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Updated: Sep 17, 2025

A Freeze-Thawing Method to Prepare Chitosan-Polyvinyl alcohol Hydrogels Without Crosslinking Agents and Diflunisal Release Studies
Published on: January 14, 2020
Preparation and Characterization of PVA/PVP/CS Bionic Hydrogels
Ziyan Zheng1, Shanhua Qian1,2, Sen Liu1
1School of Mechanical Engineering, Jiangnan University, Wuxi, Jiangsu 214122, China.
This study enhances poly(vinyl alcohol) (PVA) hydrogels using polyvinylpyrrolidone (PVP) and chitosan (CS) to mimic oral soft tissue. The resulting PVA/PVP/CS hydrogels exhibit improved mechanical, lubrication, and biocompatibility properties for oral applications.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Biomedical Engineering
Background:
- Poly(vinyl alcohol) (PVA) hydrogels possess biomimetic properties but differ significantly from natural oral soft tissues in mechanical and surface characteristics within simulated oral environments.
- Developing enhanced PVA hydrogels is crucial for creating effective oral substitutes that accurately mimic native tissue properties.
Purpose of the Study:
- To engineer a novel composite hydrogel based on PVA, polyvinylpyrrolidone (PVP), and chitosan (CS) with properties suitable for simulating oral soft tissue.
- To investigate the effects of a specific preparation strategy on the surface, mechanical, lubrication, and biocompatibility characteristics of the modified PVA hydrogels.
Main Methods:
- Preparation of PVA/PVP (APV) hydrogels via solvent exchange using DMSO, followed by cross-linking with chitosan (CS) to form PVA/PVP/CS (PPC) composite hydrogels.
- Comprehensive evaluation of APV and PPC hydrogels, including tensile strength, compression modulus, surface wettability (water contact angle), lubrication performance (friction coefficient), and in vitro biocompatibility (cell viability).
Main Results:
- Solvent exchange with DMSO enhanced the cross-linking density of PVA and PVP, with a PVA/PVP ratio of 3:1 yielding optimal tensile properties in APV hydrogels.
- PPC hydrogels demonstrated a 212% increase in compression modulus compared to PVA hydrogels, closely matching human tongue tissue.
- PPC hydrogels exhibited significantly improved superhydrophilicity (water contact angle of 27.07° for PPC2) and lubrication (62% reduction in friction coefficient for PPC2 vs. APV), maintaining stability in simulated oral conditions.
- PPC hydrogels showed enhanced biocompatibility, with a MC3T3-E1 cell survival rate of 96.18% in PPC extract after 48 hours.
Conclusions:
- The developed preparation strategy effectively enhances the comprehensive properties of PVA hydrogels, particularly mechanical strength, lubrication, and surface characteristics, without compromising biocompatibility.
- The bionic PVA/PVP/CS composite hydrogels show significant promise as advanced materials for oral substitute applications, offering valuable insights for future biomaterial development.
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