Most cited article - PubMed ID 31427136
Study of interactions between carboxylated core shell magnetic nanoparticles and polymyxin B by capillary electrophoresis with inductively coupled plasma mass spectrometry
The increasing use of engineered nanoparticles (NPs) in consumer and biomedical products has raised concern over their potential accumulation, transformation, and toxicity in biological systems. Accurate analytical methods are essential to detect, characterize, and quantify NPs in complex biological matrices. Inductively coupled plasma mass spectrometry (ICP-MS) has emerged as a leading technique due to its high sensitivity, elemental selectivity, and quantitative capabilities. This review critically evaluates recent advances (from January 2020 onward) in ICP-MS-based methods for analysis of NPs in biological samples. Two main strategies are discussed: single-particle ICP-MS (spICP-MS) and hyphenated techniques coupled to ICP-MS. spICP-MS allows direct determination of particle size, concentration, and metal content at environmentally relevant levels. It is the most widely used approach and is therefore examined in greater detail, with attention to extraction procedures, particle types, sample matrices, and inherent limitations. Advances in laser ablation spICP-MS for tissue imaging and spatially resolved NPs detection are also covered. Methods using hyphenated techniques, such as hydrodynamic chromatography, size-exclusion chromatography, capillary electrophoresis, Taylor dispersion analysis, and field-flow fractionation, are increasingly employed to address limitations spICP-MS. These approaches can provide enhanced insight into particle size distributions, aggregation behavior, and interactions with complex sample matrices. This review offers a comparative evaluation of both single-particle and hyphenated methods, discussing their respective advantages and limitations. Emphasis is placed on the complementarity of these techniques and how their combined use can offer a more complete understanding of NPs' fate in biological systems.
- Keywords
- biological samples | inductively coupled plasma mass spectrometry (ICP‐MS) | nanoparticles | separation | single particle,
- MeSH
- Mass Spectrometry * methods MeSH
- Humans MeSH
- Nanoparticles * analysis chemistry MeSH
- Particle Size MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
A novel methodology for investigating the behavior of nanoparticles in their mixtures in aqueous high-ionic strength conditions is presented in this work. Our approach utilizes Taylor dispersion analysis in capillaries connected to inductively coupled plasma mass spectrometry (ICP-MS) to probe metal-derived nanoparticles. This methodology simultaneously distinguishes between different kinds of nanoparticles and accurately determines their essential parameters, such as hydrodynamic size, diffusion coefficient, and elemental composition. Moreover, the isotope-specific ICP-MS detection allows for unique targeting of the fate of isotopically enriched nanoparticles. The complexity of our methodology opens the way for studying barely explored areas of interparticle interactions or unequivocal characterization of one type of nanoparticle in complex mixtures without any need for calibration as well as labor-consuming sample preparation.
- Publication type
- Journal Article MeSH