In Vivo Immune Cell Distribution of Gold Nanoparticles in Naive and Tumor Bearing Mice

被引:52
作者
Almeida, Joao Paulo Mattos [1 ]
Lin, Adam Yuh [1 ]
Langsner, Robert James [1 ]
Eckels, Phillip [3 ]
Foster, Aaron Edward [2 ,3 ]
Drezek, Rebekah Anna [1 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77030 USA
[2] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[3] Bellicum Pharmaceut, Houston, TX 77030 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
gold nanoparticles; immunotherapy; biodistribution; immune system; cancer; spleen; COLLOIDAL GOLD; BIODISTRIBUTION; SIZE; TOXICITY; PLATFORM; LIVER; SHAPE;
D O I
10.1002/smll.201301998
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Gold nanoparticles (AuNP) have been widely used for drug delivery and have recently been explored for applications in cancer immunotherapy. Although AuNPs are known to accumulate heavily in the spleen, the particle distribution within immune cells has not been thoroughly studied. Here, cellular distribution of Cy5 labeled 50 nm AuNPs is characterized within the immune populations of the spleen from naive and tumor bearing mice using flow cytometry. Surprisingly, approximately 30% of the detected AuNPs are taken up by B cells at 24 h, with about 10% in granulocytes, 18% in dendritic cells, and 8% in T cells. In addition, 3% of the particles are detected within myeloid derived suppressor cells, an immune suppressive population that could be targeted for cancer immunotherapy. Furthermore, it is observed that, over time, the particles traveled from the red pulp and marginal zone to the follicles of the spleen. Taking into consideration that the particle cellular distribution does not change at 1, 6 and 24 h, it is highly suggestive that the immune populations carry the particles and migrate through the spleen instead of the particles migrating through the tissue by cell-cell transfer. Finally, no difference is observed in particle distribution between naive and tumor bearing mice in the spleen, and nanoparticles are detected within 0.7% of dendritic cells of the tumor microenvironment. Overall, these results can help inform and influence future AuNP delivery design criteria including future applications for nanoparticle-mediated immunotherapy.
引用
收藏
页码:812 / 819
页数:8
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