Abdel-Rahman Laila H, Abu-Dief Ahmed M, Newair Emad F, Hamdan Samar Kamel
Chemistry Department, Faculty of Science, Sohag University, 82534 Sohag, Egypt.
Chemistry Department, Faculty of Science, Sohag University, 82534 Sohag, Egypt.
J Photochem Photobiol B. 2016 Jul;160:18-31. doi: 10.1016/j.jphotobiol.2016.03.040. Epub 2016 Apr 8.
To estimate the biological preference of synthetic small drugs towards DNA target, new metal based chemotherapeutic agents of nano-sized Cr(III), Fe(II), Co(II) and Ni(II) Schiff base complexes having N,N,O donor system were synthesized and thoroughly characterized by physic-chemical techniques. The redox behavior of the Cr(III), Fe(II) and Co(II) complex was investigated by electrochemical method using cyclic voltammetry. IR results proven that the tridentate binding of Schiff base ligand with metal center during complexation reflects the proposed structure. Magnetic and spectroscopic data give support to octahedral geometry for Cr(III) and Fe(II) complexes and tetrahedral geometry for Ni(II) and Co(II) complexes. The activation thermodynamic parameters, such as, E(⁎), ΔH(⁎), ΔS(⁎) and ΔG(⁎) are calculated using Coats-Redfern method by analyzing the TGA data. The particle size of the investigated metal complexes was estimated by TEM. In addition to, the interaction of the nanosized complexes with CT-DNA was estimated by electronic absorption, viscosity and gel electrophoresis. These techniques revealed that the complexes could bind to CT-DNA through intercalation mode. Moreover, the in vitro cytotoxic and antiviral activities of the nanosized complexes were checked against Herpes Simplex virus and Tobacco Mosaic viruses. Moreover, investigation of antioxidant activities of the new nanosized compounds was done by ABTS assay. Among the compounds tested, Fe(II) complex showed the strongest potent radical scavenging activity with percent of 58.60%. Furthermore, the antimicrobial bustle of the prepared compounds was screened against different types of bacteria and fungi and the results show that all metal complexes have superior activity than its free ligand.
为了评估合成小分子药物对DNA靶点的生物学偏好,合成了具有N,N,O供体体系的新型纳米级Cr(III)、Fe(II)、Co(II)和Ni(II)席夫碱配合物的金属基化疗药物,并通过物理化学技术对其进行了全面表征。采用循环伏安法通过电化学方法研究了Cr(III)、Fe(II)和Co(II)配合物的氧化还原行为。红外结果证明,席夫碱配体在络合过程中与金属中心的三齿结合反映了所提出的结构。磁性和光谱数据支持Cr(III)和Fe(II)配合物为八面体几何结构,Ni(II)和Co(II)配合物为四面体几何结构。利用Coats-Redfern方法通过分析热重分析数据计算了活化热力学参数,如E(⁎)、ΔH(⁎)、ΔS(⁎)和ΔG(⁎)。通过透射电子显微镜估计了所研究金属配合物的粒径。此外,通过电子吸收、粘度和凝胶电泳估计了纳米配合物与CT-DNA的相互作用。这些技术表明,配合物可以通过嵌入模式与CT-DNA结合。此外,还检测了纳米配合物对单纯疱疹病毒和烟草花叶病毒的体外细胞毒性和抗病毒活性。此外,通过ABTS法对新型纳米化合物的抗氧化活性进行了研究。在所测试的化合物中,Fe(II)配合物表现出最强的自由基清除活性,清除率为58.60%。此外,对所制备化合物对不同类型细菌和真菌的抗菌活性进行了筛选,结果表明所有金属配合物的活性均优于其游离配体。