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                <text>Faculty Publications</text>
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              <text>Thangavelu, Indumathi; Tadepalli, Srinivas</text>
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              <text>Chitosan coated multifunctional NiFe?O? nanocomposites as a promising candidate for biomedical applications</text>
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              <text>01-01-2026</text>
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              <text>Naunyn-Schmiedeberg's Archives of Pharmacology;</text>
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              <text>&lt;a href="https://doi.org/10.1007/s00210-025-04904-3" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1007/s00210-025-04904-3&lt;/a&gt; &lt;br /&gt;&lt;br /&gt;&lt;a href="https://www.scopus.com/pages/publications/105028308245?origin=resultslist" target="_blank" rel="noreferrer noopener"&gt;https://www.scopus.com/pages/publications/105028308245?origin=resultslist&lt;/a&gt;</text>
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              <text>Thangavelu I., Department of Chemistry, CHRIST (Deemed to Be University), Bangalore, 560029, India; Tadepalli S., Department of Chemical Engineering, College of Engineering, Imam Mohammad Ibn Saud Islamic University (IMSIU), 11432, Riyadh, Saudi Arabia</text>
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              <text>Nanoparticles for biomedical applications often suffer from limited stability, low biocompatibility, and suboptimal therapeutic efficacy. To address these challenges, NiFe?O? nanoparticles were functionalized with chitosan (NiFe?O?-CS) via a co-precipitation method, aiming to enhance their structural, optical, antimicrobial, and anticancer properties. XRD analysis revealed a reduction in crystallite size from 37 to 33nm after chitosan modification, indicating controlled crystal growth and increased surface area. TEM results confirmed a corresponding decrease in particle size from 35  2.1nm to 29  1.8nm, improving surface reactivity and stability. PL spectra exhibited a red-shift in green emission peaks, suggesting increased oxygen vacancies and defect states that facilitate ROS generation. Antimicrobial assays against methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans (C.albicans) demonstrated significantly higher activity for NiFe?O?-CS nanocomposites, supported by SEM imaging that showed extensive microbial membrane disruption. Furthermore, NiFe?O?-CS exhibited enhanced anticancer activity against C6 glioma cells, with an IC?? of 35.6g/mL compared to 43.6g/mL for unmodified nanoparticles. Zebrafish embryo studies confirmed the biocompatibility of NiFe?O?-CS at appropriate doses, although dose-dependent embryotoxicity was observed. These findings highlight that chitosan functionalization of dual-metal nanoparticles improves therapeutic efficacy through increased surface interactions and ROS generation while underscoring the need for careful dose optimization. This study presents a novel strategy for designing biopolymer-coated nanocomposites that balance enhanced biomedical performance with safety considerations.  The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2026.</text>
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              <text>Biocompatibility; Embryotoxic; Glioma cancer; MRSA; NiFe&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;; Zebrafish</text>
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              <text>Springer Science and Business Media Deutschland GmbH</text>
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              <text>ISSN: 281298; CODEN: NSAPC</text>
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              <text>Restricted Access; Hardcopy may be available in the library</text>
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