) and genetically similar to the novel coronavirus (SARS-CoV-2). Now, Sharp has demonstrated its effectiveness against SARS-CoV-2 in airbornedroplets.

3

Since 2000,

Sharp has promoted academic marketing*8 to demonstrate the effectiveness of Plasmacluster technology, working in collaboratio with independent third-party research organizations around the world. Thus far, numerous independent research organizations have proven its clinical efficacy in suppressing the activity of harmful substances including new pandemic influenza viruses, drug-resistant bacteria, and mite allergens, as well as in reducing bronchial inflammation levels*9 in children with asthma. At the same time, the safety of Plasmacluster ions has also been confirmed*10. Sharp will continue to contribute to society by conducting a wide range of studies demonstrating the effectiveness of Plasmacluster technology.

Comments from Dr. Jiro Yasuda, Professor, National Research Center for the Control and Prevention of Infectious Diseases, Nagasaki University

Disinfectants such as alcohol and detergents (surfactants) are well-known to be effective to reduce the risk of the virus on materials, however, for infection via aerosols (microdroplets), there are few effective countermeasures such as a mask.

Here, effective inactivation of SARS-CoV-2 in airborne droplets by Plasmacluster technology was demonstrated.- It would be expected that it is useful to reduce the risk of infection in real spaces including office, home, medical facilities and vehicles.

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Overview of Verification Test

Testing organization: National Research Center for the Control and Prevention of Infectious Diseases (CCPID)/Institute of Tropical Medicine, Nagasaki University

Verification test apparatus: Virus testing device equipped with Plasmacluster technology

Plasmacluster ion concentration: Approx. 10 million/cm3 (in the vicinity of the Plasmacluster ion generator)
Test space volume: Approx. 3 liters
Control study: Comparison using the device described above without Plasmacluster ion generation Validation virus: Novel Coronavirus (SARS-CoV-2)
Test method
1) Pass the aerosolized virus through the test devise from the generator.
2) Recover the aerosolized virus after exposure to Plasmacluster ions.
3) Calculate the infectious virus titer of the recovered virus solution by a plaque assay*.
* A standard assay to evaluate the number of infectious virus in the sample.

Verification Test Results

Without Plasmacluster ions With Plasmacluster ions Reduction
Infectious virus titer (number of plaque) 1.76 x 104 1.54 x 103 91.3%
Infectious virus titer (number of plaque)
Without Plasmacluster ions
1.76 x 104
With Plasmacluster ions
1.54 x 103
Reduction
91.3%

Table 1.
Effect of Plasmacluster ions on infectious titer of novel coronavirus (SARS-CoV-2) suspended in air

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