Abstract
Doxorubicin (DOX), a common cancer chemotherapeutics, was conjugated to folate-modified thiolated-polyethylene glycol-functionalized gold nanoparticles. The in vitro, controlled release behavior of DOX-loaded gold nanoparticles was observed using porous dialysis membranes (cut-off = 2 kDa). DOX-loaded gold nanoparticles had higher cytotoxicity for folate-receptor-positive cells (KB cells) compared to folate-receptor-negative cells (A549 cells) which were 48 and 62% viable for 10 μM doxorubicin, respectively. This indicates the potential of these nano-carriers for targeted-delivery. In addition, healthy cell viability was 69% for 10 μM free doxorubicin whereas for the same content of drug in DOX-loaded nanoparticles healthy cell viability increased to 80%.
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Acknowledgment
This project was supported by Biochemical and Bioenvironmental Centre of Sharif University of Technology, and also we wish to thank Sharif Institute of Nanoscience and Nanotechnology, Biotechnology Research Centre and Cell Bank Centre of Pasteur Institute of Iran, for their helpful contributions.
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Below is the link to the electronic supplementary material. Supplementary Fig. 1 Transmission electron microscopy (TEM) image for PEG-functionalized gold nanoparticles (PEG-SH-GdNPS) which shows the average size of the 12 nm for nanoparticles.
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Asadishad, B., Vossoughi, M. & Alamzadeh, I. In vitro release behavior and cytotoxicity of doxorubicin-loaded gold nanoparticles in cancerous cells. Biotechnol Lett 32, 649–654 (2010). https://doi.org/10.1007/s10529-010-0208-x
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DOI: https://doi.org/10.1007/s10529-010-0208-x