Abstract
The oral delivery of peptidic drugs is problematic because of their degradation in the gastrointestinal tract and low absorption through the intestinal mucosa. Earlier in vitro studies with two series of digestion-resistant, radiolabeled peptides that varied in physical properties (molecular weight, lipophilicity, and hydrogen bonding sites) had suggested that intestinal transport of these peptides was most influenced by the number of hydrogen bonding sites, the major determinant of desolvation energy. To determine whether this correlation could be confirmed in vivo, intestinal absorption was determined by comparing the biliary and urinary recovery of these radiolabeled peptides in rats given intravenous or intraduodenal doses. Absorption was inversely correlated to the number of calculated hydrogen bonding sites for the model peptides, similar to what had been found in vitro. Clearance by liver and kidneys appeared to be unaffected by desolvation energy but was well correlated with lipophilicity.
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Karls, M.S., Rush, B.D., Wilkinson, K.F. et al. Desolvation Energy: A Major Determinant of Absorption, But Not Clearance, of Peptides in Rats. Pharm Res 8, 1477–1481 (1991). https://doi.org/10.1023/A:1015882030289
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DOI: https://doi.org/10.1023/A:1015882030289