Tuning the Length of Filomicelles Prepared Via Templated Polymerization‐Induced Self‐Assembly
Year: 2026
Type: article
Abstract: High-aspect-ratio polymeric micelles (filomicelles, FMs) are attractive anisotropic nanoparticles for a wide range of applications, however, their formation is typically confined to narrow hydrophilic/hydrophobic polymer block ratios, limiting systematic structure-property investigations. Consequently, independent control over micelle width, length, and stiffness remains challenging. A supramolecular polymerization-induced self-assembly (PISA) strategy using a bis-urea core template was recently shown to robustly yield wormlike micelles across a wide range of core block lengths; however, the resulting FM lengths remained highly polydisperse. Herein, we investigate two strategies to tune the contour length: (i) Blending in polymer without the bis-urea sticker and (ii) post-micellization sonication. Unexpectedly, incorporating non-sticker polymer can increase the contour length. Transmission electron microscopy (TEM), fluorescence cross-correlation spectroscopy (FCCS), and high-resolution atomic force microscopy (AFM) were used to elucidate the key factors contributing to this peculiar self-assembly mechanism. Sonication-induced cleavage led to shortening of the particles and narrower polydispersity in length. Combined, the two strategies provide access to a wide range of anisotropic micelles with accessible aspect ratios ranging from 1 to >150. Considering their long-term (colloidal) stability, the presented system is an ideal model to study the effect of micellar anisotropy, for example, in drug delivery relevant scenarios.
Source: Small
DOI: 10.1002/smll.74648
Institutions: Utrecht University, Centre National de la Recherche Scientifique, Sorbonne Université, Institut Parisien de Chimie Moléculaire, Eindhoven University of Technology, Institut de minéralogie, de physique des matériaux et de cosmochimie, Université d'Orléans, Interfaces, Confinement, Matériaux et Nanostructures
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $5,790
OpenAlex ID: W7169526024
