Invasive brain interventions often result in complications and long recovery times. In addition, the delivery of therapeutic agents via the blood supply is often impossible because the Blood-Brain Barrier (BBB) protects the brain tissue from foreign molecules. Laboratory experiments and first clinical trials have shown that focused ultrasound (FUS) beams can be used for noninvasive interventions. However, the utilization of FUS in the brain has been seriously limited by the difficulty of delivering ultrasound through the skull bone. The hypothesis of this grant has been that transcranial therapeutic ultrasound exposures can be delivered noninvasively through an intact skull. This hypothesis has now been validated in three clinical studies that demonstrate that brain tissue can be noninvasively coagulated in the central part of the brain. During the current grant period, we furthered our initial research and developed methods to enhance FUS interaction with tissue using microbubbles, thus making whole brain sonications feasible. We have further studied the impact of ultrasound exposures on brain tissue and demonstrated chemotherapy delivery across the BBB. We, and others, have used animal tumor models to demonstrate that chemotherapy treatment significantly increases animal survival when combined with FUS induced BBB disruption. We have also developed computer simulation programs, control technology and treatment methods that will improve the delivery of ultrasound energy. Our study plan is to extend our current research and further explore the feasibility of using intravascular microbubbles to enhance the trans-skull sonications. Our goals are: First, to use our prototype phased array ultrasound system with passive acoustic monitoring to provide acoustic signal feedback, and thus localize and control bubble- enhanced treatments. Second, to utilize our computer models to develop more precise focusing, using higher and multiple frequency sonications, such that the focal volume size is reduced. This will provide better control and allow nonuniform brain tissue to be adequately exposed. Third, to construct and test the new arrays designed using the computer simulations. Fourth, to perform in vivo two-photon microscopy and behavior studies to increase our understanding of ultrasound induced BBB disruption effects on delicate brain regions. Finally, to further test the effectiveness of the ultrasound-induced BBB disruption for the delivery of chemotherapeutic agents and natural killer cells for the treatment o malignant brain tumors, and the delivery of siRNA for the treatment of Huntington's disease. Our vision is that successful trans-skull delivery of FUS could have a major impact on the treatment of many brain disorders. If successful, this research will have a major impact on patient care.

Public Health Relevance

This research develops a system that uses many high frequency sound beams for completely noninvasive brain surgery that can be performed in an out-patient setting with eventually large reduction in cost and recovery time. The system is guided by magnetic resonance imaging (MRI) and thus provides high targeting accuracy. The method may be used to target drugs to specific brain locations in the future.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB003268-18
Application #
8681438
Study Section
Special Emphasis Panel (NOIT)
Program Officer
Krosnick, Steven
Project Start
1998-02-01
Project End
2016-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
18
Fiscal Year
2014
Total Cost
$515,802
Indirect Cost
$25,363
Name
Sunnybrook & Women's Coll Health Sciences Center
Department
Type
DUNS #
200466345
City
Toronto
State
ON
Country
Canada
Zip Code
M4 3-M5
O'Reilly, Meaghan A; Hough, Olivia; Hynynen, Kullervo (2017) Blood-Brain Barrier Closure Time After Controlled Ultrasound-Induced Opening Is Independent of Opening Volume. J Ultrasound Med 36:475-483
McMahon, Dallan; Hynynen, Kullervo (2017) Acute Inflammatory Response Following Increased Blood-Brain Barrier Permeability Induced by Focused Ultrasound is Dependent on Microbubble Dose. Theranostics 7:3989-4000
Pichardo, Samuel; Moreno-Hernández, Carlos; Andrew Drainville, Robert et al. (2017) A viscoelastic model for the prediction of transcranial ultrasound propagation: application for the estimation of shear acoustic properties in the human skull. Phys Med Biol 62:6938-6962
Hughes, Alec; Hynynen, Kullervo (2017) Design of patient-specific focused ultrasound arrays for non-invasive brain therapy with increased trans-skull transmission and steering range. Phys Med Biol 62:L9-L19
O'Reilly, Meaghan Anne; Jones, Ryan Matthew; Barrett, Edward et al. (2017) Investigation of the Safety of Focused Ultrasound-Induced Blood-Brain Barrier Opening in a Natural Canine Model of Aging. Theranostics 7:3573-3584
Huang, Yuexi; Alkins, Ryan; Schwartz, Michael L et al. (2017) Opening the Blood-Brain Barrier with MR Imaging-guided Focused Ultrasound: Preclinical Testing on a Trans-Human Skull Porcine Model. Radiology 282:123-130
Jones, Ryan M; Hynynen, Kullervo (2016) Comparison of analytical and numerical approaches for CT-based aberration correction in transcranial passive acoustic imaging. Phys Med Biol 61:23-36
Hughes, Alec; Hynynen, Kullervo (2016) A Tikhonov Regularization Scheme for Focus Rotations With Focused Ultrasound-Phased Arrays. IEEE Trans Ultrason Ferroelectr Freq Control 63:2008-2017
Hynynen, Kullervo; Jones, Ryan M (2016) Image-guided ultrasound phased arrays are a disruptive technology for non-invasive therapy. Phys Med Biol 61:R206-48
O'Reilly, Meaghan A; Jones, Ryan M; Birman, Gabriel et al. (2016) Registration of human skull computed tomography data to an ultrasound treatment space using a sparse high frequency ultrasound hemispherical array. Med Phys 43:5063

Showing the most recent 10 out of 102 publications