Navas Francisco, Mendes Filipa, Santos Isabel, Navarro-Ranninger Carmen, Cabrera Silvia, Quiroga Adoración G
Departamento de Química Inorgánica, Universidad Autónoma de Madrid , ES-28049 Madrid, Spain.
Centro de Ciências e Tecnologias Nucleares, Instituto Superior Técnico, Universidade de Lisboa , 2695-066 Bobadela LRS, Portugal.
Inorg Chem. 2017 Jun 5;56(11):6175-6183. doi: 10.1021/acs.inorgchem.7b00136. Epub 2017 May 10.
Pt(IV) complexes are known as prodrugs that can potentially overcome cisplatin limitations by slowing down its reactivity and, once reduced, act as the corresponding Pt(II) drugs. We report a new approach toward trans Pt(IV) complexes, conceived to afford nonconventional active trans Pt(II) complexes with dual-targeting properties. The reduction of the complexes has been studied in the presence of ascorbic acid and glutathione, showing that different species are formed in the process. The interaction with DNA after reduction has been also studied and correlated to the formation of Pt(II) species. The cytotoxicity profile of the Pt(IV) complexes corroborated the rationale behind this approach.
铂(IV)配合物被认为是前药,它可以通过减缓其反应活性来潜在地克服顺铂的局限性,并且一旦被还原,就会作为相应的铂(II)药物起作用。我们报道了一种制备反式铂(IV)配合物的新方法,该方法旨在提供具有双靶向特性的非常规活性反式铂(II)配合物。已在抗坏血酸和谷胱甘肽存在的情况下研究了配合物的还原过程,结果表明在此过程中形成了不同的物种。还研究了还原后与DNA的相互作用,并将其与铂(II)物种的形成相关联。铂(IV)配合物的细胞毒性概况证实了该方法背后的基本原理。