A. Donnelly et al., THE INFLUENCE OF LIPOPHILICITY UPON THE NASAL ABSORPTION OF A SERIES OF HEXAPEPTIDES, International journal of pharmaceutics, 135(1-2), 1996, pp. 191-197
A series of glycine (G) and phenylalanine (F) containing hexapeptides
have been synthesised that vary only in the proportions of their const
ituent amino acids, The peptides FGGGGG (F(1)G(5)), FFGGGG (F(2)G(4))
and FFFGGG (F(3)G(3)) were characterised by their distribution coeffic
ients and it was found that a linear relationship existed between logo
and the number of phenylalanine residues. Metabolism by aminopeptidas
es is a major barrier to the nasal absorption of labile peptides. To o
vercome this the peptides were synthesised with D-phenylalanine that r
endered the peptides totally resistant to metabolism by leucine aminop
eptidase. The extent of nasal absorption of the peptides was measured
by a nasal perfusion technique. The peptides were generally poorly abs
orbed with only 20.2% (D-F(1)G(5)), 19.7% (D-F(2)G(4)) and 25.9% (D-F(
3)G(3)) disappearing from the perfusate after 105 min. The results als
o illustrate that the extent of absorption does not correspond closely
with differences in lipophilicity of the peptides.