Macroporous alginate scaffolds with calcium phosphate filler as a 3D in vitro microenvironment supporting bone cancer cells

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorBanicevic, Ivana
dc.contributor.authorMilosevic, Mia
dc.contributor.authorPetrovic, Jelena
dc.contributor.authorMilivojevic, Milena
dc.contributor.authorGasik, Michael
dc.contributor.authorStojkovska, Jasmina
dc.contributor.authorObradovic, Bojana
dc.contributor.departmentDepartment of Chemical and Metallurgical Engineeringen
dc.contributor.groupauthorMaterials Processing and Powder Metallurgyen
dc.contributor.organizationUniversity of Belgrade
dc.date.accessioned2026-02-02T09:16:31Z
dc.date.available2026-02-02T09:16:31Z
dc.date.issued2025-12-27
dc.description| openaire: EC/H2020/860462/EU//PREMUROSA | openaire: EC/H2020/952033/EU//ExcellMater
dc.description.abstractMacroporous Ca-alginate scaffolds with hydroxyapatite/β-tricalcium phosphate filler were investigated regarding possibilities to provide an adequate environment for 3D bone cancer cell cultures. Two scaffold groups were obtained from starting solutions: 1 wt.% Na-alginate, 1 wt% filler and 0.03 wt.% CaCl2 (G1) and 2 wt.% Na-alginate, 2 wt.% filler and 0.045 wt.% CaCl2 (G2). The scaffolds were produced by controlled alginate gelation followed by lyophilization, and further characterized regarding stability in culture medium, mechanical properties and biocompatibility in cultures of murine osteosarcoma cells K7M2-wt. While the scaffold porosity was the same for both groups (∼60%), G2 scaffolds exhibited higher stiffness and higher stability in the culture medium. Next, the cell seeding procedure was optimized followed by cultivation of the seeded scaffolds (1.5 × 106–4 × 106 cells/scaffold) for 7 days under continuous perfusion. The seeding strategy and scaffold architecture facilitated cell infiltration throughout the scaffold. The cells remained viable, while perfusion apparently induced higher cell metabolic activity as compared to static cultures, especially at the higher medium superficial velocity (40 μm/s vs. 15 μm/s). While few literature approaches use bioreactors, our study introduces a robust platform with scaffolds and perfusion to better mimic physiological conditions in 3D models in bone cancer research.en
dc.description.versionPeer revieweden
dc.identifier.citationBanicevic, I, Milosevic, M, Petrovic, J, Milivojevic, M, Gasik, M, Stojkovska, J & Obradovic, B 2025, 'Macroporous alginate scaffolds with calcium phosphate filler as a 3D in vitro microenvironment supporting bone cancer cells', International Journal of Polymeric Materials and Polymeric Biomaterials. https://doi.org/10.1080/00914037.2025.2608101en
dc.identifier.doi10.1080/00914037.2025.2608101
dc.identifier.issn1563-535X
dc.identifier.otherPURE UUID: fdbdc4a7-ad43-459e-b417-96d28a511df1
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/fdbdc4a7-ad43-459e-b417-96d28a511df1
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/142978
dc.identifier.urnURN:NBN:fi:aalto-202602022344
dc.language.isoenen
dc.publisherGordon and Breach Science Publishers
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/952033/EU//ExcellMater
dc.relation.fundinginfoThis work was supported by the European Union’s Horizon 2020 research and innovation programme under Marie Skłodowska-Curie ITN Grant Agreement No. 860462; the European Union’s Horizon 2020 under Grant Agreement No. 952033; and the Ministry of Science, Technological Development and Innovation of the Republic of Serbia under Contract Nos. 451-03-136/2025-03/200135, 451-03-137/2025-03/200135, 451-03-136/2025-03/200287, 451-03-136/2025-03/200042.
dc.relation.ispartofseriesInternational Journal of Polymeric Materials and Polymeric Biomaterialsen
dc.rightsrestrictedAccessen
dc.subject.keywordbeta-tricalcium phosphate
dc.subject.keywordBiomimetic
dc.subject.keywordbone tumor engineering
dc.subject.keywordhydroxyapatite
dc.subject.keywordperfusion bioreactor
dc.titleMacroporous alginate scaffolds with calcium phosphate filler as a 3D in vitro microenvironment supporting bone cancer cellsen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi

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