Quantitative evaluation of focused ultrasound with a contrast agent on blood-brain barrier disruption.
Authors: Yang FY, Fu WM, Yang RS, Liou HC, Kang KH, Lin WL
The use of an ultrasound contrast agent (UCA) with focused ultrasound sonication has the potential to disrupt the blood-brain barrier (BBB) noninvasively and reversibly at target locations. This study investigated the effects of UCA dose and ultrasound pressure on BBB disruption. Sonications were applied at 1 MHz with a burst length of 10 ms, a 1% duty cycle and a repetition frequency of 1 Hz. The duration of the sonication was 30 s. In in vivo experiments, 16 male Wistar rats were sonicated in the presence of UCA at four doses (0, 30, 60 and 90 microL/kg). BBB integrity was evaluated by injecting Evans blue (EB) into the femoral vein of anesthetized rats. The relationship between UCA dose and the region of EB extravasation was evaluated at ultrasound pressures of 0.9 and 1.2 MPa. The BBB disruption, as quantified by the amount of EB extravasation, was significantly greater in rats injected with UCA at a dose of 60 or 90 microL/kg than at a dose of 0 or 30 microL/kg. The amount of EB extravasation increased monotonically with the quantity of UCA injected into the femoral vein before sonication. Furthermore, the BBB disruption could be enhanced in the focal region relative to the surrounding region with a higher dose of UCA (60 or 90 microL/kg). This study demonstrates that BBB disruption can be both increased and localized to the focal region by injecting an appropriate quantity of UCA before performing focused ultrasound sonications.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To quantitatively evaluate the effect of focused ultrasound combined with a contrast agent on disruption of the blood–brain barrier.
Animal model / Human subject
rat, Wistar, not reported, male
Disease model
healthy
Outcomes and Safety
Summary of Outcomes
Focused ultrasound with contrast agent induced localized and reversible BBB opening.
Duration of biological effect
not reported
Safety-related matter
No safety concerns or adverse effects are mentioned in the provided text.
Brain Region
Ultrasound Parameters
Ultrasound instrument
not reported
FUS Frequency
1 MHz
FUS Intensity
not reported
FUS Pressure
0.9–1.2 MPa
FUS Mode
pulsed
Pulse duration
10 ms
Duration of a single FUS session
30 s
Treatment frequency
single
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