4.8 Article

Star-Shaped Magnetic-Plasmonic Au@Fe3O4 Nano-Heterostructures for Photothermal Therapy

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 25, Pages 29087-29098

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c04865

Keywords

core@shell; heterostructures; Au@Fe3O4; nanostar; magnetic-plasmonic; photothermal therapy

Funding

  1. European Union [823717-ESTEEM3]
  2. Russian Science Foundation [21-72-20158]
  3. Tuscany Region
  4. Russian Science Foundation [21-72-20158] Funding Source: Russian Science Foundation

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Researchers synthesized a Au@Fe3O4 core@shell structure with a unique morphology and combined plasmonic and magnetic properties. Advanced electron microscopy characterization confirmed the excellent crystallinity and uniformity of the structure. The magnetite shell exhibited a higher saturation magnetization compared to previous Au@Fe3O4 structures, attributing to the star-like morphology and large shell thickness. Cancer cells loaded with Au@Fe3O4 nanostars displayed magneto mechanical stress under a low frequency external magnetic field. The homogeneous and thick magnetite shell shifted the plasmonic resonance of the Au core to 640 nm, enabling applications in photothermal therapy and optical imaging.
Here, we synthesize a Au@Fe3O4 core@shell system with a highly uniform unprecedented star-like shell morphology with combined plasmonic and magnetic properties. An advanced electron microscopy characterization allows assessing the multifaceted nature of the Au core and its role in the growth of the peculiar epitaxial star-like shell with excellent crystallinity and homogeneity. Magnetometry and magneto-optical spectroscopy revealed a pure magnetite shell, with a superior saturation magnetization compared to similar Au@Fe3O4 heterostructures reported in the literature, which is ascribed to the star-like morphology, as well as to the large thickness of the shell. Of note, Au@Fe3O4 nanostar-loaded cancer cells displayed magneto mechanical stress under a low frequency external alternating magnetic field (few tens of Hz). On the other hand, such a uniform, homogeneous, and thick magnetite shell enables the shift of the plasmonic resonance of the Au core to 640 nm, which is the largest red shift achievable in Au@Fe3O4 homogeneous core@shell systems, prompting application in photothermal therapy and optical imaging in the first biologically transparent window. Preliminary experiments performing irradiation of a stable water suspension of the nanostar and Au@Fe3O4-loaded cancer cell culture suspension at 658 nm confirmed their optical response and their suitability for photothermal therapy. The outstanding features of the prepared system can be thus potentially exploited as a multifunctional platform for magnetic-plasmonic applications.

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