4.8 Article

Bacteria-like mesoporous silica-coated gold nanorods for positron emission tomography and photoacoustic imaging-guided chemo-photothermal combined therapy

Journal

BIOMATERIALS
Volume 165, Issue -, Pages 56-65

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.02.043

Keywords

Gold nanorods; Mesoporous silica nanoparticles; Positron emission tomography; Chemo-photothermal therapy; Cancer; Theranostics

Funding

  1. University of Wisconsin Madison, United States
  2. National Institutes of Health, United States [NIBIB/NCI 1R01CA169365, P30CA014520, 1R01CA205101, 1R01EB021336, S10-OD018505]
  3. American Cancer Society, United States [125246-RSG-13-099-01-CCE]
  4. China Scholarship Council
  5. NATIONAL CANCER INSTITUTE [R01CA169365, P30CA014520, R01CA205101] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB021336] Funding Source: NIH RePORTER
  7. OFFICE OF THE DIRECTOR, NATIONAL INSTITUTES OF HEALTH [S10OD018505] Funding Source: NIH RePORTER

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Mesoporous silica nanoshell (MSN) coating has been demonstrated as a versatile surface modification strategy for various kinds of inorganic functional nanoparticles, such as gold nanorods (GNRs), to achieve not only improved nanoparticle stability but also concomitant drug loading capability. However, limited drug loading capacity and low tumor accumulation rate in vivo are two major challenges for the biomedical applications of MSN-coated GNRs (GNR@MSN). In this study, by coating uniformly sized GNRs with MSN in an oil-water biphase reaction system, we have successfully synthesized a new bacteria-like GNR@MSN (i.e., bGNR@MSN) with a significantly enlarged pore size (4-8 nm) and surface area (470 m(2)/g). After PEGylation and highly efficient loading of doxorubicin (DOX, 40.9%, w/w), bGNR@MSN were used for positron emission tomography (PET, via facile and chelator-free Zr-89-labeling) and photoacoustic imaging-guided chemo-photothermal cancer therapy in vivo. PET imaging showed that Zr-89-labeled bGNR@MSN(DOX)-PEG can passively target to the 411 murine breast cancer-bearing mice with high efficiency (similar to 10 %ID/g), based on enhanced permeability and retention effect. Significantly enhanced chemo-photothermal combination therapy was also achieved due to excellent photo thermal effect and near-infrared-light-triggered drug release by bGNR@MSN(DOX)-PEG at the tumor site. The promising results indicate great potential of bGNR@MSN-PEG nanoplatforms for future cancer diagnosis and therapy. (C) 2018 Elsevier Ltd. All rights reserved.

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