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首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >In vivo carcinogenicity study of silver nanoparticles in transgenic rasH2 mice by one single-dose intravenous administration
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In vivo carcinogenicity study of silver nanoparticles in transgenic rasH2 mice by one single-dose intravenous administration

机译:一种单剂量静脉内给药在转基因Rash2小鼠中银纳米粒子的体内致癌性研究

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摘要

Benefited from their broad-spectrum antimicrobial property, silver nanoparticles (AgNPs) have been widely used in various daily life and medical products. Consequently, the bio-safety of AgNPs, especially long-term in vivo biological effects is of more and more importance. However, there are no correlated publications about AgNP carcinogenicity at present. Thus, in this study, we have investigated the potential carcinogenicity of polyvinylpyrrolidone (PVP)-coated AgNPs with an intermediate size (diameter similar to 42.5 nm). The C57-ras transgenic mouse model (CB6F1 Tg mice) harboring human c-Ha-ras gene was used to shorten the duration of in vivo experiments from 2 years to 22 weeks. CB6F1 Tg mice were intravenously injected by different single doses of AgNPs (0.4, 4, and 20 mg/kg body weight) during the 22-week carcinogenicity study. There were no obvious AgNP-related neoplastic lesions by microscope examination and no increase in the incidence of non-neoplastic lesions in the AgNP-treated mice in our study. Overall, these results indicate that AgNPs (<= 20 mg/kg) do not cause carcinogenesis in CB6F1 Tg mice via a single-dose intravenous injection. This provides useful toxicological information and is of great importance to more applications of AgNPs in the future.
机译:受益于其广谱抗微生物性质,银纳米粒子(AgNPS)已广泛用于各种日常生活和医疗产品。因此,AgNP的生物安全性,特别是体内生物效应的长期性更为重要。然而,目前AGNP致癌性没有相关的出版物。因此,在本研究中,我们研究了聚乙烯基吡咯烷酮(PVP)涂覆的AgNP的潜在致癌性,其中间尺寸(直径与42.5nm类似)。含有人C-HA-RA基因的C57-RAS转基因小鼠模型(CB6F1 TG小鼠)用于缩短2岁至22周的体内实验的持续时间。在22周致癌性研究期间,通过不同单剂量的agnps(0.4,4和20mg / kg体重)静脉内注射CB6F1 Tg小鼠。通过显微镜检查没有明显的AgNP相关的肿瘤病变,在我们的研究中Agnp处理的小鼠中的非肿瘤病变的发生率没有增加。总体而言,这些结果表明AgNP(<= 20mg / kg)通过单剂量静脉注射不会引起CB6F1 TG小鼠中的致癌。这提供了有用的毒理学信息,并且对未来的AGNPS应用具有重要意义。

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