Confining Effects on Semiflexible Polymers in Hollow Particles

ABSTRACT 3D entrapment of polymers in nanocavities is crucial for a variety of synthetic and biomimetic materials, including hollow particles. We evaluate the effect of chain stiffness on the properties of polymers entrapped in cavities/capsules using molecular simulation. Two confinement‐induced phenomena are found to control the polymer distribution ρ ( r ) across the closed sphere. The near‐wall entropic depletion, characteristic of flexible polymers, manifests itself in monotonous profiles similar to those around a solid sphere in open systems. Contrarily, in moderately stiff polymers, the confining surface generates distinct density enrichment in profiles due to the development of toroidal conformations. The energetics of toroidal growth in a semidilute solution is quantified by simulation. The computed bending energy confirms a simpler generation of toroids in short polymers. The observed reduction of the persistence length in a cavity facilitates the growth of toroids. The thickness of the depletion layer determined by the novel universal method is in agreement with the data from the restricted conventional method. A close relationship is demonstrated between the concentration changes in the depletion thickness and the radius of gyration. The relevance of the computed confinement effects to bioanalytical or biomedical applications of capsules/hollow particles is discussed.

Authors

Institutions

Publication Details

Journal
Journal of Polymer Science
Published
2026-01-14
DOI
https://doi.org/10.1002/pol.20251021
Primary Topic
Block Copolymer Self-Assembly
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Confining Effects on Semiflexible Polymers in Hollow Particles

Peter Cifra, Tomáš Bleha
Journal of Polymer Science
Block Copolymer Self-Assembly
article

Confining Effects on Semiflexible Polymers in Hollow Particles

Peter Cifra, Tomáš Bleha
article en

Abstract

ABSTRACT 3D entrapment of polymers in nanocavities is crucial for a variety of synthetic and biomimetic materials, including hollow particles. We evaluate the effect of chain stiffness on the properties of polymers entrapped in cavities/capsules using molecular simulation. Two confinement‐induced phenomena are found to control the polymer distribution ρ ( r ) across the closed sphere. The near‐wall entropic depletion, characteristic of flexible polymers, manifests itself in monotonous profiles similar to those around a solid sphere in open systems. Contrarily, in moderately stiff polymers, the confining surface generates distinct density enrichment in profiles due to the development of toroidal conformations. The energetics of toroidal growth in a semidilute solution is quantified by simulation. The computed bending energy confirms a simpler generation of toroids in short polymers. The observed reduction of the persistence length in a cavity facilitates the growth of toroids. The thickness of the depletion layer determined by the novel universal method is in agreement with the data from the restricted conventional method. A close relationship is demonstrated between the concentration changes in the depletion thickness and the radius of gyration. The relevance of the computed confinement effects to bioanalytical or biomedical applications of capsules/hollow particles is discussed.

Journal of Polymer ScienceVol. 64(5)
Slovak Academy of Sciences (SK), Polymer Institute of the Slovak Academy of Sciences (SK)
Openalex Percentile: Top 88%
Block Copolymer Self-Assembly
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.