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Advisor(s)
Abstract(s)
In the last decade, targeting membrane lipids in cancer cells has been a promising approach
that deserves attention in the field of anticancer drug development. To get a comprehensive un derstanding of the effect of the drug [Ru(η
5
-Cp)(PPh3
)2CN] (RuCN) on cell lipidic components, we
combine complementary analytical approaches, matrix-assisted laser desorption and ionization time of-flight mass spectrometry (MALDI TOF MS) and synchrotron radiation-based Fourier transform
infrared (SR-FTIR) spectroscopy. Techniques are used for screening the effect of potential metallodrug,
RuCN, without and with drug carriers (carbon dots (CDs) and nitrogen-doped carbon dots (N-CDs))
on the lipids of the human ovarian cancer cell line A2780. MALDI TOF MS results revealed that
the lysis of ovarian cancer membrane lipids is promoted by RuCN and not by drug carriers (CDs
and N-CDs). Furthermore, SR-FTIR results strongly suggested that the phospholipids of cancer cells
undergo oxidative stress after the treatment with RuCN that was accompanied by the disordering
of the fatty acid chains. On the other hand, using (N-)CDs as RuCN nanocarriers prevented the
oxidative stress caused by RuCN but did not prevent the disordering of the fatty acid chain packing.
Finally, we demonstrated that RuCN and RuCN/(N-)CDs alter the hydration of the membrane
surface in the membrane–water interface region.
Description
Keywords
Anticancer Ru metallodrug Carbon dots N-doped carbon dots Drug nanocarriers Lipids MALDI TOF MS SR-FTIR spectroscopy . Faculdade de Ciências Exatas e da Engenharia
Citation
Neši´c, M.D.; Duˇci´c, T.; Algarra, M.; Popovi´c, I.; Stepi´c, M.; Gonçalves, M.; Petkovi´c, M. Lipid Status of A2780 Ovarian Cancer Cells after Treatment with Ruthenium Complex Modified with Carbon Dot Nanocarriers: A Multimodal SR-FTIR Spectroscopy and MALDI TOF Mass Spectrometry Study. Cancers 2022, 14, 1182. https://doi.org/10.3390/ cancers14051182
Publisher
MDPI