| Literature DB >> 22696462 |
Satomi Onoue1, Kazuhiro Hosoi, Shinobu Wakuri, Yumiko Iwase, Toshinobu Yamamoto, Naoko Matsuoka, Kazuichi Nakamura, Tsuguto Toda, Hironori Takagi, Naoto Osaki, Yasuhiro Matsumoto, Satoru Kawakami, Yoshiki Seto, Masashi Kato, Shizuo Yamada, Yasuo Ohno, Hajime Kojima.
Abstract
A reactive oxygen species (ROS) assay was previously developed for photosafety evaluation of pharmaceuticals, and the present multi-center study aimed to establish and validate a standard protocol for ROS assay. In three participating laboratories, two standards and 42 coded chemicals, including 23 phototoxins and 19 nonphototoxic drugs/chemicals, were assessed by the ROS assay according to the standardized protocol. Most phototoxins tended to generate singlet oxygen and/or superoxide under UV-vis exposure, but nonphototoxic chemicals were less photoreactive. In the ROS assay on quinine (200 µm), a typical phototoxic drug, the intra- and inter-day precisions (coefficient of variation; CV) were found to be 1.5-7.4% and 1.7-9.3%, respectively. The inter-laboratory CV for quinine averaged 15.4% for singlet oxygen and 17.0% for superoxide. The ROS assay on 42 coded chemicals (200 µm) provided no false negative predictions upon previously defined criteria as compared with the in vitro/in vivo phototoxicity, although several false positives appeared. Outcomes from the validation study were indicative of satisfactory transferability, intra- and inter-laboratory variability, and predictive capacity of the ROS assay.Entities:
Keywords: inter-laboratory precision; photoreactivity; phototoxicity; reactive oxygen species; validation
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Year: 2012 PMID: 22696462 DOI: 10.1002/jat.2776
Source DB: PubMed Journal: J Appl Toxicol ISSN: 0260-437X Impact factor: 3.446