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                                       Details for article 51 of 143 found articles
 
 
  ELECTROCHEMICAL, SPECTRAL AND MO INVESTIGATION OF THE REDUCTIVE ACTIVATION OF ANTITUMORAL DRUGS DOXORUBICIN AND EPIRUBICIN
 
 
Title: ELECTROCHEMICAL, SPECTRAL AND MO INVESTIGATION OF THE REDUCTIVE ACTIVATION OF ANTITUMORAL DRUGS DOXORUBICIN AND EPIRUBICIN
Author: Iuliana Serbanescu
Mirela Enache
Elena Volanschi
Appeared in: Analele Universitatii Bucuresti. Chimie
Paging: Volume XII (2003) nr. I-II pages 267-278
Year: 2003
Contents: The electrochemical and chemical reduction of the antitumoral drugs doxorubicin andepirubicin is investigated in aprotic and protic media, in the presence and absence of oxygen bycoupled electrochemical and spectral techniques. The cyclic voltammetry with stationary androtating disc electrode (RDE) points out a quite similar electrochemical behaviour, consisting oftwo electron transfers and evidence as intermediate species the anion-radical (A–.), the dianion(A2–) and the protonated species AH-, AH., AH2. EPR and optical spectra registered during theelectrochemical reduction allow the identification of these species and suggest the possibility ofback oxidation of the drug by electron transfer to molecular oxygen. AM1 semiempirical MOcalculationsallow a rationalisation of the experimental results regarding the reactivity in redoxprocesses and outline the dominant role of the anthraquinone moiety. Biological implications ofthe reductive activation of molecular oxygen are also discussed.
Publisher: Ars Docendi Publishing House (provided by DOAJ)
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 51 of 143 found articles
 
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