Microemulsion-made gadolinium carbonate hollow nanospheres showing magnetothermal heating and drug release

Gadolinium carbonate (Gd (CO ) ) hollow nanospheres and their suitability for drug transport and magnetothermally-induced drug release are presented. The hollow nanospheres are prepared via a microemulsion-based synthesis using tris(tetramethylcyclopentadienyl)gadolinium(iii) and CO as the starting...

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Veröffentlicht in:Nanoscale 2017-06, Vol.9 (24), p.8362-8372
Hauptverfasser: Jung-König, J, Sanhaji, M, Popescu, R, Seidl, C, Zittel, E, Schepers, U, Gerthsen, D, Hilger, I, Feldmann, C
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Sprache:eng
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Zusammenfassung:Gadolinium carbonate (Gd (CO ) ) hollow nanospheres and their suitability for drug transport and magnetothermally-induced drug release are presented. The hollow nanospheres are prepared via a microemulsion-based synthesis using tris(tetramethylcyclopentadienyl)gadolinium(iii) and CO as the starting materials. Size, structure and composition of the as-prepared Gd (CO ) hollow nanospheres are comprehensively validated by several independent analytical methods (HRTEM, HAADF-STEM, DLS, EDXS, XRD, FT-IR, DTA-TG). Accordingly, they exhibit an outer diameter of 26 ± 4 nm, an inner cavity of 7 ± 2 nm, and a wall thickness of 9 ± 3 nm. As a conceptual study, the nanocontainer-functionality of the Gd (CO ) hollow nanospheres is validated upon filling with the anti-cancerogenic agent doxorubicin (DOX), which is straightforward via the microemulsion (ME) strategy. The resulting DOX@Gd (CO ) nanocontainers provide the option of multimodal imaging including optical and magnetic resonance imaging (OI, MRI) as well as magnetothermal heating and drug release. As a proof-of-concept, we could already prove the intrinsic DOX-based fluorescence, a low systemic toxicity according to in vitro studies as well as the magnetothermal effect and a magnetothermally-induced DOX release. In particular, the latter is new for Gd-containing nanoparticles and highly promising in view of theranostic nanocontainers and synergistic physical and chemical tumor treatment.
ISSN:2040-3364
2040-3372
DOI:10.1039/c7nr01784g