4.8 Article

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

期刊

SMALL
卷 10, 期 4, 页码 812-819

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201301998

关键词

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

资金

  1. National Institutes of Health [R01CA172836]
  2. Keck Center of the Gulf Coast Consortia, on the Nanobiology Interdisciplinary Graduate Training Program, National Institute of Biomedical Imaging and Bioengineering (NIBIB) [T32EB009379]
  3. National Science Foundation [0940902]
  4. Howard Hughes Medical Institute Med into Grad fellowship
  5. Medical Scientist Training Program at Baylor College of Medicine
  6. Edward and Josephine Hudson Scholarship
  7. NIH
  8. NCI
  9. Division Of Graduate Education
  10. Direct For Education and Human Resources [0940902] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

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