4.8 Article

A Versatile Imaging and Therapeutic Platform Based on Dual-Band Luminescent Lanthanide Nanoparticles toward Tumor Metastasis Inhibition

Journal

ACS NANO
Volume 10, Issue 2, Pages 2766-2773

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b07873

Keywords

Nd3+-sensitized lanthanide nanoparticles; upconversion emissions; NIR imaging photodynamic therapy; tumor metastasis

Funding

  1. NSFC [21425101, 21321001, 21371011, 21331001]
  2. MOST of China [2014CB643800]

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Upconversion (UC) luminescent lanthanide nanoparticles (LNPs) are expected to play an important role in imaging and photodynamic therapy (PDT) in vitro and in vivo. However, with the absorption of UC emissions by photosensitizers (PSs) to generate singlet oxygen (O-1(2)) for PDT, the imaging signals from LNPs are significantly weakened. It is important to activate another imaging route to track the location of the LNPs during PDT process. In this work, Nd3+-sensitized LNPs with dual -band visible and near -infrared (NIR) emissions under single 808 nm excitation were reported to address this issue. The UC emissions in green could trigger covalently linked rose bengal (RB) molecules for efficient PDT, and MR emissions deriving from Yb3+ and magnetic resonance imaging (MRI) were used for imaging simultaneously. Notably, the designed therapeutic platform could further effectively avoid the overheating effect induced by the laser irradiation, due to the minimized absorption of biological media at around 808 nm. TdT-mediated dUTP nick end labeling (TUNEL) assay showed serious cell apoptosis in the tumor after PDT for 2 weeks, leading to an effective tumor inhibition rate of 67%. Benefit from the PDT, the tumor growth -induced liver and spleen burdens were largely attenuated, and the liver injury was also alleviated. More importantly, pulmonary and hepatic tumor metastases were significantly reduced after PDT. The Nd3+-sensitized LNPs provide a multifunctional nanoplatform for MR light-assisted PDT with minimized heating effect and an effective inhibition of tumor growth and metastasis.

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