2010
DOI: 10.1134/s0036024410120095
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Kinetics of oxidation of bilirubin and its protein complex by hydrogen peroxide in aqueous solutions

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Cited by 4 publications
(2 citation statements)
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“…The resulting spectral and kinetic parameters suggest a general scheme of oxidative transformations in the electron‐donor DMSO medium. The significant increase in kinetics (more than 300 times) of the BR oxidation, compared to its oxidation in aqueous solution with hydrogen peroxide ( k = 18.99 × 10 −4 dm 3 mol −1 s −1 , T = 298.2 K ), is associated with the formation of another transition state form. Another important difference from aqueous solutions is that the end products of oxidation are not monopyrrolic derivatives.…”
Section: Discussionmentioning
confidence: 99%
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“…The resulting spectral and kinetic parameters suggest a general scheme of oxidative transformations in the electron‐donor DMSO medium. The significant increase in kinetics (more than 300 times) of the BR oxidation, compared to its oxidation in aqueous solution with hydrogen peroxide ( k = 18.99 × 10 −4 dm 3 mol −1 s −1 , T = 298.2 K ), is associated with the formation of another transition state form. Another important difference from aqueous solutions is that the end products of oxidation are not monopyrrolic derivatives.…”
Section: Discussionmentioning
confidence: 99%
“…The effectiveness of a BV‐reductase cycle had been clinically proved . Based on previous studies , BR oxidation by atmospheric oxygen or hydrogen peroxide in a phosphate buffer medium is studied. The proton exchange interaction mechanism is related to the interaction of NH groups with peroxyl or hydroxyl radicals leading to form an intermediate product with high reactivity and its subsequent decay to monopirrolic compounds.…”
Section: Introductionmentioning
confidence: 99%