Scientists embed antibiotics in the 3D printed implants used to regenerate damaged bone

Scientists embed antibiotics in the 3D printed implants used to regenerate damaged bone

In a ground-breaking first, researchers have fabricated 3D scaffold implants containing antibiotics at high temperatures. These scaffolds not only support bone regeneration but manage the bone infections that can arise as a result of injury or surgery.

Each year, around 4 million people worldwide develop bone infection following an open fracture or surgery. The gold standard treatment consists of a lengthy antibiotic therapy, usually delivered orally or Intravenously, and the removal of infected bone tissue, which often leaves behind a hole too large for the body to fill via normal bone regeneration. In a study published in the KeAi journal Bioactive Materials, a group of researchers from the Netherlands, Italy and Spain, outline a new treatment approach they have developed—novel antibiotic-releasing and biodegradable 3D printed scaffolds, capable of supporting bone regeneration and delivering antibiotics at the same time.

“Every person has their own individual body anatomy, which certainly requires a specific intervention in the event of bone injury,” explains one of the study’s authors, Lorenzo Moroni, professor in biofabrication for regenerative medicine at Maastricht University’s MERLN institute. “3D printed polymeric scaffolds possess several unique properties for bone regeneration: their shape can be tailored to fit the specific patient’s anatomy, they are porous to allow cell infiltration, but at the same time mechanically strong, and they can degrade over time to make space for the newly-formed bone. However, incorporating antibiotics in these scaffolds is not straightforward, since the 3D printing process consists of melting the material at high temperatures and antibiotics are heat sensitive.”

The study’s multidisciplinary team of scientists found that covering the antibiotics with lamellar inorganic protectors, prior to mixing them with the polymer and placing them in the 3D scaffolds, not only protected the antibacterial agents, it also enabled a more controlled release. This extended the period the antimicrobial were active and helped to keep local antibiotic concentrations under potentially toxic levels. At the same time, the cells in contact with these scaffolds maintained their viability and could perform normal cell functions, including bone formation—the ultimate goal of the implant.

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