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dc.date.accessioned2023-03-14T17:52:30Z
dc.date.available2023-03-14T17:52:30Z
dc.date.created2022-12-19T08:57:03Z
dc.date.issued2022
dc.identifier.citationSiribbal, Shifaa M. Ilyas, Shaista Renner, Alexander M. Iqbal, Sumiya Muñoz Vázquez, Sergio Moawia, Abubakar Valldor, Björn Martin Hussain, Muhammad S. Schomäcker, Klaus Mathur, Sanjay . Click functionalized biocompatible gadolinium oxide core-shell nanocarriers for imaging of breast cancer cells. RSC Advances. 2022, 12(49), 31830-31845
dc.identifier.urihttp://hdl.handle.net/10852/101456
dc.description.abstractSite-specific delivery using functionalized nanocarriers is in high demand in imaging applications of modern clinical research. To improve the imaging capabilities of conventionally used contrast agents and expand the targeting accuracy, functional gadolinium oxide based nanocarriers originated from homogeneous core shells structures (Gd2O3@SiO2@Fe3O4) were developed using a multilayer formation approach. The synthesis and chemical configuration for the covalent binding of macrocyclic chelating agents and estrogen targeting molecules on these nanocarriers were designed by a two-step chemical synthesis method. Initially, SiO2@Fe3O4 structures were prepared and encapsulated with a homogenous thin Gd2O3 overlayer. The exterior surface of the as-prepared carriers offered chemical binding with a breast cancer specific estrogen molecule, covalently grafted through a Click-Chemistry protocol. In the next step, to enhance the diagnostic imaging capabilities of these carriers, thiocyanate-linked chelator molecule, DOTA, was attached to the surface of estrogen bound Gd2O3@SiO2@Fe3O4 using basic reaction conditions. The active amino groups before and after conjugation of estrogen molecules on the surface were quantified using a fluorescamine based approach. Due to the covalent binding of the macrocyclic chelator to the Gd2O3@SiO2@Fe3O4 surface, core shell carriers showed potential radiolabeling efficiency using positron emitter radionuclide, gallium-68 (68Ga). Intracellular uptake of estrogen-conjugated carriers was evaluated with MCF7 breast cancer cell lines using confocal laser scanning microscopy and fluorescent flow cytometry. In addition, in vitro cytotoxicity studies of functional nanocarriers as compared to bare nanoparticles showed reduced toxicity to HEK-293 cells demonstrating the role of surface attached molecules in preventing direct exposure of the Gd2O3 surface to the cells. The as-developed gadolinium based nanocarriers presented excellent capabilities as biocompatible target-specific imaging probes which indicates great potential in the field of dual-mode contrast agents.
dc.languageEN
dc.rightsAttribution-NonCommercial 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/
dc.titleClick functionalized biocompatible gadolinium oxide core-shell nanocarriers for imaging of breast cancer cells
dc.title.alternativeENEngelskEnglishClick functionalized biocompatible gadolinium oxide core-shell nanocarriers for imaging of breast cancer cells
dc.typeJournal article
dc.creator.authorSiribbal, Shifaa M.
dc.creator.authorIlyas, Shaista
dc.creator.authorRenner, Alexander M.
dc.creator.authorIqbal, Sumiya
dc.creator.authorMuñoz Vázquez, Sergio
dc.creator.authorMoawia, Abubakar
dc.creator.authorValldor, Björn Martin
dc.creator.authorHussain, Muhammad S.
dc.creator.authorSchomäcker, Klaus
dc.creator.authorMathur, Sanjay
cristin.unitcode185,15,17,0
cristin.unitnameSenter for materialvitenskap og nanoteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2094927
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=RSC Advances&rft.volume=12&rft.spage=31830&rft.date=2022
dc.identifier.jtitleRSC Advances
dc.identifier.volume12
dc.identifier.issue49
dc.identifier.startpage31830
dc.identifier.endpage31845
dc.identifier.doihttps://doi.org/10.1039/d2ra00347c
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2046-2069
dc.type.versionPublishedVersion


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