Literature DB >> 1490488

Cross-over study of the bioavailability of a new NSAID (droxicam) versus piroxicam in healthy volunteers following single and multiple dose administration.

A Bartlett1, A Costa, L Martinez, R Roser, R Sagarra, J Sanchez.   

Abstract

Droxicam is a new anti-inflammatory drug which is a pro-drug of piroxicam and possesses delayed absorption kinetics. In this study, the comparative bioavailability of the two compounds was investigated. The study was performed following a cross-over design with single (20 mg) and multiple (20 mg/day for 30 consecutive days) administration in 25 healthy volunteers. The peak plasma concentrations of piroxicam, obtained following administration of droxicam, were lower than those calculated for administration of piroxicam, and the time taken to reach these peak concentrations was increased by approximately 5-7 h. There was no significant difference in either the elimination kinetics of piroxicam or the AUC values found following administration of the two products. Bioavailability of droxicam is equal to that of piroxicam, with a slower rate of absorption.

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Year:  1992        PMID: 1490488     DOI: 10.1007/BF03190145

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  11 in total

1.  Single and multiple dose pharmacokinetics of a new NSAID (droxicam) in healthy volunteers.

Authors:  L Martinez; J Sanchez; R Roser; J Garcia-Barbal; R Sagarra; A Bartlett
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1989 Oct-Dec       Impact factor: 2.441

Review 2.  Pharmacological profile of droxicam.

Authors:  J Esteve; A J Farré; R Roser
Journal:  Gen Pharmacol       Date:  1988

3.  Pharmacokinetics of droxicam in rat and dog.

Authors:  A Esteve; L Martínez; R Roser; R Sagarra
Journal:  Methods Find Exp Clin Pharmacol       Date:  1986-07

4.  Bioavailability--a problem in equivalence.

Authors:  C M Metzler
Journal:  Biometrics       Date:  1974-06       Impact factor: 2.571

5.  Use of confidence intervals in analysis of comparative bioavailability trials.

Authors:  W J Westlake
Journal:  J Pharm Sci       Date:  1972-08       Impact factor: 3.534

6.  Comparative study of the multiple dose pharmacokinetics and the tolerance of a new NSAID (droxicam) versus piroxicam in healthy volunteers.

Authors:  L Martínez; J Sánchez; R Roser; J García-Barbal; A Bartlett; J Estruch; R Sagarra; S Puig; A Costa
Journal:  Methods Find Exp Clin Pharmacol       Date:  1988-11

7.  Analysis of piroxicam in plasma by high-performance liquid chromatography.

Authors:  T M Twomey; S R Bartolucci; D C Hobbs
Journal:  J Chromatogr       Date:  1980-07-11

8.  Effects of droxicam on in vivo prostaglandin synthesis and ex vivo platelet aggregation.

Authors:  J Esteve; L Martínez; R Roser; R Sagarra
Journal:  Methods Find Exp Clin Pharmacol       Date:  1987-04

9.  The influence of gastric emptying on droxicam pharmacokinetics.

Authors:  J Sánchez; L Martínez; J García-Barbal; R Roser; A Bartlett; R Sagarra
Journal:  J Clin Pharmacol       Date:  1989-08       Impact factor: 3.126

10.  Pharmacological properties of droxicam, a new non-steroidal anti-inflammatory agent.

Authors:  A J Farré; M Colombo; M Fort; B Gutiérrez; L Rodríguez; R Roser
Journal:  Methods Find Exp Clin Pharmacol       Date:  1986-07
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