Evidence map›Paper›PMID 40587471›Full record

ArticlePloS one2025

Study on the relationship between viral inactivation and alkyl chain length of benzalkonium chloride.

Ikumi Takada, Atsushi Miyazaki, Chisato Igarashi, Yukiko Yamawaki, Atsuko Hayase, Takuya Mori, Takaya Sakai

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

7 authors.

Ikumi TakadaBiological Material Science Research Laboratory, Kao Corporation, Tochigi, Japan.ORCID 0000-0002-2076-6551
Atsushi MiyazakiBiological Material Science Research Laboratory, Kao Corporation, Tokyo, Japan.ORCID 0009-0000-7030-5967
Chisato IgarashiHousehold Research Laboratory, Kao corporation, Wakayama, Japan.
Yukiko YamawakiBiological Material Science Research Laboratory, Kao Corporation, Wakayama, Japan.
Atsuko HayaseBiological Material Science Research Laboratory, Kao Corporation, Tochigi, Japan.
Takuya MoriBiological Material Science Research Laboratory, Kao Corporation, Tochigi, Japan.ORCID 0000-0001-6208-0323
Takaya SakaiResearch and Development, Kao Corporation, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alkyldimethylbenzylammonium chloride (BAC), a quaternary ammonium salt surfactant, is commonly utilized as a sanitizer and disinfectant. Concerns have emerged regarding the increasing global exposure to BAC, emphasizing the need for strategies to maximize its efficacy while minimizing its usage. Therefore, it is crucial to understand BAC's effects on bacteria and viruses, and its mechanism of action. Our previous research demonstrated that BAC micelles solubilizes the lipid bilayer of viruses, significantly enhancing virus inactivation efficacy at concentrations exceeding the critical micelle concentration (CMC). We focused on the alkyl chain length of BAC to elucidate how variations in CMC, driven by differences in alkyl chain length, influence virus inactivation activity. We measured CMC and assessed influenza virus inactivation for benzyldodecyldimethylammonium chloride (C12BAC), benzyltetradecyldimethylammonium chloride (C14BAC), benzylhexadecyldimethylammonium chloride (C16BAC), and their mixtures. The results showed that both BACs with a single alkyl chain length and mixed BACs exhibited significantly enhanced inactivation activity at concentrations of the CMC or above. Notably, BAC mixtures with comparable CMC values showed similar virucidal activity, suggesting that CMC can serve as a useful indicator in designing BAC mixtures aimed at virus inactivation, leading to the development of compositions with enhanced virus inactivation at lower doses. However, when the bactericidal activity of each BAC mixture against E. coli was tested under the same conditions, a significant bactericidal effect, of at least 3 Log10, was observed even at concentrations below CMC. This suggests that the bactericidal activity of BAC is not due to the micellization at CMC, but rather to the contribution of BAC monomers, indicating a distinct difference in the mechanism of action of BAC against viruses and bacteria. Therefore, when formulating BAC-based disinfectants, it is essential to assess the inactivation efficacy against both bacteria and viruses to ensure sufficient virus inactivation.

Indexed as

Benzalkonium CompoundsDisinfectantsVirus InactivationAnimalsHumansMicellesQuaternary Ammonium CompoundsSurface-Active AgentsBenzalkonium CompoundsDisinfectantsMicellesQuaternary Ammonium CompoundsSurface-Active Agents

Identifiers

PMID40587471
PMCPMC12208410

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Registered trials

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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.