Hydrogels are attracting increasing attention due to their potential use in various fields. However, most of the existing hydrogels have limitations in either dissipating mechanical energy or maintaining high stretchability under deformation, thus do not possess high mechanical properties. Herein, poly(vinyl alcohol) (PVA)−tannic acid (TA) hydrogels with both high mechanical strength and stretchability were obtained via a step-by-step physical cross-linking and molecular alignment method. Saline-triggered physical interactions serve as "sacrifice domains" to dissipate energy and endow PVA-based hydrogel with high mechanical strength (≈16 MPa) and stretchability (≈1000%). Due to the reversible arranging and disassociating property of physical interactions, PVA−TA hydrogels show excellent shape memory performance. We further demonstrated an effective approach to fabricate strong and aligned PVA−TA thread. The resultant well-aligned PVA−TA dry thread reveals an ultrahigh mechanical tensile strength of up to 750 MPa, nearly 45 times higher than PVA−TA thread with no alignment. Wide-angle Xray two-dimensional diffraction images further confirmed the alignment of PVA fibers in stretching direction. In addition, we applied the PVA−TA hydrogel as suture and evaluated the cytotoxicity and biocompatibility of the PVA−TA suture.
In this work, we prepare guar gum-based
supramolecular hydrogel
through the formation of borate/didiol bonds. This dynamic and reversible
noncovalent borate/didiol interaction is critical for the multifunctional
properties of supramolecular hydrogel. The FT-IR and XRD analysis
verified the existence of boronate ester interactions between borax
and guar gum. Moreover, the viscoelastic and mechanical behaviors
of the hydrogels with different guar gum concentrations showed that
the storage modulus and compressive stress were highest at guar gum
concentration of 2 wt %. Besides, due to the dynamic and reservable
properties of boronate ester, these guar gum-based hydrogels had excellent
self-healing property, outstanding reformable and injectable capability.
In addition, hydrogels also exhibited reversible gel–sol transformations
by the application of physicochemical stimuli such as thermal and
pH value. The coupling of these multifunctional properties made from
low-cost, environment friendly, and readily available materials could
have potential applications in many biomedical areas in the future.
We expect that this simple strategy of fabricating the self-healing
guar gum hydrogels with multistimuli responsive properties may enrich
the avenue in the exploration of multifunctional guar gum based hydrogels
to expand their potential applications in various fields.
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