Shear thinning hydrogels hold promise in treating many diseases, including cancer

Published on November 16, 2012 at 4:43 AM · No Comments

Gels that can be injected into the body, carrying drugs or cells that regenerate damaged tissue, hold promise for treating many types of disease, including cancer. However, these injectable gels don't always maintain their solid structure once inside the body.

MIT chemical engineers have now designed an injectable gel that responds to the body's high temperature by forming a reinforcing network that makes the gel much more durable, allowing it to function over a longer period of time.

The research team, led by Bradley Olsen, an assistant professor of chemical engineering, described the new gels in a recent issue of the journal Advanced Functional Materials. Lead author of the paper is Matthew Glassman, a graduate student in Olsen's lab. Jacqueline Chan, a former visiting student at MIT, is also an author.

Olsen and his students worked with a family of gels known as shear thinning hydrogels, which have a unique ability to switch between solid-like and liquid-like states. When exposed to mechanical stress - such as being pushed through an injection needle - these gels flow like fluid. But once inside the body, the gels return to their normal solid-like state.

However, a drawback of these materials is that after they are injected into the body, they are still vulnerable to mechanical stresses. If such stresses make them undergo the transition to a liquid-like state again, they can fall apart.

"Shear thinning is inherently not durable," Olsen says. "How do you undergo a transition from not durable, which is required to be injected, to very durable, which is required for a long, useful implant life?"

The MIT team answered that question by creating a reinforcing network within their gels that is activated only when the gel is heated to body temperature (37 degrees Celsius).

Shear thinning gels can be made with many different materials (including polymers such as polyethylene glycol, or PEG), but Olsen's lab is focusing on protein hydrogels, which are appealing because they can be designed relatively easily to promote biological functions such as cellular adhesion and cell migration.

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