Fluorescence-Tagged Gold Nanoparticles for Rapidly Characterizing the Size-Dependent Biodistribution in Tumor Models

被引:89
作者
Chou, Leo Y. T. [1 ]
Chan, Warren C. W. [1 ]
机构
[1] Terrence Donnelly Ctr Cellular & Biomol Res, Inst Biomat & Biomed Engn, Toronto, ON M5S 3E1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PARTICLE-SIZE; CHAIN-LENGTH; THERMODYNAMIC CONTROL; SURFACE-PROPERTIES; SPECTRAL OVERLAP; IN-VITRO; PHARMACOKINETICS; PEG; ENHANCEMENT; ADSORPTION;
D O I
10.1002/adhm.201200084
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Nanoparticle vehicles may improve the delivery of contrast agents and therapeutics to diseased tissues, but their rational design is currently impeded by a lack of robust technologies to characterize their in vivo behavior in realtime. This study demonstrates that fluorescent-labeled gold nanoparticles can be optimized for in vivo detection, perform pharmacokinetic analysis of nanoparticle designs, analyze tumor extravasation, and clearance kinetics in tumor-bearing animals. This optical imaging approach is non-invasive and high-throughput. Interestingly, these fluorescent gold nanoparticles can be used for multispectral imaging to compare several nanoparticle designs simultaneously within the same animal and eliminates the host-dependent variabilities across measured data. Together these results describe a novel platform for evaluating the performance of tumor-targeting nanoparticles, and provide new insights for the design of future nanotherapeutics.
引用
收藏
页码:714 / 721
页数:8
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