The microencapsulation technique is being used successfully in various
types of cells for providing a substratum for long-term survival and
immunoprotection to immobilized transplanted cells. Rat hepatocytes we
re microencapsulated in alginic acid poly-l-lysine membrane and transp
lanted intraperitoneally in rabbits. The animals were followed up to s
tudy the functional capacity of transplanted hepatocytes by assessing
ureagenesis and the efficacy of the capsule membrane to provide a phys
ical barrier between the host's immune system and the encapsulated hep
atocytes, assessed by no evidence of hepatocyte rejection by the host
for up to 2 months, The transplanted animals were sacrificed by cervic
al dislocation after 15, 30, 45 and 60 days. The transplanted capsules
were retrieved and the hepatocytes were studied for their capacity fo
r ureagenesis. The capsules were found intact even after 60 days of tr
ansplantation. The retrieval was 75% with 80% of viable cells displayi
ng normal functional capacity to produce urea. Therefore, it may be co
ncluded that the microencapsulation technique is effective in maintain
ing functional capacity and providing a physical barrier between the h
ost's immune system and immobilized cells.