Acoustically-active microbubbles conjugated to liposomes: Characterization of a proposed drug delivery vehicle

被引:229
作者
Kheirolomoom, Azadeh [1 ]
Dayton, Paul A. [1 ]
Lum, Aaron F. H. [1 ]
Little, Erika [1 ]
Paoli, Eric E. [1 ]
Zheng, Hairong [1 ]
Ferrara, Katherine W. [1 ]
机构
[1] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
关键词
microbubble; liposome; ultrasound radiation forces; delivery vehicle;
D O I
10.1016/j.jconrel.2006.12.015
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
A new acoustically-active delivery vehicle was developed by conjugating liposomes and microbubbles, using the high affinity interaction between avidin and biotin. Binding between microbubbles and liposomes, each containing 5% DSPE-PEG2kBiotin, was highly dependent on avidin concentration and observed above an avidin concentration of 10 nM. With an optimized avidin and liposome concentration, we measured and calculated as high as 1000 to 10,000 liposomes with average diameters of 200 and 100 nm, respectively, attached to each microbubble. Replacing avidin with neutravidin resulted in 3-fold higher binding, approaching the calculated saturation level. High-speed photography of this new drug delivery vehicle demonstrated that the liposome-bearing microbubbles oscillate in response to an acoustic pulse in a manner similar to microbubble contrast agents. Additionally, microbubbles carrying liposomes could be spatially concentrated on a monolayer of PC-3 cells at the focal point of ultrasound beam. As a result of cell-vehicle contact, the liposomes fused with the cells and internalization of NBD-cholesterol occurred shortly after incubation at 37 degrees C, with internalization of NBD-cholesterol substantially enhanced in the acoustic focus. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 284
页数:10
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