4.7 Article

iRGD peptide as effective transporter of CuInZnxS2+x quantum dots into human cancer cells

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 146, Issue -, Pages 9-18

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2016.05.041

Keywords

CuInZnxS2+x QDs; iRGD peptide; Cell labelling; Tumor spheroids; Tumor-targeted delivery

Funding

  1. National Centre for Research and Development [PBS1/A9/13/2012]
  2. International PhD Projects Programme of Foundation for Polish Science operated within the Innovative Economy Operational Programme
  3. European Regional Development Fund

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In this paper, iRGD peptide-mediated quantum dots (QDs) delivery was studied. In the first step, dodecanethiol-capped CulnZn(x)S(2+x) (ZCIS) QDs were prepared and subsequently transferred into water using a standard and facile ligand exchange approach involving 3-mercaptopropionic acid (MPA). ZCIS@MPA nanocrystals possess a photoluminescence quantum yield (PL QY) of 25%, a PL emission centered at ca. 640nm and low distributions in size and shape. Next, the iRGD peptide was electrostatically associated to ZCIS@MPA QDs. After cytotoxicity evaluation, the tumor-targeting and penetrating activities of the iRGD/QD assembly were investigated by confocal microscopy. The experiments performed on various cancer cell lines revealed a high penetration ability of the assembly, while the bare QDs were not internalized. Additionally, imaging experiments were conducted on three-dimensional multicellular tumor spheroids in order to mimic the tumor microenvironment in vivo. iRGD/QD assemblies were found to be evenly distributed throughout the whole HeLa spheroid contrary to normal cells where they were not present. Therefore, iRGD/QD assemblies have a great potential to be used as targeted imaging agents and/or nanocarriers specific to cancer cells. (C) 2016 Elsevier B.V. All rights reserved.

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