Antiangiogenic-targeting drug-loaded microbubbles combined with focused ultrasound for glioma treatment

被引:122
作者
Fan, Ching-Hsiang [1 ]
Ting, Chien-Yu [1 ]
Liu, Hao-Li [2 ]
Huang, Chiung-Yin [3 ,4 ]
Hsieh, Han-Yi [2 ]
Yen, Tzu-Chen [4 ,5 ,6 ]
Wei, Kuo-Chen [3 ,4 ]
Yeh, Chih-Kuang [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Biomed Engn & Environm Sci, Hsinchu 30013, Taiwan
[2] Chang Gung Univ, Dept Elect Engn, Tao Yuan 33302, Taiwan
[3] Chang Gung Univ, Dept Neurosurg, Tao Yuan 33305, Taiwan
[4] Mem Hosp, Tao Yuan 33305, Taiwan
[5] Chang Gung Univ, Dept Nucl Med, Tao Yuan 33305, Taiwan
[6] Chang Gung Univ, Mol Imaging Ctr, Tao Yuan 33305, Taiwan
关键词
Targeting microbubble; Focused ultrasound (FUS); Glioblastoma multiforme (GBM); Chemotherapy; Blood-brain barrier (BBB); Antiangiogenic therapy; BLOOD-BRAIN-BARRIER; ENDOTHELIAL GROWTH-FACTOR; TUMOR ANGIOGENESIS; GLIOBLASTOMA-MULTIFORME; CONTRAST AGENT; GENE DELIVERY; MOUSE-BRAIN; THERAPY; CELLS; SONOPORATION;
D O I
10.1016/j.biomaterials.2012.11.048
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Current chemotherapeutic agents do not only kill tumor cells but also induce systemic toxicity that significantly limits their dosage. Focused ultrasound (FUS) in the presence of microbubbles (MBs) is capable of transient and local opening of the blood brain barrier (BBB) that enhances chemotherapeutic drug delivery into the brain parenchyma for glioma treatment. Our previous results demonstrated the success of combining the use of drug (1,3-bis(2-chloroethyl)-1-nitrosourea, BCNU)-loaded MBs with FUS-induced BBB opening to improve local drug delivery and reduce systemic toxicity. Here we introduce novel VEGF-targeting, drug-loaded MBs that significantly further enhance targeted drug release and reduce tumor progression in a rat model, using the FUS-BBB opening strategy. This study suggests a promising direction for future MB design aimed at targeted brain tumor therapy, and the possible future extension of MB application towards theragnostic use. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2142 / 2155
页数:14
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