Enhanced toxicity of 2,2-bis(chloromethyl) trimethylene bis[bis(2-chloroethyl) phosphate] (V6) by nanopolystyrene particles towards HeLa cells.

IF 3.6 3区 医学 Q3 NANOSCIENCE & NANOTECHNOLOGY Nanotoxicology Pub Date : 2023-04-01 DOI:10.1080/17435390.2023.2203238
Zheng Zhong, Xin Liu, Yiming Ruan, Ziwei Li, Junxian Li, Lili Sun, Sen Hou
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Abstract

2,2-bis(chloromethyl) trimethylene bis[bis(2-chloroethyl) phosphate] (V6) has been widely used as an additive in a variety of plastics due to its extremely low toxicity. However, we showed in the study that once mixed with nanopolystyrene particles (NPs), the nontoxic V6 could exhibit significant toxicity to HeLa cells. The enhanced toxicity was much higher than the toxicity of NPs alone and was related to the size of NPs. The mixture of V6 and small polystyrene NPs (10 nm and 15 nm in radius) showed obvious toxicity to HeLa cells. The toxicity increased with the concentrations of both V6 and NPs. On the contrary, the mixture of V6 and larger NPs (25 nm, 50 nm, 100 nm, and 500 nm in radius) showed almost no toxicity even at extremely high concentrations (NPs: 100 mg/L; V6: 50 mg/L). The small NPs could enter the cells and accumulated in cytoplasm. However, the larger NPs did not distribute inside the cells. NPs efficiently adsorbed V6 on the surface. The mechanism of the enhanced toxicity was attributed to the increased intracellular reactive oxygen species (ROS) production and the regulation of gene expression concerning apoptosis and ROS scavenging. Our study not only showed that a safe chemical V6 could be turned to be toxic by NPs, but also pointed out a potential risk caused by the joint toxicity of 'safe' chemicals and plastic particles with small size.

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纳米聚苯乙烯颗粒增强2,2-二(氯甲基)三亚甲基二[二(2-氯乙基)磷酸](V6)对HeLa细胞的毒性。
2,2-二(氯甲基)三亚甲基二[二(2-氯乙基)磷酸](V6)因其极低的毒性已被广泛用作各种塑料的添加剂。然而,我们在研究中发现,一旦与纳米聚苯乙烯颗粒(NPs)混合,无毒的V6可能对HeLa细胞表现出明显的毒性。其增强毒性远高于单纯NPs的毒性,且与NPs的大小有关。V6和小聚苯乙烯NPs(半径分别为10 nm和15 nm)的混合物对HeLa细胞具有明显的毒性。毒性随V6和NPs浓度的增加而增加。相反,V6和更大的NPs(半径为25 nm、50 nm、100 nm和500 nm)的混合物即使在极高浓度(NPs: 100 mg/L;V6: 50 mg/L)。小的NPs可以进入细胞并在细胞质中积累。然而,较大的NPs不分布在细胞内。NPs在表面有效吸附了V6。毒性增强的机制归因于细胞内活性氧(ROS)的产生增加以及与细胞凋亡和ROS清除有关的基因表达的调节。我们的研究不仅表明了一种安全的化学品V6可以被NPs转化为有毒物质,而且还指出了“安全”化学品与小尺寸塑料颗粒共同毒性造成的潜在风险。
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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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