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Related Experiment Video
Updated: Mar 27, 2026

Fabrication of Polymer Microspheres for Optical Resonator and Laser Applications
Published on: June 2, 2017
Polymer ejection from strong spherical confinement.
1Department of Computer Science, Aalto University, P.O. Box 15400, FI-00076 Aalto, Finland.
Polymer ejection from confined spaces is exponentially slower with more ejected monomers due to increasing free energy. This explains polymer dynamics during capsid expulsion through nanoscale pores.
Area of Science:
- Biophysics
- Polymer Physics
- Nanotechnology
Background:
- Flexible polymers are often confined within biological or synthetic capsids.
- Understanding polymer ejection dynamics is crucial for applications like drug delivery and viral assembly.
Purpose of the Study:
- To investigate the ejection dynamics of a confined flexible polymer from a spherical capsid through a nanoscale pore.
- To elucidate the relationship between polymer confinement, free energy, and ejection time.
Main Methods:
- Utilized molecular dynamics simulations at unprecedentedly high initial monomer densities.
- Measured the force exerted by the polymer at the pore during ejection.
Main Results:
- Ejection time for individual monomers increases exponentially with the number of already ejected monomers.
- Excess free energy due to confinement grows exponentially with the initial number of monomers, driving this dependence.
- Ejection time scales linearly with polymer length, dominated by internal capsid pressure.
Conclusions:
- The exponential increase in ejection time is linked to the rising free energy of confined polymers, analogous to Flory-Huggins theory predictions.
- Finite-size effects in simulations, specifically polymer tail retraction, can lead to observed superlinear dependencies in ejection times.

