Suppr超能文献

盐酸头孢马替林水合物(S-1090)的遗传毒性研究

[Genotoxicity studies of cefmatilen hydrochloride hydrate (S-1090)].

作者信息

Kondo K, Takase S, Nishimoto Y, Miyajima H, Shiratori O, Miyake Y

机构信息

Developmental Research Laboratories, Shionogi & Co., Ltd., 3-1-1 Futaba-cho, Toyonaka, Osaka 561-0825, Japan.

出版信息

J Toxicol Sci. 2001 May;26 Suppl 1:243-54.

Abstract

Cefmatilen hydrochloride hydrate (S-1090), a new non-ester type of orally active cephem antibiotic synthesized in Shionogi Research Laboratories, was evaluated for its genotoxic potential using three assay systems. In a reverse mutation test with bacteria of Salmonella typhimurium TA100, TA1535, TA98, and TA1537, and Escherichia coli WP2uvrA using the preincubation method, the number of revertant colonies in the S-1090 treated plates was almost equal to that in the negative control plates in all strains with and without metabolic activation system with S9 mix (maximum dose, 100 micrograms/plate in TA98). In a chromosomal aberration test with cultured Chinese hamster lung cells (CHL/IU), S-1090 did not induce structural chromosome aberrations or polyploid cells either in the absence or presence of S9 mix up to the 50% growth inhibition doses. The potential of inducing clastogenicity and/or disruption of mitotic apparatus in vivo by S-1090 was evaluated by a micronucleus test with bone marrow cells of male Jc1:ICR mice. S-1090 suspended in 0.5% aqueous methylcellulose was administered by oral gavage up to 2000 mg/kg/day in single and double dosing groups. No induction of micronucleated polychromatic erythrocytes was observed 24 hr after the last dosing in each group. As all three genotoxicity tests showed negative responses, S-1090 is thought to have no genotoxic potential.

摘要

盐酸头孢替米伦水合物(S - 1090)是盐野义制药研究实验室合成的一种新型非酯型口服活性头孢烯抗生素,使用三种检测系统对其遗传毒性潜力进行了评估。在采用预孵育法对鼠伤寒沙门氏菌TA100、TA1535、TA98和TA1537以及大肠杆菌WP2uvrA进行的细菌回复突变试验中,在有和没有S9混合液代谢活化系统的情况下(TA98中最大剂量为100微克/平板),用S - 1090处理的平板中回复菌落数在所有菌株中几乎与阴性对照平板中的相等。在用培养的中国仓鼠肺细胞(CHL/IU)进行的染色体畸变试验中,在高达50%生长抑制剂量时,无论有无S9混合液,S - 1090均未诱导结构染色体畸变或多倍体细胞。通过对雄性Jc1:ICR小鼠骨髓细胞进行微核试验,评估了S - 1090在体内诱导断裂作用和/或破坏有丝分裂装置的潜力。将S - 1090悬浮于0.5%甲基纤维素水溶液中,通过口服灌胃给予单剂量和双剂量组,剂量高达2000毫克/千克/天。在每组最后一次给药24小时后,未观察到微核多染红细胞的诱导。由于所有三项遗传毒性试验均显示阴性反应,因此认为S - 1090没有遗传毒性潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验