z-logo
Premium
Culture of primary rat hepatocytes within porous chitosan scaffolds
Author(s) -
Li Jieliang,
Pan Jilun,
Zhang Liguo,
Guo Xinji,
Yu Yaoting
Publication year - 2003
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.10076
Subject(s) - chitosan , biopolymer , monolayer , materials science , scanning electron microscope , membrane , biophysics , albumin , hepatocyte , chemical engineering , porosity , biomedical engineering , nanotechnology , chemistry , biochemistry , in vitro , polymer , composite material , biology , medicine , engineering
Chitosan is considered to be a very promising biopolymer for various biomedical and pharmaceutical uses because of its nontoxic and biocompatible natures (Chandy T, Shama P. Biomater Artif Cells Artif Org 1990;18:1–24). In this study, we prepared porous chitosan scaffolds by lyophilization of chitosan solution. The scaffolds were modified with water‐soluble polyanionic species such as alginate and heparin. The pore structures of these scaffolds were viewed via light and scanning electron microscopy. The scaffolds prepared have a high porosity of ∼90% with mean pore sizes from 50 to 200 μm. They were used as substrates for hepatocytes culture. The cell attachment ratio was much higher than on monolayer membrane and hepatocytes exhibited a round cellular morphology with many microvilli evident on the surface of the cells. Metabolic activities of the cells were evaluated in terms of albumin secretion and urea synthesis. It was found that hepatocytes cultured on the modified scaffolds showed an increase in albumin secretion during the first 4 days and were more stable than those on monolayer membrane and nonmodified scaffolds. Therefore, primary rat hepatocytes cultured on modified scaffolds would be beneficial to liver assist device. © 2003 Wiley Periodicals, Inc. J Biomed Mater Res 67A: 938–943, 2003

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom