This diagram shows the artificial tendon material versus real tendons at different scales. Image: Mutian Hua, Shuwang Wu, and Ximin He/UCLA.Materials scientists at the University of California, Los Angeles (UCLA) and their colleagues have developed a new method for making synthetic biomaterials that mimic the internal structure, stretchiness, strength and durability of tendons and other biological tissues.
The researchers developed a two-pronged process to enhance the strength of existing hydrogels, which could then be used to create artificial tendons, ligaments and cartilage that are 10 times tougher than the natural tissues. Although the hydrogels contain mostly water with little solid content (about 10% polymer), they are more durable than Kevlar and rubber, which are both 100% polymer.
This kind of breakthrough, reported in a paper in Nature, has never been achieved in water-laden polymers before. The new hydrogels could also provide coating for implanted or wearable medical devices to improve their fit, comfort and long-term performance.
"This work shows a very promising pathway toward artificial biomaterials that are on par with, if not stronger than, natural biological tissues," said study leader Ximin He, an assistant professor of materials science and engineering at the UCLA Samueli School of Engineering.
Hydrogels are a broad class of materials with interior structures made up of crisscrossing polymers or gels. They show promise for use as replacement tissues, either to temporarily close wounds or as a long-term or even permanent solution. In addition, the gels may have applications for soft robots and wearable electronics.
However, current hydrogels are not strong or durable enough to mimic or replace tissues that need to move and flex repeatedly while bearing weight. To address these issues, the UCLA-led team employed a combination of molecular and structural engineering approaches that had not previously been utilized together to make hydrogels.
First, the researchers used a method called 'freeze-casting' – a solidifying process that results in porous and concentrated polymers, similar to a sponge. Second, they used a 'salting-out' treatment to aggregate and crystalize the polymer chains into strong fibrils.
This produced hydrogels with a series of connecting structures across several different scales – from molecular levels up to a few millimeters. The hierarchy of these multiple structures, similar to that of biological counterparts, enables the material to be stronger and more stretchable. As demonstrated by the team, this versatile method is highly customizable and could replicate various soft tissues in the human body.
The researchers used polyvinyl alcohol, a material already approved by the US Food and Drug Administration, to make their hydrogel prototype. On testing its durability, they saw no signs of deterioration after 30,000 cycles of stretch testing. Under light, the new hydrogel produced a vivid shimmer, similar to real tendons, confirming the micro/nano structures that formed in the gel.
In additional to biomedical applications, this advance may hold potential for surgical machines or bioelectronics that operate innumerable cycles, and for 3D printing of previously unachievable configurations, thanks to the hydrogel's flexibility. In fact, the team demonstrated that such 3D-printed hydrogel architectures could transform into other shapes pending changes in temperature, acidity or humidity. Acting as artificial muscles, they are much more resilient and could exert great force.
This story is adapted from material from the University of California, Los Angeles, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.