Pulsed Focal Ultrasound as a Non-Invasive Method to Deliver Exosomes in the Brain/Stroke.
Authors: Alptekin A, Khan MB, Ara R, Rashid MH, Kong F, Parvin M, Frank JA, Chopra R, Dhandapani K, Arbab AS
Exosomes, a component of extracellular vesicles, are shown to carry important small RNAs, mRNAs, protein, and bioactive lipid from parent cells and are found in most biological fluids. Investigators have demonstrated the importance of mesenchymal stem cells derived exosomes in repairing stroke lesions. However, exosomes from endothelial progenitor cells have not been tested in any stroke model, nor has there been an evaluation of whether these exosomes target/home to areas of pathology. Targeted delivery of intravenous administered exosomes has been a great challenge, and a targeted delivery system is lacking to deliver naïve (<i>unmodified</i>) exosomes from endothelial progenitor cells to the site of interest. Pulsed focused ultrasound is being used for therapeutic and experimental purposes. There has not been any report showing the use of low-intensity pulsed focused ultrasound to deliver exosomes to the site of interest in stroke models. In this proof of principle study, we have shown different parameters of pulsed focused ultrasound to deliver exosomes in the intact and stroke brain with or without intravenous administration of nanobubbles. The study results showed that administration of nanobubbles is detrimental to the brain structures (micro bleeding and white matter destruction) at peak negative pressure of >0.25 megapascal, despite enhanced delivery of intravenous administered exosomes. However, without nanobubbles, pulsed focused ultrasound enhances the delivery of exosomes in the stroke area without altering the brain structures.
Introduction
Purpose
Drug delivery WITHOUT BBB opening
Study Objective
To determine whether low-intensity pulsed focused ultrasound can enhance targeted delivery of endothelial progenitor cell-derived exosomes to intact and stroke brain tissue with or without intravenous nanobubbles and to assess associated tissue effects.
Animal model / Human subject
mouse, C57BL/6, 8–10 weeks, male
Disease model
stroke
Targeted brain region(s)
Cortex
Cargo name and characteristics
nanoparticle
Route of administration
intravenous
Outcomes and Safety
Summary of Outcomes
PFUS alone enhanced the delivery of EPC-derived exosomes to ischemic brain tissue; adding nanobubbles further boosted delivery but caused tissue damage at pressures >0.25 MPa.
Duration of biological effect
not reported
Safety-related matter
PFUS alone enhanced the delivery of EPC-derived exosomes to ischemic brain tissue; adding nanobubbles further boosted delivery but caused tissue damage at pressures >0.25 MPa.
Brain Region
Ultrasound Parameters
Ultrasound instrument
single-element focused ultrasound transducer
FUS Frequency
1.0 MHz
FUS Intensity
not reported
FUS Pressure
0.25 MPa
FUS Mode
pulsed
Pulse duration
100 ms
Duration of a single FUS session
5 min
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