TY - JOUR
T1 - Monitoring of acoustic cavitation in microbubble-presented focused ultrasound exposure using gradient-echo MRI
AU - Wu, Chen Hua
AU - Liu, Hao Li
AU - Ho, Cheng Tao
AU - Hsu, Po Hung
AU - Fan, Ching Hsiang
AU - Yeh, Chih Kuang
AU - Kang, Shih Tsung
AU - Chen, Wen Shiang
AU - Wang, Fu Nien
AU - Peng, Hsu Hsia
N1 - Funding Information:
Contract grant sponsor: Ministry of Science and Technology, Taiwan; Contract grant numbers: MOST 107-2221-E-182-002; MOST 106-2314-B-007-006-MY3. We thank the assistance from the Center for Advanced Molecular Imaging and Translation, Chang Gung Memorial Hospital, Taoyuan, Taiwan. Parts of this work were presented at the 22nd and 23rd Annual Meeting of the International Society for Magnetic Resonance in Medicine.
Funding Information:
Contract grant sponsor: Ministry of Science and Technology, Taiwan; Contract grant numbers: MOST 107-2221-E-182-002; MOST 106-2314-B-007-006-MY3.
Publisher Copyright:
© 2019 International Society for Magnetic Resonance in Medicine
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: Gadolinium-based contrast agents can be used to identify the blood–brain barrier (BBB) opening after inducing a focused ultrasound (FUS) cavitation effect in the presence of microbubbles. However, the use of gadolinium may be limited for frequent routine monitoring of the BBB opening in clinical applications. Purpose: To use a gradient-echo sequence without contrast agent administration for monitoring of acoustic cavitation. Study Type: Animal and phantom prospective. Phantom/Animal Model: Static and flowing gel phantoms; six normal adult male Sprague–Dawley rats. Field Strength/Sequence: 3T, 7T; fast low-angle shot sequence. Assessment: Burst FUS with acoustic pressures = 1.5, 2.2, 2.8 MPa; pulse repetition frequencies = 1, 10,100 Hz; and duty cycles = 2%, 5%, 10% were transmitted to the chamber of a static phantom with microbubble concentrations = 10%, 1%, 0.1%. MR slice thicknesses = 3, 6, 8 mm were acquired. In flowing phantom experiments, 0.1%, 0.25%, 0.5%, 0.75%, and 1% microbubbles were infused and transmitted by burst FUS with an acoustic pressure = 0.4 and 1 MPa. In in vivo experiments, 0.25% microbubbles was infused and 0.8 MPa burst FUS was transmitted to targeted brain tissue beneath the superior sagittal sinus. The mean signal intensity (SI) was normalized using the mean SI from pre-FUS. Statistical Tests: Two-tailed Student's t-test. P < 0.05 was considered statistically significant. Results: In the static phantom, the time courses of normalized SI decreases to minimum SI levels of 70–80%. In the flowing phantom, substantial normalized SI of 160–230% was present with variant acoustic pressures and microbubble concentrations. Compared with in vivo control rats, the brain tissue of experimental rats with transmission of FUS pulses exhibited considerable decreases of normalized SI (P < 0.001) because of the cavitation-induced perturbation of flow. Data Conclusion: Observing gradient-echo SI changes can help monitor the targeted location of microbubble-enhanced FUS, which in turn assists the monitoring of the BBB opening. Level of Evidence: 2. Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2020;51:311–318.
AB - Background: Gadolinium-based contrast agents can be used to identify the blood–brain barrier (BBB) opening after inducing a focused ultrasound (FUS) cavitation effect in the presence of microbubbles. However, the use of gadolinium may be limited for frequent routine monitoring of the BBB opening in clinical applications. Purpose: To use a gradient-echo sequence without contrast agent administration for monitoring of acoustic cavitation. Study Type: Animal and phantom prospective. Phantom/Animal Model: Static and flowing gel phantoms; six normal adult male Sprague–Dawley rats. Field Strength/Sequence: 3T, 7T; fast low-angle shot sequence. Assessment: Burst FUS with acoustic pressures = 1.5, 2.2, 2.8 MPa; pulse repetition frequencies = 1, 10,100 Hz; and duty cycles = 2%, 5%, 10% were transmitted to the chamber of a static phantom with microbubble concentrations = 10%, 1%, 0.1%. MR slice thicknesses = 3, 6, 8 mm were acquired. In flowing phantom experiments, 0.1%, 0.25%, 0.5%, 0.75%, and 1% microbubbles were infused and transmitted by burst FUS with an acoustic pressure = 0.4 and 1 MPa. In in vivo experiments, 0.25% microbubbles was infused and 0.8 MPa burst FUS was transmitted to targeted brain tissue beneath the superior sagittal sinus. The mean signal intensity (SI) was normalized using the mean SI from pre-FUS. Statistical Tests: Two-tailed Student's t-test. P < 0.05 was considered statistically significant. Results: In the static phantom, the time courses of normalized SI decreases to minimum SI levels of 70–80%. In the flowing phantom, substantial normalized SI of 160–230% was present with variant acoustic pressures and microbubble concentrations. Compared with in vivo control rats, the brain tissue of experimental rats with transmission of FUS pulses exhibited considerable decreases of normalized SI (P < 0.001) because of the cavitation-induced perturbation of flow. Data Conclusion: Observing gradient-echo SI changes can help monitor the targeted location of microbubble-enhanced FUS, which in turn assists the monitoring of the BBB opening. Level of Evidence: 2. Technical Efficacy: Stage 1 J. Magn. Reson. Imaging 2020;51:311–318.
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U2 - 10.1002/jmri.26801
DO - 10.1002/jmri.26801
M3 - Article
C2 - 31125166
AN - SCOPUS:85066902642
SN - 1053-1807
VL - 51
SP - 311
EP - 318
JO - Journal of Magnetic Resonance Imaging
JF - Journal of Magnetic Resonance Imaging
IS - 1
ER -