L. Illum et al., NASAL ADMINISTRATION OF MORPHINE-6-GLUCURONIDE IN SHEEP - A PHARMACOKINETIC STUDY, Biopharmaceutics & drug disposition, 17(8), 1996, pp. 717-724
The pharmacokinetics of morphine-6-glucuronide (M6G) after both intrav
enous dosing and nasal administration were studied in sheep. The nasal
formulation consisted of M6G in combination with an absorption promot
ing delivery system in the form of chitosan. The mean half-life of M6G
after intravenous administration was 51.0 +/- 8.2 min and that after
intranasal dosing was 45.0 +/- 5.5 min. M6G clearance and volume of di
stribution were 5.4 +/- 1.5 mL min(-1)kg(-1) and 0.4 +/- 0.1 L kg(-1)
respectively. The plasma profile after nasal administration demonstrat
ed rapid absorption of M6G. The bioavailability of M6G in the chitosan
formulation was found to be 31.4%. These results suggest that M6G adm
inistered in combination with the chitosan delivery system may be cons
idered as a suitable non-parenteral means of administering this analge
sic.