Siribbal, Shifaa M., Ilyas, Shaista, Renner, Alexander M., Iqbal, Sumiya, Munoz Vazquez, Sergio, Moawia, Abubakar, Valldor, Martin, Hussain, Muhammad S., Schomaecker, Klaus and Mathur, Sanjay (2022). Click functionalized biocompatible gadolinium oxide core-shell nanocarriers for imaging of breast cancer cells. RSC Adv., 12 (49). S. 31830 - 31846. CAMBRIDGE: ROYAL SOC CHEMISTRY. ISSN 2046-2069

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Abstract

Site-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 (Ga-68). 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.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Siribbal, Shifaa M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ilyas, ShaistaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Renner, Alexander M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Iqbal, SumiyaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Munoz Vazquez, SergioUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Moawia, AbubakarUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Valldor, MartinUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hussain, Muhammad S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Schomaecker, KlausUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mathur, SanjayUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-678136
DOI: 10.1039/d2ra00347c
Journal or Publication Title: RSC Adv.
Volume: 12
Number: 49
Page Range: S. 31830 - 31846
Date: 2022
Publisher: ROYAL SOC CHEMISTRY
Place of Publication: CAMBRIDGE
ISSN: 2046-2069
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
MAGNETIC-RESONANCE; SURFACE MODIFICATION; FE3O4 NANOPARTICLES; CONTRAST AGENTS; LUMINESCENCE; RELAXIVITY; FACILE; T-1; CUMultiple languages
Chemistry, MultidisciplinaryMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/67813

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