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Position 1 sodium channel blockers, such as tetrodotoxin and saxitoxin are small molecule drugs with powerful local anesthetic properties
Encapsulating these drugs in a safe delivery system has always been a challenge: because they are extremely soluble in water, they tend to enter the water surrounding the body
Daniel Kohane, MD, director of the Biomaterials and Drug Delivery Laboratory at Boston Children's Hospital and associate director of anesthesiology, intensive care and pain medicine research, said: "Toxicities are dose-limited, and you won't suffer long-lasting nerve blocks
Dr.
The Kohane laboratory has created many slow-release systems, including systems to deliver tetrodotoxin, but this is the first system to hijack a natural design
Get clues from nature
In order to create a sustained-release system, Ji Wanchang, co-first author Dr.
The research team modified P1 and P2 with long-chain hydrophobic molecules
Kohane explained: "When you add a hydrophobic chain, the peptide will form a long fiber with thousands of p1 and p2 dancing around
When this structure is injected near the target nerve, tetrodotoxin slowly releases itself through diffusion and other processes, and binds to the P1 and P2 of the nerve itself
Put the design into practice
Then, the research team tested the tetrodotoxin-carrying nanostructures and injected them near the sciatic nerve of living mice
"By hijacking nature's design, we created a synthetic anesthetic drug receptor as a delivery and release system," Ji said
The team has applied for a patent for their method