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Chemical Reactions and Stability of Riboflavin in Foods

Choe, Eunok, Huang, Rongmin, Min, David B.·2005·Journal of Food Science

Abstract

ABSTRACT: Riboflavin is relatively stable during thermal and nonthermal food processing and storage but is very sensitive to light. It can accept or donate a pair of hydrogen atoms. It can act as a photosensitizer (through either Type I or Type II mechanism) or a prooxidant for food components under light. Photosensitization of riboflavin causes production of reactive oxygen species such as superoxide anion, singlet oxygen, hydroxy radical, and hydrogen peroxide. Radicals and reactive oxygen species accelerate the decomposition of proteins, lipids, carbohydrates, and vitamins, and could cause significant nutrient loss in foods. Carbohydrates are less sensitive to riboflavinphotosensitized oxidation than proteins, lipids, or vitamins. Riboflavin is an excellent photosensitizer for singlet oxygen formation and a superb reactant for singlet oxygen, with the reaction rate of 1.01 ± 10 10 /M/s.

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Metadata

Authors
Choe, E., Huang, R., & Min, D. B.
Venue
Journal of Food Science
Publisher
Wiley
Published
2005-01
Volume
70
Issue
1
ISSN
  • 0022-1147 (ISSN-L)
  • 1750-3841
OpenAlex
W2018211718
Cited by
195
References
0
FWCI
2.81
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Chemical Reactions and Stability of Riboflavin in Foods. https://app.cochat.ai/papers/10.1111/j.1365-2621.2005.tb09055.x
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Choe, E., Huang, R., & Min, D. B. (2005). Chemical Reactions and Stability of Riboflavin in Foods. Journal of Food Science. https://doi.org/10.1111/j.1365-2621.2005.tb09055.x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.