THE PERMEABILITY OF EUDRAGIT RL AND HEMA MMA MICROCAPSULES TO GLUCOSE AND INULIN

Measurement of the rate of glucose diffusion from EUDGRAGIT RL and HEMA‐MMA microcapsules coupled with a Thiele modulus/Biot number analysis of the glucose utilization rate suggests that pancreatic islets and CHO (Chinese hamster ovary) cells (at moderate to high cell densities) should not be adversely affected by the diffusion restrictions associated with these capsule membranes. The mass transfer coefficients for glucose at 20 °C were of the same order of magnitude for both capsules, based on release measurements: ∼5 × 10−6 cm/s for EUDRAGIT RL and ∼2 × 10−6 for HEMA‐MMA. Inulin release from EUDRAGIT RL was slower than for glucose (mass transfer coefficient 14 ± 4 × 10−8 cm/s). The Thiele moduli were much less than 1, either for a single islet at the center of a capsule or CHO cells uniformly distributed throughout a capsule at 10−6 cells/ mL, so that diffusion restrictions within the cells in EUDRAGIT RL or 800 μm HEMA‐MMA capsules should be negligible. The ratio of external to internal diffusion resistance (Biot number) was less than 1, so that at most, only a small diffusion effect on glucose utilization should be expected (i.e., the overall effectiveness factors were greater than 0.8). These calculations were consistent with experimental observation of encapsulated islet behavior but not fully with CHO cell behavior. Permeability restricted cell viability and growth is potentially a major limitation of encapsulated cells; further analysis is warranted. Copyright © 1990 John Wiley & Sons, Inc.