A method for processing and embedding alginate-polylysine microencapsu
lated pancreatic tissue in glycol methacrylate resin (GMA) is describe
d. Fixation in 4% phosphate buffered formaldehyde, processing in ascen
ding concentrations of glycol methacrylate monomer and embedding in Te
chnovit 7100 results in well preserved morphological details of hydrog
els, hydrogel-cell interfaces, and encapsulated pancreatic tissue, Rou
tine staining with Loeffler's methylene blue, hematoxylin and eosin, a
nd Romanovsky-Giemsa gave excellent images of the GMA embedded alginat
e polylysine membrane and tissues allowing cells on the outside of the
capsule to be analyzed effectively as part of the foreign body reacti
on against the capsule membrane.