{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T17:33:19Z","timestamp":1790098399591,"version":"4.0.1"},"reference-count":47,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2016,1,19]],"date-time":"2016-01-19T00:00:00Z","timestamp":1453161600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Cosmetics Europe"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Contact Dermatitis"],"published-print":{"date-parts":[[2016,3]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Methylisothiazolinone (<jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>) [with methylchloroisothiazolinone (<jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content>) in a ratio of 1:3, a well\u2010recognized allergenic preservative] was released as an individual preservative in the 2000s for industrial products and in 2005 for cosmetics. The high level of exposure to <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content> since then has provoked an epidemic of contact allergy to <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>, and an increase in <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> allergy. There are questions concerning the <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> cross\u2010reaction pattern.<\/jats:p><\/jats:sec><jats:sec><jats:title>Objectives<\/jats:title><jats:p>To bring a new perspective on the <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> cross\u2010reactivity issue by studying their <jats:italic>in\u2009situ<\/jats:italic> chemical behaviour in <jats:styled-content style=\"fixed-case\">3D<\/jats:styled-content> reconstructed human epidermis (<jats:styled-content style=\"fixed-case\">RHE<\/jats:styled-content>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> were synthesized with <jats:styled-content style=\"fixed-case\"><jats:sup>13<\/jats:sup>C<\/jats:styled-content> substitution at positions <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\u20104\/<jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\u20105 and <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\u20105, respectively. Their <jats:italic>in\u2009situ<\/jats:italic> chemical behaviours in an <jats:styled-content style=\"fixed-case\">RHE<\/jats:styled-content> model were followed by use of the high\u2010resolution magic angle spinning nuclear magnetic resonance technique.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content> was found to react exclusively with cysteine thiol residues, whereas <jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> reacted with histidines and lysines. The reaction mechanisms were found to be different for <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content>, and the adducts formed had different molecular structures.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>In <jats:styled-content style=\"fixed-case\">RHE<\/jats:styled-content>, different <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content> reactions towards different nucleophilic amino acids were observed, making it difficult to explain cross\u2010reactivity between <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MCI<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/cod.12524","type":"journal-article","created":{"date-parts":[[2016,1,19]],"date-time":"2016-01-19T10:10:52Z","timestamp":1453198252000},"page":"159-167","source":"Crossref","is-referenced-by-count":38,"title":["<i>In\u2009situ<\/i> chemical behaviour of methylisothiazolinone (<scp>MI<\/scp>) and methylchloroisothiazolinone (<scp>MCI<\/scp>) in reconstructed human epidermis: a new approach to the cross\u2010reactivity issue"],"prefix":"10.1111","volume":"74","author":[{"given":"Camille","family":"Debeuckelaere","sequence":"first","affiliation":[{"name":"Dermatochemistry Laboratory, Institut de Chimie de Strasbourg, UMR 7177\/Universit\u00e9 de Strasbourg\u00a0\u2013\u00a0CNRS  67081 Strasbourg France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fran\u00e7ois\u2010Marie","family":"Moussallieh","sequence":"additional","affiliation":[{"name":"Dermatochemistry Laboratory, Institut de 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