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Hepatic Cellular Distribution of Silica Nanoparticles by Surface Energy Modification.
Lee, A-Rang; Nam, Kibeom; Lee, Byeong Jun; Lee, Seoung-Woo; Baek, Su-Min; Bang, Jun-Sun; Choi, Seong-Kyoon; Park, Sang-Joon; Kim, Tae-Hwan; Jeong, Kyu-Shik; Lee, Dong Yun; Park, Jin-Kyu.
Afiliação
  • Lee AR; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Nam K; Department of Polymer Science and Engineering, Kyungpook National University, Daegu 41566, Korea.
  • Lee BJ; Department of Polymer Science and Engineering, Kyungpook National University, Daegu 41566, Korea.
  • Lee SW; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Baek SM; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Bang JS; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Choi SK; Core Protein Resources Center, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea.
  • Park SJ; Laboratory of Veterinary Histology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Kim TH; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Jeong KS; Department of Veterinary Pathology, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea.
  • Lee DY; Stem Cell Therapeutic Research Institute, Kyungpook National University, Daegu 41566, Korea.
  • Park JK; Department of Polymer Science and Engineering, Kyungpook National University, Daegu 41566, Korea. dongyunlee@knu.ac.kr.
Int J Mol Sci ; 20(15)2019 Aug 05.
Article em En | MEDLINE | ID: mdl-31387201
ABSTRACT
The cellular distribution of silica nanoparticles (NPs) in the liver is not well understood. Targeting specific cells is one of the most important issues in NP-based drug delivery to improve delivery efficacy. In this context, the present study analyzed the relative cellular distribution pattern of silica NPs in the liver, and the effect of surface energy modification on NPs. Hydrophobic NP surface modification enhanced NP delivery to the liver and liver sinusoid fFendothelial cells (LSECs). Conversely, hydrophilic NP surface modification was commensurate with targeting hepatic stellate cells (HSCs) rather than other cell types. There was no notable difference in NP delivery to Kupffer cells or hepatocytes, regardless of hydrophilic or hydrophobic NP surface modification, suggesting that both the targeting of hepatocytes and evasion of phagocytosis by Kupffer cells are not associated with surface energy modification of silica NPs. This study provides useful information to target specific cell types using silica NPs, as well as to understand the relationship between NP surface energy and the NP distribution pattern in the liver, thereby helping to establish strategies for cell targeting using various NPs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Sistemas de Liberação de Medicamentos / Dióxido de Silício / Nanopartículas / Fígado Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Sistemas de Liberação de Medicamentos / Dióxido de Silício / Nanopartículas / Fígado Idioma: En Ano de publicação: 2019 Tipo de documento: Article