Characterization Challenges of Self-Assembled Polymer-SPIONs Nanoparticles: Benefits of Orthogonal Methods

Int J Mol Sci. 2022 Dec 17;23(24):16124. doi: 10.3390/ijms232416124.

Abstract

Size and zeta potential are critical physicochemical properties of nanoparticles (NPs), influencing their biological activity and safety profile. These are essential for further industrial upscale and clinical success. However, the characterization of polydisperse, non-spherical NPs is a challenge for traditional characterization techniques (ex., dynamic light scattering (DLS)). In this paper, superparamagnetic iron oxide nanoparticles (SPIONs) were coated with polyvinyl alcohol (PVAL) exhibiting different terminal groups at their surface, either hydroxyl (OH), carboxyl (COOH) or amino (NH2) end groups. Size, zeta potential and concentration were characterized by orthogonal methods, namely, batch DLS, nanoparticle tracking analysis (NTA), tunable resistive pulse sensing (TRPS), transmission electron microscopy (TEM), asymmetric flow field flow fractionation (AF4) coupled to multi-angle light scattering (MALS), UV-Visible and online DLS. Finally, coated SPIONs were incubated with albumin, and size changes were monitored by AF4-MALS-UV-DLS. NTA showed the biggest mean sizes, even though DLS PVAL-COOH SPION graphs presented aggregates in the micrometer range. TRPS detected more NPs in suspension than NTA. Finally, AF4-MALS-UV-DLS could successfully resolve the different sizes of the coated SPION suspensions. The results highlight the importance of combining techniques with different principles for NPs characterization. The advantages and limitations of each method are discussed here.

Keywords: SPIONs; asymmetric flow field flow fractionation; characterization; dynamic light scattering; nanoparticle tracking analysis; orthogonal characterization techniques; polydispersity; tunable resistive pulse sensing.

MeSH terms

  • Dynamic Light Scattering
  • Magnetic Iron Oxide Nanoparticles
  • Nanoparticles* / chemistry
  • Particle Size
  • Polymers*
  • Polyvinyl Alcohol

Substances

  • Polymers
  • Polyvinyl Alcohol

Grants and funding

The authors acknowledge support from the Bourgogne Franche-Comté Graduate School EUR-EIPHI (contract ANR-17-EURE-0002) and the ANER project “Nanoprot” no. 2019-Y-10648. This work was also supported by the French National Research Agency (ANR) as part of the “Investments d’Avenir” Programme (ANR-21-CE18-0015-01 and ANR-10-EQPX-05-01/IMAPPI Equipex).