Evidence map›Paper›PMID 41634676›Full record

ArticleBMC biotechnology2026

Berberine-ZnO loaded chitosan nanoparticles inhibits biofilm formation in Pseudomonas aeruginosa PAO1 through targeting extracellular polymeric substances.

Fatemeh Esnaashari, Fatemeh Azizi Alidoust, Nastaran Jafari, Mohebat Ghasemi, Fatemeh Asadi Rahmani, Sara Sedaghat Safsari, Hossein Zahmatkesh

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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.

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5 · Who and what money

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7 authors.

Fatemeh EsnaashariDepartment of Biology, La. C., Islamic Azad University, Lahijan, Iran.
Fatemeh Azizi AlidoustDepartment of Microbiology, La. C., Islamic Azad University, Lahijan, Iran.
Nastaran JafariDepartment of Plant Protection, Faculty of Agriculture, University of Tabriz, Tabriz, Iran.
Mohebat GhasemiDepartment of Microbiology, La. C., Islamic Azad University, Lahijan, Iran.
Fatemeh Asadi RahmaniDepartment of Microbiology, La. C., Islamic Azad University, Lahijan, Iran.
Sara Sedaghat SafsariDepartment of Genetics, La. C., Islamic Azad University, Lahijan, Iran.
Hossein ZahmatkeshDepartment of Biology, University of Guilan, Rasht, Iran. hza.zahmatkesh@gmail.com.ORCID 0000-0003-2765-7718

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiofilm formation is an important strategy for coping with antimicrobial agents and worsening bacterial infections. In this investigation, we synthesized berberine-zinc oxide-loaded chitosan nanoparticles (CS-ZnO-Ber NPs) and explored their potential as anti-biofilm agents against Pseudomonas aeruginosa PAO1.

resultsCS-ZnO-Ber NPs exhibited an amorphous structure with particle sizes ranging from 34.7 to 407.7 nm and a zeta potential of − 38.5 mV. The biofilm inhibitory activity of the fabricated NPs was validated using a crystal violet staining assay. Based on the SEM imaging, cells treated with NPs displayed thin biofilms with low aggregation, whereas the untreated group exhibited robust biofilms with dense architecture. Moreover, at sub-inhibitory concentration of CS-ZnO-Ber NPs, the production levels of extracellular matrix components, including exopolysaccharides, pellicle, and alginate, decreased by 92.81 ± 0.84%, 81.45 ± 3.1%, and 31.74 ± 2.91%, respectively. Additionally, exposure to CS-ZnO-Ber NPs resulted in a significant reduction in pyocyanin production and attenuation of bacterial motility, including swimming, swarming, and twitching. CS-ZnO NPs and CS-ZnO-Ber NPs also decreased the EtBr MIC four-fold and eight-fold, respectively, indicating their efflux pump–inhibitory activity. Furthermore, molecular docking simulations revealed a favorable binding orientation of berberine with biofilm-associated proteins (AlgD, PelD, and PslG), as well as with quorum-sensing regulators LasI and LasR.

conclusionOverall, CS-ZnO-Ber NPs substantially diminished extracellular matrix components, leading to the formation of weak and unstable biofilms. Pending further investigation, these findings suggest that CS-ZnO-Ber NPs hold promise as effective agents for controlling biofilm-related infections caused by P. aeruginosa.

Indexed as

Anti-Bacterial AgentsBerberineBiofilmsChitosanExtracellular Polymeric Substance MatrixNanoparticlesPseudomonas aeruginosaZinc OxideAlginatesBacterial ProteinsMolecular Docking SimulationParticle SizePyocyanineAlginatesAnti-Bacterial AgentsBacterial ProteinsBerberineChitosanPyocyanineZinc OxideAlginateAntibiofilmExopolysaccharidesMotilityPyocyaninQuorum-sensing

Identifiers

PMID41634676
PMCPMC12958632

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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.