Foreign body reaction

It has also been proposed that the mechanical property of the interface between an implant and its surrounding tissues is critical for the host response.

For example, a lithopedion is a rare phenomenon which occurs most commonly when a fetus dies during an abdominal pregnancy,[5] is too large to be reabsorbed by the body, and calcifies.

The end stage of the foreign body reaction is the fibrous capsule formation around the implanted biomaterial.

[9] The composition and conformation of adsorbed proteins on the implant surface is critical to the foreign body reaction.

Platelets from the blood-biomaterial interaction release inflammatory cytokines that cause monocytes and macrophages to extravasate and migrate to the implant site.

[11] Foreign body giant cell formation depends on the biomaterial surface properties and on the presence of interleukin-4 and interleukin-13.

[11] Foreign body giant cells release reactive oxygen intermediates, degradative enzymes, and acid onto the biomaterial surface.

[11] Adherent macrophages and foreign body giant cells degrade biomaterials and can lead to device failure.

[13] Thicker cylindrical implants on the millimeter scale were shown to produce greater fibrous encapsulation.

[14] The sustained release of certain anti-inflammatory drugs from the biomaterial, such as dexamethasone, is shown to increase implant life by preventing inflammation and fibrosis.

[13] Commonly used biomaterials like polyethylene glycol and polyhydroxyethylmethacrylate resist nonspecific protein adsorption but are easily degraded in the in vivo oxidative environment.

[13] Zwitterionic polymers have the ability to reduce nonspecific adsorption of proteins and cells at biological interfaces.

Nazarova and coworkers synthesized MPC copolymers with 2-methacrylamido-D-glucose, N-vinylpyrrolidone, and N-vinyl-N-methyl-acetamide and grafted them onto the surface of carbon fibre biosorbent using γ-radiation.

[13] There are a few triazole-containing alginate derivative microspheres that remain clear of fibrotic deposition in mice, but more studies are required to explore the relationship between triazole groups and the inflammatory response.

Protein adsorption on the surface of the implant attracts immune cells that ultimately result in the fibrous encapsulation of the implant. [ 8 ]