Photochemistry and Photobiology 2012-01-01

Investigation of the sunscreen octocrylene's interaction with amino acid analogs in the presence of UV radiation.

Isabella Karlsson, Elin Persson, Jerker Mårtensson, Anna Börje

文献索引:Photochem. Photobiol. 88(4) , 904-12, (2012)

全文:HTML全文

摘要

Octocrylene is an organic UV filter, commonly used in sunscreens and cosmetics, which can give rise to both contact and photocontact allergy. Our aim was to investigate octocrylene's interaction with amino acid analogs in the presence of UV radiation to better understand the reason for octocrylene's photoallergenic capacity. The amino acid analogs were photolysed in presence and absence of octocrylene for 1 h in cyclohexane. The rate of degradation was considerably slower for all amino acid analogs when octocrylene was present in the mixture. Benzylamine, the lysine analog, did react with octocrylene during the photolysis and the corresponding amide was formed in an acylation reaction. By varying the benzylamine concentration and keeping the octocrylene concentration fixed the reaction rate was shown to be independent of the amine concentration. The same type of acylation reaction took place when octocrylene alone was photolysed in ethanol in which the ethyl ester was formed from octocrylene and ethanol. Our results suggest that octocrylene's ability to cause photocontact allergy could be due to its photoinduced reactivity toward primary amines and alcohols.© 2012 Wiley Periodicals, Inc. Photochemistry and Photobiology © 2012 The American Society of Photobiology.


相关化合物

  • 4-丙基苯酚
  • 奥克立林
  • 苄胺
  • 1-辛硫醇
  • 3-甲基吲哚
  • 苄胺盐酸盐

相关文献:

Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins

2009-01-01

[Bioorg. Med. Chem. 17 , 896-904, (2009)]

A convenient screening method to differentiate phenolic skin whitening tyrosinase inhibitors from leukoderma-inducing phenols.

2015-10-01

[J. Dermatol. Sci. 80 , 18-24, (2015)]

Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study.

2005-11-17

[J. Med. Chem. 48 , 7234-42, (2005)]

Inhibition of rat, mouse, and human glutathione S-transferase by eugenol and its oxidation products.

1996-01-05

[Chem. Biol. Interact. 99(1-3) , 85-97, (1996)]

更多文献...