4.8 Article

Sub-100 nm hollow Au-Ag alloy urchin-shaped nanostructure with ultrahigh density of nanotips for photothermal cancer therapy

期刊

BIOMATERIALS
卷 35, 期 13, 页码 4099-4107

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.01.053

关键词

Cancer; Photothermal therapy; Nanourchins; Hollow Au-Ag alloy; Photothermal conversion efficiency

资金

  1. National Natural Science Foundation of China [51171139, 51222203, 51002100, 51132006, 51302180]
  2. Tengfei Talent Project of Xi'an Jiaotong University
  3. New Century Excellent Talents in University (NCET)
  4. Scientific New Star Program in Shaanxii Province [2012KJXX-03]
  5. Fundamental Research Funds for the Central Universities [08142008]
  6. Doctoral Fund of Ministry of Education of China [20110201120039, 20130201110032]
  7. National 973 Program of China [2011CB911002, 2012C8932601]
  8. Priority Academic Program Development of Jiangsu Higher Education Institutions
  9. National Natural Science Foundation of Jiangsu Province [BK20130305]
  10. Postdoctoral science foundation of China [2013M531400]
  11. Postdoctoral research program of Jiangsu Province [1202044C]

向作者/读者索取更多资源

The 'sea urchin nanostructures with particular small size (<100 nm) and abundant multi-tips have not yet been employed for the cancer photothermal therapy (PTT). Here we report sub-100 nm hollow Au-Ag alloy nanourchins (HAAA-NUs) with ultrahigh density of nanotips synthesized via a facile seed-mediated growth. The HAAA-NUs exhibit a remarkably integrated high-quality photothermal feature including well-defined but tunable surface plasmon resonance peak, strong absorption (2.2 x 10(10) M-1 cm(-1)) as well as high photothermal conversion efficiency (80.4%) in the near-infrared region. Importantly, the HAAA-NUs demonstrate improved photothermal stability verified via continuous exposition and cyclic irradiation of laser beam. The cell assay, in vitro cell ablation and in vivo breast cancer treatment verify that the HAAA-NUs are superior photothermal agent for photothermal tumor ablation therapy owing to low toxicity and high cell destruction capability. (c) 2014 Elsevier Ltd. All rights reserved.

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