Understanding the self-assembly of the polymeric drug solubilizer Soluplus®

J Colloid Interface Sci. 2022 Apr:611:224-234. doi: 10.1016/j.jcis.2021.12.016. Epub 2021 Dec 16.

Abstract

Hypothesis: Soluplus® is one of the most widely used amphiphilic copolymers in drug delivery and has been reported to strongly enhance the adsorption of model drugs. However, there is still a limited understanding of its micellar behavior as it responds to the different routes of administration, which involve important changes in concentration.

Experiments: The microstructure of Soluplus aqueous solutions has been investigated at a wide range of polymer concentrations (2 × 10-6 - 0.2 g/mL) by a combination of diffusion NMR (dNMR), small angle X-ray scattering (SAXS), static (SLS) dynamic (DLS) light scattering and viscosity measurements. These techniques have been coupled with surface tension measurements to frame the polymer's critical micellar concentration (cmc).

Findings: We demonstrate the presence at all tested concentrations of two forms of Soluplus, with hydrodynamic radii of 3 and 26 nm, where the fraction of smaller objects accounts for as much as 60-70%. dNMR, SAXS, DLS and SLS indicate that Soluplus spontaneously self-assembles into large spherical particles with a core-shell structure. However, self-assembly takes place three orders of magnitude above the cmc evaluated via surface tension measurements. Instead of the traditional cooperative micellization process, we propose a thermal-activated isodesmic self-assembly of the small aggregates into core-shell micelles.

Keywords: Diffusion NMR; Hard spheres interactions; Isodesmic self-assembly; Light scattering; Polymeric micelles; small angle X-ray scattering (SAXS).

MeSH terms

  • Micelles*
  • Polyethylene Glycols
  • Polymers*
  • Polyvinyls
  • Scattering, Small Angle
  • X-Ray Diffraction

Substances

  • Micelles
  • Polymers
  • Polyvinyls
  • polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer
  • Polyethylene Glycols