研究目的
The objective of this paper is to determine the limitations of the isotopic labelling technique for ENPs in biological matrices, which should be an important step prior to any future fate and toxicity study.
研究成果
The study demonstrated the advantages of the isotopic labelling method for working at very low concentrations of QDs in biological media. The QD-LOQ values were significantly lower than conventional LOQ values, enabling future studies on ENP fate and toxicity at realistic concentrations. The QD-RLOQ concept was introduced to better assess the efficiency of the spiking method by considering the background concentration in the matrix.
研究不足
The limitations include the poor recovery rates for Se due to the need for high resolution in ICP-MS measurements, which results in lower count numbers. The method's sensitivity is affected by the background concentration of elements in the matrices and the dilution factor required for analysis.
1:Experimental Design and Method Selection:
The study involved the synthesis of multi-isotopically labelled CdSe/ZnS quantum dots (QDs) and their dispersion in various biological matrices to assess the limits of isotopic labelling technique.
2:Sample Selection and Data Sources:
Biological matrices included synthetic saliva, synthetic urine, plasma, and DPBS growth medium.
3:List of Experimental Equipment and Materials:
Chemicals with natural and modified isotopic compositions were used. Instruments included HR-ICP-MS (ThermoScientific Element II), TEM (JEOL 2100 F), UV-Vis spectrometer (Thermo Scientific Evolution 600), and spectrofluorometer (Horiba Scientific FluoroMax-4).
4:4). Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: QDs were synthesized, characterized, and dispersed in biological matrices at very low concentrations. Isotopic compositions were determined by HR-ICP-MS.
5:Data Analysis Methods:
Statistical data treatment was used to determine the limits of quantification of the method (QD-LOQ).
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