Akcay Ogur Fatma, Mamasoglu Sezin, Perry Sarah L, Akin Fatma Ahu, Kayitmazer A Basak
Department of Chemistry, Bogazici University, Bebek, Istanbul 34342, Turkiye.
Department of Chemical Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
J Phys Chem B. 2024 Sep 19;128(37):9022-9035. doi: 10.1021/acs.jpcb.4c03930. Epub 2024 Sep 9.
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.
透明质酸(HA)/壳聚糖(CHI)复合凝聚层最近因其聚合物的pH依赖性电离和半柔性以及在组织工程中的适用性而受到关注。在此,我们应用等温滴定量热法(ITC)来了解HA/CHI凝聚的表观热力学与pH、离子强度和链长的关系。我们将这些ITC实验与电位滴定得到的HA和CHI电荷状态的知识相结合,以了解复合物形成的机理。我们的数据表明,HA和CHI复合凝聚的驱动力本质上是熵驱动的,并且这种驱动力随着离子强度的增加而降低。我们还观察到随着离子强度的增加,离子配对的化学计量比降低,我们认为这是由于在较高离子强度下HA电离程度变化的结果。尽管在测试的最低pH值下观察到更强的相互作用,这可能是由于HA和CHI之间氢键的贡献,但推测与pH值相互作用强度的增加也是HA电离程度变化的结果。