Updated Aspects of Safety Regulations for Biomedical Applications of Aerogel Compounds—Compendia-Like Evaluation

IF 1.8 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Safety Pub Date : 2023-11-20 DOI:10.3390/safety9040080
Monica Neagu, F. Grisi, Alfio Pulvirenti, R. Simón‐Vázquez, C. García-González, A. Boccia
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引用次数: 0

Abstract

Aerogels have recently started to be considered as “advanced materials”; therefore, as a general consideration, aerogels’ toxicity testing should focus on their functionality which resides in their nanoscale open internal porosity. To assess the hazards of organic aerogels, testing at three levels may characterize their biophysical, in vitro and in vivo toxicity, defining distinct categories of aerogels. At the first level of testing, their abiotic characteristics are investigated, and the best aerogel(s) is forwarded to be tested at level 2, wherein in vitro methodologies may mainly evaluate the aerogels’ cellular behavior. Within level 2 of testing, the main characteristics of toxicity are investigated and the selected aerogels are introduced to in vivo animal models at level 3. In the animal model testing, target organs are investigated along with systemic parameters of toxicity. Some study cases are presented for organic or anorganic aerogels. Within this tiered workflow, aerogels-based materials can be tested in terms of human health hazard.
气凝胶化合物生物医学应用安全法规的最新方面--类似《简编》的评价
气凝胶最近开始被视为 "先进材料";因此,作为一般考虑因素,气凝胶的毒性测试应侧重于其纳米级开放内部孔隙的功能。为评估有机气凝胶的危害,可从三个层面对其生物物理、体外和体内毒性进行测试,从而确定气凝胶的不同类别。在第一级测试中,将对气凝胶的非生物特性进行调查,并将最佳气凝胶送至第二级测试,其中体外方法主要评估气凝胶的细胞行为。在第二级测试中,将对毒性的主要特征进行调查,并将选定的气凝胶引入第三级的体内动物模型中。在动物模型测试中,将对目标器官和系统毒性参数进行调查。一些研究案例是针对有机或无机气凝胶的。在这种分级工作流程中,可以对气凝胶材料的人体健康危害进行测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Safety
Safety Social Sciences-Safety Research
CiteScore
3.20
自引率
5.30%
发文量
71
审稿时长
7 weeks
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