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Stanford Demonstrates Sugar-Stabilized Liposomes for Ultrasound-Controlled Drug Release

A sugar-stabilized liposome platform that can be triggered by focused ultrasound to localize drug release is pending FDA approval for a first human trial.

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Overview

  • In rat experiments, focused ultrasound targeting the medial prefrontal cortex delivered about three times more ketamine to that region and produced measurable reductions in anxious behavior.
  • A 2.5-minute ultrasound session to the sciatic nerve released encapsulated ropivacaine, inducing localized anesthesia for over an hour without systemic effects.
  • The nanoparticles feature a 5 percent sucrose core and phospholipid shell—leveraging mRNA vaccine–grade liposome technology to enhance stability and drug loading.
  • Encapsulation significantly lowered off-target ketamine concentrations across organs including liver, kidney and heart compared with equivalent free-drug injections.
  • Researchers are refining particle design to further reduce drug leakage and elucidate the ultrasound-triggered release mechanism while preparing for FDA clearance of a ketamine trial in chronic pain patients.