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Contact allergens formed on air exposure of linalool. Identification and quantification of primary and secondary oxidation products and the effect on skin sensitization.

Sköld, Maria, 1976 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Börje, Anna, 1961 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Harambasic, Elma, 1973 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
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Karlberg, Ann-Therese, 1947 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
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 (creator_code:org_t)
2004-11-25
2004
Engelska.
Ingår i: Chemical research in toxicology. - : American Chemical Society (ACS). - 0893-228X .- 1520-5010. ; 17:12, s. 1697-705
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Linalool (3,7-dimethyl-1,6-octadien-3-ol) is an important fragrance chemical, frequently used in scented products because of its fresh, flowery odor. Linalool is an unsaturated hydrocarbon and is therefore susceptible to oxidation in the presence of air. The primary oxidation products, that is, hydroperoxides, formed in the autoxidation process, are reactive compounds that can be suspected to act as sensitizers. In the present investigation, we studied the autoxidation of linalool with emphasis on the formation of hydroperoxides. The oxidation products were isolated using flash chromatography and preparative HPLC and were identified with NMR and GC/MS, using synthesized reference compounds. Two hydroperoxides and several different secondary oxidation products were identified, among which some contain structural features that make them potential allergens. The amounts of linalool and the major oxidation products were quantified over time, using GC and an HPLC-method, suitable for the analysis of thermolabile primary oxidation products. The hydroperoxide 7-hydroperoxy-3,7-dimethylocta-1,5-diene-3-ol was found to be present in 15% in an oxidized sample. The local lymph node assay (LLNA) was used to investigate the sensitizing potential of pure linalool, two samples of air-exposed linalool, and oxidation products of linalool (an alpha,beta-unsaturated aldehyde, a mixture of two hydroperoxides, and an alcohol). Pure linalool showed no sensitizing potential. The air-exposed samples of linalool produced clearly positive responses, and the hydroperoxides were the strongest allergens of the tested oxidation products. The study demonstrates the importance of autoxidation on the sensitizing potential of linalool. We also conclude that the sensitizing potential differs with the composition of the oxidation mixture and thus with the air exposure time.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Läkemedelskemi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medicinal Chemistry (hsv//eng)

Nyckelord

Allergens
chemistry
immunology
Chromatography
High Pressure Liquid
Dermatitis
Allergic Contact
immunology
Humans
Hydrogen Peroxide
analysis
Local Lymph Node Assay
Monoterpenes
chemistry
immunology
metabolism
Oxidation-Reduction
Perfume
chemistry
Time Factors

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