4.4 Article

Photodegradation of trimeprazine triggered by self-photogenerated singlet molecular oxygen

Journal

JOURNAL OF SAUDI CHEMICAL SOCIETY
Volume 20, Issue 5, Pages 543-546

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ELSEVIER
DOI: 10.1016/j.jscs.2012.07.016

Keywords

Trimeprazine; Phenothiazine; Singlet oxygen; Phototoxicity

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The antihistaminic drug trimeprazine (1, also known as alimemazine) is photolabile under UV-A light in aerobic conditions. Irradiation of a methanol solution of trimeprazine produces two photoproducts which were isolated as N, N2-trimethyl-3-(10H-phenothiazin-10-yl sulfoxide) propan-1-amine (2) and N, 2-dimethyl-3-(10H-phenothiazin-10-yl) propan-1-amine (4). The formation of products was explained by the oxidative photodegradation of trimeprazine in an irreversible trapping of the self-photogenerated O-1(2) by the type II photodynamic action of the drug. The generation of singlet oxygen during photolysis of trimeprazine was confirmed by singlet oxygen scavenger 2,5-dimethylfuran (2,5-DMF). (C) 2012 Production and hosting by Elsevier B.V. on behalf of King Saud University.

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