A 3D printable and highly stretchable tough hydrogel is developed by combining poly(ethylene glycol) and sodium alginate, which synergize to. Hydrogels are used as scaffolds for tissue engineering, vehicles for drug delivery, actuators for optics and fluidics, and model extracellular matrices for biological. In this investigation, we successfully prepared extremely stretchable, transparent and tough DN hydrogels by using neutral synthetic polymer–poly(vinyl alcohol).

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Crack blunting and the strength of soft elastic solids. An alginate chain consists of mannuronic acid M unit and guluronic acid G unitarranged in blocks rich in G units, blocks rich in M units, and blocks of alternating G and M units.

However, the critical stretch at rupture reached the maximum when acrylamide was 89 wt. A local damage model for anomalous high toughness of double-network gels. When the gel contains a notch and is stretched, the deformation is inhomogeneous: Measurement of the fracture toughness of some contact lens hydrogels. The covalent crosslinker, MBAA, was fixed at 0.

On the basis of our experimental findings, we discuss mechanisms of deformation and energy dissipation. High-water-content and resilient PEG-containing hydrogels with low fibrotic response. Vlassak1 and Zhigang Suo 1, 5.

Hybrid gels dissipate energy effectively, as shown by pronounced hysteresis. The strength of highly elastic materials. For the notch to turn into a running crack, only the chains directly ahead the hough needs to break. After the first loading and unloading, the hybrid gel was much weaker if the second loading was applied immediately, and recovered somewhat if the second loading was applied 1 day later Fig.

From thermally activated to viscosity controlled fracture of biopolymer hydrogels. Hydrogels are used as scaffolds for tissue engineering [ 1 ], vehicles for drug delivery [ 2 annd, actuators for optics and fluidics [ 3 ], and model extracellular matrices for biological studies [ 4 ].

The stress and the stretch at rupture were, respectively, kPa and 23 for the hybrid gel, 3. Direct observation wtretchable damage zone around crack tips in double-network gels.


New Process for 3D Printing of Highly Stretchable and Tough Hydrogels

A similar trend was observed for samples with notches Fig. Long-term stable hydrogels for biorelevant dissolution testing of drug-eluting stents Beatrice SemmlingStefan NagelK. Growth factors, matrices, and forces combine and control stem cells. J Am Ceram Soc.

Supplelementary Data Click here to view. Environment-sensitive hydrogels for drug delivery. In addition to biomedical applications, the same technique could be applied to printing a variety of soft but tough structural materials, he says, such as actuators for soft robotic systems. When the hybrid gel is stretched, the polyacrylamide network remains intact and stabilizes the deformation, while the alginate network unzips progressively, with closely spaced ionic crosslinks unzipping at a small stretch, followed by more and more widely spaced ionic crosslinks unzipping as the stretch increases.

Most hydrogels do not exhibit high stretchability; for example, an alginate hydrogel ruptures when stretched to about 1. The new biocompatible tough hydrogel can be printed into diverse 3-D structures such as a hollow cube, hemisphere, pyramid, twisted bundle, multilayer mesh, or physiologically relevant shapes, such as a human nose or ear.

Highly stretchable and tough hydrogels

Showing of extracted citations. The next step in the research will be to improve the resolution of the printer, which is currently limited to details about micrometers in size, and to test the printed hydrogel structures in animal models. That a tough material can be made of brittle constituents is reminiscent of transformation-toughening ceramics, as well as composites made of ceramic fibers and ceramic matrices. Hydrogels Search for additional papers on this topic.

The densities of ionic and covalent crosslinks also strongly affect the mechanical behavior of the hybrid gels Supplementary Figs. The composition greatly affects the behavior of the hybrid gel a, Stress-strain curves of gels of various weight ratios of acrylamide and alginate. Hydrogels, defined by water molecules encased in rubbery polymer networks that provide shape and structure, are similar to natural tissues such as cartilage, which is used by the body as a natural shock absorber.


Proc R Soc Lond A.

New Process for 3D Printing of Highly Stretchable and Tough Hydrogels

That is, the properties at rupture of the hybrid gel far exceeded those of either of its parents. When the stretch was small, the elastic modulus of the hybrid gel was 29kPa, which was close to the sum of the elastic modulus of the alginate gel 17kPa and that of the polyacrylamide gel 8kPa. An elastic gel is known to be brittle and notch-sensitive—that is, the high stretchability and strength drop markedly when samples ans notches, or any other features that cause inhomogeneous deformation [ 19 ].

All authors commented on the manuscript. When the gel is stretched, the glassy domains remain intact, while the ionic crosslinks break and dissipate energy. Enhanced proliferation of human bone marrow derived mesenchymal stem cells on tough hydrogel substrates.

Most hydrogels do not exhibit high stretchability. National Center for Biotechnology InformationU. Hydrogels with enhanced mechanical properties will expand the scope of their applications. The authors declare no competing financial interests. Ad data suggest that the fracture energy of hydrogels can be dramatically enhanced by combining weak and strong crosslinks.

For example, an alginate hydrogel ruptures when stretched to about 1.

After one pair of G blocks unzip, the high stress shifts to the neighboring pair of G blocks and causes them to unzip also Supplementary Fig. The ionic crosslinks reform during a period of time after the first loading [ 22 ].

Gels of various proportions of alginate and acrylamide were prepared to study why the hybrids were much more stretchable and stronger than either of their parents. Fracture and large strain behavior of self-assembled triblock copolymer hoghly.