Skip to main content
Log in

S-Ibuprofen versus ibuprofen-racemate

A randomized double-blind study in patients with rheumatoid arthritis

  • Originals
  • Published:
Rheumatology International Aims and scope Submit manuscript

Summary

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Adams SS, Bresloff P, Mason CG (1976) Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (-)-isomer. J Pharm Pharmacol 28:256–257

    Google Scholar 

  2. Geisslinger G, Schuster O, Stock KP, Loew D, Bach GL, Brune K (1990) Pharmacokinetics of S(+)-and R(-)-ibuprofen in volunteers and first clinical experience with S(+)-ibuprofen in rheumatoid arthritis. Eur J Clin Pharmacol 38:493–497

    Google Scholar 

  3. Lee EJD, Williams K, Day R, Graham G, Champion D (1985) Stereoselective disposition of ibuprofen enantiomers in man. Br J Clin Pharmacol 19:669–674

    Google Scholar 

  4. Ariens EJ (1986) Stereochemistry: a source of problems in medical chemistry. Med Res Rev 6:451–466

    Google Scholar 

  5. Williams K, Day R, Knihinicki R, Duffield K (1986) The stereoselective uptake of ibuprofen enantiomers into adipose tissue. Biochem Pharmacol 35:3403–3405

    Google Scholar 

  6. Peskar BM, Hoppe U, Lange K, Peskar BA (1985) Effects of non-steroidal anti-inflammatory drugs on rat gastric mucosal leukotriene C4 and prostanoid release: relation to ethanol-induced injury. Br J Pharmacol 93:669–674

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Stock, K.P., Geisslinger, G., Loew, D. et al. S-Ibuprofen versus ibuprofen-racemate. Rheumatol Int 11, 199–202 (1991). https://doi.org/10.1007/BF00332562

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00332562

Key words

Navigation