Hydrophobic cyanine dye-doped micelles for optical in vivo imaging of plasma leakage and vascular disruption

被引:10
作者
Botz, Balint
Boelcskei, Kata
Kemeny, Agnes
Sandor, Zoltan
Tekus, Valeria
Setalo, Gyoergy, Jr.
Csepregi, Janka
Mocsai, Attila
Pinter, Erika
Kollar, Laszlo
Helyes, Zsuzsanna
机构
[1] University of Pécs, School of Medicine, Department of Pharmacology and Pharmacotherapy, Szigeti út 12, Pécs
[2] University of Pécs, János Szentágothai Research Centre, Molecular Pharmacology Research Team, Ifjúság útja 20, Pécs
[3] University of Pécs, School of Medicine, Department of Medical Biology, Szigeti út 12, Pécs
[4] University of Pécs, János Szentágothai Research Centre, Signal Transduction Research Team, Ifjúság útja 20, Pécs
[5] Semmelweis University School of Medicine, MTA-SE Lendület Inflammation Physiology Research Group, Department of Physiology, Tzoltó u. 37-47, Budapest
[6] University of Pécs, Department of Inorganic Chemistry, Ifjúság útja. 6, Pécs
[7] MTA-PTE NAP B Pain Research Group, Szigeti út 12, Pécs
基金
欧洲研究理事会; 英国惠康基金;
关键词
animal model; inflammation; plasma leakage; fluorescence; micelle; optical imaging; fluorescence tomography; NEAR-INFRARED FLUORESCENCE; INDOCYANINE GREEN; PERMEABILITY; ARTHRITIS; MODEL; FLUOROPHORES; INFLAMMATION; TOXICITY; RECEPTOR; SYSTEM;
D O I
10.1117/1.JBO.20.1.016022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Vascular leakage is an important feature of various disease conditions. In vivo optical imaging provides a great opportunity for the evaluation of this phenomenon. In the present study, we focus on the development and validation of a near-infrared (NIR) imaging formula to allow reliable, cost-efficient evaluation of vascular leakage in diverse species using the existing small-animal fluorescence imaging technology. IR-676, a moderately hydrophobic NIR cyanine dye, was doped into self-assembling aqueous micelles using a widely employed and safe nonionic emulsifier (Kolliphor HS 15), and was tested in several acute and chronic inflammatory disease models in both mice and rats. The imaging formula is stable and exerts no acute toxic effects in vitro. It accumulated specifically in the inflamed regions in all models, which could be demonstrated by both conventional epifluorescence imaging, and fluorescence tomography both as a standalone technique and also by merging it with computed tomography scans. Ex vivo verification of dye accumulation by confocal fluorescence microscopy was also possible. The present formula allows sensitive and specific detection of inflammatory plasma leakage in diverse models. Its potential for imaging larger animals was also demonstrated. IR-676-doped micelles offer an excellent opportunity to image inflammatory vascular leakage in various models and species. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License.
引用
收藏
页数:9
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