Literature DB >> 24115675

In vivo immune cell distribution of gold nanoparticles in naïve and tumor bearing mice.

Joao Paulo Mattos Almeida1, Adam Yuh Lin, Robert James Langsner, Phillip Eckels, Aaron Edward Foster, Rebekah Anna Drezek.   

Abstract

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 naïve 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 naïve 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.
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  biodistribution; cancer; gold nanoparticles; immune system; immunotherapy; spleen

Mesh:

Substances:

Year:  2013        PMID: 24115675      PMCID: PMC3962812          DOI: 10.1002/smll.201301998

Source DB:  PubMed          Journal:  Small        ISSN: 1613-6810            Impact factor:   13.281


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