The goal of oral insulin delivery devices is to protect the sensitive drug
from proteolytic degradation in the stomach and upper portion of the small
intestine. In this work, we investigate the use of pH-responsive, poly(meth
acrylic-g-ethylene glycol) hydrogels as oral delivery vehicles for insulin.
Insulin was loaded into polymeric microspheres and administered orally to
healthy and diabetic Wistar rats, In the acidic environment of the stomach,
the gels were unswollen due to the formation of intermolecular polymer com
plexes. The insulin remained in the gel and was protected from proteolytic
degradation. In the basic and neutral environments of the intestine, the co
mplexes dissociated which resulted in rapid gel swelling and insulin releas
e. Within 2 h of administration of the insulin-containing polymers, strong
dose-dependent hypoglycemic effects were observed in both healthy and diabe
tic rats. These effects lasted for up to 8 h following administration.