Abstract

Polyvinylpyrrolidone (PVP) is a hydrophilic polymer that is widely used in various biomedical applications owing to its excellent biocompatibility. It has been suggested that water-polymer interactions play a key role in controlling biocompatibility, although the molecular-level consequences of these interactions remain unknown. In this study, the hydrogen-bonded structures of water molecules hydrating PVP were investigated using X-ray absorption spectroscopy (XAS) and X-ray emission spectroscopy (XES). XAS spectral profiles revealed that the CO bonds in highly concentrated PVP aqueous solutions have at least two states: one where hydrogen bonds are formed with water molecules and the other where they are not. In the XES profile of water extracted from a solution with a stoichiometric ratio of nw = 1.0, increased hydrogen bonding and hydrogen bond distortion were identified from the enhancement of 1b1′ and 3a1 peaks, respectively. Because it is difficult for water molecules to form strong hydrogen-bonded structures in tetrahedral coordination at nw = 1.0, these findings suggest that the presence of strong hydrogen bonds between the CO sites and water prevents the formation of tetrahedrally coordinated hydrogen-bonded structures among water molecules.

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