# Destruction/Inactivation of SARS-CoV-2 Virus Using Ultrasound Excitation: A Preliminary Study

**Authors:** Almunther Alhasawi, Fajer Alassaf, Alshimaa Hassan

PMC · DOI: 10.3390/v18020152 · Viruses · 2026-01-23

## TL;DR

This study explores using high-frequency ultrasound to inactivate the SARS-CoV-2 virus in water, showing promising results in reducing viral load.

## Contribution

The study introduces ultrasound as a novel non-pharmacological method to target and inactivate SARS-CoV-2 virus variants.

## Key findings

- Ultrasound exposure significantly increased PCR cycle threshold values, indicating reduced amplifiable viral genomic material.
- 85.7% of high-viral-load samples shifted to low or moderate content after ultrasound treatment.
- The intervention showed a large effect size (Cohen’s d = 2.422) in reducing viral load.

## Abstract

SARS-CoV-2, the causative virus of the COVID-19 pandemic, is a highly transmissible, enveloped, single-stranded RNA virus that has mutated into several variants, complicating vaccine strategies and drug resistance. Novel treatment modalities targeting conserved structural vulnerable points are essential to combat these variants. The primary aim of the current study is to test the mechanical vulnerability of the SARS-CoV-2 virus envelope and spike proteins to focused, high-frequency ultrasound waves (25 MHz) in vitro. Utilizing a preliminary pretest and posttest study design, the study was conducted on a virus sample within a distilled water matrix, under controlled laboratory biosafety conditions. Since detailed imaging tools were unavailable, viral disruption was indirectly measured using real-time PCR cycle threshold (Ct) values. Ct values increased significantly after high-frequency ultrasound exposure, indicating a reduction in amplifiable viral genomic material. A paired t-test indicated a significant difference between the pretest and posttest Ct (p < 0.001), which is supported by Monte Carlo test results that revealed statistically significant shifting in viral load categories (p = 0.001, two-sided). Specifically, 85.7% of high-viral-load samples converted to low or moderate content, 46.7% of low or moderate samples were shifted to negative content. This intervention produced a large effect size (Cohen’s d = 2.422). These results indicate that ultrasound may offer a promising non-pharmacological approach to destroy or inactivate SARS-CoV-2 variants in an aqueous environment.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, ORF1ab (ORF1a polyprotein;ORF1ab polyprotein) [NCBI Gene 43740578], E (envelope protein) [NCBI Gene 43740570]
- **Diseases:** influenza (MESH:D007251), injury to (MESH:D014947), fatigue (MESH:D005221), cytomegalovirus (MESH:D003586), dengue (MESH:D003715), varicella-zoster virus (MESH:D000073618), Ebola (MESH:D019142), MERS-CoV (MESH:D018352), deaths (MESH:D003643), kidney stones (MESH:D007669), herpes simplex virus (MESH:D006561), COVID-19 (MESH:D000086382), infected (MESH:D007239), Zika virus disease (MESH:D000071243)
- **Chemicals:** MB (MESH:D008751), water (MESH:D014867), VTM:2.5 (-), lipid (MESH:D008055), reactive oxygen species (MESH:D017382)
- **Species:** hepatitis C virus [taxon 11103], Human respirovirus 3 (no rank) [taxon 11216], Human papillomavirus (species) [taxon 10566], Ebola virus [taxon 186536], Variola virus (smallpox virus, no rank) [taxon 10255], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Hepatitis B virus (no rank) [taxon 10407], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human immunodeficiency virus (species) [taxon 12721], Molluscum contagiosum virus (no rank) [taxon 10279], Respiratory syncytial virus (no rank) [taxon 12814], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944889/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944889/full.md

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Source: https://tomesphere.com/paper/PMC12944889