Characterization of the distribution of matter in hybrid liver support devices where cells are cultured in a 3-D membrane network or on flat substrata

Citation
G. Catapano et al., Characterization of the distribution of matter in hybrid liver support devices where cells are cultured in a 3-D membrane network or on flat substrata, INT J ARTIF, 24(2), 2001, pp. 102-109
Citations number
15
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology
Journal title
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS
ISSN journal
03913988 → ACNP
Volume
24
Issue
2
Year of publication
2001
Pages
102 - 109
Database
ISI
SICI code
0391-3988(200102)24:2<102:COTDOM>2.0.ZU;2-M
Abstract
Bioreactors for liver assist tested on small animal models are generally sc aled-up to treat humans by increasing their size to host a given liver cell mass. In this process, liver cell function in different culture devices is often established based on the metabolite concentration difference between the bioreactor inlet and outlet irrespective of how matter distributes in the bioreactor. In this paper, we report our investigation aimed at establishing whether bi oreactor design and operating conditions influence the distribution of matt er in two bioreactors proposed for liver assist. We investigated a clinical -scale bioreactor where liver cells are cultured around a three-dimensional network of hollow fiber membranes and a laboratory-scale bioreactor with c ells adherent on collagen-coated flat substrata. The distribution of matter was characterized under different operating modes and conditions in terms of the bioreactor residence time distribution evaluated by means of tracer experiments and modeled as a cascade of N stirred tanks with the same volum e. Under conditions recommended by the manufacturers, matter distributed un iformly in the clinical-scale bioreactor as a result of the intense backmix ing (N=1) whereas axial mixing was negligible in the laboratory-scale biore actor (N=8). Switching from recycle to single-pass operation definitely red uced axial mixing in the clinical-scale bioreactor (N=2). Increasing feed f low rate significantly enhanced axial mixing in the laboratory-scale biorea ctor (N=4). The effects of design, operating mode and conditions on matter distribution in bioreactors for liver cell culture suggest that characteriz ation of the distribution of matter is a necessary step in the scale-up of bioreactors for liver assist and when function of liver cells cultured in d ifferent bioreactors is evaluated and compared.