Effects of acoustic parameters and ultrasound contrast agent dose on focused-ultrasound induced blood-brain barrier disruption

被引:225
作者
Mcdannold, Nathan [1 ,2 ]
Vykhodtseva, Natalia [1 ,2 ]
Hynynen, Kullervo [3 ,4 ]
机构
[1] Harvard Univ, Sch Med, Dept Radiol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[3] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[4] Sunnybrook Hlth Sci Ctr, Discipline Imaging Res, Toronto, ON M4N 3M5, Canada
关键词
ultrasound; blood-brain barrier; drug delivery; ultrasound contrast agents; MRI;
D O I
10.1016/j.ultrasmedbio.2007.11.009
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Previously, it was shown that low-intensity focused ultrasound pulses applied along with an ultrasound contrast agent results in temporary blood-brain barrier (BBB) disruption. This effect could be used for targeted drug delivery in the central nervous system. This study examined the effects of burst length, pulse repetition frequency (PRF), and ultrasound contrast agent dose on the resulting BBB disruption. One hundred nonoverlapping brain locations were sonicated through a craniotomy in experiments in 26 rabbits (ultrasound frequency: 0.69 MHz, burst: 0.1, 1, 10 ms, PRF: 0.5, 1, 2, 5 Hz, duration: 20 s, peak negative pressure amplitude: 0.1 to 1.5 MPa, Optison dosage 50, 100, 250 mu l/kg). For each sonication, BBB disruption was evaluated using contrast-enhanced magnetic resonance imaging. The BBB disruption threshold (the pressure amplitude yielding a 50% probability for BBB disruption) was determined using probit regression for the three burst lengths tested. Tissue effects were examined in light microscopy for representative locations with similar amounts of contrast enhancement from each group. While changing the PRF or the Optison dosage did not result in a significant difference in the magnitude of the BBB disruption (p > 0.05), reducing the burst length resulted in significantly less contrast enhancement (p < 0.01). The BBB disruption thresholds were estimated to be 0.69, 0.47 and 0.36 MPa for 0.1, 1 and 10 ms bursts, respectively. No difference was detected in histology between any experimental groups. This data suggests that over the range of parameters tested, BBB disruption is not affected by PRF or ultrasound contrast agent dose. However, both the BBB disruption magnitude and its threshold depend on the burst length. (E-mail: njm@bwh.harvard.edu) (c) 2008 World Federation for Ultrasound in Medicine & Biology.
引用
收藏
页码:930 / 937
页数:8
相关论文
共 25 条
[1]   Transporting therapeutics across the blood-brain barrier [J].
Abbott, NJ ;
Romero, IA .
MOLECULAR MEDICINE TODAY, 1996, 2 (03) :106-113
[2]   CONVECTION-ENHANCED DELIVERY OF MACROMOLECULES IN THE BRAIN [J].
BOBO, RH ;
LASKE, DW ;
AKBASAK, A ;
MORRISON, PF ;
DEDRICK, RL ;
OLDFIELD, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2076-2080
[3]   Noninvasive, transcranial and localized opening of the blood-brain barrier using focused ultrasound in mice [J].
Choi, James J. ;
Pernot, Mathieu ;
Small, Scott A. ;
Konofagou, Elisa E. .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2007, 33 (01) :95-104
[4]  
Doolittle ND, 2000, CANCER, V88, P637, DOI 10.1002/(SICI)1097-0142(20000201)88:3<637::AID-CNCR22>3.0.CO
[5]  
2-Y
[6]  
Finney D.J., 1977, PROBIT ANAL, VIII
[7]   COMPREHENSIVE COMPILATION OF EMPIRICAL ULTRASONIC PROPERTIES OF MAMMALIAN-TISSUES [J].
GOSS, SA ;
JOHNSTON, RL ;
DUNN, F .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1978, 64 (02) :423-457
[8]   Recent advances in brain tumor therapy: local intracerebral drug delivery by polymers [J].
Guerin, C ;
Olivi, A ;
Weingart, JD ;
Lawson, HC ;
Brem, H .
INVESTIGATIONAL NEW DRUGS, 2004, 22 (01) :27-37
[9]   Local and reversible blood-brain barrier disruption by noninvasive focused ultrasound at frequencies suitable for trans-skull sonications [J].
Hynynen, K ;
McDannold, N ;
Sheikov, NA ;
Jolesz, FA ;
Vykhodtseva, N .
NEUROIMAGE, 2005, 24 (01) :12-20
[10]   500-element ultrasound phased array system for noninvasive focal surgery of the brain: A preliminary rabbit study with ex vivo human skulls [J].
Hynynen, K ;
Clement, GT ;
McDannold, N ;
Vykhodtseva, N ;
King, R ;
White, PJ ;
Vitek, S ;
Jolesz, FA .
MAGNETIC RESONANCE IN MEDICINE, 2004, 52 (01) :100-107