Yokoyama Hideaki, Hattori Norimichi, Ohtsuka Hirohiko, Murata Eiji, Kobayashi Akio, Muta Kyotaka, Takumi Asuka, Kitaura Harumi, Jinno Fumihiro, Iwai Atsushi, Nakai Keiko, Mori Kanae, Saito Kosuke, Saito Yoshiro
Japan Tobacco Inc.
Ajinomoto Co., Inc.
J Toxicol Sci. 2020;45(6):319-325. doi: 10.2131/jts.45.319.
Due to finalization of the ICH S3A Q&A focusing on microsampling, application of microsampling technique to regular non-clinical animal studies is expected for non-clinical safety assessment of pharmaceuticals. In Europe, microsampling from the tail vein or saphenous vein has often been used, whereas sampling from the jugular vein is thought to be more common for non-clinical studies in Japan. Therefore, we assessed the toxicological effects of serial microsampling from the jugular vein of SD rats in a common 28-day study at 4 independent organizations. Fifty microliter sampling was performed at 6 timepoints on day 1 to 2 and 7 timepoints on day 27 to 28 and its toxicological influences on body weight, food consumption, hematological and clinical chemistry parameters, and organ weights (on day 29 for 3 and day 28 for 1 organizations) were evaluated. The serial microsampling was shown to have no or minimal influences on the assessed parameters. The observed statistical differences for the 18 parameters were sporadic and did not appear to be systemically associated with microsampling. However, the sporadic changes were more often observed in females (14/18 parameters) than in males (6/18), suggesting the possibility that female rats were more susceptible to treatment-based influences. The current results indicate that serial 50 μL sampling from the jugular vein of SD rats had no or very slight toxicological effects, suggesting that this microsampling condition is applicable for toxicokinetic evaluation of non-clinical rat toxicity studies.
由于聚焦微量采样的国际人用药品注册技术协调会(ICH)S3A问答最终定稿,预计在药物非临床安全性评价的常规非临床动物研究中会应用微量采样技术。在欧洲,经常采用从尾静脉或隐静脉进行微量采样,而在日本,非临床研究中从颈静脉采样更为常见。因此,我们在4个独立机构开展的一项常见的28天研究中,评估了从SD大鼠颈静脉进行连续微量采样的毒理学效应。在第1至2天的6个时间点以及第27至28天的7个时间点进行50微升采样,并评估其对体重、食物摄入量、血液学和临床化学参数以及器官重量(3个机构在第29天,1个机构在第28天)的毒理学影响。结果表明,连续微量采样对所评估参数没有或只有极小的影响。观察到的18个参数的统计学差异是零星出现的,似乎与微量采样没有系统性关联。然而,零星变化在雌性大鼠(14/18个参数)中比在雄性大鼠(6/18个参数)中更常出现,这表明雌性大鼠可能更容易受到基于处理的影响。目前的结果表明,从SD大鼠颈静脉连续进行50微升采样没有或只有非常轻微的毒理学效应,这表明这种微量采样条件适用于非临床大鼠毒性研究的毒代动力学评价。