Drug-loaded bubbles with matched focused ultrasound excitation for concurrent blood-brain barrier opening and brain-tumor drug delivery

被引:81
作者
Fan, Ching-Hsiang [1 ]
Ting, Chien-Yu [1 ]
Chang, Yuan-Chih [2 ]
Wei, Kuo-Chen
Liu, Hao-Li [6 ,3 ]
Yeh, Chih-Kuang [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Biomed Engn & Environm Sci, Hsinchu, Taiwan
[2] Acad Sinica, Inst Cellular & Organism Biol, Taipei 115, Taiwan
[3] Chang Gung Univ, Coll Med, Dept Neurosurg, Tao Yuan, Taiwan
关键词
Blood-brain barrier; Chemotherapy; Focused ultrasound; Intracerebral hemorrhage; Inertial cavitation reduction; INTRACEREBRAL HEMORRHAGE; MALIGNANT GLIOMAS; DISRUPTION; MICROBUBBLES; GLIOBLASTOMA; BCNU; CHEMOTHERAPY; CAVITATION; RABBITS; DOXORUBICIN;
D O I
10.1016/j.actbio.2014.12.026
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Focused ultrasound (FUS) with microbubbles has been used to achieve local blood-brain barrier opening (BBB opening) and increase the penetration of therapeutic drugs into brain tumors. However, inertial cavitation of microbubbles during FUS-induced BBB opening causes intracerebral hemorrhaging (ICH), leading to acute and chronic brain injury and limiting the efficiency of drug delivery. Here we investigated whether induction of drug (1,3-bis(2-chloroethyl)-1-nitrosourea, BCNU)-loaded bubbles (BCNU bubbles) to oscillate at their resonant frequency would reduce inertial cavitation during BBB opening, thereby eliminating ICH and enhancing drug delivery in a rat brain model. FUS was tested at I and 10 MHz, over a wide range of pressure (mechanical index ranging from 0.16 to 1.42) in the presence of BCNU bubbles. Excitation of BCNU bubbles by resonance frequency-matched FUS (10 MHz) resulted in predominantly stable cavitation and significantly reduced the occurrence of potential hazards of exposure to biological tissues during the BBB opening process. In addition, the drug release process could be monitored by acoustic emission obtained from ultrasound imaging. In tumor-bearing animals, BCNU bubbles with PUS showed significant control of tumor progression and improved maximum survival from 26 to 35 days. This study provides useful advancements toward the goal of successfully translating FUS theranostic bubble-enhanced brain drug delivery into clinical use. (C) 2015 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:89 / 101
页数:13
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