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Water-Soluble Ruthenium(III)-Dimethyl Sulfoxide Complexes:Chemical Behaviour and Pharmaceutical Properties

机译:水溶性钌(III)-二甲基亚砜配合物:化学行为和药物特性

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摘要

In this paper we report a review of the results obtained in the last few years by our group in the development of ruthenium(III) complexes characterized by the presence of sulfoxide ligands and endowed with antitumor properties. In particular, we will focus on ruthenates of general formula Na[trans-RuCl4(R1R2SO)(L)], where R1R2SO = dimethylsulfoxide (DMSO) or tetramethylenesulfoxide (TMSO) and L = nitrogen donor ligand. The chemical behavior of these complexes has been studied by means of spectroscopic techniques both in slightly acidic distilled water and in phosphate buffered solution at physiological pH. The influence of biological reductants on the chemical behavior is also described. The antitumor properties have been investigated on a number of experimental tumors. Out of the effects observed, notheworthy appears the capability of the tested ruthenates to control the metastatic dissemination of solid metastasizing tumors. The analysis of the antimetastatic action, made in particular on the MCa mammary carcinoma of CBA mouse, has demonstrated a therapeutic value for these complexes which are able to significantly prolong the survival time of the treated animals. The antimetastatic effect is not attributable to a specific cytotoxicity for metastatic tumor cells although in vitro experiments on pBR322 double stranded DNA has shown that the test ruthenates bind to the macromolecule, causing breakscorresponding to almost all bases, except than thymine, and are able to cause interstrandbonds, depending on the nature of the complex being tested, some of which results activeas cisplatin itself.
机译:在本文中,我们报告了我们小组最近几年在开发以亚砜配体为特征并具有抗肿瘤特性的钌(III)配合物方面取得的成果的综述。特别是,我们将重点关注通式Na [反式RuCl4(R1R2SO)(L)]的钌酸盐,其中R1R2SO =二甲基亚砜(DMSO)或四亚甲基亚砜(TMSO),L =氮供体配体。这些配合物的化学行为已通过光谱技术在微酸性蒸馏水和生理pH的磷酸盐缓冲液中进行了研究。还描述了生物还原剂对化学行为的影响。已经对许多实验性肿瘤研究了抗肿瘤特性。从观察到的效果中,被测试的钌酸酯控制实体转移肿瘤的转移扩散的能力显得格外重要。对特别是对CBA小鼠的MCa乳癌的抗转移作用的分析表明,这些复合物具有治疗价值,其能够显着延长被治疗动物的存活时间。尽管对pBR322双链DNA的体外实验显示测试的钌酸盐与大分子结合,导致断裂,但抗转移作用并非归因于转移性肿瘤细胞的特定细胞毒性。对应于除胸腺嘧啶以外的几乎所有碱基,并且能够引起链间键,取决于所测试复合物的性质,其中某些结果有效作为顺铂本身。

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