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Research article summary (published 30 May 1996):

Pharmacokinetic aspects of rectal formulations of temazepam.

Full Abstract

An in vitro/in vivo study was carried out with different rectal formulations of temazepam. Pharmacokinetic data were determined in a cross-over study in 10 volunteers after rectal administration of 10 mg temazepam as a polyethylene glycol based suppository (selected from in vitro data), a liquid-filled capsule and a micro-enema respectively, using oral administration of a liquid-filled capsule as a reference. Serum levels of temazepam indicate an instantaneous and complete release from the micro-enema (Frel = 0.94 +/- 0.21, Cmax 205 +/- 36.9 micrograms/l, tmax 0.49 +/- 0.31 hour) and a slower but complete release of temazepam from the suppository (Frel = 1.10 +/- 0.25, Cmax 202 +/- 41.3 micrograms/l, tmax 1.48 +/- 0.41 hour). A high interindividual variation in absorption profiles was observed after rectal administration of the liquid-filled capsule (Frel 0.72 +/- 0.36, Cmax 182 +/- 122 micrograms/l, tmax 4.08 +/- 4.28 hour), which makes it less suitable for rectal use. The micro-enema and suppository appear to be useful as rectal formulations for temazepam.

 

Author information

Author/s: Hanff, L M (LM); Rutten, W J (WJ);

Affiliation: Department of Pharmacy, University Hospital Rotterdam, The Netherlands.

Journal and publication information

Publication Type: Comparative Study; Journal Article

Journal: Pharmacy world & science : PWS (Pharm World Sci), published in NETHERLANDS. (Language: eng)

Reference: 1996-Jun; vol 18 (issue 3) : pp 114-9

Dates: Created 1997/04/02; Completed 1997/04/02; Revised 2006/11/15;

PMID: 8826537, status: MEDLINE (last retrieved date: 2/18/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

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Associated Chemicals: Anti-Anxiety Agents (0) ; Capsules (0) ; Excipients (0) ; Polyethylene Glycols (0) ; Solutions (0) ; Suppositories (0) ; Temazepam (846-50-4)

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