4.6 Article

Cellular distribution of injected PLGA-nanoparticles in the liver

Journal

NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
Volume 12, Issue 5, Pages 1365-1374

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2016.01.013

Keywords

nanomedicine; Kupffer cells; Liver sinusoidal endothelial cells; Hepatic stellate cells; Hepatocytes

Funding

  1. NIH [R01 DK082600, P30 DK045735, R21 AA023599, CT DPH 2015-0901, AI112443]
  2. JSPS KAKENHI of Ministry of Education, Sport, Culture, Science and Technology in Japan [26440055]
  3. Grants-in-Aid for Scientific Research [26440055] Funding Source: KAKEN

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The cellular fate of nanoparticles in the liver is not fully understood. Because the effectiveness and safety of nanoparticles in liver therapy depends on targeting nanoparticles to the right cell populations, this study aimed to determine a relative distribution of PLGA-nanoparticles (sizes 271 +/- 1.4 nm) among liver cells in vivo. We found that Kupffer cells were the major cells that took up nanoparticles, followed by liver sinusoidal endothelial cells and hepatic stellate cells. Nanoparticles were found in only 7% of hepatocytes. Depletion of Kupffer cells by clodronate liposomes increased nanoparticle retention in liver sinusoidal endothelial cells and hepatic stellate cells, but not in hepatocytes. It is importantly suggested that studies of drug-loaded nanoparticle delivery to the liver have to demonstrate not only uptake of nanoparticles by the target cell type but also non-uptake by other cell types to assess their effect as well as ensure their safety. (C) 2016 Elsevier Inc. All rights reserved.

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