Oxygen transfer in a diffusion-limited hollow fiber bioartificial liver

被引:75
作者
Hay, PD
Veitch, AR
Smith, MD
Cousins, RB
Gaylor, JDS
机构
[1] Univ Strathclyde, Bioengn Unit, Wolfson Ctr, Glasgow G4 0NW, Lanark, Scotland
[2] Univ Strathclyde, Dept Stat & Modelling Sci, Glasgow G4 0NW, Lanark, Scotland
[3] Univ Strathclyde, Dept Chem & Proc Engn, Glasgow G4 0NW, Lanark, Scotland
关键词
bioartifical liver; oxygen transport; hollow fiber; modeling;
D O I
10.1046/j.1525-1594.2000.06499.x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A mathematical model was developed to predict oxygen transport in a hollow fiber bioartificial liver device. Model parameters were taken from the Hepatix ELAD configuration; a blood perfused hollow fiber cartridge with hepatocytes seeded in the extracapillary space. Cellular oxygen uptake is based on Michaelis-Menten kinetics, and nonlinear oxygen transport in the blood is considered. The effect of modulating three important parameters is investigated, namely, the Michaelis-Menten constants V-m (volumetric oxygen consumption of the hepatocytes) and K-m (half-saturation constant), and hollow fiber oxygen permeability. A computer implementation of the model is used to assess whether a given cell mass could be maintained within such a device. The results suggest that liver cell lines possessing low rates of oxygen consumption could be maintained if membranes of sufficiently high oxygen permeability are used. For primary hepatocytes, which have much higher oxygen demands, radial transport of oxygen is rate limiting, and the axial-flow hollow fiber cartridge is thus an inappropriate design fur use as a bioartificial liver with primary hepatocytes.
引用
收藏
页码:278 / 288
页数:11
相关论文
共 25 条
[1]  
BHATIA SN, 1996, CELL ENG, V1, P125
[2]   Modeling of axial-flow hollow fiber cell culture bioreactors [J].
Brotherton, JD ;
Chau, PC .
BIOTECHNOLOGY PROGRESS, 1996, 12 (05) :575-590
[3]  
BUERK DG, 1978, ADV EXP MED BIOL, V94, P225
[4]   Technique for the kinetic characterization of the metabolic reactions of hepatocytes in adhesion culture [J].
Catapano, G ;
De Bartolo, L .
BIOTECHNOLOGY PROGRESS, 1998, 14 (03) :500-507
[5]   Mass transfer limitations to the performance of membrane bioartificial liver support devices [J].
Catapano, G .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1996, 19 (01) :18-35
[6]   OPTIMUM FIBER SPACING IN A HOLLOW FIBER BIOREACTOR [J].
CHRESAND, TJ ;
GILLIES, RJ ;
DALE, BE .
BIOTECHNOLOGY AND BIOENGINEERING, 1988, 32 (08) :983-992
[7]  
De Groot H., 1988, OXYGEN SENSING TISSU, P49
[8]  
DEGROOT H, 1985, ARCH BIOCHEM BIOPHYS, V243, P563
[9]   Pilot-controlled trial of the extracorporeal liver assist device in acute liver failure [J].
Ellis, AJ ;
Hughes, RD ;
Wendon, JA ;
Dunne, J ;
Langley, PG ;
Kelly, JH ;
Gislason, GT ;
Sussman, NL ;
Williams, R .
HEPATOLOGY, 1996, 24 (06) :1446-1451
[10]   In vitro evaluation of a novel bioreactor based on an integral oxygenator and a spirally wound nonwoven polyester matrix for hepatocyte culture as small aggregates [J].
Flendrig, LM ;
laSoe, JW ;
Jorning, GGA ;
Steenbeek, A ;
Karlsen, OT ;
Bovee, WMMJ ;
Ladiges, NCJJ ;
teVelde, AA ;
Chamuleau, RAFM .
JOURNAL OF HEPATOLOGY, 1997, 26 (06) :1379-1392