栓塞金属及偶氮金属配合物的合成、表征及生物学特性

R. Aravindhan, T. Sreelatha, P. Perumal, A. Gnanamani
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引用次数: 18

摘要

本研究重点介绍了血管内皮素、血管内皮-金属(EM)和血管内皮-偶氮金属(EAM)配合物的合成和生物谱分析。EM配合物采用纯embelin和d-嵌段过渡元素Mn、Fe、Co、Ni、Cu和Zn制备。同样地,用苯基偶氮栓塞与上述过渡金属合成了EAM配合物。对Embelin、EM和EAM配合物进行了紫外可见光谱、傅里叶变换红外光谱、核磁共振、电喷雾电离质谱、热重分析、碳氢氮硫分析。在生物分析方面,研究了测试配合物的抗氧化和抗菌活性。结果表明,制备的EM和EAM配合物与栓塞形成八面体配合物,产率在45 ~ 75%之间。所有的仪器分析都证实了金属与双齿动脉的相互作用,通过它的烯醛和醌氧原子[M(Emb)2(H2O)2]H2O和[M(Emb-偶氮)2(H2O)2]。抗氧化谱研究表明,与金属络合后,栓塞的自由基清除能力明显降低。但是,在抗菌活性方面,钴和镍栓塞复合物与单独栓塞相比,显示出>80%的生长抑制作用。溶血活性研究表明,栓塞和金属配合物均无溶血作用。详细讨论了其抗氧化活性降低、抗菌活性增加的原因。
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Synthesis, characterization and biological profile of metal and azo-metal complexes of embelin
The present study emphasizes synthesis and bioprofiling of embelin, embelin-metal (EM) and embelin-azo-metal (EAM) complexes in detail. EM complexes were prepared using pure embelin and d-block transition elements, namely Mn, Fe, Co, Ni, Cu, and Zn. Similarly, EAM complexes were synthesized using phenyl azo-embelin with the said transition metals. Embelin, EM, and EAM complexes were subjected to ultra violet visible spectroscopy, Fourier transform infrared spectroscopy, nuclear magnetic resonance, electrospray ionization mass spectrometry, thermogravimetric analysis, carbon hydrogen nitrogen sulfur analysis. With regard to bioprofiling, the test complexes were studied for the antioxidant and antimicrobial activities. Results revealed that the prepared EM and EAM complexes form octahedral complexes with embelin with the yield in the range of 45–75%. All the instrumental analyses authenticate the interaction of metals with bidentate embelin through its enolic and quinonic oxygen atoms as [M(Emb)2(H2O)2]H2O and [M(Emb-Azo)2(H2O)2]. The antioxidant profile studies suggested that upon complexation with metals, the free radical scavenging activity of embelin reduced significantly. But, with regard to antimicrobial activity, cobalt and nickel embelin complexes displayed>80% growth inhibition in comparison with embelin alone. The hemolytic activity studies suggested that both embelin and the metal complexes are non-hemolytic. The reason for the reduction in antioxidant and an increase in antimicrobial activities were discussed in detail.
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