The purpose of the present study of buprenorphine is to add information abo
ut the correlation between various animal models and nasal bioavailabilitie
s in man. PEG 300 was added to one formulation to study whether the additio
n of the co-solvent results in the same absorption pattern as seen for shee
p. The bioavailability of intranasal buprenorphine 0.6 mg in PEG 300 and 5%
dextrose was assessed in a cross-over study in six rabbits. The mean bioav
ailabilities, T-max and C-max were 46% (S.D. +/- 13) and 53% (S.D. +/- 17),
8 and 12 min, 28 and 27 ng/ml for 30% PEG 300 and 5% dextrose, respectivel
y. No significant differences were found between the nasal buprenorphine fo
rmulations. The bioavailabilities in rabbit and sheep, respectively, were a
pproximate to2.5 and four times higher than for man. The absorption rate wa
s faster for rabbit and sheep than for man. It appears that rabbit and shee
p bioavailability differ from humans, especially with respect to rate. PEG
300 do not increase the bioavailability of buprenorphine. (C) 2001 Elsevier
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