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Evaluation Methods and Design for Bioartificial Liver Based on Perfusion Model  

Park Yueng Guen (Radiation Application Research Division)
Ryu Hwa-Won (Faculty of Applied Chemical Engineering, Chonnam National University, Institute of Bioindustrial Technology, Chonnam National University)
Publication Information
Biotechnology and Bioprocess Engineering:BBE / v.10, no.1, 2005 , pp. 9-15 More about this Journal
Abstract
A bioartificial liver (BAL) is a medical device entrapping living hepatocytes or immortalized cells derived from hepatocytes. Many efforts have already been made to maintain the functions of the hepatocytes in a BAL device over a long term. However, there is still some uncertainty as to their efficacy. and their limitations are unclear. Therefore, it is important to quantitatively evaluate the metabolic functions of a BAL. In previous studies on in vitro BAL devices, two test methods, an initial bolus loading and constant-rate infusion plus initial bolus loading, were theoretically carried out to obtain physiologic data on drugs. However, in the current study, the same two methods were used as a perfusion model and derived the same clearance characterized by an interrelationship between the perfusate flow rate and intrinsic clearance. The interrelationship indicated that the CL increased with an increasing perfusate flow rate and approached its maximum value, i.e. intrinsic clearance. In addition, to set up an in vivo BAL system, the toxic plateau levels in the BAL system were calculated for both series and parallel circuit models. The series model had a lower plateau level than the parellel model. The difference in the toxic plateau levels between the parallel and series models increased with an increasing number of BAL cartridges.
Keywords
bioartificial liver; perfusion model; clearance; flow rate; mass transfer;
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1 de Bartolo, L., S. G. Jarosch-Von, A. Haverich, and A. Bader (2000) A novel full-scale flat membrane bioreactor utilizing porcine hepatocytes: Cell viability and tissuespecific functions. Biotechnol. Prog. 16: 102-108   DOI   ScienceOn
2 Tilles, A. W., H. Baskaran, P. Roy, M. L. Yarmush, and M. Toner (2001) Effect of oxygenation and flow on the viability and function of rat hepatocytes cocultured in a microchannel flat-plate bioreactor. Biotechnol. Bioeng. 73: 379- 389   DOI   ScienceOn
3 Patankar, D. and T. Oolman (1991) Wall-growth hollow fiber reactor for tissue culture: I. Preliminary experiments. Biotechnol. Bioeng. 37: 80-92   DOI   PUBMED
4 Rowland, M. and T. N. Tozer (1989) Clinical Pharmacokinetics: Concepts an Applications. Lea & Febiger, Philadelphia, USA
5 Gion, T., M. Shimada, K. Shirabe, K. Nakazawa, H. Ijima, T. Matsushita, and K. Funatsu (1999) Evaluation of a hybrid artificial liver using a polyurethane foam packed-bed culture system in dogs. J. Surg. Res. 82: 131-136   DOI   ScienceOn
6 Lanza, R. P., D. H. Butler, K. M. Borland, J. E. Staruk, D. L. Faustman, B. A. Solomen, T. E. Muller, R. G. Rupp, T. Maki, A. P. Monaco, and W. L. Chick (1991) Xeno transplantation of canine, bovine, and porcine islets in diabetic rats without immunosuppression. Proc. Natl. Acad. Sci. USA 88: 11100-11104   DOI   ScienceOn
7 Park, Y. G., H. Iwata, S. Satoh, T. Uesugi, and H.–W. Ryu (2003) Method for evaluating metabolic functions of drugs in bioartificial liver. Biotechnol. Bioprocess Eng. 8: 41-46   DOI   ScienceOn
8 Hughes, R. D. and R. Williams (1996) Use of bioartificial and artificial liver support devices. Sem. Liver Dis. 16: 435-444   DOI   ScienceOn
9 Nyberg, S. L., W. D. Payne, B. Amiot, K. Shirabe, R. P. Remmel, W. S. Hu, and F. B. Cerra (1993) Demonstration of biochemical function by extracorporeal xenohepatocytes in an anhepatic animal model. Transplant. Proc. 25: 1944-1945
10 Demetriou, A. A., J. Rozga, L. Podesta, E. Lepage, E. Morsiani, A. D. Moscioni, A. Hoffman, M. McGrath, L. Kong, H. Rosen, F. Villamil, G. Woolf, J. Vierling, and L. Makowka (1995) Early clinical experience with a hybrid bioartificial liver. Scand. J. Gastroenterol. 30: 111-117   DOI   PUBMED
11 Sakai, Y., K. Naruse, I. Nagashima, T. Muto, and M. Suzuki (1999) A new bioartificial liver using porcine hepatocytes spheroids in high-cell-density suspension perfusion culture: In vivo performance in synthesized culture medium and in 100% human plasma. Cell Transplant. 8: 531- 541   DOI
12 Sardonini, C. A. and D. DiBiasio (1992) An investigation of the diffusion-limited growth of animal cells around single hollow fibers. Biotechnol. Bioeng. 40: 1233-1242   DOI   PUBMED
13 Yarmush, M. L., J. C. Dunn, and R. G. Tompkins (1992) Assessment of artificial liver support technology. Cell Transplant. 1: 323-341   DOI
14 Park, Y. G., Y. S. Son, and H.-W. Ryu (2003) Perfusion model for detoxification of drugs in a bioartificial liver. Int. J. Artif. Organs 26: 224-231
15 Rozga, J., E. Morsiani, H. Fujioka, and A. A. Demetriou (1993) Anhepatic pig-evaluation of a model. J. Hepatol. 18: S72-S79   DOI
16 Sussman, N. L., G. T. Gislason, C. A. Conlin, and J. H. Kelly (1994) The hepatix extracorporeal liver assist device: Initial clinical experience. Artif. Organs. 18: 390-396   DOI   ScienceOn
17 Asonuma, K., J. C. Gibert, J. E. Stein, T. Takeda, and J. P. Vacanti (1992) Quantitation of transplanted hepatic mass necessary to cure the gunn rate model of hyperbilirubinemia. J. Pediat. Surg. 27: 298-301   DOI   ScienceOn
18 Kamlot, A., J. Rozga, F. D. Watanabe, and A. A. Demetriou (1996) Review: Artificial liver support system. Biotechnol. Bioeng. 50: 382-391   DOI   PUBMED   ScienceOn