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dc.creatorOgnjanović, Miloš
dc.creatorBošković, Marko
dc.creatorStanojković, Tatjana
dc.creatorDojčinović, Biljana P.
dc.creatorAbeykoon, A. M. Milinda
dc.creatorTomić, Aleksandra
dc.creatorJanković, Drina
dc.creatorVranješ-Đurić, Sanja
dc.creatorBozin, Emil S.
dc.creatorAntić, Bratislav
dc.date.accessioned2025-09-03T09:26:42Z
dc.date.available2025-09-03T09:26:42Z
dc.date.issued2025
dc.identifier.issn1944-8244
dc.identifier.issn1944-8252
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsami.5c12439
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/15348
dc.description.abstractThe development of nanoplatforms capable of efficient heat generation and stable radionuclide delivery is essential for effective bimodal cancer therapy. In this study, binary (Fe–M) and ternary (Fe–M–M′) metal oxide nanoparticles were synthesized via a polyol method optimized to produce flower-like γ-Fe2O3 (maghemite) structures, with M and M′ representing Zn and/or Mn. Comprehensive structural and magnetic characterization was conducted to explain the relationship between composition, defect structure, and hyperthermic performance. The analyses revealed that cation substitution induced an Fe-site vacancy, primarily at octahedral positions, leading to local structural distortions, as confirmed by powder X-ray diffraction and pair distribution function analysis. The optimized composition, with Zn/Mn/Fe = 0.040:0.182:1, exhibited the highest concentration of vacancies and structural disorder. These vacancies altered the bonding environment, enhancing magnetic interactions at tetrahedral sites while weakening those at the octahedral positions. The resulting multicore nanoflowers (20–63 nm; core size 13–18 nm) displayed strong heating performance, with intrinsic loss power ranging from 0.34 to 5.77 nHm2 kg–1. The optimized sample achieved a temperature increase of 30 °C within 2 min and a specific absorption rate of 369 W g–1. This composition was further coated with citrate (CA) and successfully radiolabeled with 177Lu, achieving a radiolabeling yield of 92.7% and excellent stability, thus forming a robust nanoplatform for combined magnetic hyperthermia and radionuclide therapy. Biological evaluation of the optimized S5 composition revealed selective cytotoxicity toward HeLa and LS174 cells, while toxicity was significantly lower to A549, A375, and normal MRC-5 cells. Citrate coating of S5 nanoparticles (S5@CA) drastically reduced their cytotoxicity across all tested cell lines (IC50 > 200 μg mL–1), confirming their enhanced biocompatibility for therapeutic applications. In HeLa cells subjected to magnetic hyperthermia, the viability decreased to approximately 84% after 30 min and 61% after 60 min of treatment, demonstrating the sustained hyperthermic effect at a controlled working temperature of 48 °C. These results underscore the effectiveness of cation substitution and vacancy engineering in tailoring the functional properties of maghemite-based nanomaterials for advanced multimodal cancer therapies.en
dc.language.isoen
dc.relationinfo:eu-repo/grantAgreement/ScienceFundRS/Prizma2023_TT/7282/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200017/RS//
dc.relationbilateral Serbia-NR China project No. 003417078 2024 013440 003 000 620 021
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200043/RS//
dc.relationHIP-2D-QM - ERA Chair project by the European Union’s Horizon Europe research and innovation program under grant agreement No. 101185375
dc.rightsrestrictedAccess
dc.sourceACS Applied Materials & Interfaces
dc.subjectmulticore nanoparticlesen
dc.subjectmicrostructureen
dc.subjectmagnetic hyperthermiaen
dc.subjectin vitroen
dc.subjectradiolabelingen
dc.subjectDefects in solidsen
dc.subjectHyperthermiaen
dc.subjectMagnetic propertiesen
dc.subjectNanoparticlesen
dc.subjectTransition metalsen
dc.titleFrom Structure to Function: Zn/Mn-Modified Maghemite as an Advanced Nanoplatform for Magnetic Hyperthermia and Radionuclide Therapyen
dc.typearticleen
dc.rights.licenseARR
dc.citation.volume17
dc.citation.issue33
dc.citation.spage46836
dc.citation.epage46849
dc.identifier.doi10.1021/acsami.5c12439
dc.citation.rankM21a
dc.description.otherCorrection to the article: [https://doi.org/10.1021/acsami.5c21701]
dc.type.versionpublishedVersion


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    [PRIZMA] Design of RADIOactive MAGnetic nanoconstructs for tumour therapy by synergy of nanobrachytherapy and magnetic hyperthermia

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