TY - JOUR
T1 - Effect of Dynamically Arrested Domains on the Phase Behavior, Linear Viscoelasticity and Microstructure of Hyaluronic Acid - Chitosan Complex Coacervates
AU - Es Sayed, Julien
AU - Caïto, Clément
AU - Arunachalam, Abinaya
AU - Amirsadeghi, Armin
AU - van Westerveld, Larissa
AU - Maret, Denise
AU - Mohamed Yunus, Roshan Akdar
AU - Calicchia, Eleonora
AU - Dittberner, Olivia
AU - Portale, Giuseppe
AU - Parisi, Daniele
AU - Kamperman, Marleen
N1 - Funding Information:
Marleen Kamperman gratefully acknowledges the European Research Council (ERC) for the financial support under the European Union’s Horizon 2020 research and innovation program under the Consolidator grant agreement no. 864982.
Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society.
PY - 2023/8/8
Y1 - 2023/8/8
N2 - Complex coacervates make up a class of versatile materials formed as a result of the electrostatic associations between oppositely charged polyelectrolytes. It is well-known that the viscoelastic properties of these materials can be easily altered with the ionic strength of the medium, resulting in a range of materials from free-flowing liquids to gel-like solids. However, in addition to electrostatics, several other noncovalent interactions could influence the formation of the coacervate phase depending on the chemical nature of the polymers involved. Here, the importance of intermolecular hydrogen bonds on the phase behavior, microstructure, and viscoelasticity of hyaluronic acid (HA)-chitosan (CHI) complex coacervates is revealed. The density of intermolecular hydrogen bonds between CHI units increases with increasing pH of coacervation, which results in dynamically arrested regions within the complex coacervate, leading to elastic gel-like behavior. This pH-dependent behavior may be very relevant for the controlled solidification of complex coacervates and thus for polyelectrolyte material design.
AB - Complex coacervates make up a class of versatile materials formed as a result of the electrostatic associations between oppositely charged polyelectrolytes. It is well-known that the viscoelastic properties of these materials can be easily altered with the ionic strength of the medium, resulting in a range of materials from free-flowing liquids to gel-like solids. However, in addition to electrostatics, several other noncovalent interactions could influence the formation of the coacervate phase depending on the chemical nature of the polymers involved. Here, the importance of intermolecular hydrogen bonds on the phase behavior, microstructure, and viscoelasticity of hyaluronic acid (HA)-chitosan (CHI) complex coacervates is revealed. The density of intermolecular hydrogen bonds between CHI units increases with increasing pH of coacervation, which results in dynamically arrested regions within the complex coacervate, leading to elastic gel-like behavior. This pH-dependent behavior may be very relevant for the controlled solidification of complex coacervates and thus for polyelectrolyte material design.
UR - http://www.scopus.com/inward/record.url?scp=85166432467&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.3c00269
DO - 10.1021/acs.macromol.3c00269
M3 - Article
AN - SCOPUS:85166432467
SN - 0024-9297
VL - 56
SP - 5891
EP - 5904
JO - Macromolecules
JF - Macromolecules
IS - 15
ER -