4.6 Article

Theranostics With Multifunctional Magnetic Gold Nanoshells Photothermal Therapy and T2* Magnetic Resonance Imaging

期刊

INVESTIGATIVE RADIOLOGY
卷 46, 期 2, 页码 132-140

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RLI.0b013e3181f8e7d8

关键词

theranostics; gold nanoshells; T-2* magnetic resonance imaging; photothermal ablation; ultrasmall paramagnetic iron oxide

资金

  1. NCI Cancer Center [CA016672]
  2. Odyssey Program
  3. Cockrell Foundation for Scientific Achievement at The University of Texas M. D. Anderson Cancer Center
  4. National Institutes of Health [R01 CA119387]
  5. John S. Dunn Foundation
  6. Odyssey Fellowship
  7. SPORE Head and Neck Career Development Award [P50CA097007]

向作者/读者索取更多资源

Objectives: To investigate the multifunctional imaging and therapeutic capabilities of core-shell nanoparticles composed of a superparamagnetic iron oxide (SPIO) core and a gold shell (SPIO@AuNS). Materials and Methods: The magnetic/optical properties of SPIO@AuNS were examined both in an agar gel phantom and in vivo by evaluating contrast-enhanced magnetic resonance imaging (MRI) and by measuring near-infrared (NIR) light-induced temperature changes mediated by SPIO@AuNS. In addition, the biodistribution and pharmacokinetics of In-111-labeled SPIO@AuNS after intravenous injection in mice bearing A431 tumors were evaluated in the presence and absence of an external magnet. Results: In agar phantoms containing SPIO@AuNS, a significant contrast enhancement in T2-weighted MRI was observed and a linear increase in temperature was observed with increasing concentration and laser output power when irradiated with NIR light centered at an 808 nm. In vivo, T-2*-MRI delineated SPIO@AuNS and magnetic resonance temperature imaging of the same tumors revealed significant temperature elevations when intratumorally injected with SPIO@AuNS (1 x 10(11) particles/mouse) and irradiated with NIR light (65.70 degrees C +/- 0.69 degrees C vs. 44.23 degrees C +/- 0.24 degrees C for saline + laser). Biodistribution studies in mice intravenously injected with In-111-labeled-SPIO@AuNS(1 x 10(13) particles/mouse) had an approximately 2-fold increase in SPIO@AuNS delivered into tumors in the presence of an external magnet compared with tumors without the magnet. Conclusions: Owing to its ability to mediate efficient photothermal ablation of cancer cells under MRI guidance, as well as the ability to be directed to solid tumors with an external magnetic field gradient, multifunctional SPIO@AuNS is a promising theranostic nanoplatform.

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