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Assessment of 8-methosypsoralen, lomefloxacin, sparfloxacin, and Pirfenidone phototoxicity in Long-Evans rats.
Adachi, Tamiko; Satou, Yuko; Satou, Hiroko; Shibata, Hiroshi; Miwa, Satoko; Iwase, Yumiko; Yamamoto, Toshinobu; Nishida, Atsuyuki; Masutomi, Naoya.
Affiliation
  • Adachi T; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Satou Y; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Satou H; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Shibata H; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Miwa S; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Iwase Y; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Yamamoto T; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Nishida A; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan.
  • Masutomi N; Research Division, Safety Research Laboratories, Mitsubishi Tanabe Pharma Corporation, Kisarazu, Chiba, Japan masutomi.naoya@mm.mt-pharma.co.jp.
Int J Toxicol ; 34(1): 16-23, 2015.
Article de En | MEDLINE | ID: mdl-25432946
ABSTRACT
Phototoxicity has a strong impact on drug development. Although several animal models have been developed to quantitatively assess human risks, none have been validated for standardized use. In this study, we validated an in vivo phototoxicity model using Long-Evans (LE) rats treated with 4 well-known phototoxic drugs, namely 8-methoxypsoralen, lomefloxacin, sparfloxacin, and pirfenidone. Daily macroscopic observations of skin and eyes, ophthalmological examinations 4 days after dosing, and blood sampling for toxicokinetics (TKs) were performed after exposure of treated animals to ultraviolet, and dose-dependent eye and/or skin reactions were noted for all compounds. Margins of safety were calculated when possible and correlated well with known relative phototoxicity of the 4 compounds. We conclude that the present in vivo phototoxicity assay using LE rats with TK analysis can be used to quantitatively predict the risk of pharmaceutical phototoxicity in humans.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Furocoumarines / Pyridones / Rayons ultraviolets / Dermatite phototoxique / Fluoroquinolones Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Int J Toxicol Sujet du journal: TOXICOLOGIA Année: 2015 Type de document: Article Pays d'affiliation: Japon

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Furocoumarines / Pyridones / Rayons ultraviolets / Dermatite phototoxique / Fluoroquinolones Type d'étude: Prognostic_studies Limites: Animals Langue: En Journal: Int J Toxicol Sujet du journal: TOXICOLOGIA Année: 2015 Type de document: Article Pays d'affiliation: Japon