In vivo transcranial cavitation threshold detection during ultrasound-induced blood-brain barrier opening in mice.
Authors: Tung YS, Vlachos F, Choi JJ, Deffieux T, Selert K, Konofagou EE
The in vivo cavitation response associated with blood-brain barrier (BBB) opening as induced by transcranial focused ultrasound (FUS) in conjunction with microbubbles was studied in order to better identify the underlying mechanism in its noninvasive application. A cylindrically focused hydrophone, confocal with the FUS transducer, was used as a passive cavitation detector (PCD) to identify the threshold of inertial cavitation (IC) in the presence of Definity® microbubbles (mean diameter range: 1.1-3.3 µm, Lantheus Medical Imaging, MA, USA). A vessel phantom was first used to determine the reliability of the PCD prior to in vivo use. A cerebral blood vessel was simulated by generating a cylindrical channel of 610 µm in diameter inside a polyacrylamide gel and by saturating its volume with microbubbles. The microbubbles were sonicated through an excised mouse skull. Second, the same PCD setup was employed for in vivo noninvasive (i.e. transdermal and transcranial) cavitation detection during BBB opening. After the intravenous administration of Definity® microbubbles, pulsed FUS was applied (frequency: 1.525 or 1.5 MHz, peak-rarefactional pressure: 0.15-0.60 MPa, duty cycle: 20%, PRF: 10 Hz, duration: 1 min with a 30 s interval) to the right hippocampus of twenty-six (n = 26) mice in vivo through intact scalp and skull. T1 and T2-weighted MR images were used to verify the BBB opening. A spectrogram was generated at each pressure in order to detect the IC onset and duration. The threshold of BBB opening was found to be at a 0.30 MPa peak-rarefactional pressure in vivo. Both the phantom and in vivo studies indicated that the IC pressure threshold had a peak-rarefactional amplitude of 0.45 MPa. This indicated that BBB opening may not require IC at or near the threshold. Histological analysis showed that BBB opening could be induced without any cellular damage at 0.30 and 0.45 MPa. In conclusion, the cavitation response could be detected without craniotomy in mice and IC may not be required for BBB opening at relatively low pressures.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To investigate the in vivo cavitation response during transcranial focused ultrasound-induced blood–brain barrier opening with microbubbles and determine whether inertial cavitation is required.
Animal model / Human subject
Mouse (Mus musculus), C57BL/6, adult, male
Disease model
Healthy
MRI or image guidance method
Vertical-bore 9.4 T MRI (Bruker Biospin, Billerica, MA, USA); T1-weighted and 3D T2* weighted MRI
Targeted brain region(s)
Thalamus
Target coordinates
3 mm beneath the skull
Outcomes and Safety
Summary of Outcomes
BBB opening occurred at 0.3 Mpa without histological damage, while inertial cavitation onset was detected at 0.45 Mpa, indicating BBBO did not require inertial cavitation at threshold pressures
Safety-related matter
Histological analysis showed no cellular damage at 0.30 and 0.45 MPa, indicating BBB opening was achieved without adverse effects; inertial cavitation may not be required at these low pressures.
Brain Region
Ultrasound Parameters
Ultrasound instrument
Single-element focused ultrasound transducer: Transducer A (Riverside Research Institute); Transducer B, model cdc7411-3 (Imasonic)
FUS Frequency
1.525 MHz, 1.5 MHz
FUS Pressure
0.15–0.60 MPa (applied range); 0.30 MPa (BBB opening threshold); 0.45 MPa (inertial cavitation threshold)
FUS Mode
pulsed
Pulse duration
20 ms
Duration of a single FUS session
1 min (with a 30 s interval)
Focal Characteristics
Transducer A: focal depth: 90 mm, focal length: None, aperture size: 60 mm; Transducer B: focal depth: 60 mm, focal length: None, aperture size: 60 mm;
Treatment frequency
Single
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