等温滴定量热法
凝聚
壳聚糖
离子强度
电位滴定法
滴定法
聚合物
量热法
化学
离子键合
无机化学
热力学
有机化学
色谱法
离子
物理化学
水溶液
物理
作者
Fatma Akcay Ogur,Sezin Mamasoglu,Sarah L. Perry,F. Ahu Akin,A. Basak Kayitmazer
标识
DOI:10.1021/acs.jpcb.4c03930
摘要
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.
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