Literature DB >> 6747022

Absolute bioavailability and effect of food and antacid on diazepam absorption from a slow-release preparation.

A Locniskar, D J Greenblatt, M A Zinny, J S Harmatz, R I Shader.   

Abstract

A series of healthy volunteers received a single 7.5-mg intravenous dose of diazepam on one occasion and a single 15-mg oral dose of slow-release diazepam (DZ-SR) on another occasion. Diazepam concentrations were measured by gas chromatography in multiple plasma samples drawn during seven days after each dose. Absorption of diazepam from DZ-SR was slow, with mean +/- S.E. peak concentrations attained at 3.8 +/- 0.5 hours after dosage. Absolute bioavailability of DZ-SR averaged 0.98 +/- 0.06. In two other studies, diazepam absorption from DZ-SR was evaluated when coadministered with a standard breakfast or with an antacid preparation (Maalox). Neither food nor antacid altered the rate of diazepam absorption and did not impair the completeness of absorption. Higher peak total plasma diazepam concentrations occurred in the postprandial as opposed to the fasting state, but this was an artifact of reduced protein binding (increased free fraction) due to fasting. Thus, diazepam absorption from DZ-SR is slow and essentially complete.

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Year:  1984        PMID: 6747022     DOI: 10.1002/j.1552-4604.1984.tb02782.x

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  2 in total

1.  Intermittent drug dosing intervals guided by the operational multiple dosing half lives for predictable plasma accumulation and fluctuation.

Authors:  Anita Grover; Leslie Z Benet
Journal:  J Pharmacokinet Pharmacodyn       Date:  2011-04-16       Impact factor: 2.745

2.  Effect of food on the pharmacokinetics of once-daily cyclobenzaprine extended-release 30 mg: a randomized, open-label, crossover, single-centre study.

Authors:  Mona Darwish; Fang Xie
Journal:  Clin Drug Investig       Date:  2009       Impact factor: 2.859

  2 in total

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