Competence Unit Molecular Diagnostics, Austrian Institute of Technology GmbH, 1210 Vienna, Austria.
Smart Materials, Istituto Italiano di Tecnologia, via Morego 30, 16163 Genova, Italy.
Int J Environ Res Public Health. 2020 Nov 27;17(23):8832. doi: 10.3390/ijerph17238832.
The exposure of humans to nano-and microplastic particles (NMPs) is an issue recognized as a potential health hazard by scientists, authorities, politics, non-governmental organizations and the general public. The concentration of NMPs in the environment is increasing concomitantly with global plastic production and the usage of plastic materials. NMPs are detectable in numerous aquatic organisms and also in human samples, therefore necessitating a risk assessment of NMPs for human health. So far, a comprehensive risk assessment of NMPs is hampered by limited availability of appropriate reference materials, analytical obstacles and a lack of definitions and standardized study designs. Most studies conducted so far used polystyrene (PS) spheres as a matter of availability, although this polymer type accounts for only about 7% of total plastic production. Differently sized particles, different concentration and incubation times, and various biological models have been used, yielding hardly comparable data sets. Crucial physico-chemical properties of NMPs such as surface (charge, polarity, chemical reactivity), supplemented additives and adsorbed chemicals have been widely excluded from studies, although in particular the surface of NMPs determines the interaction with cellular membranes. In this manuscript we give an overview about the critical parameters which should be considered when performing risk assessments of NMPs, including novel reference materials, taking into account surface modifications (e.g., reflecting weathering processes), and the possible role of NMPs as a substrate and/or carrier for (pathogenic) microbes. Moreover, we make suggestions for biological model systems to evaluate immediate toxicity, long-term effects and the potential of NMPs to cross biological barriers. We are convinced that standardized reference materials and experimental parameters along with technical innovations in (nano)-particle sampling and analytics are a prerequisite for the successful realization of conclusive human health risk assessments of NMPs.
人类暴露于纳米和微塑料颗粒(NMPs)被科学家、当局、政治、非政府组织和公众认为是一个潜在的健康危害问题。随着全球塑料生产和塑料材料的使用,NMPs 在环境中的浓度也在增加。NMPs 在许多水生生物以及人类样本中都可检测到,因此需要对 NMPs 对人类健康的风险进行评估。到目前为止,由于缺乏适当的参考材料、分析障碍以及缺乏定义和标准化的研究设计,对 NMPs 的全面风险评估受到了阻碍。到目前为止,大多数研究都使用聚苯乙烯(PS)球作为可用材料,尽管这种聚合物类型仅占总塑料产量的约 7%。不同大小的颗粒、不同的浓度和孵育时间,以及不同的生物模型已经被使用,产生的数据集几乎无法进行比较。NMPs 的关键物理化学性质,如表面(电荷、极性、化学反应性)、补充添加剂和吸附化学物质,在研究中被广泛排除在外,尽管特别是 NMPs 的表面决定了与细胞膜的相互作用。在本文中,我们概述了在进行 NMPs 风险评估时应考虑的关键参数,包括新型参考材料,考虑到表面改性(例如,反映风化过程),以及 NMPs 作为(致病)微生物的基质和/或载体的可能作用。此外,我们还对生物模型系统提出了建议,以评估即时毒性、长期影响以及 NMPs 穿透生物屏障的潜力。我们相信,标准化参考材料和实验参数以及(纳米)颗粒采样和分析方面的技术创新是成功实现 NMPs 人类健康风险评估的先决条件。