Evidence map›Paper›PMID 42852200›Full record

ArticleACS omega2026

Oleic Acid-Modified Oligochitosan Nanoparticles Preserve Bacteriophage Lytic Activity against Clinical

Joselyn Aime García-Mar, Patricia Dolores Martínez-Flores, David Encinas-Basurto, Gerardo García-González, Gerardo E Rodea-Montealegre, Refugio Pérez-González, Viviana Reyes-Márquez, Marco Antonio López-Mata, Natalia Hassan, Antonio Topete and 1 more

Abstract read
In one paragraph

Article in ACS omega, 2026. 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

11 authors.

Joselyn Aime García-MarDepartamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Sonora, Hermosillo CP 83000, México.
Patricia Dolores Martínez-FloresDepartamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Sonora, Hermosillo CP 83000, México.
David Encinas-BasurtoDepartamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Sonora, Hermosillo CP 83000, México.
Gerardo García-GonzálezDepartamento de Microbiología, Facultad de Medicina y Hospital Universitario "Dr. José Eleuterio González", Universidad Autónoma de Nuevo León, Monterrey 64460, México.
Gerardo E Rodea-MontealegreLaboratorio de Investigación en Microbiología y Resistencia Bacteriana, Hospital Infantil de México, Federico Gómez, Ciudad de México 06720, Mexico.
Refugio Pérez-GonzálezDepartamento de Investigación en Polímeros y Materiales, Universidad de Sonora, Hermosillo CP 83000, México.
Viviana Reyes-MárquezDepartamento de Ciencias Químico-Biológicas, Facultad Interdisciplinaria de Ciencias Biológicas y de Salud, Universidad de Sonora, Hermosillo CP 83000, México.
Marco Antonio López-MataDepartamento de Ciencias de la Salud, Facultad Interdisciplinaria de Ciencias Biológicas y de Salud, Universidad de Sonora, Cajeme CP 85010, México.
Natalia HassanPrograma Institucional de Fomento a la Investigación, Desarrollo e Innovación, Universidad Tecnológica Metropolitana, Santiago 8330383, Chile.ORCID https://orcid.org/0000-0001-5001-5102
Antonio TopeteDepartamento de Física de Partículas, Instituto de Materiales (iMATUS) e Instituto deInvestigación Sanitaria (IDIS), Universidad de Santiago de Compostela, Santiago de Compostela 15782, España.
Josué JuárezDepartamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Sonora, Hermosillo CP 83000, México.ORCID https://orcid.org/0000-0003-1801-0349

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) lung infections are recurrent and frequently associated with multidrug-resistant bacteria, limiting the efficacy of the currently available antibiotic therapies. Bacteriophages have emerged as a promising alternative; however, their clinical translation is constrained by their limited stability and inefficient delivery within the airway microenvironment. Here, oleic acid-modified oligochitosan (OCS-OA) nanoparticles were developed as controlled-release nanocarriers to promote bacterial clearance during infection. Three OCS-OA formulations (10, 20, and 30% OA substitution) were modified via an amidation reaction and confirmed by attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). Surface tension analysis demonstrated the amphiphilic behavior and self-assembly of the modified oligosaccharides into micelle-like nanostructures. The bacteriophage (vB_Eco_K-02) was efficiently encapsulated (>90%), and the resulting formulations were characterized by scanning transmission electron microscopy (STEM), atomic force microscopy (AFM), dynamic light scattering (DLS), and ζ-potential. Formulations prepared with 10 and 20% OCS-OA preserved phage lytic activity against a clinical

Identifiers

PMID42852200
PMCPMC13647333

What OpenQuestion holds

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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.