Hazard assessment of hexagonal boron nitride and hexagonal boron nitride reinforced thermoplastic polyurethane composites using human skin and lung cells

哈卡特 材料科学 热塑性聚氨酯 氮化硼 促炎细胞因子 复合材料 化学 医学 免疫学 炎症 生物化学 体外 弹性体
作者
Michela Carlin,Jasreen Kaur,Dinu Zinovie Ciobanu,Zheng‐Mei Song,Magnus Olsson,Tiberiu Totu,Govind Gupta,Guotao Peng,Viviana Jehová González,Iwona Janica,Victor Fuster Pozo,Savvina Chortarea,Marija Buljan,Tina Buerki‐Thurnherr,Antonio Esaú Del Río Castillo,Sanjay Thorat,Francesco Bonaccorso,Aurelia Tubaro,Ester Vázquez,Maurizio Prato,Andrea Armirotti,Peter Wick,Alberto Bianco,Bengt Fadeel,Marco Pelin
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:473: 134686-134686
标识
DOI:10.1016/j.jhazmat.2024.134686
摘要

Hexagonal boron nitride (hBN) is an emerging two-dimensional material attracting considerable attention in the industrial sector given its innovative physicochemical properties. Potential risks are associated mainly with occupational exposure where inhalation and skin contact are the most relevant exposure routes for workers. Here we aimed at characterizing the effects induced by composites of thermoplastic polyurethane (TPU) and hBN, using immortalized HaCaT skin keratinocytes and BEAS-2B bronchial epithelial cells. The composite was abraded using a Taber® rotary abraser and abraded TPU and TPU-hBN were also subjected to photo-Fenton-mediated degradation mimicking potential weathering across the product life cycle. Cells were exposed to the materials for 24 h (acute exposure) or twice per week for 4 weeks (chronic exposure) and evaluated with respect to material internalization, cytotoxicity, and proinflammatory cytokine secretion. Additionally, comprehensive mass spectrometry-based proteomics and metabolomics (secretomics) analyses were performed. Overall, despite evidence of cellular uptake of the material, no significant cellular and/or protein expression profiles alterations were observed after acute or chronic exposure of HaCaT or BEAS-2B cells, identifying only few pro-inflammatory proteins. Similar results were obtained for the degraded materials. These results support the determination of hazard profiles associated with cutaneous and pulmonary hBN-reinforced polymer composites exposure.
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