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Redox potential of the active bleomycin-Fe(III) complex by cyclic voltammetry
Institution:1. MIIT Key Laboratory of Thermal Control of Electronic Equipment, School of Energy and Power Engineering, Nanjing University of Science and Technology, Nanjing 210094, People’s Republic of China;2. Advanced Combustion Laboratory, School of Energy and Power Engineering, Nanjing University of Science and Technology, Nanjing 210094, People’s Republic of China;3. Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy & Environment, Southeast University, Nanjing 210096, People’s Republic of China;1. Departamento de Ingeniería Mecánica, Energética y de los Materiales Universidad de Extremadura, 06006 Badajoz, Spain;2. Departamento de Física Aplicada, Universidad de Extremadura, 06006 Badajoz, Spain;3. LiqTech International AS,Industriparken 22C, 2750 Ballerup, Denmark;4. Department of Energy Conversion and Storage, Technical University of Denmark, Risø Campus, Frederiksborgvej 399, DK-4000 Roskilde, Denmark;1. Technological Institute of Aeronautics (ITA), Physics Department, São José dos Campos, SP, Brazil;2. Federal University of São Paulo - ICT, São José dos Campos, SP, Brazil;1. Department of Chemistry and Chemical Engineering, Chalmers University of Technology, S-412 96 Göteborg, Sweden;2. Department of Energy and Environment, Chalmers University of Technology, S-412 96 Göteborg, Sweden;1. School of Pure and Applied Physics, M.G. University, Kottayam 686560, India;2. Raman Research Institute, C.V. Raman Avenue, Bangalore 560080, India;3. Department of Optoelectronics, University of Kerala, Kariavattom, Thiruvananthapuram, Kerala 695581, India
Abstract:The redox potential of the active Fe(III) complex of bleomycin (BLM), which is a DNA cleaving species, was measured by cyclic voltammetry at 25 °C under a hydrogen atmosphere. The cyclic voltammogram showed the reversible one-electron Fe(III)/Fe(II) coupled redox reaction at −0.225 V versus SCE. Under the same conditions the redox potentials of the iso-BLM—Fe(III) complex and the deglyco-BLM—Fe(III) complex were also observed, but the cyclic voltammogram for the inactive Fe(III) complex of BLM could not be obtained.
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