4.8 Article

Elimination Pathways of Nanoparticles

Journal

ACS NANO
Volume 13, Issue 5, Pages 5785-5798

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b01383

Keywords

nanoparticle; elimination; liver; Kupffer cell; liver sinusoidal endothelial cell; hepatocyte; hepatobiliary

Funding

  1. CIHR [FDN-159932, MOP-130143]
  2. OGS
  3. NSERC [2015-06397]
  4. Wildcat Foundation
  5. Vanier Canada Graduate Scholarship
  6. McLaughlin Centre
  7. Donnelly Centre
  8. Royal Bank of Canada (RBC)
  9. Canadian Research Chairs program [950-223824]
  10. CHRP program [CPG-146468]
  11. Canadian Cancer Society [705185-1]

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Understanding how nanoparticles are eliminated from the body is required for their successful clinical translation. Many promising nanoparticle formulations for in vivo medical applications are large (>5.5 nm) and nonbiodegradable, so they cannot be eliminated renally. A proposed pathway for these nanoparticles is hepatobiliary elimination, but their transport has not been well-studied. Here, we explored the barriers that determined the elimination of nanoparticles through the hepatobiliary route. The route of hepatobiliary elimination is usually through the following pathway: (1) liver sinusoid, (2) space of Disse, (3) hepatocytes, (4) bile ducts, (5) intestines, and (6) out of the body. We discovered that the interaction of nanoparticles with liver nonparenchymal cells (e.g., Kupffer cells and liver sinusoidal endothelial cells) determines the elimination fate. Each step in the route contains cells that can sequester and chemically or physically alter the nanoparticles, which influences their fecal elimination. We showed that the removal of Kupffer cells increased fecal elimination by >10 times. Combining our results with those of prior studies, we can start to build a systematic view of nanoparticle elimination pathways as it relates to particle size and other design parameters. This is critical to engineering medically useful and translatable nanotechnologies.

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