Hepatocytes Immobilised by Microencapsulation in Artificial Cells: Effects on Hyperbilirubihemia in Gunn Rats
- 1 January 1989
- journal article
- research article
- Published by Taylor & Francis in Biomaterials, Artificial Cells and Artificial Organs
- Vol. 17 (4) , 403-411
- https://doi.org/10.3109/10731198909118855
Abstract
The possibility of using hepatocytes encapsulated in a calciumalginate-polylysine matrix to lower bilirubin levels in hyperbilirubinemia was investigated. The animal model was the Gunn rat. The microencapsulated hepatocytes were injected intraperitoneally. 15×106 microencapsulated hepatocytes from Wistar rats, lowered the bilirubin from 14 mg/100 ml to 6 mg/100 ml after 20 days. The bilirubin is still depressed after 90 days. After encapsulation, Sprague-Dawley hepatocytes were as effective as free hepatocytes in lowering bilirubin levels in Gunn rats. After 68 days, the free Sprague-Dawley hepatocytes were not rejected.This publication has 15 references indexed in Scilit:
- The Viability and Regeneration of Artificial Cell Microencapsulated Rat Hepatocyte Xenograft Transplants in MiceBiomaterials, Artificial Cells and Artificial Organs, 1988
- Microencapsulated Hepatocytes: an in Vitro and in Vivo StudyBiomaterials, Artificial Cells and Artificial Organs, 1987
- Replacement of Liver Function in Rats by Transplantation of Microcarrier-Attached HepatocytesScience, 1986
- SPONTANEOUS LONG-TERM ACCEPTANCE OF RT-1-INCOMPATIBLE LIVER ALLOGRAFTS IN INBRED RATSTransplantation, 1983
- Microencapsulated Islets as Bioartificial Endocrine PancreasScience, 1980
- SPECIFIC TRANSPLANTATION TOLERANCE INDUCED BY SPONTANEOUSLY TOLERATED LIVER ALLOGRAFT IN INBRED STRAINS OF RATSTransplantation, 1980
- Chapter 4 Preparation of Isolated Rat Liver CellsPublished by Elsevier ,1976
- SEMIPERMEABLE AQUEOUS MICROCAPSULES: I. PREPARATION AND PROPERTIESCanadian Journal of Physiology and Pharmacology, 1966
- Semipermeable MicrocapsulesScience, 1964
- METABOLISM AND DISPOSITION OF C14-BILIRUBIN IN CONGENITAL NONHEMOLYTIC JAUNDICE*Journal of Clinical Investigation, 1963