4.8 Article

Biologically Inspired Polydopamine Capped Gold Nanorods for Drug Delivery and Light-Mediated Cancer Therapy

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 8, 期 37, 页码 24368-24384

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b05907

关键词

polydopamine; gold nanorods; drug delivery; photodynamic; photothermal; chemotherapy; light-mediated therapy

资金

  1. National Basic Research Program of China (973 Program) [2013CB834704]
  2. National Natural Science Foundation of China [61275190, 61178062, 61008052, 91233208]
  3. Program of Zhejiang Leading Team of Science and Technology Innovation [2010R50007]
  4. Fundamental Research Funds for the Central Universities
  5. Swedish Research Council

向作者/读者索取更多资源

Multifunctional drug delivery and combined multi modal therapy strategies are very promising in tumor theranostic applications. In this work, a simple and versatile nanoplatform based on biologically inspired polydopamine capped gold nanorods (GNR-PDA) is developed. Dopamine, a well-known neurotransmitter associated with many neuronal disorders, can undergo self-polymerization on the surface of GNRs to form a stable PDA shell. Its unique molecular adsorption property, as well as its high chemical stability and biocompatibility, facilitate GNR-PDA as an ideal candidate for drug delivery. Methylene blue (MB) and doxorubicin (DOX) are directly adsorbed on GNR-PDA via electrostatic and/or pi-pi stacking interactions, forming GNR-PDA-MB and GNR-PDA-DOX nanocomposites, respectively. The GNR-PDA-MB can generate reactive oxygen species (ROS, from MB) or hyperthermia (from GNR-PDA) with high efficiency under deep-red/NIR laser irradiation, while the GNR-PDA-DOX exhibits light-enhanced drug release under NIR laser irradiation. The combined dual modal light-mediated therapy, by using GNR-PDA-MB [photodynamic/photothermal therapy (PDT/PTT)] and GNR-PDA-DOX (Chemo/PTT), is carried out and shows remarkable cancer cell killing efficiency in vitro and significant suppression of tumor growth in vivo, which are much more distinct than any single-modal therapy strategy. Our work illustrates that GNR-PDA could be a promising nanoplatform for multifunctional drug delivery and multimodal tumor theranostics in the future.

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