Evidence map›Paper›PMID 40569371›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

Chitosan and L-histidine coated biofunctional TiO₂ composite with enhanced ROS-mediated antimicrobial and anticancer efficacy for biomedical applications.

Indumathi Thangavelu, Srinivas Tadepalli, AbdulAziz A AlGhamdi, Thalakulam Shanmugam Boopathi

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Indumathi ThangaveluDepartment of Chemistry, CHRIST (Deemed to Be University), Bangalore, Karnataka, 560029, India.
Srinivas TadepalliDepartment of Chemical Engineering, College of Engineering, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, 11432, Kingdom of Saudi Arabia. stadepalli@imamu.edu.sa.
AbdulAziz A AlGhamdiDepartment of Chemical Engineering, College of Engineering, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, 11432, Kingdom of Saudi Arabia.
Thalakulam Shanmugam BoopathiDepartment of Chemistry, Amrita School of Physical Sciences Coimbatore, Amrita Vishwa Vidyapeetham, Coimbatore, India, 641112.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Societies continue to face the urgent challenge of developing effective, safe, and stable nanoparticles with promising biomedical applications. Herein, the present study synthesis chitosan and L-Histidine dually coated titanium dioxide (TiCSLH) nanocomposite (NC) by chemical co-precipitation method. The antimicrobial performance of TiO₂ nanoparticles is closely linked to their physicochemical properties, such as reduced particle size, increased bandgap, and the presence of oxygen vacancies, all of which collectively enhance reactive oxygen species (ROS) generation and inhibit microbial growth. Structural analyses using XRD and TEM confirmed that TiCSLH nanoparticles possess an anatase phase and a spherical morphology. Compared to TiO₂, TiCSLH nanoparticles demonstrated significantly enhanced antimicrobial activity against MRSA, E. coli, K. pneumoniae, P. aeruginosa and C. albicans strains, as evidenced by larger zones of inhibition from 23-24 mm. This enhanced efficacy is attributed to their smaller particle size (~ 26 ± 3 nm), wider bandgap (3.34 eV), and prominent oxygen vacancy-related emissions at 518 and 531 nm, which facilitate increased ROS production, resulting in cellular membrane disruption and microbial death. Furthermore, compared to TiO

Indexed as

Anti-Infective AgentsAntineoplastic AgentsChitosanHistidineNanocompositesReactive Oxygen SpeciesTitaniumAnimalsCell Line, TumorCell SurvivalHumansMiceMicrobial Sensitivity TestsParticle SizeAnti-Infective AgentsAntineoplastic AgentsChitosanHistidineReactive Oxygen SpeciesTitaniumtitanium dioxideBreast cancer cellChitosanL-HistidineMRSATiO2

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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.