Determination of pore size distribution at the cell-hydrogel interface

<p>Abstract</p> <p>Background</p> <p>Analyses of the pore size distribution in 3D matrices such as the cell-hydrogel interface are very useful when studying changes and modifications produced as a result of cellular growth and proliferation within the matrix, as pore si...

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Main Authors: Nowicki Marcin, Díaz-Cuenca Aránzazu, Dietrich-Braumann Ulf, Leal-Egaña Aldo, Bader Augustinus
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Journal of Nanobiotechnology
Online Access:http://www.jnanobiotechnology.com/content/9/1/24
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spelling doaj-bea66c43121c44c58cb60fcacbce8d242020-11-25T01:39:11ZengBMCJournal of Nanobiotechnology1477-31552011-05-01912410.1186/1477-3155-9-24Determination of pore size distribution at the cell-hydrogel interfaceNowicki MarcinDíaz-Cuenca AránzazuDietrich-Braumann UlfLeal-Egaña AldoBader Augustinus<p>Abstract</p> <p>Background</p> <p>Analyses of the pore size distribution in 3D matrices such as the cell-hydrogel interface are very useful when studying changes and modifications produced as a result of cellular growth and proliferation within the matrix, as pore size distribution plays an important role in the signaling and microenvironment stimuli imparted to the cells. However, the majority of the methods for the assessment of the porosity in biomaterials are not suitable to give quantitative information about the textural properties of these nano-interfaces.</p> <p>Findings</p> <p>Here, we report a methodology for determining pore size distribution at the cell-hydrogel interface, and the depth of the matrix modified by cell growth by entrapped HepG<sub>2 </sub>cells in microcapsules made of 0.8% and 1.4% w/v alginate. The method is based on the estimation of the shortest distance between two points of the fibril-like network hydrogel structures using image analysis of TEM pictures. Values of pore size distribution determined using the presented method and those obtained by nitrogen physisorption measurements were compared, showing good agreement. A combination of these methodologies and a study of the cell-hydrogel interface at various cell culture times showed that after three days of culture, HepG<sub>2 </sub>cells growing in hydrogels composed of 0.8% w/v alginate had more coarse of pores at depths up to 40 nm inwards (a phenomenon most notable in the first 20 nm from the interface). This coarsening phenomenon was weakly observed in the case of cells cultured in hydrogels composed of 1.4% w/v alginate.</p> <p>Conclusions</p> <p>The method purposed in this paper allows us to obtain information about the radial deformation of the hydrogel matrix due to cell growth, and the consequent modification of the pore size distribution pattern surrounding the cells, which are extremely important for a wide spectrum of biotechnological, pharmaceutical and biomedical applications.</p> http://www.jnanobiotechnology.com/content/9/1/24
collection DOAJ
language English
format Article
sources DOAJ
author Nowicki Marcin
Díaz-Cuenca Aránzazu
Dietrich-Braumann Ulf
Leal-Egaña Aldo
Bader Augustinus
spellingShingle Nowicki Marcin
Díaz-Cuenca Aránzazu
Dietrich-Braumann Ulf
Leal-Egaña Aldo
Bader Augustinus
Determination of pore size distribution at the cell-hydrogel interface
Journal of Nanobiotechnology
author_facet Nowicki Marcin
Díaz-Cuenca Aránzazu
Dietrich-Braumann Ulf
Leal-Egaña Aldo
Bader Augustinus
author_sort Nowicki Marcin
title Determination of pore size distribution at the cell-hydrogel interface
title_short Determination of pore size distribution at the cell-hydrogel interface
title_full Determination of pore size distribution at the cell-hydrogel interface
title_fullStr Determination of pore size distribution at the cell-hydrogel interface
title_full_unstemmed Determination of pore size distribution at the cell-hydrogel interface
title_sort determination of pore size distribution at the cell-hydrogel interface
publisher BMC
series Journal of Nanobiotechnology
issn 1477-3155
publishDate 2011-05-01
description <p>Abstract</p> <p>Background</p> <p>Analyses of the pore size distribution in 3D matrices such as the cell-hydrogel interface are very useful when studying changes and modifications produced as a result of cellular growth and proliferation within the matrix, as pore size distribution plays an important role in the signaling and microenvironment stimuli imparted to the cells. However, the majority of the methods for the assessment of the porosity in biomaterials are not suitable to give quantitative information about the textural properties of these nano-interfaces.</p> <p>Findings</p> <p>Here, we report a methodology for determining pore size distribution at the cell-hydrogel interface, and the depth of the matrix modified by cell growth by entrapped HepG<sub>2 </sub>cells in microcapsules made of 0.8% and 1.4% w/v alginate. The method is based on the estimation of the shortest distance between two points of the fibril-like network hydrogel structures using image analysis of TEM pictures. Values of pore size distribution determined using the presented method and those obtained by nitrogen physisorption measurements were compared, showing good agreement. A combination of these methodologies and a study of the cell-hydrogel interface at various cell culture times showed that after three days of culture, HepG<sub>2 </sub>cells growing in hydrogels composed of 0.8% w/v alginate had more coarse of pores at depths up to 40 nm inwards (a phenomenon most notable in the first 20 nm from the interface). This coarsening phenomenon was weakly observed in the case of cells cultured in hydrogels composed of 1.4% w/v alginate.</p> <p>Conclusions</p> <p>The method purposed in this paper allows us to obtain information about the radial deformation of the hydrogel matrix due to cell growth, and the consequent modification of the pore size distribution pattern surrounding the cells, which are extremely important for a wide spectrum of biotechnological, pharmaceutical and biomedical applications.</p>
url http://www.jnanobiotechnology.com/content/9/1/24
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