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吸入纳米颗粒的致癌性。

Carcinogenicity of inhaled nanoparticles.

机构信息

Advisory Office for Risk Assessment, Dortmund, Germany.

出版信息

Inhal Toxicol. 2009 Jul;21 Suppl 1:144-57. doi: 10.1080/08958370902942541.

Abstract

Large epidemiological studies in the United States have shown a statistical association between air concentration of the fine dust fraction PM(2.5) in the general environment and increased risk of lung cancer. A quantitative risk assessment for lung cancer based on these studies corresponds to risk estimates based on studies at workplaces with exposure to diesel engine emissions; its magnitude cannot be explained by the known carcinogenicity of organic substances or metals adsorbed to the insoluble particle core. Carcinogenic effects of diesel particles were observed after inhalation in rats independently in several studies. The surprisingly strong effect of diesel particles was partially attributed to their small size. This hypothesis was corroborated by inhalation studies with synthetic nanoparticles virtually free of organic compounds. IARC found sufficient evidence for the carcinogenicity of carbon black and of titanium dioxide in experimental animals. Long-term studies by the method of intratracheal instillation confirmed the carcinogenic effects in rats for an even broader spectrum of synthetic nanoparticles. Non-positive studies with hamsters are not valid because hamsters did not develop lung tumors after inhalation of some known human carcinogens. In recent years, the number of publications reporting in vitro genotoxicity of TiO(2) and of carbon black nanomaterials has increased. Overall, there is clear positive evidence for carcinogenicity in rats, together with supporting evidence from human data of structurally related substances. Therefore, the European Union (EU) criteria for category 2 of carcinogenic substances appear to be fulfilled for bio-durable nanoparticles consisting of matter without known significant specific toxicity.

摘要

美国的大型流行病学研究表明,一般环境中细粉尘 PM(2.5)的空气浓度与肺癌风险增加之间存在统计学关联。基于这些研究的肺癌定量风险评估与基于工作场所接触柴油发动机排放的研究的风险估计相对应;其大小不能用吸附在不溶性颗粒核心上的有机物质或金属的已知致癌性来解释。在几项研究中,大鼠吸入柴油颗粒后独立观察到致癌作用。柴油颗粒的惊人强烈作用部分归因于其粒径小。这项假设通过使用几乎不含有机化合物的合成纳米颗粒进行吸入研究得到了证实。IARC 发现了足够的证据表明碳黑和二氧化钛在实验动物中具有致癌性。通过气管内滴注法进行的长期研究证实,对于更广泛的合成纳米颗粒,甚至具有致癌作用。与仓鼠的非阳性研究是无效的,因为仓鼠在吸入一些已知的人类致癌物后没有发展出肺癌。近年来,报告 TiO(2)和碳黑纳米材料体外遗传毒性的出版物数量有所增加。总体而言,大鼠的致癌性有明确的阳性证据,同时还有结构相关物质的人类数据提供的支持证据。因此,对于由无已知显著特定毒性的物质组成的生物持久纳米颗粒,欧盟 2 类致癌物质标准似乎得到了满足。

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