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Focused ultrasound augments the delivery and penetration of model therapeutics into cerebral cavernous malformations.

Authors: Fisher DG, Hoch MR, Gorick CM, Huchthausen C, Breza VR, Sharifi KA, Tvrdik P, Miller GW, Price RJ

Cerebral cavernous malformations (CCMs) are vascular neoplasms in the brain that can cause debilitating symptoms. Current treatments pose significant risks to some patients, motivating the development of new nonsurgical options. We recently discovered that focused ultrasound-microbubble treatment (FUS) arrests CCM formation and growth. Here, we build on this discovery and assess the ability of FUS to deliver model therapeutics into CCMs. T1 mapping MRI was used with 1 kDa (MultiHance; MH) and 17 kDa (GadoSpin D; GDS) contrast agents to assess the FUS-mediated delivery and penetration of model small molecule drugs and biologics, respectively, into CCMs of Krit1 mutant mice. FUS elevated MH delivery rate in lesion cores (4.6-fold) and perilesional spaces (6.7-fold). For the model biologic (i.e. GDS), FUS was of greater relative benefit, resulting in 21.7-fold and 3.8-fold delivery increases to the intralesional and perilesional spaces, respectively. These findings indicate that FUS can serve as a powerful non-invasive platform for augmenting therapeutic delivery to CCM.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To assess whether focused ultrasound-microbubble treatment (FUS) can enhance delivery and penetration of model small-molecule and biologic therapeutics into cerebral cavernous malformations in Krit1 mutant mice using T1 mapping MRI.
Animal model / Human subject Mouse (Krit1, age: 2-3 months)
Disease model Cerebral cavernous malformations
MRI or image guidance method T1 mapping MRI
Targeted brain region(s) Cerebral Cavernous Malformations (Ccms) (6 Targets In The Frontal Hemisphere)
Cargo name and characteristics MultiHance (MH) contrast agent
Route of administration intravenous

Outcomes and Safety

Summary of Outcomes Focused ultrasound with microbubbles markedly increased delivery of a 1 kDa tracer (MultiHance) by 4.6-fold in lesion cores and 6.7-fold perilesionally, and a 17 kDa tracer (GadoSpin D) by 21.7-fold intralesionally and 3.8-fold perilesionally into CCMs in Krit1 mutant mice.
Safety-related matter No adverse effects were reported

Brain Region

Ultrasound Parameters

Ultrasound instrument RK-300 small bore FUS device (FUS Instruments, Toronto, CA)
FUS Frequency 1.1 MHz
FUS Pressure 0.2, 2.5, 3, 3.5, 4
FUS Mode pulsed
Pulse duration 10 ms
Duration of a single FUS session 2 min
Focal Characteristics NR
Treatment frequency multiple

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