posted on 2024-09-09, 13:04authored byFatma Akcay Ogur, Sezin Mamasoglu, Sarah L. Perry, Fatma Ahu Akin, A. Basak Kayitmazer
Hyaluronic acid (HA)/chitosan (CHI) complex coacervates
have recently
gained interest due to the pH-dependent ionization and semiflexibility
of the polymers as well as their applicability in tissue engineering.
Here, we apply isothermal titration calorimetry (ITC) to understand
the apparent thermodynamics of coacervation for HA/CHI as a function
of the pH, ionic strength, and chain length. We couple these ITC experiments
with the knowledge of the charge states of HA and CHI from potentiometric
titration to understand the mechanistic aspects of complex formation.
Our data demonstrate that the driving force for the complex coacervation
of HA and CHI is entropic in nature and this driving force decreased
with increasing ionic strength. We also observed a decrease in the
stoichiometry for ion-pairing with increasing ionic strength, which
we suggest is a consequence of the changing degree of ionization for
HA at higher ionic strengths. An increase in the strength of interactions
with pH was hypothesized to also be a result of changes in the degree
of ionization of HA, though stronger interactions were observed at
the lowest pH tested, likely due to contributions from hydrogen bonding
between HA and CHI.