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Home NEWS Science News Technology

Quick way to test air disinfection effectiveness: Watch it glow

Bioengineer by Bioengineer
April 2, 2026
in Technology
Reading Time: 4 mins read
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Quick way to test air disinfection effectiveness: Watch it glow
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A groundbreaking advancement in the rapid assessment of air disinfection efficacy heralds a significant leap forward in managing airborne viral pathogens. Researchers at the University of Michigan Engineering have pioneered a novel technique leveraging viral aerosol fluorescence for the near real-time evaluation of virus inactivation. This method harnesses ultraviolet (UV) fluorescence properties intrinsic to viral particles suspended in aerosol form, enabling scientists to bypass the conventional, laborious processes that have long impeded rapid testing and deployment of effective air disinfection technologies.

Traditional approaches to measuring the performance of air disinfectants involve collecting airborne pathogens pre- and post-treatment, followed by culturing these organisms in host cells. This process demands meticulous laboratory work, including microscopic examination for viral infectivity—steps that introduce significant delays and limit throughput. By contrast, the newly developed fluorescence-based method measures the intensity of UV-induced fluorescence emitted by viral aerosols, capitalizing on the fact that virus-laden particles exhibit a distinctive glow whose intensity diminishes as viruses are inactivated.

The principle underpinning this advancement relies on the electronic properties of molecules within viral aerosols. When exposed to UV light, these molecules absorb photons and re-emit light at different wavelengths—a phenomenon termed fluorescence. Importantly, the fluorescence intensity of viral aerosols correlates with their infectivity status; active viruses fluoresce more brightly compared to their non-infectious counterparts following inactivation treatment. This correlation enables rapid inference of disinfection efficacy without the need for direct viral culture, thereby transforming evaluation timelines from hours to mere minutes.

The researchers’ methodology incorporates continuous sampling of air both upstream and downstream of an air purifier or disinfection chamber. Aerosol particles are individually sized and then subjected to excitation via UV illumination. The emitted fluorescence is quantitatively measured, generating thousands of data points that form a distribution characterized by a bell-shaped curve. As the fraction of inactivated viral aerosols increases, this distribution shifts notably towards lower fluorescence intensities. By calibrating this spectral shift against known infectivity benchmarks of specific pathogens, researchers achieve rapid, indirect quantification of virus inactivation efficacy.

This acceleration of analysis stands to revolutionize the iterative design and optimization of antiviral air-sanitizing devices. The technique permits a high-resolution investigation of how disinfection performance varies under myriad environmental conditions—such as fluctuations in airflow dynamics, temperature gradients, and relative humidity—parameters that traditionally required extensive experimentation over protracted durations. Consequently, the development pipeline for new plasma-based or other non-filtering air disinfection technologies is expected to contract substantially.

The research team, led by Herek Clack, Associate Professor of Civil and Environmental Engineering, has focused on nonthermal plasma technologies for air disinfection. Nonthermal plasmas generate highly reactive charged species that disrupt viral structural components without significant heating of the surrounding air. Their prior work demonstrated that these plasmas can deactivate up to 99.9% of infectious viral particles in flowing air streams, a performance verified in both controlled laboratory settings and practical applications such as enclosed livestock facilities. This plasma-based approach represents a promising avenue for scalable, energy-efficient airborne pathogen mitigation.

Clack’s entrepreneurial efforts have translated this technology into prototype respiratory protective equipment through his startup, Taza Aya. Currently undergoing field trials in a Michigan turkey processing plant, these prototypes harness plasma-generated reactive species to neutralize viruses directly in the air breathed by workers, offering enhanced protection against airborne pathogens. The ability to rapidly quantify device performance using fluorescence measurements will expedite iterative improvements to these wearables, tailoring them for diverse occupational health contexts.

While this fluorescence-based monitoring excels in evaluating plasma, ozone, and chlorine-mediated disinfection methods, it shows limitations for ultraviolet germicidal irradiation (UVGI) techniques. UVGI primarily inflicts damage on viral nucleic acids deep within the viral capsid, a locus not readily interrogated by fluorescence emissions from surface-exposed molecular groups. Thus, fluorescence signatures remain largely unaltered following UV genome targeting, rendering this approach less effective for monitoring UVGI disinfection.

Fundamentally, this technique offers a paradigm shift in airborne pathogen research by enabling high temporal resolution monitoring of aerosol infectivity changes without reliance on direct pathogen culture. This capacity provides critical data for public health authorities refining guidelines on indoor ventilation, air purification, and pandemic preparedness. As respiratory viruses continue to pose global health challenges, tools that facilitate rapid, accurate evaluation of transmission mitigation strategies become indispensable.

By removing a major bottleneck in air disinfection verification, this fluorescence-based detection methodology empowers researchers and engineers to innovate more swiftly and effectively. Its implications extend from laboratory investigations to real-world applications, promising safer indoor environments through enhanced air purification technologies. As this technology gains broader adoption, it may become integral to strategies combating future viral outbreaks and respiratory disease epidemics worldwide.

In sum, the University of Michigan team’s work exemplifies the confluence of advanced photonics, aerosol science, and plasma chemistry in solving pressing public health challenges. This approach not only accelerates fundamental research but also bridges the gap to practical solutions, underscoring the critical role of multidisciplinary engineering efforts in global health innovation.

Subject of Research: Viral aerosol infectivity monitoring and air disinfection technology evaluation
Article Title: Using Viral Aerosol Fluorescence for Detection of Virus Infectivity Change Induced by Non-thermal Plasma
News Publication Date: Not specified
Web References:

https://link.springer.com/article/10.1007/s11090-026-10648-6
https://taza-aya.com
References:
University of Michigan Engineering study published in Plasma Chemistry and Plasma Processing
Image Credits: Not specified

Keywords: Viral aerosols, air disinfection, UV fluorescence, nonthermal plasma, virus inactivation, airborne transmission, biosensors, pathogen detection, aerosol science, respiratory disease mitigation, air purification technology, plasma chemistry

Tags: air disinfection effectiveness testingairborne pathogen control methodsfluorescence-based virus infectivity testingimproving airborne virus detection speednovel air disinfection measurement techniquesrapid virus inactivation assessmentreal-time air sanitizer evaluationultraviolet fluorescence for virus monitoringUniversity of Michigan air quality researchUV-induced viral particle glowviral aerosol fluorescence detectionviral aerosol fluorescence properties

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