Literature DB >> 1784888

S-ibuprofen versus ibuprofen-racemate. A randomized double-blind study in patients with rheumatoid arthritis.

K P Stock1, G Geisslinger, D Loew, W S Beck, G L Bach, K Brune.   

Abstract

Ibuprofen (ibu) is a racemic 2-arylpropionic acid non-steroidal anti-inflammatory drug whose activity is due mainly to the S-enantiomer. So far only the racemic compound is in clinical use. A double-blind randomized trial was carried out for a 2-week period in 50 patients with classical rheumatoid arthritis (RA) (Steinbrocker II-III) to compare the effectiveness and tolerance of S-ibu (400 mg T.I.D.) with that of the racemic compound (600 mg T.I.D.). Ritchie-index, limitation of movement, joint pain on pressure and pain at night decreased significantly in both groups. Due to lack of effectiveness, the dose had to be increased in 3 patients from the S-ibu group as well as in 6 patients from the racemic group resulting in mean daily doses of 1220 mg S-ibuprofen and 1870 mg racemic ibu. No statistically significant difference could be found between both groups concerning efficacy and unwanted effects. Therefore, S-ibu given alone may be advantageous because the metabolic load to the human body is reduced and patients are more likely to comply with drug doses of 1.2 g/day as compared to 1.8 g/day.

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Year:  1991        PMID: 1784888     DOI: 10.1007/bf00332562

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  6 in total

1.  Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (-)-isomer.

Authors:  S S Adams; P Bresloff; C G Mason
Journal:  J Pharm Pharmacol       Date:  1976-03       Impact factor: 3.765

2.  The stereoselective uptake of ibuprofen enantiomers into adipose tissue.

Authors:  K Williams; R Day; R Knihinicki; A Duffield
Journal:  Biochem Pharmacol       Date:  1986-10-01       Impact factor: 5.858

Review 3.  Stereochemistry: a source of problems in medicinal chemistry.

Authors:  E J Ariëns
Journal:  Med Res Rev       Date:  1986 Oct-Dec       Impact factor: 12.944

4.  Stereoselective disposition of ibuprofen enantiomers in man.

Authors:  E J Lee; K Williams; R Day; G Graham; D Champion
Journal:  Br J Clin Pharmacol       Date:  1985-05       Impact factor: 4.335

5.  Pharmacokinetics of S(+)- and R(-)-ibuprofen in volunteers and first clinical experience of S(+)-ibuprofen in rheumatoid arthritis.

Authors:  G Geisslinger; O Schuster; K P Stock; D Loew; G L Bach; K Brune
Journal:  Eur J Clin Pharmacol       Date:  1990       Impact factor: 2.953

6.  Effects of non-steroidal anti-inflammatory drugs on rat gastric mucosal leukotriene C4 and prostanoid release: relation to ethanol-induced injury.

Authors:  B M Peskar; U Hoppe; K Lange; B A Peskar
Journal:  Br J Pharmacol       Date:  1988-04       Impact factor: 8.739

  6 in total
  5 in total

Review 1.  Clinical pharmacokinetics of ibuprofen. The first 30 years.

Authors:  N M Davies
Journal:  Clin Pharmacokinet       Date:  1998-02       Impact factor: 6.447

Review 2.  Nonsteroidal anti-inflammatory drugs in perisurgical pain management. Mechanisms of action and rationale for optimum use.

Authors:  J Cashman; G McAnulty
Journal:  Drugs       Date:  1995-01       Impact factor: 9.546

3.  Variability in the stereoselective disposition of ibuprofen in patients with rheumatoid arthritis.

Authors:  G Geisslinger; K P Stock; D Loew; G L Bach; K Brune
Journal:  Br J Clin Pharmacol       Date:  1993-06       Impact factor: 4.335

4.  The stereoselective disposition of the enantiomers of ibuprofen in blood, blister and synovial fluid.

Authors:  P Seideman; F Lohrer; G G Graham; M W Duncan; K M Williams; R O Day
Journal:  Br J Clin Pharmacol       Date:  1994-09       Impact factor: 4.335

Review 5.  Metabolic-Hydroxy and Carboxy Functionalization of Alkyl Moieties in Drug Molecules: Prediction of Structure Influence and Pharmacologic Activity.

Authors:  Babiker M El-Haj; Samrein B M Ahmed
Journal:  Molecules       Date:  2020-04-22       Impact factor: 4.411

  5 in total

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