College of Chemistry and Chemical Engineering, Liaoning Normal University, No. 850, Huanghe Road, Dalian 116029, PR China; Regenerative Medicine Centre, First Affiliated Hospital of Dalian Medical University, No. 222 Zhongshan Road, Dalian 116011, PR China.
J Inorg Biochem. 2013 Nov;128:57-67. doi: 10.1016/j.jinorgbio.2013.07.018. Epub 2013 Jul 19.
Three novel complexes, [La(phen)2(IAA)2]·NO3 (1), [Sm(phen)2(IAA)2]·NO3 (2) and [Sm(IBA)3(phen)]·phen·HNO3·H2O (3) (phen: 1,10-phenanthroline, IAA: indole-3-acetic acid, IBA: indole-3-butyric acid), were synthesized and characterized with spectroscopy (infrared and UV-visible), X-ray crystal diffraction and elemental analysis. Structural analysis revealed that each lanthanide atom in complexes 1-3 held a distorted tricapped trigonal prism geometry in a nine-coordinate mode. There were two types of coordination modes of the IAA ligand in complexes 1 and 2: a μ2-η(1):η(2) bridging mode linking two lanthanide atoms and a μ2-η(1):η(1) double monodentate bridging mode. There were three types of coordination modes of the IBA ligand: a μ2-η(1):η(1) double monodentate bridging mode, a μ1-η(2) bridging mode and a μ2-η(1):η(2) bridging mode linking two lanthanide atoms. Adjacent Sm atoms were linked via the μ2-bridging carboxylate groups of the IBA ligands to generate a binuclear building unit. The biological activity of the complexes was evaluated in human adipose tissue-derived stem cells (hADSCs) and Chang liver cells using a multiple parallel perfused microbioreactor. The results showed that cytotoxicity increased as the concentrations of complexes 1-3 increased.
三种新型配合物,[La(phen)2(IAA)2]·NO3(1)、[Sm(phen)2(IAA)2]·NO3(2)和[Sm(IBA)3(phen)]·phen·HNO3·H2O(3)(phen:1,10-邻菲啰啉,IAA:吲哚-3-乙酸,IBA:吲哚-3-丁酸),通过光谱学(红外和紫外-可见)、X 射线晶体衍射和元素分析进行了合成和表征。结构分析表明,配合物 1-3 中的每个镧系元素原子在九配位模式下呈扭曲的三角双锥几何形状。IAA 配体在配合物 1 和 2 中有两种配位模式:μ2-η(1):η(2)桥联模式连接两个镧系元素原子和μ2-η(1):η(1)双单齿桥联模式。IBA 配体有三种配位模式:μ2-η(1):η(1)双单齿桥联模式、μ1-η(2)桥联模式和μ2-η(1):η(2)桥联模式连接两个镧系元素原子。相邻的 Sm 原子通过 IBA 配体的μ2-桥联羧基连接,生成双核构建单元。通过多平行灌流微生物反应器在人脂肪组织来源的干细胞(hADSCs)和 Chang 肝细胞中评估了配合物的生物活性。结果表明,随着配合物 1-3 浓度的增加,细胞毒性增加。