Department of Nanoengineering, University of California San Diego, San Diego, California, USA.
Nanomedicine. 2010 Dec;6(6):797-807. doi: 10.1016/j.nano.2010.06.005. Epub 2010 Jul 3.
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.
我们在此报告多功能药物递送纳米粒子的体内联合模态成像。这些基于葡聚糖核心的隐形脂质体纳米粒子(纳米囊)含有阿霉素、用于磁共振成像(MRI)对比的氧化铁和用于荧光的 BODIPY。由于表面用聚乙二醇修饰并掺入乙酰化脂质,这些粒子在体内具有长寿命,这些乙酰化脂质经过紫外线交联以获得物理稳定性。我们开发了一种啮齿动物背部皮肤窗室,可方便地对同一肿瘤中纳米粒子积累进行 MRI 和非侵入性光学成像。室肿瘤通过 DsRed-2 进行基因标记,这使得可以对 MR 图像、肿瘤的红色荧光和纳米粒子的蓝色荧光进行共定位。然后,使用窗室开发的纳米粒子设计和磁共振成像被扩展到表达 DsRed-2 的原位胰腺肿瘤。使用氧化铁-葡聚糖脂质体和荧光对肿瘤进行磁共振成像,以证明这些纳米粒子的深层成像能力。