4.3 Article

Construction and evaluation of tumor nucleus-targeting nanocomposite for cancer dual-mode imaging - Guiding photodynamic therapy/photothermal therapy

出版社

ELSEVIER
DOI: 10.1016/j.msec.2019.04.088

关键词

WS2 nanoparticles; Au-25 nanoclusters; Single excitation laser; Nucleus targeting; PTT/PDT

资金

  1. National Natural Science Foundation of China [81402893]
  2. Key Scientific Research Project Plan of Colleges and Universities in Henan Province [17A350015]
  3. Training Program of Young Key Teachers in Colleges and Universities in Henan Province [2017GGJS010]
  4. Center for Modern Analysis and Computing of Zhengzhou University

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To tackle the barrier of the insufficient intra-cellular delivery of reactive oxygen species (ROS) and heat, we designed a multifunctional nanoplatform to release ROS and heat directly in the cell nucleus for enhancing combined photodynamic therapy (PDT) and photothermal therapy (PTT) of tumors. As a photothermal agent, WS2 nanoparticles were adsorbed photosensitive Au-25(Captopril)(18)(-) (Au-25) nanoclusters via electrostatic interaction. And Dexamethasone (Dex), a glucocorticoid with nucleus targeting capability, played a key role in the intra-nuclear process of heat and ROS. PTT can increase intra-tumoral blood flow to promote Au-25 produce more ROS for PDT. Under near infrared (NIR) laser irradiation at a single 808 nm, these nucleus targeting WS2 nanoplatforms showed a significant decreased cell viability of 18.2 +/- 1.7% and a high DNA damage degree of 59.6 +/- 8.3%. Furthermore, the WS2 nanoplatform could be further used for X-ray computed tomography (CT) images. Taken together, our study provided a new prospect for effectively diagnostic and enhancing PTT/PDT efficacy.

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