Evidence map›Paper›PMID 41923040›Full record

ArticleBMC biotechnology2026

Preparation, characterization, and evaluation of chitosan-thymol nanoparticles for antibacterial and antibiofilm activities against catheter-associated uropathogenic Escherichia coli.

Yasaman Dini, Mohamad Javad Mirzaei-Parsa, Mehrdad Halaji, Farzin Sadeghi, Abazar Pournajaf, Hoda Shirafkan, Mehdi Rajabnia

Abstract read
In one paragraph

Article in BMC biotechnology, 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

7 authors.

Yasaman DiniStudent Research Committee, Babol University of Medical Sciences, Babol, Iran.
Mohamad Javad Mirzaei-ParsaPathology and Stem Cell Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Mehrdad HalajiInfectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran. mehrdad.md69@gmail.com.
Farzin SadeghiCellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Abazar PournajafInfectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Hoda ShirafkanSocial Determinants of Health Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Mehdi RajabniaInfectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran. ramazan69@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uropathogenic Escherichia coli (UPEC) is a major cause of urinary tract infections (UTIs) and is capable of forming biofilms on inert surfaces, contributing to persistent and recurrent infections. Given the limitations of conventional antibiotics, alternative strategies are needed to control multidrug-resistant (MDR) UPEC. This study aimed to evaluate the antibacterial and antibiofilm effects of thymol-loaded chitosan nanoparticles (TLCNPs) against MDR UPEC isolates urinary catheters. TLCNPs were prepared using the ionotropic gelation method and characterized by scanning electron microscopy (SEM), dynamic light scattering (DLS), and Fourier-transform infrared spectroscopy (FTIR). The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined using the broth microdilution method. Antibiofilm activity was assessed by the microtiter plate crystal violet assay. The relative expression of fimA and fimH genes was evaluated using real-time PCR. Cytotoxicity was assessed by the MTT assay on a human bladder carcinoma cell line (EJ138). The results showed that TLCNPs exhibited antibacterial activity against MDR UPEC isolates, with MIC and MBC values of 625 µg/mL. Biofilm formation was reduced by up to 76.2 ± 0.6% at ½ MIC concentration. Although a decrease in the relative expression of fimA and fimH genes was observed following treatment with TLCNPs, these changes were not statistically significant. Cytotoxicity assays indicated that more than 70% of EJ138 cells remained viable after 24 h, and over 50% after 48 h at ½ MIC. Overall, this study evaluated the antibacterial, antibiofilm, and preliminary safety profile of thymol-loaded chitosan nanoparticles against MDR UPEC, providing experimental data for their further investigation as a potential adjunct approach for biofilm-associated UTIs.

Indexed as

Anti-Bacterial AgentsBiofilmsChitosanNanoparticlesThymolUropathogenic Escherichia coliHumansMicrobial Sensitivity TestsUrinary CathetersUrinary Tract InfectionsAnti-Bacterial AgentsChitosanThymol

Identifiers

PMID41923040
PMCPMC13173837

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.