Ohuchida A, Yoshida R
Drug Safety Laboratory, Taiho Pharmaceutical Co., Ltd., Tokushima, Japan.
J Toxicol Sci. 1988 Jun;13 Suppl 1:245-56. doi: 10.2131/jts.13.supplementi_245.
The mutagenicity of cefodizime sodium (THR-221) was investigated by the reverse mutation test using seven bacterial strains (Salmonella typhimurium strains TA100, TA98, TA1535, TA1537 and TA1538, and Escherichia coli strains WP2 and WP2uvrA) and the chromosomal aberration test with cultured Chinese hamster lung (CHL) cells. The reverse mutation test was carried out in dose range from 0.0025 to 5.0 micrograms/plate in the absence and presence of mammalian metabolic activation system. Antibacterial effects were observed at concentrations more than 0.25 microgram/plate, and no significant increases in the number of revertants were observed at the dose levels where antibacterial effects were not detected. THR-221 caused no increases in the number of chromosomal aberrants at dose levels of 0.75, 1.5, 3.0 and 6.0 mg/ml in the absence and presence of the metabolic activation. These results indicate that THR-221 has no mutagenic activity.
采用七种菌株(鼠伤寒沙门氏菌TA100、TA98、TA1535、TA1537和TA1538株,以及大肠杆菌WP2和WP2uvrA株)进行回复突变试验,并对培养的中国仓鼠肺(CHL)细胞进行染色体畸变试验,以研究头孢地嗪钠(THR - 221)的致突变性。在不存在和存在哺乳动物代谢活化系统的情况下,回复突变试验在0.0025至5.0微克/平板的剂量范围内进行。在浓度超过0.25微克/平板时观察到抗菌作用,在未检测到抗菌作用的剂量水平下,未观察到回复子数量的显著增加。在不存在和存在代谢活化的情况下,THR - 221在0.75、1.5、3.0和6.0毫克/毫升的剂量水平下均未导致染色体畸变数量增加。这些结果表明THR - 221没有致突变活性。