Investigation of the Therapeutic Effect of Doxorubicin Combined With Focused Shockwave on Glioblastoma.
Authors: Liao WH, Hsiao MY, Kung Y, Huang AP, Chen WS
Glioblastoma multiforme (GBM) is currently the most devastating brain tumor globally and produces a high mortality rate. GBM is also challenging to eradicate using surgery due to its invasive characteristics. Moreover, the blood-brain barrier (BBB) increases the difficulty of transporting most therapeutic drugs to tumor sites. The use of transcranial focused ultrasound (FUS) has recently been investigated for opening the BBB to facilitate drug delivery. A special form of FUS, the shockwave (SW), has also been shown to open BBB efficiently. SW has several advantages including no heating effect, less reactive oxygen species production, good transcranial ability, and no need to supply microbubbles. We employed a commercial SW device, which is a common tool used for musculoskeletal disorders, to improve doxorubicin delivery across the BBB and evaluated its therapeutic efficacy on GBM rat models. SW emits relatively short but stronger mechanical pulses comparing with FUS. The results demonstrated that doxorubicin combined with SW treatment substantially inhibited tumor growth and prolonged overall survival. The present study shows the non-invasive transcranial SW may have potential for the treatment of GBM in future clinical setting.
Introduction
Purpose
Other
Study Objective
To determine whether transcranial shockwave treatment enhances doxorubicin delivery across the blood–brain barrier and improves therapeutic efficacy against glioblastoma in rat models.
Animal model / Human subject
Rat, Sprague–Dawley, 8 weeks old, male
Disease model
Glioblastoma multiforme (glioma)
Targeted brain region(s)
Striatum
Target coordinates
AP +0.5 mm (anterior to bregma), ML 2.0 mm (lateral to bregma), DV 5.0 mm deep
Cargo name and characteristics
drug
Route of administration
intravenous
Outcomes and Safety
Summary of Outcomes
Shockwave treatment enhanced doxorubicin delivery across the BBB, reduced tumor growth, and prolonged survival in glioma-bearing rats.
Duration of biological effect
26 days
Safety-related matter
No tissue damage reported.
Brain Region
Ultrasound Parameters
Ultrasound instrument
PiezoWave (Richard Wolf GmbH, Knittlingen, Germany); transducer aperture/diameter: not reported
FUS Frequency
5 Hz
FUS Intensity
0.21 mJ/mm²
FUS Pressure
not reported
FUS Mode
pulsed
Pulse duration
not reported
Duration of a single FUS session
approximately 40 seconds
Focal Characteristics
focal depth: none; focal length: none; aperture size: 1 (f/stop)
Treatment frequency
Multiple
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