4.8 Article

Ultrafast synthesis of ultrasmall polyethylenimine-protected AgBiS2 nanodots by rookie method for in vivo dual-modal CT/PA imaging and simultaneous photothermal therapy

Journal

NANOSCALE
Volume 10, Issue 35, Pages 16765-16774

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8nr04870c

Keywords

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Funding

  1. National Natural Science Foundation of China [21590794, 21210001, 21521092]
  2. Youth Innovation Promotion Association of Chinese Academy of Sciences [2015181]
  3. CAS [YZDY-SSW-JSC018]
  4. Jilin Province Science and Technology Development Plan Project [20180101172JC]

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Developing a biocompatible nanotheranostic platform integrating diagnostic and therapeutic functions is a great prospect for cancer treatment. However, it is still a great challenge to synthesize nanotheranostic agents using an ultra-facile method. In the research reported here, ultrasmall polyethylenimine-protected silver bismuth sulfide (PEI-AgBiS2) nanodots were successfully synthesized using an ultra-facile and environmentally friendly strategy (1 min only at room temperature), which could be described as a rookie method. PEI-AgBiS2 nanodots show good monodispersity and biocompatibility. For the first time, PEI-AgBiS2 nanodots were reported as a powerful and safe nanotheranostic agent for cancer treatment. PEI-AgBiS2 nanodots exhibit excellent computed tomography (CT) and photoacoustic (PA) dual-modal imaging ability, which could effectively guide photothermal cancer therapy. Furthermore, PEI-AgBiS2 nanodots exhibit a high photothermal conversion efficiency (n = 35.2%). The photothermal therapy (PTT) results demonstrated a highly efficient tumor ablation ability. More importantly, the blood biochemistry and histology analyses verify that the PEI-AgBiS2 nanodots have negligible long-term toxicity. This work highlights that PEI-AgBiS2 nanodots produced using this extremely effective method are a high-performance and safe PTT agent. These findings open a new gateway for synthesizing nanotheranostic agents by using this ultra-facile method in the future.

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