Photochemical and Pharmacokinetic Characterization of Orally Administered Chemicals to Evaluate Phototoxic Risk.
Administration, Oral
Animals
Dermatitis, Phototoxic
/ diagnosis
Feasibility Studies
Male
Methoxsalen
/ administration & dosage
Pyridones
/ administration & dosage
Rats
Rats, Sprague-Dawley
Reactive Oxygen Species
/ metabolism
Risk Assessment
/ methods
Skin
/ drug effects
Structure-Activity Relationship
Tissue Distribution
Toxicity Tests, Acute
/ methods
Trifluoperazine
/ administration & dosage
Ultraviolet Rays
/ adverse effects
Voriconazole
/ administration & dosage
cassette-dosing pharmacokinetic study
photosafety assessment
phototoxicity
reactive oxygen species
structural diversity
Journal
Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
13
08
2018
revised:
17
09
2018
accepted:
08
10
2018
pubmed:
20
10
2018
medline:
12
5
2020
entrez:
19
10
2018
Statut:
ppublish
Résumé
This study aimed to verify the applicability of a proposed photosafety screening system based on a reactive oxygen species (ROS) assay and a cassette-dosing pharmacokinetic (PK) study to chemicals with wide structural diversity. The orally taken chemicals, erythromycin, gatifloxacin, 8-methoxypsoralen (MOP), pirfenidone (PFD), trifluoperazine (TFP), and voriconazole (VRZ), were selected as test compounds. The ROS assay was conducted to evaluate their photoreactivity, and all test compounds excluding erythromycin generated significant ROS under simulated sunlight exposure. According to the ROS data, TFP had potent photoreactivity, and the photoreactivity of 4 other compounds was judged to be moderate. Regarding the oral cassette-dosing PK test in rats, the skin deposition of MOP, PFD, and VRZ was relatively high, and gatifloxacin and TFP exhibited moderate skin deposition properties. Based on the ROS and PK data of test compounds, PFD and TFP were judged to be potent phototoxic compounds, and MOP and VRZ were deduced to have phototoxic risk. The predicted phototoxic risk of test compounds by proposed screening was mostly in agreement with observed in vivo phototoxicity in the rat skin. The proposed screening system could provide reliable photosafety information on orally administered compounds with wide structural diversity.
Identifiants
pubmed: 30336153
pii: S0022-3549(18)30613-0
doi: 10.1016/j.xphs.2018.10.013
pii:
doi:
Substances chimiques
Pyridones
0
Reactive Oxygen Species
0
Trifluoperazine
214IZI85K3
pirfenidone
D7NLD2JX7U
Voriconazole
JFU09I87TR
Methoxsalen
U4VJ29L7BQ
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1303-1308Informations de copyright
Copyright © 2019 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.