{"title":"Methodological foundations for substantiating safe levels of exposure to artificial nanomaterials (for example, carbon nanotubes) (literature review)","authors":"G. A. Timerbulatova, L. Fatkhutdinova","doi":"10.36946/0869-7922-2021-29-6-5-15","DOIUrl":null,"url":null,"abstract":"Introduction. The unique physicochemical properties of carbon nanotubes allow them to be used in many fields. The global nanomaterials market is growing every year. An important step in introducing products to the domestic and world markets is to determine the safe exposure levels of CNTs. Establishing a corporate standard can serve as a preliminary stage before the approval of a state hygiene standard. Material and methods. The material for the analysis was the sources of information on the available standards for the content of CNTs in the air of the working area using information from regulatory agencies, research centers, CNT manufacturers, bibliographic and abstract databases Web of Science, Scopus, PubMed, RSCI. Results. A scheme for justifying safe levels of exposure to CNTs (corporate standard) has been developed, consisting of several stages: characterization of CNTs in the air at workplaces, selection of experimental doses of CNTs, preparation of CNT dispersions, and conducting toxicological and hygienic experiments. Justification of the corporate standard is carried out in in vitro and in vivo experiments. The planning of experiments should be carried out taking into account the target organ under the influence of CNT - the respiratory system. The recommended dose / concentration range for experiments should include doses / concentrations derived from calculated and literature data. A necessary step is to obtain homogeneous dispersions in which CNTs become bioavailable for biological systems. In vitro and in vivo experiments determine the level of exposure at which no harmful effect is observed and / or the lowest level of exposure at which there is a harmful effect on the cell culture / respiratory tract of animals. After the stage of substantiating the corporate standard, the enterprise should take measures for several years to adjust the corporate standard based on data from clinical and hygienic studies, during which the working conditions and health status of workers are monitored, and extended toxicological and hygienic studies. Conclusion. The presence of a corporate standard will allow the manufacturer of CNTs to carry out activities for the development and implementation of a production control program with the introduction of monitoring the air condition in the working area. The development of a corporate regulation can be seen as a preparatory stage before the establishment of a government regulation.","PeriodicalId":23128,"journal":{"name":"Toxicological Review","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicological Review","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36946/0869-7922-2021-29-6-5-15","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction. The unique physicochemical properties of carbon nanotubes allow them to be used in many fields. The global nanomaterials market is growing every year. An important step in introducing products to the domestic and world markets is to determine the safe exposure levels of CNTs. Establishing a corporate standard can serve as a preliminary stage before the approval of a state hygiene standard. Material and methods. The material for the analysis was the sources of information on the available standards for the content of CNTs in the air of the working area using information from regulatory agencies, research centers, CNT manufacturers, bibliographic and abstract databases Web of Science, Scopus, PubMed, RSCI. Results. A scheme for justifying safe levels of exposure to CNTs (corporate standard) has been developed, consisting of several stages: characterization of CNTs in the air at workplaces, selection of experimental doses of CNTs, preparation of CNT dispersions, and conducting toxicological and hygienic experiments. Justification of the corporate standard is carried out in in vitro and in vivo experiments. The planning of experiments should be carried out taking into account the target organ under the influence of CNT - the respiratory system. The recommended dose / concentration range for experiments should include doses / concentrations derived from calculated and literature data. A necessary step is to obtain homogeneous dispersions in which CNTs become bioavailable for biological systems. In vitro and in vivo experiments determine the level of exposure at which no harmful effect is observed and / or the lowest level of exposure at which there is a harmful effect on the cell culture / respiratory tract of animals. After the stage of substantiating the corporate standard, the enterprise should take measures for several years to adjust the corporate standard based on data from clinical and hygienic studies, during which the working conditions and health status of workers are monitored, and extended toxicological and hygienic studies. Conclusion. The presence of a corporate standard will allow the manufacturer of CNTs to carry out activities for the development and implementation of a production control program with the introduction of monitoring the air condition in the working area. The development of a corporate regulation can be seen as a preparatory stage before the establishment of a government regulation.
介绍。碳纳米管独特的物理化学性质使其在许多领域得到应用。全球纳米材料市场每年都在增长。将产品引入国内和国际市场的一个重要步骤是确定碳纳米管的安全暴露水平。企业标准的制定可以作为国家卫生标准批准前的预备阶段。材料和方法。分析的材料是工作区域空气中碳纳米管含量可用标准的信息来源,使用的信息来自监管机构、研究中心、碳纳米管制造商、书目和摘要数据库Web of Science、Scopus、PubMed、RSCI。结果。已经制定了证明碳纳米管暴露安全水平的方案(公司标准),包括几个阶段:工作场所空气中碳纳米管的表征、碳纳米管实验剂量的选择、碳纳米管分散体的制备以及进行毒理学和卫生实验。在体外和体内实验中对公司标准进行了论证。实验计划应考虑到靶器官在碳纳米管的影响下-呼吸系统。实验的推荐剂量/浓度范围应包括从计算数据和文献数据得出的剂量/浓度。一个必要的步骤是获得均匀的分散体,使碳纳米管成为生物系统的生物可利用性。体外和体内实验确定没有观察到有害影响的暴露水平和/或对细胞培养/动物呼吸道有有害影响的最低暴露水平。企业在确定企业标准后,应在数年内采取措施,根据监测工人劳动条件和健康状况的临床和卫生研究数据,以及扩展的毒理学和卫生研究,对企业标准进行调整。结论。企业标准的存在将使碳纳米管制造商能够开展活动,制定和实施生产控制计划,并引入对工作区域空气状况的监测。公司法规的制定可以看作是政府法规建立之前的一个准备阶段。