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Improving Mechanical Properties of Starch-Based Hydrogels Using Double Network Strategy
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This work aims to improve the mechanical properties of starch-based hydrogels using a double-network (DN) strategy. The single network (SN) starch hydrogel was first prepared using glutaraldehyde as a crosslinker. The compressive properties of the SN hydrogels were influenced by both crosslinker content and crosslinking time. The SN starch hydrogel possessing the best mechanical properties was then fabricated into DN hydrogels. Poly(vinyl alcohol) (PVA) and borax were used as a secondary polymer and a crosslinker, respectively. The PVA–borax complexation partly enhanced the DN hydrogel’s compressive modulus by 30% and its toughness by 39%. DN hydrogels were found to have denser microstructures than SN hydrogels. To be specific, their walls thickened and grew more continuous while their pores shrank. The increased crosslinking density resulted in changes to the microstructure, which were well correlated with their porosity and water uptake capacity. An in vitro cytotoxicity test of the DN hydrogels revealed that they were non-toxic to chondrocytes. This work demonstrated that double networking is a simple but effective strategy for improving mechanical properties of starch-based hydrogels without sacrificing their biocompatibility. This approach can be used to tailor hydrogel properties to fulfill requirements for biomedical applications, such as tissue engineering and other related fields.
Title: Improving Mechanical Properties of Starch-Based Hydrogels Using Double Network Strategy
Description:
This work aims to improve the mechanical properties of starch-based hydrogels using a double-network (DN) strategy.
The single network (SN) starch hydrogel was first prepared using glutaraldehyde as a crosslinker.
The compressive properties of the SN hydrogels were influenced by both crosslinker content and crosslinking time.
The SN starch hydrogel possessing the best mechanical properties was then fabricated into DN hydrogels.
Poly(vinyl alcohol) (PVA) and borax were used as a secondary polymer and a crosslinker, respectively.
The PVA–borax complexation partly enhanced the DN hydrogel’s compressive modulus by 30% and its toughness by 39%.
DN hydrogels were found to have denser microstructures than SN hydrogels.
To be specific, their walls thickened and grew more continuous while their pores shrank.
The increased crosslinking density resulted in changes to the microstructure, which were well correlated with their porosity and water uptake capacity.
An in vitro cytotoxicity test of the DN hydrogels revealed that they were non-toxic to chondrocytes.
This work demonstrated that double networking is a simple but effective strategy for improving mechanical properties of starch-based hydrogels without sacrificing their biocompatibility.
This approach can be used to tailor hydrogel properties to fulfill requirements for biomedical applications, such as tissue engineering and other related fields.
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