Concanavalin A-conjugated gold nanoparticle/silica quantum dot (AuNPs/SiQDs-Con A)-based platform as a fluorescent nanoprobe for the bioimaging of glycan-positive cancer cells.
Somayeh JafarzadehNasrin BargahiHassan Bagherpour ShamlooJafar SoleymaniPublished in: RSC advances (2022)
The glycan receptor is a glycosylphosphatidylinositol glycoprotein that is overexpressed on the surface of various cancer cells and has been utilized for wide applications. In the present work, the surface of citrate-capped gold nanoparticles (cit-AuNPs) was modified with mercaptopropionic acid (MPA) molecules to provide carboxylic groups for secondary functionalization with amine anchored-silica quantum dots (Si-NH 2 QDs) to produce cit-AuNPs-MPA/Si-NH 2 QDs fluorescent nanoparticles. Concanavalin A (Con A) molecules were attached through thiol-AuNP bonds to produce the final cit-AuNPs/MPA/Si-NH 2 QDs/Con A smart nanoparticles. The synthesized novel cit-AuNPs/MPA/Si-NH 2 QDs/Con A nanoparticles were utilized for the bioimaging of glycan-overexpressed breast cancer cells. Fluorescence microscopy and flow cytometry results revealed that the cit-AuNPs/MPA/Si-NH 2 QDs/Con A NPs can be efficiently taken up by cancer cells, with differentiating ability between overexpressed cancer cells and low-expressed normal cells. The cellular viability of the cit-AuNPs/MPA/Si-NH 2 QDs/Con A NPs was tested by the MTT test, proving their biocompatible nature at the 200 μg mL -1 level. In conclusion, the fabricated cit-AuNPs/MPA/Si-NH 2 QDs/Con A NPs could be utilized for the bioimaging of MCF-7 cancer cells even in the clinical setting after proper in vivo validation.
Keyphrases
- room temperature
- quantum dots
- ionic liquid
- living cells
- breast cancer cells
- gold nanoparticles
- flow cytometry
- single molecule
- fluorescent probe
- sensitive detection
- perovskite solar cells
- energy transfer
- induced apoptosis
- computed tomography
- oxidative stress
- high resolution
- mass spectrometry
- oxide nanoparticles
- cell proliferation
- cell surface
- cell death
- magnetic resonance
- cell cycle arrest
- high speed
- endoplasmic reticulum stress
- signaling pathway
- walled carbon nanotubes