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Perfluorocarbon nanoemulsions for quantitative molecular imaging and targeted therapeutics.

作者信息

Kaneda Megan M, Caruthers Shelton, Lanza Gregory M, Wickline Samuel A

机构信息

Department of Biomedical Engineering, Washington University, St Louis, MO, USA.

出版信息

Ann Biomed Eng. 2009 Oct;37(10):1922-33. doi: 10.1007/s10439-009-9643-z. Epub 2009 Jan 30.


DOI:10.1007/s10439-009-9643-z
PMID:19184435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2745515/
Abstract

A broad array of nanomaterials is available for use as contrast agents for molecular imaging and drug delivery. Due to the lack of endogenous background signal in vivo and the high NMR sensitivity of the (19)F atom, liquid perfluorocarbon nanoemulsions make ideal agents for cellular and magnetic resonance molecular imaging. The perfluorocarbon core material is surrounded by a lipid monolayer which can be functionalized with a variety of agents including targeting ligands, imaging agents and drugs either individually or in combination. Multiple copies of targeting ligands (approximately 20-40 monoclonal antibodies or 200-400 small molecule ligands) serve to enhance avidity through multivalent interactions while the composition of the particle's perfluorocarbon core results in high local concentrations of (19)F. Additionally, lipophilic drugs contained within molecularly targeted nanoemulsions can result in contact facilitated drug delivery to target cells. Ultimately, the dual use of perfluorocarbon nanoparticles for both site targeted drug delivery and molecular imaging may provide both imaging of disease states as well as conclusive evidence that drug delivery is localized to the area of interest. This review will focus on liquid perfluorocarbon nanoparticles as (19)F molecular imaging agents and for targeted drug delivery in cancer and cardiovascular disease.

摘要

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本文引用的文献

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