Abstract

In order to improve the performance of traditional sodium alginate (SA) hydrogels cross-linked by Ca2+ ions to meet greater application demand, a strategy was designed to structure novel SA-based gels (named OP-PN gels) to achieve both stimulus responsiveness and improved mechanical strength. In this strategy, the SA chains are co-cross-linked by CaCl2 and cationic octa-ammonium polyhedral oligomeric silsesquioxane (Oa-POSS) particles as the first network, and an organically cross-linked poly(N-isopropyl acrylamide) (PNIPA) network is introduced into the gels as the second network. Several main results are obtained from the synthesis and characterization of the gels. For OP-PN gels, their properties depend on the content of both uniformly dispersed Oa-POSS and PNIPA network directly. The increased Oa-POSS and PNIPA network content significantly improves both the strength and resilience of gels. Relatively, the increased Oa-POSS is greatly beneficial to the modulus of gels, and the increased PNIPA network is more favorable to advancing the tensile deformation of gels. The gels with hydrophilic PNIPA network exhibit better swelling ability and remarkable temperature responsiveness, and their volume phase transition temperature can be adjusted by altering the content of Oa-POSS. The deswelling rate of gels increases gradually with the increase of POSS content due to the hydrophobic Si–O skeleton of POSS. Moreover, the enhanced drug loading and sustained release ability of the target drug bovine serum albumin displays great potential for this hybrid gel in the biomedical field.

Highlights

  • Hydrogels are physically or chemically cross-linked three-dimensional hydrophilic polymeric networks capable of absorbing large amounts of water and swelling

  • To structure interpenetrating polymer network (IPN) hydrogels based on sodium alginate (SA), NIPA was chosen to be cross-linked first to form a precursor gel with SA, and the SA network was formed inside the precursor gel by immersing the gel into the solution with abundant exchangeable ions

  • Our concern here is the successful introduction of POSS particles and their link type inside the gels, and several characterizations were used to analyze this problem

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Summary

Introduction

Hydrogels are physically or chemically cross-linked three-dimensional hydrophilic polymeric networks capable of absorbing large amounts of water (or biological fluids) and swelling. These soft materials have similar properties to human tissue and show responsiveness to special stimuli, attracting growing interest in recent years due to their potential application in tissue engineering [1,2], soft robotics [3,4], biosensing [5,6], flexible displays [7,8], and drug delivery [9,10]. SA hydrogels contain carboxylate anions on their hydrophilic surface similar to the characteristics of cell surfaces in vertebrates, which could minimize the effect on immunity, advancing biocompatibility [20,21]

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