| Literature DB >> 26774224 |
Yi-Nan Zhang1, Wilson Poon1, Anthony J Tavares1, Ian D McGilvray2, Warren C W Chan3.
Abstract
30-99% of administered nanoparticles will accumulate and sequester in the liver after administration into the body. This results in reduced delivery to the targeted diseased tissue and potentially leads to increased toxicity at the hepatic cellular level. This review article focuses on the inter- and intra-cellular interaction between nanoparticles and hepatic cells, the elimination mechanism of nanoparticles through the hepatobiliary system, and current strategies to manipulate liver sequestration. The ability to solve the "nanoparticle-liver" interaction is critical to the clinical translation of nanotechnology for diagnosing and treating cancer, diabetes, cardiovascular disorders, and other diseases.Entities:
Keywords: Hepatobiliary clearance; Liver; Macrophage; Nanoparticle
Mesh:
Year: 2016 PMID: 26774224 DOI: 10.1016/j.jconrel.2016.01.020
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776