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EMF Studies

25 August 2014

Blood-Brain-Barrier Disruption with High-Frequency Pulsed Electric Fields

A cortical microvessel stained
for blood-brain-barrier protein
ZO-1  (credit: Nathan S. Ivey/
Wikimedia Commons)
Blood-brain-barrier disruption with high-frequency pulsed electric fields
kurzveilai.net, 14 August 2014

A team of researchers from Virginia Tech and Wake Forest University School of Biomedical Engineering and Sciences have developed a new technique for using pulsed electric energy to open the blood-brain-barrier (BBB) for treating brain cancer and neurological disorders.

Their Vascular Enabled Integrated Nanosecond pulse (VEIN pulse) procedure consists of inserting minimally invasive needle electrodes into the diseased tissue and applying multiple bursts of 850-nanosecond pulsed electric energy with alternating polarity.

The researchers think the bursts disrupt tight junction proteins responsible for maintaining the integrity of the BBB, but without causing damage to the surrounding tissue.

This technique will be described in the upcoming issue of the journal TECHNOLOGY.

Treating brain diseases

For the treatment of brain cancer, “VEIN pulses could be applied at the same time as biopsy or through the same track as the biopsy probe in order to mitigate damage to the healthy tissue by limiting the number of needle insertions,” says Rafael V. Davalos, Ph.D, director of the Bioelectromechanical Systems Laboratory at Virginia Tech.

The BBB is a network of tight junctions that normally acts to protect the brain from foreign substances by preventing them from leaking from blood vessels into neural structures. But that also limits the effectiveness of drugs to treat brain disease. Temporarily opening the BBB is a way to ensure that drugs can still be effective.

Pathologic and MRI evidence of blood-brain-barrier (BBB) disruption induced by the VEIN (Vascular Enabled Integrated Nanosecond) pulse generation system. Two minimally invasive needle electrodes with 1 mm active length were spaced 4.0 mm apart and inserted into the right cerebral hemisphere 1.5 mm beneath the surface of the dura. A burst of 200, 500 ns duration square pulses of alternating polarity with a voltage-to-distance ratio of 250 V/cm were applied through the electrodes. In the case shown above, bursts were repeated once per second for 10 min. The extent of BBB disruption is shown by the dotted line surrounding Evans blue-albumin complex uptake on the gross brain slice preparation (left) and the corresponding fluorescent image (middle). Additionally, areas of BBB disruption appear as hyperintense (white) on the T1-weighted MRI exam, due to the uptake of a gadolinium-Evans blue tracer. Scale bar represents 5 mm. (Credit: John H. Rossmeisl Jr., Neurology and Neurosurgery, Virginia-Maryland Regional College of Veterinary Medicine and Virginia Tech-Wake Forest University School of Biomedical Engineering and Sciences).

The research also shows that VEIN pulses can be applied without causing muscle contractions, which may dislodge the electrodes and require the use of a neuroblocker and general anesthesia. According to Christopher B. Arena, Ph.D., co-lead author on the paper, “the fact that the pulses alternate in polarity helps to avoid unwanted, electrically induced movement. Therefore, it could be possible to perform this procedure without using a neuroblocker and with patients under conscious sedation. This is similar to how deep brain stimulation is implemented clinically to treat Parkinson’s disease.”

The team now plans to translate the technology into clinical applications through a university spin-out company, VoltMed, Inc.

Researchers at Virginia-Maryland Regional College of Veterinary Medicine where also involved in the study.

This research was supported in part by grants from the National Science Foundation, the Golfers Against Cancer, and the Center for Biomolecular Imaging in the Wake Forest School of Medicine.

Abstract of Technology paper

The blood-brain-barrier (BBB), a network of tight junctions that impedes large molecule transport, limits the usefulness of systemic chemotherapeutic delivery for the treatment of malignant gliomas and other neurological diseases. Here, we present a tool for BBB disruption that uses bursts of sub-microsecond bipolar pulses to enhance the transfer of large molecules to the brain. Blunt needle electrodes were advanced into the motor cortex of anesthetized adult rats, and a series of 90–900 bursts were delivered with voltage-to-distance ratios of 250 or 2000 V/cm, a total programmed energized time of 100 μs, and a repetition rate of 1 Hz. BBB disruption was assessed via a gadolinium-Evans blue albumin tracer, and all experimental conditions were found to cause BBB disruption immediately following treatment without inducing local or distal muscle contractions. The lowest energy condition, 300 bursts consisting of 850 ns bipolar pulses, resulted in significant BBB disruption (0.51 cm3), without displaying necrotic or apoptotic damage to neurological tissue.

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