CAT.INIST
Accueil du sitewww.cnrs.frwww.inist.frOther CNRS


COMMANDER / ORDER
PARTAGER / SHARE
EXPORT
Bookmark and Share
Mendeley    EndNote

Titre du document / Document title

Comparison of two different preparations of ibuprofen with regard to the time course of their analgesic effect: A randomised, placebo-controlled, double-blind cross-over study using Laser somatosensory evoked potentials obtained from UV-irritated skin in healthy volunteers

Auteur(s) / Author(s)

SEIBEL Klaus (1) ; SCHAFFLER Klaus (1) ; REEH Peter (2) ; REITMEIR Peter (3) ;

Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)

(1) HPR-Human Pharmacodynamic Research GmbH, Munich, ALLEMAGNE
(2) Department of Physiology (1) and Pathophysiology, University of Erlangen, Erlangen, ALLEMAGNE
(3) Biostatistician, Munich, ALLEMAGNE

Résumé / Abstract

In the treatment of painful conditions the time to onset of a drug's analgesic effect is of great relevance. Plain ibuprofen acid (Ibu, CAS 15687-27-1) is relatively slowly absorbed after oral administration (tmax is about 90-120 min). If, however, ibuprofen is given in form of a lysine salt, absorption is much quicker. It has been shown in pharmacokinetic studies that the maximum plasma concentration after administration of an ibuprofen lysine tablet (IbuLys) is reached at about 35 min after oral administration. The aim of this study was to evaluate the onset and extent of the analgesic effect of 400 mg ibuprofen administered as marketed ibuprofen lysine tablets (two tablets of Dolormin® as a single dose) in comparison with standard Ibu tablets (two tablets as a single dose) and placebo (PIc) utilising the objective, quantitative (high resolution) method of Laser algesimetry. The N1-P2 peak-to-peak amplitude of the Laser-induced somatosensory evoked potentials (LSEPs) - measured during the first two hours after administration of study drugs - was the main efficacy parameter for the onset of the analgesic effects. The values obtained during 5 h after administration of the study drugs were used to measure the extent of the analgesic effects. As a main result with respect to the onset of analgesic action, the reduction of the N1-P2 peak-to-peak amplitude was significantly and relevantly more pronounced during the first 2 h after administration of IbuLys than after Ibu (IbuLys vs. Plc: p ≤ 0.0020, IbuLys vs. Ibu: p ≤ 0.0366). During the same time the amplitudes of the single N1-components of the LSEPs were also significantly smaller after IbuLys than after Plc (p ≤ 0.0031) whereas the difference between plain Ibu and Plc was not significant (p ≤ 0.1027). As a measure of the extent of analgesic action, the N1-P2 peak-to-peak amplitudes recorded during 5 h after medication were more effectively reduced by IbuLys than by Ibu (IbuLys vs. Plc: p ≤ 0.0001, IbuLys vs. Ibu: p ≤ 0.0041, Ibu vs. Plc: p ( 0.383). The reduction of the amplitudes of the single N1-components by IbuLys was significant in comparison to Plc (p ≤ 0.0031), but not in comparison to Ibu. During the time of 5 h after medication the attenuating (analgesic) effect of IbuLys on the amplitude of the P2 component of the LSEPs was stronger than that of Plc (p ≤ 0.0053) and stronger than that of Ibu (p ≤ 0.0058). In summary IbuLys was significantly superior to Ibu with respect to the onset and extent of the analgesic effect.

Revue / Journal Title

Arzneimittel-Forschung   ISSN 0004-4172   CODEN ARZNAD 

Source / Source

2004, vol. 54, no8, pp. 444-451 [8 page(s) (article)] (22 ref.)

Langue / Language

Anglais

Editeur / Publisher

Cantor, Aulendorf, ALLEMAGNE  (1951) (Revue)

Mots-clés anglais / English Keywords

Aminoacid ; Electrophysiology ; Enzyme ; Oxidoreductases ; Prostaglandin-endoperoxide synthase ; Enzyme inhibitor ; Arylpropionic acid derivatives ; Drug ; Non steroidal antiinflammatory agent ; Lysine ; Healthy subject ; Skin ; Evoked potential ; Crossover study ; Double blind study ; Randomization ; Analgesic ; Ibuprofen ; Comparative study ;

Mots-clés français / French Keywords

Aminoacide ; Electrophysiologie ; Enzyme ; Oxidoreductases ; Prostaglandin-endoperoxide synthase ; Inhibiteur enzyme ; Arylpropionique acide dérivé ; Médicament ; Antiinflammatoire non stéroïde ; Lysine ; Individu sain ; Peau ; Potentiel évoqué ; Essai croisé ; Etude double insu ; Randomisation ; Analgésique ; Ibuprofène ; Etude comparative ;

Mots-clés espagnols / Spanish Keywords

Aminoácido ; Electrofisiología ; Enzima ; Oxidoreductases ; Prostaglandin-endoperoxide synthase ; Inhibidor enzima ; Arilpropionico ácido derivado ; Medicamento ; Antiinflamatorio no esteroide ; Lisina ; Individuo sano ; Piel ; Potencial evocado ; Ensayo cruzado ; Estudio doble ciego ; Aleatorización ; Analgésico ; Ibuprofeno ; Estudio comparativo ;

Mots-clés d'auteur / Author Keywords

CAS 15687-27-1 Dolormin® Ibuprofen ; analgesic effect ; lysine salt ; plain Laser algesimetry Non-steroidal anti- inflammatory drugs Somatosensory evoked potentials UV-induced hyperalgesia ;

Localisation / Location

INIST-CNRS, Cote INIST : 565, 35400012023934.0030

Nº notice refdoc (ud4) : 16059757

COMMANDER / ORDER
PARTAGER / SHARE
EXPORT
Bookmark and Share
Mendeley    EndNote

CAT.INIST