Ultrasonic drug uncaging and debris clearance for noninvasive neurointervention
5th March 2026
Timing : 1 pm ET
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For a list of all talks at the NanoBio seminar series Spring'26, see here
For targeted, noninvasive interventions in the nervous system, ultrasound is a near ideal modality given its relative lack of attenuation through biological tissues.
Towards a translatable and versatile ultrasound-gated targeted drug delivery vehicle, we have developed and validated acoustically-activatable liposomes for targeted uncaging of small molecule drugs at millimetrically-resolved regions of interest in the body and brain. The clinical translation potential of this vehicle is supported by it being composed only of validated, common, and safe pharmaceutical excipients. We anticipate opening a first-in-human trial in mid-2026 using this vehicle to enable targeted delivery of ketamine to the dorsal anterior cingulate in patients with chronic pain.
Additionally, we have developed a low-intensity ultrasound protocol that upregulates mediators of the glymphatic system and modulates key neuroinflammatory markers. Via noninvasive activation of mechanosensitive channels expressed by microglia and astrocytes, we shift the phenotype of these key non-neuronal cells to enable these positive bioeffects. In hemorrhagic stroke models, these effects were sufficient to reduce neuroinflammation and edema, increase functional recovery, reduce morbidity, and increase survival. We are now also clinically translating this protocol and will open a first-in-human trial of it in early 2026.
Overall, we envision each of these technologies - ultrasonic drug uncaging from acoustically activatable liposomes, and ultrasonic debris clearance - as key additions to the armament of clinicians who may use therapeutic ultrasound to noninvasively treat myriad neurologic and psychiatric disorders.