Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells

10.3390/ijms20010035

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Main Authors:	Tee, J.K, Ng, L.Y, Koh, H.Y, Leong, D.T, Ho, H.K
Other Authors:	CHEMICAL & BIOMOLECULAR ENGINEERING
Format:	Article
Published:	2020
Subjects:	nanoparticle titanium dioxide protein kinase B titanium apoptosis Article cell adhesion cell proliferation cell viability chronic liver disease disease exacerbation drug delivery system drug penetration endothelium cell enzyme linked immunosorbent assay flow cytometry human human cell immunofluorescence liver cell liver sinusoidal endothelial cell oxidative stress particle size protein expression real time polymerase chain reaction signal transduction Western blotting zeta potential cell communication cell culture cell survival chemistry cytology drug effect liver metabolism pathology permeability Cell Communication Cell Survival Cells, Cultured Endothelial Cells Hepatocytes Humans Liver Nanoparticles Oxidative Stress Permeability Proto-Oncogene Proteins c-akt Signal Transduction Titanium
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/176190
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1761902024-04-05T09:03:50Z Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells Tee, J.K Ng, L.Y Koh, H.Y Leong, D.T Ho, H.K CHEMICAL & BIOMOLECULAR ENGINEERING PHARMACY nanoparticle titanium dioxide protein kinase B titanium titanium dioxide apoptosis Article cell adhesion cell proliferation cell viability chronic liver disease disease exacerbation drug delivery system drug penetration endothelium cell enzyme linked immunosorbent assay flow cytometry human human cell immunofluorescence liver cell liver sinusoidal endothelial cell oxidative stress particle size protein expression real time polymerase chain reaction signal transduction Western blotting zeta potential cell communication cell culture cell survival chemistry cytology drug effect endothelium cell liver liver cell metabolism pathology permeability Cell Communication Cell Survival Cells, Cultured Endothelial Cells Hepatocytes Humans Liver Nanoparticles Oxidative Stress Permeability Proto-Oncogene Proteins c-akt Signal Transduction Titanium 10.3390/ijms20010035 International Journal of Molecular Sciences 20 1 35 2020-09-14T08:25:48Z 2020-09-14T08:25:48Z 2019 Article Tee, J.K, Ng, L.Y, Koh, H.Y, Leong, D.T, Ho, H.K (2019). Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells. International Journal of Molecular Sciences 20 (1) : 35. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms20010035 1661-6596 https://scholarbank.nus.edu.sg/handle/10635/176190 Unpaywall 20200831
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	nanoparticle titanium dioxide protein kinase B titanium titanium dioxide apoptosis Article cell adhesion cell proliferation cell viability chronic liver disease disease exacerbation drug delivery system drug penetration endothelium cell enzyme linked immunosorbent assay flow cytometry human human cell immunofluorescence liver cell liver sinusoidal endothelial cell oxidative stress particle size protein expression real time polymerase chain reaction signal transduction Western blotting zeta potential cell communication cell culture cell survival chemistry cytology drug effect endothelium cell liver liver cell metabolism pathology permeability Cell Communication Cell Survival Cells, Cultured Endothelial Cells Hepatocytes Humans Liver Nanoparticles Oxidative Stress Permeability Proto-Oncogene Proteins c-akt Signal Transduction Titanium
spellingShingle	nanoparticle titanium dioxide protein kinase B titanium titanium dioxide apoptosis Article cell adhesion cell proliferation cell viability chronic liver disease disease exacerbation drug delivery system drug penetration endothelium cell enzyme linked immunosorbent assay flow cytometry human human cell immunofluorescence liver cell liver sinusoidal endothelial cell oxidative stress particle size protein expression real time polymerase chain reaction signal transduction Western blotting zeta potential cell communication cell culture cell survival chemistry cytology drug effect endothelium cell liver liver cell metabolism pathology permeability Cell Communication Cell Survival Cells, Cultured Endothelial Cells Hepatocytes Humans Liver Nanoparticles Oxidative Stress Permeability Proto-Oncogene Proteins c-akt Signal Transduction Titanium Tee, J.K Ng, L.Y Koh, H.Y Leong, D.T Ho, H.K Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
description	10.3390/ijms20010035
author2	CHEMICAL & BIOMOLECULAR ENGINEERING
author_facet	CHEMICAL & BIOMOLECULAR ENGINEERING Tee, J.K Ng, L.Y Koh, H.Y Leong, D.T Ho, H.K
format	Article
author	Tee, J.K Ng, L.Y Koh, H.Y Leong, D.T Ho, H.K
author_sort	Tee, J.K
title	Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
title_short	Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
title_full	Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
title_fullStr	Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
title_full_unstemmed	Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
title_sort	titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/176190
_version_	1800914420576026624

Titanium dioxide nanoparticles enhance leakiness and drug permeability in primary human hepatic sinusoidal endothelial cells

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