AI Article Synopsis

  • The study explores the synthesis of conjugates formed by tetrakis benzo[d]thiazol-2-yl phthalocyaninato zinc(II) and indium(III) chloride linked to gold speckled silica nanoparticles, using gold-sulfur and gold-nitrogen bonds.
  • The characterization of these conjugates reveals changes in photophysical properties, specifically an increase in singlet and triplet oxygen quantum yields, which are crucial for their effectiveness in photodynamic therapy (PDT) against MCF-7 breast cancer cells.
  • The results demonstrate that the conjugate 2-GSS significantly enhances PDT activity, killing more cancer cells while maintaining higher viability in dark conditions compared to the individual components.

Article Abstract

This work reports on the linkage of 2(3),9(10),16(17),23(24) tetrakis [(benzo[d]thiazol-2-yl phenoxy) phthalocyaninato] zinc(II) (1) and indium(III) chloride (2) to gold speckled silica (GSS) nanoparticles via gold to sulphur (Au-S) and gold to nitrogen (Au-N) self-assembly to form the conjugates: 1-GSS and 2-GSS. The formed conjugates were characterized using microscopic and spectroscopic techniques, and the photophysicochemical properties and photodynamic therapy (PDT) activity against human breast adenocarcinoma cell line (MCF-7 cells) were studied. The conjugates afforded decrease in fluorescence quantum yields with corresponding increase in triplet and singlet oxygen quantum yields when compared to phthalocyanines alone. Singlet oxygen is cytotoxic to cancer cells hence it is important for PDT. The in vitro dark toxicity of complex 2 and 2-GSS against MCF-7 cells showed ≥93% viable cells within concentration ranges of 10-160 μg/mL. 2-GSS showed enhanced PDT activity with less than 50% viable cells at 80 μg/mL as compared to 2 and GSS alone which showed >60% viable cells within 10-160 μg/mL. The observed improvements in the PDT activity of 2-GSS could be attributed to the high singlet oxygen generation of 2-GSS compared to 2 alone in addition to the phototoxicity of GSS.

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Source
http://dx.doi.org/10.1016/j.pdpdt.2019.01.019DOI Listing

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