A new brain drug delivery strategy: focused ultrasound-enhanced intranasal drug delivery.
Authors: Chen H, Chen CC, Acosta C, Wu SY, Sun T, Konofagou EE
Central nervous system (CNS) diseases are difficult to treat because of the blood-brain barrier (BBB), which prevents most drugs from entering into the brain. Intranasal (i.n.) administration is a promising approach for drug delivery to the brain, bypassing the BBB; however, its application has been restricted to particularly potent substances and it does not offer localized delivery to specific brain sites. Focused ultrasound (FUS) in combination with microbubbles can deliver drugs to the brain at targeted locations. The present study proposed to combine these two different platform techniques (FUS+i.n.) for enhancing the delivery efficiency of intranasally administered drugs at a targeted location. After i.n. administration of 40 kDa fluorescently-labeled dextran as the model drug, FUS targeted at one region within the caudate putamen of mouse brains was applied in the presence of systemically administered microbubbles. To compare with the conventional FUS technique, in which intravenous (i.v.) drug injection is employed, FUS was also applied after i.v. injection of the same amount of dextran in another group of mice. Dextran delivery outcomes were evaluated using fluorescence imaging of brain slices. The results showed that FUS+i.n. enhanced drug delivery within the targeted region compared with that achieved by i.n. only. Despite the fact that the i.n. route has limited drug absorption across the nasal mucosa, the delivery efficiency of FUS+i.n. was not significantly different from that of FUS+i.v.. As a new drug delivery platform, the FUS+i.n. technique is potentially useful for treating CNS diseases.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To evaluate whether focused ultrasound combined with intranasal administration (FUS+IN) can enhance targeted delivery of an intranasally administered model drug to the mouse brain and to compare its delivery efficiency with FUS plus intravenous injection (FUS+IV).
Animal model / Human subject
Mouse; strain: C57BL/6; age not specified; sex male
Disease model
Healthy
Targeted brain region(s)
Caudate Putamen
Cargo name and characteristics
40 kDa fluorescently-labeled dextran (polysaccharide polymer macromolecule tracer, 40 kDa)
Route of administration
Intranasal and Intravenous
Outcomes and Safety
Summary of Outcomes
Focused ultrasound (FUS) targeted to the caudate putamen in the presence of systemically administered microbubbles produced an ~8-fold increase in intranasally delivered 40 kDa dextran at the targeted site and achieved similar delivery efficiency to FUS with intravenous dosing. The successful/tested FUS condition was a single targeted sonication delivered with systemic microbubbles (stable and inertial cavitation measured); no other FUS parameter variations were reported, and minor, comparable microhemorrhages were observed for both FUS+IN and FUS+IV.
Safety-related matter
Minor microhemorrhages (small clusters of erythrocyte extravasation) were observed in the FUS-targeted regions of both FUS+IN and FUS+IV groups, with no tissue damage on the contralateral non-sonicated sides and similar cavitation doses between groups; damage correlated with acoustic exposure rather than administration route. Prior studies and non-human primate behavioral data suggest these effects are minor/transient and can potentially be eliminated by reducing FUS exposure.
Brain Region
Ultrasound Parameters
Ultrasound instrument
Single-element FUS transducer (Imasonic)
FUS Frequency
1.5 MHz
FUS Pressure
0.45 MPa
FUS Mode
pulsed
Pulse duration
6.7 ms
Duration of a single FUS session
60 s
Focal Characteristics
Focal depth: 60 mm; Focal length: None; Aperture size: 60 mm
Treatment frequency
single
Mechanical index
0.3674234614174768
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