Journal of Kermanshah University of Medical Sciences
Peer-reviewed Medical Quarterly
Image Credit:J Kermanshah Univ Med Sci
Outline
Cytotoxic effects of palladium complexes containing squaric ligands and sulfosuccinic acid on cancer cell lines
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Abstract
Background: Some metal complex derivatives can have an effective role in cancer treatment. The most common used components are platinum complexes which have numerous side effects, whereas, palladium complexes have shown fewer toxicity rate.
Methods: Some of palladium complexes were designed and synthesized for biological evaluation based on the squaric and sulfosuccinic acid ligands.
Results: the cytotoxic effects of the synthesized complexes, including 2-iodo squarato palladium (II), 2-iodo sulfosuccinate palladium (II) and 2-amino squarato palladium (II) on different cell lines (Hela, MCF-7, K562, and HUVEC) were examined. To determine the toxicity effect, lactate dehydrogenase (LDH) and trypan blue staining technique were used and the results were compared with cis-platinum.
Conclusion: the analysis of binding of new groups to palladium showed higher toxicity of 2-iodo sulfosuccinate palladium on normal cells than control compound. The comparison of compounds indicated that amino group increased the efficacy. Replacement of ion atoms by amino group in 2-amino squarato palladium enhanced the efficacy of the compound on cancer cell lines. 2-amino squarato palladium exerted the maximum effect on PC3 cell line and the minimum effect on Hela with IC50s of 4.33 µM and 18.88µM, respectively. Moreover, 2-amino squarato palladium (II) indicated less toxicity on HUVEC in comparison to cis-platinum.
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© 2015, Journal of Kermanshah University of Medical Sciences. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.
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