Human whole blood assay for rapid and routine testing of non-steroidal anti-inflammatory drugs (NSAIDs) on cyclo-oxygenase-2 activity

. Aim of this study was to present a simple, fast and reliable method to examine the capacity of NSAIDs to inhibiting COX-2 activity that uses rapid (stimulation takes only 5 h compared to other existing protocols) and routine testing. The assay includes elimination of COX-1-activity using ASS (a se...

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Veröffentlicht in:Inflammopharmacology 2008-08, Vol.16 (4), p.155-161
Hauptverfasser: Laufer, S., Greim, C., Luik, S., Ayoub, S. S., Dehner, F.
Format: Artikel
Sprache:eng
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Zusammenfassung:. Aim of this study was to present a simple, fast and reliable method to examine the capacity of NSAIDs to inhibiting COX-2 activity that uses rapid (stimulation takes only 5 h compared to other existing protocols) and routine testing. The assay includes elimination of COX-1-activity using ASS (a selective COX-1 inhibitor) and the thromboxane synthetase inhibitor (TXBSI), COX-2 induction via LPS and measurement of PGE 2 . Using TXBSI reduces the amount of LPS and results in higher prostaglandin production. Cremophor EL ® -EtOH was used as vehicle instead of DMSO because within a defined concentration range, Cremophor EL ® -EtOH allows even very hydrophobic drugs to be solubilized and applied in vitro without cell damage. Cremophor EL ® -EtOH at 0.2% was optimal as at this relatively low concentration excellent drug dissolution was obtained whereas many hydrophobic substances precipitate in 0.2% DMSO. Our results demonstrate that the IC 50 values for the tested NSAIDs are in the range of published data.
ISSN:0925-4692
1568-5608
DOI:10.1007/s10787-008-8007-x