ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Designing Scalable Mechano-Virucidal Nanostructured Acrylic Surfaces for Enhanced Viral Inactivation.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Synergistic control of viral persistence via wettability and ion release on antiviral coatings.Materials today. Bio · 2026Article
- Nanostructured surfaces for enveloped virus inactivation: mechanisms and fabrication strategies.Frontiers in bioengineering and biotechnology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
Abstract
The transmission of viral pathogens via contaminated surfaces remains a critical public health concern, particularly in shared environments. Conventional antiviral coatings incorporating biocidal compounds face limitations due to cytotoxicity, environmental persistence, degradation, and the risk of promoting antiviral resistance. Nanostructured mechano-bactericidal surfaces have proven effective in preventing bacterial colonization, motivating exploration of their antiviral potential. In this study, flexible nanostructured acrylic films with nanopillar arrays are fabricated using anodized aluminum oxide (AAO) molds and ultraviolet nanoimprint lithography (UV-NIL), providing a scalable mechano-virucidal platform, capable of physically rupturing viral particles. Systematic variation of nanopillar pitch and height reveals that interpillar spacing is the dominant determinant of antiviral efficacy. Dense arrays with a 60 nm pitch reduce human parainfluenza virus type 3 (hPIV-3) infectivity by up to 1.2-log (∼94%) within 1 h. Finite element method (FEM) simulations demonstrate that these arrays generate localized stresses exceeding the estimated ∼10 MPa rupture threshold of the viral envelope. In contrast, increasing the pitch to 100 nm results in diminished antiviral activity that is influenced by nanopillar height, while a 200 nm pitch abolishes antiviral activity. These findings offer a chemical-free, mechano-virucidal strategy for scalable antiviral surface protection across healthcare, consumer, and environmental applications.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.