研究目的
Investigating the biodissolution and cellular response to MoO3 nanoribbons and proposing a new framework for early hazard screening for 2D materials.
研究成果
The study demonstrates that MoO3 nanoribbons undergo rapid dissolution in biological simulant fluids and cell culture, placing them in Class D (biosoluble with low-hazard degradation products). This suggests they are a low priority for further nanotoxicology testing. The proposed framework for early hazard screening could accelerate the risk assessment of 2D materials and promote their safe design and commercialization.
研究不足
The study focuses on MoO3 nanoribbons as a case study, and the proposed framework may require validation with a broader range of 2D materials. The dissolution screening does not capture all possible biological interactions, and long-term in vitro or in vivo studies may be needed for comprehensive risk assessment.
1:Experimental Design and Method Selection:
The study involved synthesizing MoO3 nanoribbons and characterizing their stability and dissolution in various biological and environmental simulant fluids.
2:Sample Selection and Data Sources:
MoO3 nanoribbons were synthesized and characterized using SEM, TEM, ICP-OES, Raman analysis, and XRD.
3:List of Experimental Equipment and Materials:
Equipment included SEM (Zeiss LEO 1530 and FEI Scios Dual Beam FIB/SEM), TEM (JEOL 2500), ICP-OES (Thermo Scientific iCAP? 7400), Raman analysis, and XRD (Bruker Eco Advance).
4:Experimental Procedures and Operational Workflow:
The nanoribbons were tested in six fluid environments (nanopure water, EPA moderately-hard water, PBS, RPMI, simulated lung fluid, and phagolysosomal simulant fluid) to monitor dissolution and aggregation.
5:Data Analysis Methods:
Dissolution rates were determined by ICP-OES, and DLS was used to monitor changes in particle size distribution.
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