In situ conversion of porphyrin microbubbles to nanoparticles for multimodality imaging

被引:0
|
作者
Huynh E. [1 ,2 ]
Leung B.Y.C. [3 ]
Helfield B.L. [2 ,3 ]
Shakiba M. [1 ,2 ]
Gandier J.-A. [4 ]
Jin C.S. [1 ,5 ,6 ]
Master E.R. [4 ]
Wilson B.C. [1 ,2 ]
Goertz D.E. [2 ,3 ]
Zheng G. [1 ,2 ,5 ,6 ]
机构
[1] Princess Margaret Cancer Center, Techna Institute, University Health Network, Toronto, M5G 2M9, ON
[2] Department of Medical Biophysics, University of Toronto, Toronto, M5G 1L7, ON
[3] Sunnybrook Health Sciences Center, Toronto, M4N 3M5, ON
[4] Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, M5S 3E5, ON
[5] Department of Pharmaceutical Sciences, University of Toronto, Toronto, M5S 3M2, ON
[6] Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, M5G 1L7, ON
基金
加拿大创新基金会; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1038/nnano.2015.25
中图分类号
学科分类号
摘要
Converting nanoparticles or monomeric compounds into larger supramolecular structures by endogenous or external stimuli is increasingly popular because these materials are useful for imaging and treating diseases. However, conversion of microstructures to nanostructures is less common. Here, we show the conversion of microbubbles to nanoparticles using low-frequency ultrasound. The microbubble consists of a bacteriochlorophyll-lipid shell around a perfluoropropane gas. The encapsulated gas provides ultrasound imaging contrast and the porphyrins in the shell confer photoacoustic and fluorescent properties. On exposure to ultrasound, the microbubbles burst and form smaller nanoparticles that possess the same optical properties as the original microbubble. We show that this conversion is possible in tumour-bearing mice and could be validated using photoacoustic imaging. With this conversion, our microbubble can potentially be used to bypass the enhanced permeability and retention effect when delivering drugs to tumours. © 2015 Macmillan Publishers Limited. All rights reserved.
引用
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页码:325 / 332
页数:7
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