Technology ID

Diffusion Through Skull as Route of Delivery for Treatment of Brain Injury and Disease

Lead Inventor
McGavern, Dorian (NINDS)
Roth, Theodore (Stanford University (aka Leland Stanford Junior University))
Therapeutic Areas
Development Status
  • In vitro data available
  • In vivo data available (animal)
Lead IC
Traumatic Brain injury (TBI) often results from head impact and is a major cause of death and disability. Brain injuries vary in severity and can be associated with hemorrhaging, swelling, inflammation, and death of brain tissue. Inventors at NINDS developed a novel approach to treating brain injuries that involves transcranial application of small molecules. They discovered, using two photon laser scanning microscopy, that compounds as large as 40,000 molecular weight (MW) can pass directly through the intact skull into the underlying cerebral spinal fluid (CSF) that circulates through the brain and spinal cord. Small molecular weight compounds (e.g. 600 MW) pass through the skull more quickly than large ones and appear to do so by simple diffusion. Researchers have shown that application of a variety of agents, including glutathione, TNP-ATP hydrase (P2X4 inhibitor), oxidated ATP (P2X7 inhibitor), MRS2578 (P2Y6 inhibitor), MeSAMP (P2Y12 inhibitor) and Carbenoxelone (Connexin Hemichannel Inhibitor) directly to the head results in delivery of the agents to the brain. Transcranial drug application can be used to pharmacologically target several tiers of brain injury responses, from the toxic mediators that cause cell death to the molecular signals that drive inflammation. Application can be by direct application to the skull through the scalp (e.g. rubbing it in), transdermal patch, or subcutaneous injection under the scalp.
Commercial Applications
  • Treating Traumatic Brain Injury
  • Treating stroke
  • Treating other acute CNS conditions, including encephalitis and meningitis
  • Treating chronic CNS disorders such as brain tumors, Alzheimer’s, Parkinson’s, and multiple sclerosis
Competitive Advantages
  • Quickly achieves a high local drug concentration at the site of brain injury.
  • Bypasses the blood brain barrier and allows rapid administration of therapeutic agents directly into injured or inflamed brain.
  • Current therapies to treat Traumatic Brain Injury with neuroprotective agents are often limited by ability to achieve therapeutic concentrations of therapeutic agent in the brain.
Licensing Contact:
Sharma, Smita
Phone: 301-435-7761