Toxicity dose descriptors from animal inhalation studies of 13 nanomaterials and their bulk and ionic counterparts and variation with primary particle characteristics.

IF 3.6 3区 医学 Q3 NANOSCIENCE & NANOTECHNOLOGY Nanotoxicology Pub Date : 2023-06-01 DOI:10.1080/17435390.2023.2221728
Niels Hadrup, Nicklas Sahlgren, Nicklas R Jacobsen, Anne T Saber, Karin S Hougaard, Ulla Vogel, Keld A Jensen
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Abstract

This study collects toxicity data from animal inhalation studies of some nanomaterials and their bulk and ionic counterparts. To allow potential grouping and interpretations, we retrieved the primary physicochemical and exposure data to the extent possible for each of the materials. Reviewed materials are compounds (mainly elements, oxides and salts) of carbon (carbon black, carbon nanotubes, and graphene), silver, cerium, cobalt, copper, iron, nickel, silicium (amorphous silica and quartz), titanium (titanium dioxide), and zinc (chemical symbols: Ag, C, Ce, Co, Cu, Fe, Ni, Si, Ti, TiO2, and Zn). Collected endpoints are: a) pulmonary inflammation, measured as neutrophils in bronchoalveolar lavage (BAL) fluid at 0-24 hours after last exposure; and b) genotoxicity/carcinogenicity. We present the dose descriptors no-observed-adverse-effect concentrations (NOAECs) and lowest-observed-adverse-effect concentrations (LOAECs) for 88 nanomaterial investigations in data-library and graph formats. We also calculate 'the value where 25% of exposed animals develop tumors' (T25) for carcinogenicity studies. We describe how the data may be used for hazard assessment of the materials using carbon black as an example. The collected data also enable hazard comparison between different materials. An important observation for poorly soluble particles is that the NOAEC for neutrophil numbers in general lies around 1 to 2 mg/m3. We further discuss why some materials' dose descriptors deviate from this level, likely reflecting the effects of the ionic form and effects of the fiber-shape. Finally, we discuss that long-term studies, in general, provide the lowest dose descriptors, and dose descriptors are positively correlated with particle size for near-spherical materials.

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13种纳米材料及其体积和离子对应物的动物吸入毒性剂量描述符以及主要颗粒特征的变化。
本研究收集了一些纳米材料及其体积和离子对应物的动物吸入研究的毒性数据。为了进行潜在的分组和解释,我们尽可能地检索了每种材料的主要物理化学和暴露数据。所审查的材料是碳(炭黑、碳纳米管和石墨烯)、银、铈、钴、铜、铁、镍、硅(无定形二氧化硅和石英)、钛(二氧化钛)和锌(化学符号:Ag、C、Ce、Co、Cu、Fe、Ni、Si、Ti、TiO2和Zn)的化合物(主要是元素、氧化物和盐)。收集的终点是:a)肺部炎症,在最后一次暴露后0-24小时以支气管肺泡灌洗液(BAL)中的中性粒细胞测量;b)遗传毒性/致癌性。我们以数据库和图表格式介绍了88种纳米材料研究的剂量描述符无观察到的不良反应浓度(NOAECs)和最低观察到的不良反应浓度(loecs)。我们还为致癌性研究计算了“25%的暴露动物产生肿瘤的值”(T25)。我们描述了如何将数据用于以炭黑为例的材料的危害评估。收集的数据还可以进行不同材料之间的危害比较。对难溶性颗粒的一个重要观察结果是,中性粒细胞数目的NOAEC一般在1至2毫克/立方米左右。我们进一步讨论了为什么一些材料的剂量描述符偏离了这个水平,可能反映了离子形式和纤维形状的影响。最后,我们讨论了长期研究通常提供最低剂量描述符,并且剂量描述符与近球形材料的粒径正相关。
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来源期刊
Nanotoxicology
Nanotoxicology 医学-毒理学
CiteScore
10.10
自引率
4.00%
发文量
45
审稿时长
3.5 months
期刊介绍: Nanotoxicology invites contributions addressing research relating to the potential for human and environmental exposure, hazard and risk associated with the use and development of nano-structured materials. In this context, the term nano-structured materials has a broad definition, including ‘materials with at least one dimension in the nanometer size range’. These nanomaterials range from nanoparticles and nanomedicines, to nano-surfaces of larger materials and composite materials. The range of nanomaterials in use and under development is extremely diverse, so this journal includes a range of materials generated for purposeful delivery into the body (food, medicines, diagnostics and prosthetics), to consumer products (e.g. paints, cosmetics, electronics and clothing), and particles designed for environmental applications (e.g. remediation). It is the nano-size range if these materials which unifies them and defines the scope of Nanotoxicology . While the term ‘toxicology’ indicates risk, the journal Nanotoxicology also aims to encompass studies that enhance safety during the production, use and disposal of nanomaterials. Well-controlled studies demonstrating a lack of exposure, hazard or risk associated with nanomaterials, or studies aiming to improve biocompatibility are welcomed and encouraged, as such studies will lead to an advancement of nanotechnology. Furthermore, many nanoparticles are developed with the intention to improve human health (e.g. antimicrobial agents), and again, such articles are encouraged. In order to promote quality, Nanotoxicology will prioritise publications that have demonstrated characterisation of the nanomaterials investigated.
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