» Articles » PMID: 33755563

Transcranial MR-Guided Histotripsy System

Abstract

Histotripsy has been previously shown to treat a wide range of locations through excised human skulls in vitro. In this article, a transcranial magnetic resonance (MR)-guided histotripsy (tcMRgHt) system was developed, characterized, and tested in the in vivo pig brain through an excised human skull. A 700-kHz, 128-element MR-compatible phased-array ultrasound transducer with a focal depth of 15 cm was designed and fabricated in-house. Support structures were also constructed to facilitate transcranial treatment. The tcMRgHt array was acoustically characterized with a peak negative pressure up to 137 MPa in free field, 72 MPa through an excised human skull with aberration correction, and 48.4 MPa without aberration correction. The electronic focal steering range through the skull was 33.5 mm laterally and 50 mm axially, where a peak negative pressure above the 26-MPa cavitation intrinsic threshold can be achieved. The MR compatibility of the tcMRgHt system was assessed quantitatively using SNR, B0 field map, and B1 field map in a clinical 3T magnetic resonance imaging (MRI) scanner. Transcranial treatment using electronic focal steering was validated in red blood cell phantoms and in vivo pig brain through an excised human skull. In two pigs, targeted cerebral tissue was successfully treated through the human skull as confirmed by MRI. Excessive bleeding or edema was not observed in the peri-target zones by the time of pig euthanasia. These results demonstrated the feasibility of using this preclinical tcMRgHt system for in vivo transcranial treatment in a swine model.

Citing Articles

A pre-clinical MRI-guided all-in-one focused ultrasound system for murine brain studies.

Kaovasia T, Duclos S, Gupta D, Kalayeh K, Fabiilli M, Noll D Sci Rep. 2025; 15(1):144.

PMID: 39747938 PMC: 11696467. DOI: 10.1038/s41598-024-84078-9.


A novel transcranial MR Guided focused ultrasound method based on the ultrashort echo time skull acoustic model and phase retrieval techniques.

Kong D, Liu G, Cheng B, Qi X, Zhu J, He Q Sci Rep. 2024; 14(1):11876.

PMID: 38789537 PMC: 11636931. DOI: 10.1038/s41598-024-62500-6.


Neuronavigation-Guided Transcranial Histotripsy (NaviTH) System.

Choi S, Komaiha M, Choi D, Lu N, Gerhardson T, Fox A Ultrasound Med Biol. 2024; 50(8):1155-1166.

PMID: 38789304 PMC: 11822949. DOI: 10.1016/j.ultrasmedbio.2024.04.001.


Ultrasound imaging guided precision histotripsy: Effects of pulse settings on ablation properties in rat brain.

Landry T, Brown J J Acoust Soc Am. 2024; 155(4):2860-2874.

PMID: 38682916 PMC: 11175660. DOI: 10.1121/10.0025832.


Revolutionizing brain interventions: the multifaceted potential of histotripsy.

Verma Y, Perera Molligoda Arachchige A Neurosurg Rev. 2024; 47(1):124.

PMID: 38509320 DOI: 10.1007/s10143-024-02353-9.


References
1.
Gerhardson T, Sukovich J, Pandey A, Hall T, Cain C, Xu Z . Effect of Frequency and Focal Spacing on Transcranial Histotripsy Clot Liquefaction, Using Electronic Focal Steering. Ultrasound Med Biol. 2017; 43(10):2302-2317. PMC: 5580808. DOI: 10.1016/j.ultrasmedbio.2017.06.010. View

2.
Khokhlova V, Fowlkes J, Roberts W, Schade G, Xu Z, Khokhlova T . Histotripsy methods in mechanical disintegration of tissue: towards clinical applications. Int J Hyperthermia. 2015; 31(2):145-62. PMC: 4448968. DOI: 10.3109/02656736.2015.1007538. View

3.
Coluccia D, Fandino J, Schwyzer L, OGorman R, Remonda L, Anon J . First noninvasive thermal ablation of a brain tumor with MR-guided focused ultrasound. J Ther Ultrasound. 2015; 2:17. PMC: 4322509. DOI: 10.1186/2050-5736-2-17. View

4.
Parsons J, Cain C, Fowlkes J . Cost-effective assembly of a basic fiber-optic hydrophone for measurement of high-amplitude therapeutic ultrasound fields. J Acoust Soc Am. 2006; 119(3):1432-40. DOI: 10.1121/1.2166708. View

5.
Jezzard P, Balaban R . Correction for geometric distortion in echo planar images from B0 field variations. Magn Reson Med. 1995; 34(1):65-73. DOI: 10.1002/mrm.1910340111. View