Evidence map›Paper›PMID 40143304›Full record

ArticleViruses2025

Inhibitory Activity of Hydroxypropyl Methylcellulose on Rhinovirus and Influenza A Virus Infection of Human Nasal Epithelial Cells.

Hsiao-Hui Ong, YongChiat Wong, Jayant Khanolkar, Belinda Paine, Daniel Wood, Jing Liu, Mark Thong, Vincent T Chow, De-Yun Wang

Abstract read
In one paragraph

Article in Viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hsiao-Hui OngDepartment of Otolaryngology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.ORCID 0000-0002-9753-2059
YongChiat WongPersonal Health Care, Procter & Gamble International Operations SA Singapore Branch, Singapore 138547, Singapore.ORCID 0009-0003-2281-8663
Jayant KhanolkarPersonal Health Care, Procter & Gamble UK, Reading RG2 0RX, UK.
Belinda PainePersonal Health Care, Procter & Gamble UK, Reading RG2 0RX, UK.
Daniel WoodPersonal Health Care, Procter & Gamble UK, Reading RG2 0RX, UK.
Jing LiuDepartment of Otolaryngology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.
Mark ThongDepartment of Otolaryngology-Head & Neck Surgery, National University Health System, Singapore 119228, Singapore.ORCID 0000-0001-7060-4270
Vincent T ChowInfectious Diseases Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.ORCID 0000-0003-2634-6213
De-Yun WangDepartment of Otolaryngology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.ORCID 0000-0002-0909-2963

Funding

Agency for Science, Technology and Research R-190-000-064-305The Procter & Gamble Company R-190-000-064-597
6 · The paper itself

Abstract

The nasal epithelium is the primary site for entry of respiratory viruses. In comparison to oral administration, nasal drug applications directed locally to the site of infection can serve as early interventional barriers against respiratory virus pathogenesis by limiting viral spread in the upper airway. Experiments on the diffusion of methylene blue and nanoparticles in both water and low pH conditions revealed that hydroxypropyl methylcellulose (HPMC) can act as an effective physical barrier. This study also evaluated the activity of HPMC as a barrier against common respiratory viruses, i.e., rhinovirus (RV) and influenza A virus (IAV) using the in vitro human nasal epithelial cell (hNEC) model. Utilizing the hNEC infection model, we assessed the protective effects of HPMC in pH 3.5 and pH 7 buffers against RV and IAV. Acidic and pH-neutral buffers and HPMC dissolved in acidic and pH-neutral buffers were administered for 4 h prior to virus infection and at 4 h post-infection (hpi). The apical supernatant was harvested at 24 hpi to determine the viral loads of RV and IAV (H1N1 and H3N2). HPMC was demonstrated to exert protective effects in the infected hNECs independent of acidic pH. Pre-treatment with HPMC in acidic buffer significantly diminished viral loads for both RV and IAV infections of hNECs. Similarly, direct treatment of HPMC in acidic buffer after infection (4 hpi) also effectively decreased viral loads of both RV and IAV. Moreover, treatment using HPMC in acidic buffer before or after infection did not affect the epithelial integrity and ciliary function of hNECs. This study demonstrates the protective effects of HPMC in acidic buffer against RV and IAV infections of the human nasal epithelium.

Indexed as

Antiviral AgentsEpithelial CellsHypromellose DerivativesInfluenza A virusNasal MucosaRhinovirusCell LineHumansHydrogen-Ion ConcentrationInfluenza, HumanViral LoadVirus ReplicationAntiviral AgentsHypromellose Derivativesacidic bufferHPMChydroxypropyl methylcelluloseinfluenza A virusesnasal epitheliumrhinovirus

Identifiers

PMID40143304
PMCPMC11946253

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LicenceCC BY
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Registered trials

None linked

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.