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Human whole blood assay for rapid and routine testing of non-steroidal anti-inflammatory drugs (NSAIDs) on cyclo-oxygenase-2 activity
- Source :
- Inflammopharmacology. 16:155-161
- Publication Year :
- 2008
- Publisher :
- Springer Science and Business Media LLC, 2008.
-
Abstract
- 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.
- Subjects :
- Glycerol
Lipopolysaccharides
Allergy
Routine testing
Immunology
Stimulation
Pharmacology
Inhibitory Concentration 50
Humans
Medicine
Pharmacology (medical)
Cyclo oxygenase 2
Whole blood
Cyclooxygenase 2 Inhibitors
Ethanol
business.industry
Anti-Inflammatory Agents, Non-Steroidal
Prostaglandin production
Reproducibility of Results
medicine.disease
Solubility
Non steroidal anti inflammatory
Cyclooxygenase 2
Biological Assay
lipids (amino acids, peptides, and proteins)
Pharmaceutical Vehicles
Cyclo-oxygenase
business
Hydrophobic and Hydrophilic Interactions
Subjects
Details
- ISSN :
- 15685608 and 09254692
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Inflammopharmacology
- Accession number :
- edsair.doi.dedup.....977e4fe04bbb04ac02badc157b02294a
- Full Text :
- https://doi.org/10.1007/s10787-008-8007-x