Citation: QIU Na, SHI Xiao, YANG Yiyi, SONG Nannan, LI Jiajia, GE Zhenying, ZHANG Lei. Synthesis and Anti-colorectal Cancer Activity of Amphipathic Trimethine Indocyanine Dyes[J]. Chinese Journal of Applied Chemistry, ;2020, 37(11): 1262-1267. doi: 10.11944/j.issn.1000-0518.2020.11.200126 shu

Synthesis and Anti-colorectal Cancer Activity of Amphipathic Trimethine Indocyanine Dyes

  • Corresponding author: GE Zhenying, 15890986202@139.com ZHANG Lei, zhlei@henu.edu.cn
  • Received Date: 29 April 2020
    Revised Date: 10 June 2020
    Accepted Date: 21 July 2020

    Fund Project: the Key R&D and Promotion Projects in Henan Province 202102310155the National Natural Science Foundation of China 81803573China Postdoctoral Science Foundation 2018M640672Supported by the National Natural Science Foundation of China(No.81803573), China Postdoctoral Science Foundation(No.2018M640672), and the Key R&D and Promotion Projects in Henan Province(No.202102310155)

Figures(4)

  • The improvement of the amphipathicity of cyanine dyes is conducive to the improvement of its own antitumor activity. In this paper, the feasibility of converting trimethine indocyanine dye (Cy3) into multifunctional small-molecule chemotherapy drug was explored for the first time. Two amphipathic trimethine indocyanine dyes of Cy3-DIPEG and Cy3-SO3-DIPEG containing polyethylene glycol(PEG) chains on the indol "N" were designed and synthesized in yields of about 40%. The structure of the product was identified by 1H NMR and 13C NMR spectroscopy and mass spectroscopy. The maximal fluorescence emission wavelengths of Cy3-DIPEG and Cy3-SO3-DIPEG in water are about 570 nm, and their fluorescence quantum yields (Ф) are 0.06 and 0.13, respectively. The antitumor activities of two dyes on human colorectal cancer cell lines (SW480 and HCT-116) were tested in vitro by the thiazole blue (MTT) assay and the antitumor mechanism was initially explored by subcellular localization experiments. The results show that Cy3-DIPEG can accumulate in mitochondria through the tumor cell membrane, and significantly inhibit the proliferation of human colorectal cancer cells, but Cy3-SO3-DIPEG cannot penetrate into the tumor cell and has no antitumor activity.
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