Literature DB >> 8728505

Photochemical formation of singlet molecular oxygen in illuminated aqueous solutions of several commercially available sunscreen active ingredients.

J M Allen1, C J Gossett, S K Allen.   

Abstract

Evidence is presented for the photochemical formation of singlet molecular oxygen (1O2) in air-saturated aqueous solutions of several sunscreen active ingredients using sunlight-range illumination. This is of significance because (1) 1O2 is known to be cytotoxic, and (2) there have been several reports of toxic effects associated with the use of some sunscreens; most notably, with p-aminobenzoic acid (PABA). Illuminated aqueous solutions of PABA, 2-ethylhexyl p-(dimethylamino)benzate (ODPABA), 2-hydroxy-4-methoxybenzophenone (BZ3), 2,2'-dihydroxy-4-methoxybenzophenone (BZ8), 2-ethylhexyl 2-cyano-3,3-diphenylacrylate (OCR), 2-ethylhexyl p-methoxycinnamate (OMC), and 2-ethylhexyl salicylate (OCS) were evaluated individually for 1O2 formation. Furfuryl alcohol (FFA), a well-known chemical trap for 1O2, was added to each of the aqueous sunscreen solutions. The FFA was consumed when solutions of PABA, ODPABA, OMC, and OCR were illuminated, but no loss of FFA other than by direct photolysis occurred in solutions of BZ3, BZ8, or OCS. There was also no significant loss of FFA in any of these solutions kept in the dark. Further evidence for the formation of 1O2 in illuminated aqueous sunscreen solutions is provided by the results of experiments in which individual solutions containing sunscreen active ingredients and FFA that were diluted with D2O exhibited an increased rate of FFA consumption while the addition of azide ion (N3-) reduced the rate of FFA consumption. Continuous sunlight-range illumination of aqueous PABA solutions produced significantly higher steady-state concentrations of 1O2 than in solutions containing any of the other sunscreen active ingredients evaluated. The substituted benzophenone compounds (BZ3 and BZ8) and the salicylate-based compound (OCS) not only appear to produce no 1O2, but they also appear to produce no other reactive oxidant species that are capable of consuming FFA. This indicates that BZ3, BZ8, and OCS may be peferable, from the standpoint of toxic oxidant formation, for use as sunscreen active ingredients when compared to the other compounds evaluated in this study.

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Year:  1996        PMID: 8728505     DOI: 10.1021/tx950197m

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  8 in total

1.  Sunscreens and their usefulness: have we made any progress in the last two decades?

Authors:  Nick Serpone
Journal:  Photochem Photobiol Sci       Date:  2021-02-18       Impact factor: 3.982

2.  Non-Euclidean phasor analysis for quantification of oxidative stress in ex vivo human skin exposed to sun filters using fluorescence lifetime imaging microscopy.

Authors:  Sam Osseiran; Elisabeth M Roider; Hequn Wang; Yusuke Suita; Michael Murphy; David E Fisher; Conor L Evans
Journal:  J Biomed Opt       Date:  2017-12       Impact factor: 3.170

3.  Studies on the formation of formaldehyde during 2-ethylhexyl 4-(dimethylamino)benzoate demethylation in the presence of reactive oxygen and chlorine species.

Authors:  Waldemar Studziński; Alicja Gackowska; Maciej Przybyłek; Jerzy Gaca
Journal:  Environ Sci Pollut Res Int       Date:  2017-01-29       Impact factor: 4.223

Review 4.  A Perspective on Femtosecond Pump-Probe Spectroscopy in the Development of Future Sunscreens.

Authors:  Abigail L Whittock; Temitope T Abiola; Vasilios G Stavros
Journal:  J Phys Chem A       Date:  2022-04-08       Impact factor: 2.944

5.  Identification of the Biotransformation Products of 2-Ethylhexyl 4-(N,N-Dimethylamino)benzoate.

Authors:  Zacarias León; Jon de Vlieger; Alberto Chisvert; Amparo Salvador; Henk Lingeman; Hubertus Irth; Martin Giera
Journal:  Chromatographia       Date:  2009-11-12       Impact factor: 2.044

6.  Octyl methoxycinnamate modulates gene expression and prevents cyclobutane pyrimidine dimer formation but not oxidative DNA damage in UV-exposed human cell lines.

Authors:  Nur Duale; Ann-Karin Olsen; Terje Christensen; Shamas T Butt; Gunnar Brunborg
Journal:  Toxicol Sci       Date:  2010-01-13       Impact factor: 4.849

7.  Photophysics of sunscreen molecules in the gas phase: a stepwise approach towards understanding and developing next-generation sunscreens.

Authors:  Natércia D N Rodrigues; Michael Staniforth; Vasilios G Stavros
Journal:  Proc Math Phys Eng Sci       Date:  2016-11       Impact factor: 2.704

Review 8.  Photostability of Topical Agents Applied to the Skin: A Review.

Authors:  Agata Kryczyk-Poprawa; Anna Kwiecień; Włodzimierz Opoka
Journal:  Pharmaceutics       Date:  2019-12-20       Impact factor: 6.321

  8 in total

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