Literature DB >> 26774224

Nanoparticle-liver interactions: Cellular uptake and hepatobiliary elimination.

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.
Copyright © 2016. Published by Elsevier B.V.

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


  198 in total

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Review 4.  Progress on Modulating Tumor-Associated Macrophages with Biomaterials.

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Journal:  Adv Mater       Date:  2019-09-27       Impact factor: 30.849

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Authors:  David T White; Meera T Saxena; Jeff S Mumm
Journal:  Adv Drug Deliv Rev       Date:  2019-02-12       Impact factor: 15.470

Review 6.  Selective tissue targeting of synthetic nucleic acid drugs.

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7.  Locally Trapping the C-C Chemokine Receptor Type 7 by Gene Delivery Nanoparticle Inhibits Lymphatic Metastasis Prior to Tumor Resection.

Authors:  Sai An; Karthik Tiruthani; Ying Wang; Ligeng Xu; Mengying Hu; Jingjing Li; Wantong Song; Hongnan Jiang; Jirui Sun; Rihe Liu; Leaf Huang
Journal:  Small       Date:  2019-01-28       Impact factor: 13.281

8.  Comparison of silver nanoparticle-induced inflammatory responses between healthy and metabolic syndrome mouse models.

Authors:  Lisa Kobos; Saeed Alqahtani; Li Xia; Vincent Coltellino; Riley Kishman; Daniel McIlrath; Carlos Perez-Torres; Jonathan Shannahan
Journal:  J Toxicol Environ Health A       Date:  2020-04-12

9.  Toxicological Profiling of Metal Oxide Nanoparticles in Liver Context Reveals Pyroptosis in Kupffer Cells and Macrophages versus Apoptosis in Hepatocytes.

Authors:  Vahid Mirshafiee; Bingbing Sun; Chong Hyun Chang; Yu-Pei Liao; Wen Jiang; Jinhong Jiang; Xiangsheng Liu; Xiang Wang; Tian Xia; André E Nel
Journal:  ACS Nano       Date:  2018-03-19       Impact factor: 15.881

10.  One-year chronic toxicity evaluation of single dose intravenously administered silica nanoparticles in mice and their Ex vivo human hemocompatibility.

Authors:  Raziye Mohammadpour; Darwin L Cheney; Jason W Grunberger; Mostafa Yazdimamaghani; Jolanta Jedrzkiewicz; Kyle J Isaacson; Marina A Dobrovolskaia; Hamidreza Ghandehari
Journal:  J Control Release       Date:  2020-05-25       Impact factor: 9.776

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