Affiliations 

  • 1 Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center; Engineering Research Center of Key Technology and Industrialization of Cell-based Vaccine, Ministry of Education; Gansu Tech Innovation Center of Animal; China-Malaysia National Joint Laboratory, Northwest Minzu University, Lanzhou, Gansu 730030, P. R. China
  • 2 The Second Clinical Medical College, Lanzhou University, Lanzhou, Gansu 730000, P. R. China
  • 3 College of Life Science and Engineering, Northwest Minzu University, Lanzhou, Gansu 730030, P. R. China
  • 4 School of Life Science and Engineering, Lanzhou University of Technology, Lanzhou, Gansu 730050, P. R. China
  • 5 State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metals Chemistry and Resources Utilization of Gansu Province, Department of Chemistry, Lanzhou University, Lanzhou, Gansu 730000, P. R. China
  • 6 Beijing Key Laboratory for Green Catalysis and Separation, Department of Chemistry and Chemical Engineering, Center of Excellence for Environmental Safety and Biological Effects, Beijing University of Technology, Beijing 100124, P. R. China
Anal Chem, 2024 Feb 06;96(5):1913-1921.
PMID: 38266028 DOI: 10.1021/acs.analchem.3c04062

Abstract

2D nanosheets (NSs) have been widely used in drug-related applications. However, a comprehensive investigation into the cytotoxicity mechanism linked to the redox activity is lacking. In this study, with cytochrome c (Cyt c) as the model biospecies, the cytotoxicity of 2D NSs was evaluated systematically based on their redox effect with microfluidic techniques. The interface interaction, dissolution, and redox effect of 2D NSs on Cyt c were monitored with pulsed streaming potential (SP) measurement and capillary electrophoresis (CE). The relationship between the redox activity of 2D NSs and the function of Cyt c was evaluated in vitro with Hela cells. The results indicated that the dissolution and redox activity of 2D NSs can be simultaneously monitored with CE under weak interface interactions and at low sample volumes. Both WS2 NSs and MoS2 NSs can reduce Cyt c without significant dissolution, with reduction rates measured at 6.24 × 10-5 M for WS2 NSs and 3.76 × 10-5 M for MoS2 NSs. Furthermore, exposure to 2D NSs exhibited heightened reducibility, which prompted more pronounced alterations associated with Cyt c dysfunction, encompassing ATP synthesis, modifications in mitochondrial membrane potential, and increased reactive oxygen species production. These observations suggest a positive correlation between the redox activity of 2D NSs and their redox toxicity in Hela cells. These findings provide valuable insight into the redox properties of 2D NSs regarding cytotoxicity and offer the possibility to modify the 2D NSs to reduce their redox toxicity for clinical applications.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.