Magnetic resonance and fluorescence imaging of doxorubicin-loaded nanoparticles using a novel in vivo model

被引:41
作者
Erten, Ahmet [2 ]
Wrasidlo, Wolf [1 ]
Scadeng, Miriam [3 ]
Esener, Sadik [2 ]
Hoffman, Robert M. [4 ,5 ]
Bouvet, Michael [1 ,4 ]
Makale, Milan [1 ]
机构
[1] Univ Calif San Diego, Moores Canc Ctr, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Nanoengn, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Dept Radiol, San Diego, CA 92103 USA
[4] Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA
[5] AntiCancer Inc, San Diego, CA USA
基金
美国国家卫生研究院;
关键词
Multifunctional nanoparticle; MRI; Dorsal skinfold window chamber; CYTOSINE-ANALOG CS-682; PANCREATIC-CANCER; CONTRAST AGENTS; ORTHOTOPIC MODEL; DRUG-DELIVERY; LIPOSOMES; CIRCULATION; DEXTRAN; PROTEIN; PARTICLES;
D O I
10.1016/j.nano.2010.06.005
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report here the in vivo combined-modality imaging of multifunctional drug delivery nanoparticles. These dextran core-based stealth liposomal nanoparticles (nanosomes) contained doxorubicin, iron oxide for magnetic resonance imaging (MRI) contrast, and BODIPY for fluorescence. The particles were long-lived in vivo because of surface decoration with polyethylene glycol and the incorporation of acetylated lipids that were ultraviolet cross-linked for physical stability. We developed a rodent dorsal skinfold window chamber that facilitated both MRI and non-invasive optical imaging of nanoparticle accumulation in the same tumors. Chamber tumors were genetically labeled with DsRed-2, which enabled co-localization of the MR images, the red fluorescence of the tumor, and the blue fluorescence of the nanoparticles. The nanoparticle design and MR imaging developed with the window chamber were then extended to orthotopic pancreatic tumors expressing DsRed-2. The tumors were MR-imaged using iron oxide-dextran liposomes and by fluorescence to demonstrate the deep imaging capability of these nanoparticles. From the Clinical Editor: In vivo combined-modality imaging of multifunctional drug delivery nanoparticles is discussed in this proof of principle paper. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:797 / 807
页数:11
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