淋巴
淋巴系统
体内分布
淋巴结
材料科学
脾脏
生物医学工程
药物输送
病理
核医学
医学
化学
纳米技术
免疫学
生物化学
体外
作者
Yu Cheng Tseng,Zhenghong Xu,Kevin Guley,Hong Yuan,Leaf Huang
出处
期刊:Biomaterials
[Elsevier BV]
日期:2014-05-01
卷期号:35 (16): 4688-4698
被引量:95
标识
DOI:10.1016/j.biomaterials.2014.02.030
摘要
A lipid/calcium/phosphate (LCP) nanoparticle (NP) formulation (particle diameter ∼25 nm) with superior siRNA delivery efficiency was developed and reported previously. Here, we describe the successful formulation of (111)In into LCP for SPECT/CT imaging. Imaging and biodistribution studies showed that, polyethylene glycol grafted (111)In-LCP preferentially accumulated in the lymph nodes at ∼70% ID/g in both C57BL/6 and nude mice when the improved surface coating method was used. Both the liver and spleen accumulated only ∼25% ID/g. Larger LCP (diameter ∼67 nm) was less lymphotropic. These results indicate that 25 nm LCP was able to penetrate into tissues, enter the lymphatic system, and accumulate in the lymph nodes via lymphatic drainage due to 1) small size, 2) a well-PEGylated lipid surface, and 3) a slightly negative surface charge. The capability of intravenously injected (111)In-LCP to visualize an enlarged, tumor-loaded sentinel lymph node was demonstrated using a 4T1 breast cancer lymph node metastasis model. Systemic gene delivery to the lymph nodes after IV injection was demonstrated by the expression of red fluorescent protein cDNA. The potential of using LCP for lymphatic drug delivery is discussed.
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