INVESTIGADORES
GAMBETTA Carolina
artículos
Título:
Methyl anthranilate as generator and quencher of reactive oxygen species. A photochemical study.
Autor/es:
GAMBETTA, CAROLINA; NATERA, JOSÉ; MASSAD, WALTER; GARCÍA, NORMAN
Revista:
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
Editorial:
ELSEVIER SCIENCE SA
Referencias:
Lugar: Philadelphia; Año: 2013 p. 27 - 33
ISSN:
1010-6030
Resumen:
Methyl anthranilate (MA) is a naturally occurring aromatizer and flavorant agent frequently employed in food industry and in personal care products. Due to the property of MA of being a UV-A radiation- absorber it is incorporated to topical sunscreen formulations. Within the framework of the wide variety of practical uses and applications, the photodegradation of MA becomes a topic of interest from health to an economic point of view. In this context, kinetics and mechanistic aspects of its photo-oxidation has been studied, in order to know the degradation pathways of MA under natural-like photoirradiation. The assays were performed in the absence and in the presence of riboflavin (Rf, vitamin B2) acting the later as a native photosensitizer. The results showed that MA is capable to generate singlet molecular oxygen (O2(1Δg)) upon direct UV-A irradiation, with a quantum yield value of 0.13 ± 0.02. The anthranilate also quenches the oxidative species with an overall rate constant value kt = 2.1 ± 0.2 x107 M-1s-1 while the reactive interaction between MA and O2(1g) showed a rate constant value in the range of 5.9 ? 6.8 x106 M-1s-1. The kr/kt ratio, lower than 0.35 indicates that only one third of the O2(1g)-quenching events effectively lead to oxidation of the scavenger, being this an acceptable property for a sunscreen component. Regarding the Rf-photosensitized visible-light irradiation of MA-Rf mixtures, the anthranilate quenches the electronically excited singlet and triplet states of the vitamin. As a result the oxidative species O2?? and H2O2, are generated, being the later effectively deactivated by MA. At first, the described results would show MA as a candidate for UV-A and visible-light mediated degradation. Nevertheless, at the same time MA acts as a moderate physical scavenger of photogenerated oxidative species in a sort of self-protector against photoinduced degradation and protector of oxidizable surrounding compounds.