DNA binding, antibacterial, hemolytic and anticancer studies of some fluorescent emissive surfactant-ruthenium(II) complexes
| Autor: | Siva Kalaiselvam, Selvakumar Veeralakshmi, Selvan Nehru, S. P. Subin David, Sankaralingam Arunachalam, Jayakumar Sandhya |
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| Rok vydání: | 2020 |
| Předmět: |
0303 health sciences
Circular Dichroism 030303 biophysics chemistry.chemical_element DNA General Medicine Fluorescence Combinatorial chemistry Ruthenium Anti-Bacterial Agents Surface-Active Agents 03 medical and health sciences chemistry.chemical_compound chemistry Pulmonary surfactant Coordination Complexes Structural Biology Amphiphile Drug carrier Molecular Biology |
| Zdroj: | Journal of Biomolecular Structure and Dynamics. 39:2242-2256 |
| ISSN: | 1538-0254 0739-1102 |
| DOI: | 10.1080/07391102.2020.1747547 |
| Popis: | Designing the effective metallodrugs with amphiphilic nature is an active approach for the biomedical applications such as chemotheraphy, bioimaging, drug carrier, etc. To elaborate this, some fluorescent emissive surfactant-ruthenium(II) complexes and its precursor ruthenium(II) complexes have been interacted with calf thymus DNA (CT-DNA) for understanding the biophysical impacts of head and tail parts of the metallosurfactants. Here, DNA binding studies were examined by UV-visible absorption, fluorescence, circular dichroism and viscosity measurements. The obtained results showed that surfactant-ruthenium(II) complexes effectively bind with CT-DNA through hydrophobic interactions dominated moderate intercalation, whereas precursor ruthenium(II) complexes interact CT-DNA through electrostatic interactions dominated moderate intercalation. Also, increase of hydrophobic alkyl amine chain length as well as size of the head group in surfactant-ruthenium(II) complexes increased the binding affinity with CT-DNA, in which tail group played a dominant role. Further investigations of antibacterial, hemolytic and anticancer activities showed that desired biological activities could be obtained by tuning the head and tail groups of the metallodrugs in near future.Communicated by Ramaswamy H. Sarma. |
| Databáze: | OpenAIRE |
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