Generation of Nano/Microplastics for Immunological Assessments

Q2 Materials Science
Yoshitaka Nakanishi , Yukio Fujiwara , Yuta Nakashima
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引用次数: 1

Abstract

This study aimed to develop a method to generate nano/microplastics (NPs/MPs), whose morphology and constituents are clarified for various biological tests. NPs/MPs were generated using a pin-on-disc machine, where a pin made of polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), or polyethylene terephthalate (PET) was pressed onto a quartz glass disc. Relative motion between the pin and disc was then applied in a saline solution. An ultraviolet lamp (UV-B) was used to irradiate the frictional surfaces through a quartz glass disc to investigate the degradation of the plastic materials. A microtextured glass surface was used to induce fatigue failure of plastic materials and adjust the crack propagation of plastic materials. UV degradation was confirmed for all the plastic materials and UV irradiation increased the equivalent circle diameter (D) of PE, PVC, and PET but decreased the equivalent circle diameter (D) of PP. However, it was thought that UV irradiation did not affect the aspect ratio (R) and complexity (C) of all plastic materials. The physical degradation mechanism of using the microtextured glass surface may increase the generation of NPs/MPs, and the surface profile of microtextured glass may adjust the crack propagation of plastic material surfaces. Notably, almost all the NPs/MPs generated were fragment-shaped. The NPs/MPs were compared to the particles found in the environment or generated by milling, cutting or chemical degradation in vitro. It was concluded that the fragment-shaped NPs/MPs were similar to the particles found in the environment or generated by milling in vitro, through visual inspection, aspect ratios, and complexity. As the presence of NPs/MPs in the human body can pose a serious health risk, a microchamber device capable of both quantitative and time-dependent assessments of inflammatory cytokine (TNF-α) secretion from human monocyte-derived macrophages (HMDMs) was proposed. The microchamber was constructed with a height of 200 μm and a diameter of 15 mm. This configuration enabled the NPs/MPs to pass near the HMDM, which is important in the phagocytosis of NPs/MPs and contributes to quantitative assessment. Although approximately the same morphological aspects of NPs/MPs were administered, the secretion of TNF-α differed depending on the plastic material.

用于免疫学评估的纳米/微塑料的产生
本研究旨在开发一种制备纳米/微塑料(NPs/MPs)的方法,澄清其形态和成分,用于各种生物试验。NPs/MPs是使用针盘机生成的,其中由聚乙烯(PE),聚丙烯(PP),聚氯乙烯(PVC)或聚对苯二甲酸乙二醇酯(PET)制成的针被压在石英玻璃盘上。然后在生理盐水溶液中应用针和盘之间的相对运动。用紫外灯(UV-B)通过石英玻璃圆盘照射摩擦表面,研究塑料材料的降解情况。采用微织构玻璃表面诱导塑性材料疲劳破坏,调节塑性材料裂纹扩展。所有塑料材料均被证实有紫外线降解作用,并且紫外线照射增加了PE、PVC和PET的等效圆直径(D),但降低了PP的等效圆直径(D),但认为紫外线照射对所有塑料材料的纵横比(R)和复杂度(C)没有影响。微织构玻璃表面的物理降解机制可能会增加NPs/MPs的生成,微织构玻璃的表面轮廓可能会调节塑料材料表面的裂纹扩展。值得注意的是,几乎所有生成的np / mp都是碎片状的。将NPs/MPs与在环境中发现的颗粒或通过铣削、切割或体外化学降解产生的颗粒进行比较。通过目视检查、纵横比和复杂性,得出的结论是,碎片状的NPs/MPs与在环境中发现的颗粒或通过体外碾磨产生的颗粒相似。由于NPs/MPs在人体内的存在可能会造成严重的健康风险,因此提出了一种能够定量和时间依赖性评估人单核细胞源性巨噬细胞(HMDMs)炎症细胞因子(TNF-α)分泌的微室装置。微室高度为200 μm,直径为15 mm。这种结构使NPs/MPs能够在HMDM附近通过,这对NPs/MPs的吞噬非常重要,有助于定量评估。尽管给予NPs/MPs的形态学方面大致相同,但TNF-α的分泌因塑料材料而异。
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
Biotribology
Biotribology Materials Science-Surfaces, Coatings and Films
CiteScore
4.20
自引率
0.00%
发文量
17
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