Intranasal bioavailability of buprenorphine in rabbit correlated to sheep and man

Citation
K. Lindhardt et al., Intranasal bioavailability of buprenorphine in rabbit correlated to sheep and man, INT J PHARM, 217(1-2), 2001, pp. 121-126
Citations number
20
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
ISSN journal
03785173 → ACNP
Volume
217
Issue
1-2
Year of publication
2001
Pages
121 - 126
Database
ISI
SICI code
0378-5173(20010417)217:1-2<121:IBOBIR>2.0.ZU;2-M
Abstract
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 Science B.V. All rights reserved.