Molecular and colloidal transport in bacterial cellulose hydrogels

TL;DR

This study investigates the microstructure of bacterial cellulose films and how their layered nanofiber networks influence the diffusion of particles and molecules, providing insights for biomedical and industrial applications.

Contribution

It combines microscopy and diffusion experiments to characterize the microstructure and transport properties of bacterial cellulose films, revealing how structural features affect permeability.

Findings

Porous layers allow micron-sized particle diffusion.

Dense layers significantly hinder particle penetration.

Structural periodicity influences transport dynamics.

Abstract

Bacterial cellulose biofilms are complex networks of strong interwoven nanofibers that control transport and protect bacterial colonies in the film. Design of diverse applications of bacterial cellulose films also relies on understanding and controlling transport through the fiber mesh, and transport simulations of the films are most accurate when guided by experimental characterization of the structures and the resultant diffusion inside. Diffusion through such films is a function of their key microstructural length scales, determining how molecules, as well as particles and microorganisms, permeate them. We use microscopy to study the unique bacterial cellulose film structure and quantify the mobility dynamics of various sizes of tracer particles and macromolecules. Mobility is hindered within the films, as confinement and local movement strongly depend on void size relative to diffusing tracers. The biofilms have a naturally periodic structure of alternating dense and porous layers of nanofiber mesh, and we tune the magnitude of the spacing via fermentation conditions. Micron-sized particles can diffuse through the porous layers, but can not penetrate the dense layers. Tracer mobility in the porous layers is isotropic, indicating a largely random pore structure there. Molecular diffusion through the whole film is only slightly reduced by the structural tortuosity. Knowledge of transport variations within bacterial cellulose networks can be used to guide design of symbiotic cultures in these structures and enhance their use in applications biomedical implants, wound dressings, lab-grown meat, and sensors.