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富勒烯C60纳米颗粒的体外和体内遗传毒性试验。

In vitro and in vivo genotoxicity tests on fullerene C60 nanoparticles.

作者信息

Shinohara Naohide, Matsumoto Kyomu, Endoh Shigehisa, Maru Junko, Nakanishi Junko

机构信息

Research Institute of Science for Safety and Sustainability, AIST, 16-1, Onogawa, Tsukuba, Ibaraki 305-8569, Japan.

出版信息

Toxicol Lett. 2009 Dec 15;191(2-3):289-96. doi: 10.1016/j.toxlet.2009.09.012. Epub 2009 Sep 20.

Abstract

There are several conflicting reports on the genotoxicity of fullerene C(60) in the literature. To determine the genotoxic potential of C(60) nanoparticles, we prepared stable nano-sized C(60) suspensions using 0.1% carboxymethylcellulose sodium (CMC-Na) or 0.1% Tween 80 aqueous solution. We conducted a bacterial reverse mutation test with Ames Salmonella typhimurium TA98, TA100, TA1535, and TA1537 strains and Escherichia coli strain and a chromosomal aberration test with cultured Chinese hamster CHL/IU cells in the presence and absence of metabolic activation under dark conditions and visible light irradiation using a stable C(60) nanoparticle suspension with CMC-Na. In addition, we performed a bone marrow micronucleus test using a stable C(60) nanoparticle suspension with Tween 80 on ICR mice. C(60) nanoparticles did not show a positive mutagenic response up to the maximum dose of 1000 microg/plate with any tester strain in the bacterial reverse mutation test regardless of metabolic activation and irradiation, although a slight but not significant increase in the number of revertants was observed in TA100 and WP2 uvrA/pKM101. No increase in the incidence of chromosomal aberrations was observed at any C(60) nanoparticle dose regardless of metabolic activation and irradiation in the chromosomal aberration test up to the maximum doses of 100 and 200 microg/mL. In addition, the micronucleus test showed that the in vivo clastogenic ability of the C(60) nanoparticles was negative up to the maximum dose of 88 mg/kg x 2. Therefore, we concluded that the stable and well-characterized C(60) nanoparticles did not have genotoxic ability in the bacterial reverse mutation assay, in vitro chromosome aberration assay, nor in vivo micronucleus assay.

摘要

文献中关于富勒烯C(60)的遗传毒性有几份相互矛盾的报告。为了确定C(60)纳米颗粒的遗传毒性潜力,我们使用0.1%羧甲基纤维素钠(CMC-Na)或0.1%吐温80水溶液制备了稳定的纳米级C(60)悬浮液。我们用鼠伤寒沙门氏菌TA98、TA100、TA1535和TA1537菌株以及大肠杆菌菌株进行了细菌回复突变试验,并用培养的中国仓鼠CHL/IU细胞在黑暗条件和可见光照射下,在有和没有代谢激活的情况下,使用含有CMC-Na的稳定C(60)纳米颗粒悬浮液进行了染色体畸变试验。此外,我们使用含有吐温80的稳定C(60)纳米颗粒悬浮液对ICR小鼠进行了骨髓微核试验。在细菌回复突变试验中,无论有无代谢激活和照射,C(60)纳米颗粒在高达1000微克/平板的最大剂量下,对任何测试菌株均未显示出阳性诱变反应,尽管在TA100和WP2 uvrA/pKM101中观察到回复突变体数量有轻微但不显著的增加。在染色体畸变试验中,无论有无代谢激活和照射,在高达100和200微克/毫升的最大剂量下,任何C(60)纳米颗粒剂量均未观察到染色体畸变发生率增加。此外,微核试验表明,C(60)纳米颗粒在高达88毫克/千克×2的最大剂量下,体内致断裂能力为阴性。因此,我们得出结论,稳定且特性良好的C(60)纳米颗粒在细菌回复突变试验、体外染色体畸变试验和体内微核试验中均没有遗传毒性能力。

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