Magnetic Enhancement of Stem Cell-Targeted Delivery into the Brain Following MR-Guided Focused Ultrasound for Opening the Blood-Brain Barrier.
Authors: Shen WB, Anastasiadis P, Nguyen B, Yarnell D, Yarowsky PJ, Frenkel V, Fishman PS
Focused ultrasound (FUS)-mediated blood-brain barrier disruption (BBBD) can enable even large therapeutics such as stem cells to enter the brain from the bloodstream. However, the efficiency is relatively low. Our previous study showed that human neural progenitor cells (hNPCs) loaded with superparamagnetic iron oxide nanoparticles (SPIONs) in culture were attracted by an external magnetic field. In vivo, enhanced brain retention was observed near a magnet mounted on the skull in a rat model of traumatic brain injury, where BBBD also occurs. The goal of the current study was to determine whether magnetic attraction of SPION-loaded hNPCs would also enhance their retention in the brain after FUS-mediated BBBD. A small animal magnetic resonance imaging (MRI)-guided FUS system operating at 1.5 MHz was used to treat rats (∼120 g) without tissue damage or hemorrhage. Evidence of successful BBBD was validated with both radiologic enhancement of gadolinium on postsonication TI MRI and whole brain section visualization of Evans blue dye. The procedure was then combined with the application of a powerful magnet to the head directly after intravenous injection of the hNPCs. Validation of cells within the brain was performed by staining with Perls' Prussian blue for iron and by immunohistochemistry with a human-specific antigen. By injecting equal numbers of iron oxide (SPIONs) and noniron oxide nanoparticles-loaded hNPCs, each labeled with a different fluorophore, we found significantly greater numbers of SPIONs-loaded cells retained in the brain at the site of BBBD as compared to noniron loaded cells. This result was most pronounced in regions of the brain closest to the skull (dorsal cortex) in proximity to the magnet surface. A more powerful magnet and a Halbach magnetic array resulted in more effective retention of SPION-labeled cells in even deeper brain regions such as the striatum and ventral cortex. There, up to 90% of hNPCs observed contained SPIONs compared to 60% to 70% with the less powerful magnet. Fewer cells were observed at 24 h posttreatment compared to 2 h (primarily in the dorsal cortex). These results demonstrate that magnetic attraction can substantially enhance the retention of stem cells after FUS-mediated BBBD. This procedure could provide a safer and less invasive approach for delivering stem cells to the brain, compared to direct intracranial injections, substantially reducing the risk of bleeding and infection.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To determine whether magnetic attraction of SPION-loaded human neural progenitor cells enhances their delivery and retention in the brain following focused ultrasound–mediated blood–brain barrier disruption.
Animal model / Human subject
Female Sprague-Dawley rats, 100-120 g
Disease model
Healthy
MRI or image guidance method
MRI-guided
Targeted brain region(s)
Striatum
Cargo name and characteristics
Human neural progenitor cells (hNPCs) loaded with superparamagnetic iron oxide nanoparticles (SPIONs)
Route of administration
Intravenous
Outcomes and Safety
Summary of Outcomes
Combining FUS-mediated BBBD with magnetic targeting significantly increased the retention of SPION-loaded hNPCs in the targeted brain region. Retention was highest near the magnet and varied by magnet strength, but declined by 24 hours post-treatment.
Duration of biological effect
24 h
Safety-related matter
FUS at 0.45 MPa opened the BBB safely without tissue damage, but higher pressures (≥0.75 MPa) produced localized red blood cell extravasation and hemorrhage proportional to the pressure.
Brain Region
Ultrasound Parameters
Ultrasound instrument
MRgFUS system (Image Guided Therapy)
FUS Frequency
1.5 MHz
FUS Pressure
0.45 MPa, 0.60 MPa, 0.75 MPa, and 0.90 Mpa
FUS Mode
pulsed
Pulse duration
5 ms
Duration of a single FUS session
60 s
Focal Characteristics
Focal depth: 7-8 mm
Treatment frequency
Single session
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