The use of different forms of human red blood cells as ol al carrier s
ystems for human insulin in vivo was the subject of this investigation
. Male Wistar rats were made diabetic by a single intraperitoneal inje
ction of streptozocin (100 mg/kg). Three days after the injection, rat
s were found diabetic as evidenced by elevated fasted blood glucose co
ncentration (200 mg/dl or higher). Rats received orally one of the fol
lowing (100 U, 2 mi): an insulin solution, a ghosts-insulin suspension
, a vesicles-insulin suspension, a liposomes-ghosts-insulin suspension
, or a liposomes-vesicles-insulin suspension. Free carrier suspensions
or sodium chloride solution (0.9%) were also given orally as controls
. Blood glucose concentration was determined just before administratio
n and at 1, 2, 3, 4, 5, 6, and 7 hr post administration. The results s
how that all treatment groups, except liposomes-ghosts-insulin, were s
ignificantly different statistically from their respective controls (i
.e., the free carriers).