Investigations of riboflavin photolysis via coloured light in the nitro blue tetrazolium assay for superoxide dismutase activity

[Display omitted] •Blue light is efficient in photochemical reaction of riboflavin.•Blue light is critical for photo-decomposition of riboflavin in visible region.•Optimal condition for the riboflavin/nitro blue tetrazolium method by blue-light irradiation was determined. Determination of the supero...

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Veröffentlicht in:Journal of photochemistry and photobiology. B, Biology Biology, 2015-07, Vol.148, p.262-267
Hauptverfasser: Cheng, Chien-wei, Chen, Liang-yü, Chou, Chan-wei, Liang, Ji-yuan
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Sprache:eng
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Zusammenfassung:[Display omitted] •Blue light is efficient in photochemical reaction of riboflavin.•Blue light is critical for photo-decomposition of riboflavin in visible region.•Optimal condition for the riboflavin/nitro blue tetrazolium method by blue-light irradiation was determined. Determination of the superoxide dismutase activity is an important issue in the fields of biochemistry and the medical sciences. In the riboflavin/nitro blue tetrazolium (B2/NBT) method, the light sources used for generating superoxide anion radicals from light-excited riboflavin are normally fluorescent lamps. However, the conditions of B2/NBT experiments vary. This study investigated the effect of the light source on the light-excitation of riboflavin. The effectiveness of the photolysis was controlled by the wavelength of the light source. The spectra of fluorescent lamps are composed of multiple colour lights, and the emission spectra of fluorescent lamps made by different manufacturers may vary. Blue light was determined to be the most efficient for the photochemical reaction of riboflavin in visible region. The quality of the blue light in fluorescent lamps is critical to the photo-decomposition of riboflavin. A blue light is better than a fluorescent lamp for the photo-decomposition of riboflavin. The performance of the B2/NBT method is thereby optimized.
ISSN:1011-1344
1873-2682
DOI:10.1016/j.jphotobiol.2015.04.028