Curcumin-conjugated magnetic nanoparticles for detecting amyloid plaques in Alzheimer's disease mice using magnetic resonance imaging (MRI)

被引:208
作者
Cheng, Kwok Kin [1 ]
Chan, Pui Shan [1 ]
Fan, Shujuan [2 ,3 ,4 ]
Kwan, Siu Ming [5 ]
Yeung, King Lun [5 ]
Wang, Yi-Xiang J. [6 ]
Chow, Albert Hee Lum [1 ]
Wu, Ed X. [2 ,3 ,4 ]
Baum, Larry [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Sch Pharm, Shatin, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Elect & Elect Engn, Lab Biomed Imaging & Signal Proc, Pokfulam, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Med, Pokfulam, Hong Kong, Peoples R China
[4] Univ Hong Kong, Dept Anat, Pokfulam, Hong Kong, Peoples R China
[5] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Univ Hong Kong, Fac Med, Dept Imaging & Intervent Radiol, Shatin, Hong Kong, Peoples R China
关键词
Alzheimer's disease; Curcumin; Iron oxide nanoparticles; Amyloid plaques; Tg2576; mice; MRI; IRON-OXIDE NANOPARTICLES; BLOOD-BRAIN-BARRIER; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; PEGYLATED POLYCYANOACRYLATE NANOPARTICLES; IN-VIVO MRI; TRANSGENIC MICE; AQUEOUS DISPERSIONS; CONTRAST AGENTS; CELLULAR UPTAKE; CLINICAL-TRIAL;
D O I
10.1016/j.biomaterials.2014.12.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Diagnosis of Alzheimer's disease (AD) can be performed with the assistance of amyloid imaging. The current method relies on positron emission tomography (PET), which is expensive and exposes people to radiation, undesirable features for a population screening method. Magnetic resonance imaging (MRI) is cheaper and is not radioactive. Our approach uses magnetic nanoparticles (MNPs) made of superparamagnetic iron oxide (SPIO) conjugated with curcumin, a natural compound that specifically binds to amyloid plaques. Coating of curcumin-conjugated MNPs with polyethylene glycol-polylactic acid block copolymer and polyvinylpyrrolidone by antisolvent precipitation in a multi-inlet vortex mixer produces stable and biocompatible curcumin magnetic nanoparticles (Cur-MNPs) with mean diameter <100 nm. These nanoparticles were visualized by transmission electron microscopy and atomic force microscopy, and their structure and chemistry were further characterized by X-ray diffraction, thermogravimetric analysis, X-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry, and Fourier transform infrared spectroscopy. Cur-MNPs exhibited no cytotoxicity in either Madin-Darby canine kidney (MDCK) or differentiated human neuroblastoma cells (SH-SY5Y). The P-app of Cur-MNPs was 1.03 x 10(-6) cm/s in an in vitro blood brain barrier (BBB) model. Amyloid plaques could be visualized in ex vivo T2*-weighted magnetic resonance imaging (MRI) of Tg2576 mouse brains after injection of Cur -MNPs, and no plaques could be found in non-transgenic mice. Immunohistochemical examination of the mouse brains revealed that Cur-MNPs were co-localized with amyloid plaques. Thus, Cur-MNPs have the potential for non-invasive diagnosis of AD using MRI. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:155 / 172
页数:18
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