3.8 Article

Polydopamine Nanoparticles for Deep Brain Ablation via Near-Infrared Irradiation

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 6, Issue 1, Pages 664-672

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.9b01097

Keywords

photothermal therapy; ablation; polydopamine; nanoparticles

Funding

  1. National Natural Science Foundation of China [81701267, 81701684, 81903165]
  2. Interdisciplinary Program of Shanghai Jiao Tong University [YG2016QN01]
  3. Science Foundation from Sci-Tech Office of Guangdong Province China [2017A020215090]
  4. Science and Technology Foundation from Health and Family Planning commission of Guangdong Province China [A2017299]

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Local resection or ablation remains an important approach to treat drug-resistant central neurological disease. Conventional surgical approaches are designed to resect the diseased tissues. The emergence of photothermal therapy (PTT) offers a minimally invasive alternative. However, their poor penetration and potential off-target effect limit their clinical application. Here, polydopamine nanoparticles (PDA-NPs) were prepared and characterized. Studies were performed to evaluate whether PDA-NPs combined with near-infrared (NIR) light can be used to ablate deep brain structures in vitro and in vivo. PDA-NPs were prepared with a mean diameter of similar to 150 nm. The particles show excellent photothermal conversion efficiency. PDA-NPs did not show remarkable cytotoxicity against neuronallike SH-SYSY cell lines. However, it can cause significant cell death when combined with NIR irradiation. Transcranial NIR irradiation after PDA-NPs administration induced enhanced local hyperthermia as compared with NIR alone. Local temperature exceeded 60 degrees C after 6 min of irradiation plus PDA while it can only reach 48 degrees C with NIR alone. PTT with PDA (10 mg/mL, 3 mu L) and NIR (1.5 W/cm(2)) can ablate deep brain structures precisely with an ablation volume of similar to 6.5 mm(3). Histological analysis confirmed necrosis and apoptosis in the targeted area. These results demonstrate the potential of NP-assisted PTT for the treatment against nontumorous central neurological diseases.

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