AI Article Synopsis

  • Emerging contaminants like nanoplastics and plasticizers raise global health concerns, especially related to respiratory tissue, due to their low biodegradability.
  • Cell culture techniques are crucial for studying the toxic effects of these substances on lung cells and help reveal their potential dangers.
  • A systematic review of 10 studies shows that exposure to nanoplastics and plasticizers can harm cell viability in a dose-dependent way, emphasizing the need for further research on their combined effects.

Article Abstract

Emerging contaminants such as nanoplastics (NPs), as well as manufacturing by-products such as plasticizers, have gained global attention and concern due to their limited biodegradability and their potential impact on human health, in particular the effects on respiratory tissue. In parallel, cell culture techniques are key to the assessment and characterization of toxic effects and cellular mechanisms in different types of tissues and should provide relevant information to understand the hazardous potential of these emergent contaminants. This systematic review presents the main results on the current knowledge of the effects of NPs and plasticizers on lung cells, as assessed with the use of cell culture techniques. From the selected studies ( = 10), following the PRISMA approach, it was observed that cell viability was the most frequently assessed endpoint and that most studies focused on epithelial cells and exposures to polystyrene (PS). It was observed that exposure to NPs or plasticizers induces cytotoxicity in a dose-dependent manner, regardless of the size of the NPs. Furthermore, there is evidence that the characteristics of NPs can affect the toxic response by promoting the association with other organic compounds. As such, further studies focusing on the combination of NPs with plasticizers will be essential for the understanding of mechanisms of NPs toxicity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315584PMC
http://dx.doi.org/10.3390/toxics10070402DOI Listing

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