This paper investigates the nasal absorption of the LHRH-analogue, gosereli
n, and the feasibility of producing a formulation with improved nasal bioav
ailability. It is shown that the use of chitosan in a nasal delivery system
has the ability of providing significantly enhanced nasal absorption in th
e sheep model. Bioavailability of 11.6, 25.6 and 36.6%, respectively, were
obtained for a goserelin chitosan solution formulation, a dry blend of chit
osan and goserelin, or goserelin freeze-dried with a cross-linked chitosan
microsphere formulation. It is concluded that nasal goserelin formulations
that show highly therapeutically relevant serum goserelin levels can be pro
duced. Such formulations would be of great benefit to the treatment of vari
ous diseases such as endometriosis, prostate cancer and cryptorchidism or i
n NF treatment regimens.