4.6 Article

PEGylated FePt@Fe2O3 core-shell magnetic nanoparticles: Potential theranostic applications and in vivo toxicity studies

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出版社

ELSEVIER
DOI: 10.1016/j.nano.2013.02.010

关键词

Magnetic nanoparticles; FePt@Fe2O3 core-shell nanoparticles; Magnetic resonance imaging; Drug delivery; Toxicology

资金

  1. National Basic Research Program (973 Program) of China [2012CB932600, 2011CB911002]
  2. National Natural Science Foundation of China [51132006, 51002100, 81171394, 81171392, k112218511]
  3. Natural Science Fund of Jiangsu Province [BK2011307]
  4. Natural Science Fund for colleges and Universities in Jiangsu Province [09KJB320016]
  5. Jiangsu Province's Key Discipline of Medicine [XK201118]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions

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Herein, we develop FePt@Fe2O3 core-shell magnetic nanoparticles as a T-2 magnetic resonance (MR) imaging contrast agent as well as a drug carrier for potential cancer theranostic applications. The FePt@Fe2O3 core-shell nanoparticles are synthesized and then functionalized with polyethylene glycol (PEG). Folic acid (FA) is conjugated on the surface of FePt@Fe2O3-PEG nanoparticles for effective targeting of folate receptor (FR)-positive tumor cells. A chemotherapy drug, doxorubicin (DOX), is then loaded onto those nanoparticles via hydrophobic physical adsorption, for targeted intracellular drug delivery and selective cancer cell killing. We then use those FePt@ Fe2O3-PEG nanoparticles for in vivo MR imaging, observing obvious tumor MR contrasts, which resulted from both passive tumor accumulation and active tumor targeting of nanoparticles. Moreover, both in vitro and in vivo studies uncover no obvious toxicity for FePt@Fe2O3-PEG nanoparticles. Therefore, our PEGylated FePt@Fe2O3 core-shell nanoparticles could serve as a promising multifunctional theranostic nanoplatform in imaging guided cancer therapy. (C) 2013 Elsevier Inc. All rights reserved.

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