Copper(II) and Platinum(II) Naproxenates: Insights on Synthesis, Characterization and Evaluation of Their Antiproliferative Activities

Author:

Silva Amanda A.1,Frajácomo Silmara C. L.2,Cruz Állefe B.3,Buglio Kaio Eduardo4,Affonso Daniele Daiane4ORCID,Portes Marcelo Cecconi5ORCID,Ruiz Ana Lúcia T. G.4ORCID,de Carvalho João Ernesto4,Lustri Wilton R.2,Pereira Douglas H.3ORCID,da Costa Ferreira Ana M.5ORCID,Corbi Pedro P.1

Affiliation:

1. Institute of Chemistry, University of Campinas—UNICAMP, Campinas 13083-970, SP, Brazil

2. Department of Biological and Health Sciences, University of Araraquara—UNIARA, Araraquara 14801-320, SP, Brazil

3. Chemistry Collegiate, Federal University of Tocantins—UFT, Gurupi 77402-970, TO, Brazil

4. Faculty of Pharmaceutical Sciences, University of Campinas-UNICAMP, Campinas 13083-871, SP, Brazil

5. Department of Fundamental Chemistry, Institute of Chemistry, University of São Paulo—USP, São Paulo 05508-000, SP, Brazil

Abstract

The growth of antibiotic resistance is a matter of worldwide concern. In parallel, cancer remains one of the main causes of death. In the search for new and improved antiproliferative agents, one of the strategies is the combination of bioactive ligands and metals that are already consolidated in the synthesis of metallopharmaceutical agents. Thus, this work deals with the synthesis, characterization, and study of naproxen (Nap)-based complexes of copper(II) and platinum(II) as antiproliferative agents. The copper complex (Cu–Nap) presents a binuclear paddle-wheel structure in a 1 Cu:2 Nap:1 H2O molar composition, in which Cu(II) is bonded to the carboxylate oxygens from naproxenate in a bidentate bridging mode. The platinum complex (Pt–Nap) was identified as the square planar cis-[Pt(Nap)2(DMSO)2] isomer, in which Pt(II) is bonded to the carboxylate oxygen atom of Nap in a monodentate fashion. Both complexes were inactive against the Gram-positive and Gram-negative bacterial strains assessed. Pt–Nap presented low cytostatic behavior over a set of tumor cells, but good viability for normal cells, while Cu–Nap was cytotoxic against all cells, with a cytocidal activity against glioma tumor cells.

Funder

CAPES

FAPESP

FAEPEX

CNPq

CEPID-Redoxoma

National Council for Scientific and Technological Development

São Paulo Research Foundation

Fund for Support to Teaching, Research and Outreach Activities of the University of Campinas

Publisher

MDPI AG

Subject

Inorganic Chemistry

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