# Impact of ultraviolet radiation on filtering facepiece respirators and SARS-CoV-2 detection

**Authors:** Khaled Al-Hadyan, Najla Al-Harbi, Sara Bin Judia, Maha Al-Ghamdi, Ibtihaj Alsharif, Layla Alharbi, Maha Al-Mozaini, Belal Moftah, Salem Al-Ghamdi, Ghazi Alsbeih

PMC · DOI: 10.3389/fpubh.2025.1537742 · Frontiers in Public Health · 2025-03-06

## TL;DR

This study shows that UV-C light can effectively decontaminate face masks without reducing their filtering ability and degrades most SARS-CoV-2 RNA genes.

## Contribution

The study provides empirical evidence on UV-C's impact on mask filtration and specific SARS-CoV-2 RNA gene degradation.

## Key findings

- UV-C irradiation did not significantly reduce filtration efficiency of FFRs across all tested particle sizes.
- UV-C significantly degraded E, RdRp2, and RdRp4 SARS-CoV-2 RNA genes but not the N gene.
- Results support UV-C as a viable decontamination method for FFRs during shortages.

## Abstract

The global coronavirus disease (COVID-19) pandemic of 2020 caused by SARS-CoV-2 resulted in a shortage of filtering facepiece respirators (FFRs), such as N95 and KN95 masks. Ultraviolet-C (UV-C) irradiation has been proposed as a potential decontamination method to enable FFR reuse and mitigate the shortage. This study aims to evaluate the impact of UV-C irradiation on the filtration efficiency (FE) of various FFR types and SARS-CoV-2 RNA degradation.

We evaluated the effect of UV-C irradiation (60–900 mJ/cm2) on the FE using various particle sizes (PSs, 0.3–5 μm) representing seven common FFR types (3M-8210, 3M-1860, Gerson 1730, Medline, Benehal, KN95 “duck shape,” and KN95 “molded shape”) and the stability of the SARS-CoV-2 RNA genes (E, RdRp2, RdRp4, and N) using reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR).

Following UV-C exposure, the FE of the FFRs at all PSs was >98%, with no significant differences among them (p > 0.05). UV-C irradiation significantly increased the RT-qPCR cycle threshold values (ΔCt) for the E, RdRp2, and RdRp4 SARS-CoV-2 genes (p ≤ 0.001) compared with the control, indicating marked RNA degradation; however, it did not significantly affect N gene stability (p = 0.612).

These results support the use of UV-C as an effective decontamination technique for FFRs, particularly during periods of shortage.

## Linked entities

- **Genes:** e (ebony) [NCBI Gene 42521], RdRP-2 (RNA-dependent RNA polymerase RdRP) [NCBI Gene 29004526], N (Notch) [NCBI Gene 31293]
- **Diseases:** SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], E (envelope protein) [NCBI Gene 43740570]
- **Diseases:** coronavirus disease (MESH:D018352), COVID-19 (MESH:D000086382)
- **Chemicals:** N95 (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11922867/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11922867/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC11922867/full.md

---
Source: https://tomesphere.com/paper/PMC11922867