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Updated: May 1, 2026

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Crystallinity-driven morphological ripening processes for poly(ethylene oxide)-block-polycaprolactone micelles in
Georgios Rizis1, Theo G M van de Ven, Adi Eisenberg
1Department of Chemistry and Centre for Self-Assembled Chemical Structures (CSACS), McGill University, 801 Sherbrooke Street West, H3A 2K6, Montreal, Canada. theo.vandeven@mcgill.ca adi.eisenberg@mcgill.ca.
Abstract:
A set of morphological transformations induced by core crystallization within spherical micelle-like aggregates of poly(ethylene oxide)-block-polycaprolactone (PEO-b-PCL) is described in the present article. The initial self-assembly step, in which individual copolymer chains associate to form the spheres, can be performed reproducibly; the stability of these spheres, however, seems to be limited, as both transmission electron microscopy and light scattering data suggest that the primary spheres transform slowly into elongated rod-like or ribbon-like aggregates when suspended in deionized water at room temperature. Although the sphere-to-rod transition takes place typically over a time scale of several days, the formation of individual rods from spheres is very rapid, as evidenced by the progressive increase in the number of long rods and the conspicuous absence of short rods.
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