Document Type: Research article
Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences
Department of Medicinal Chemistry, School of Pharmacy, Shahid Beheshti University of Medical Sciences
School of Pharmacy, Shahid Beheshti University of Medical Sciences
Coxibs such as celecoxib, rofecoxib and valdecoxib are introduced as selective COX-2 inhibitors to the market. It has been reported that inhibition of COX-2 beside traditional effects of NSAIDs, reduces the risk of colorectal, breast and lung cancers and slow the progress of Alzheimer’s disease. Zarghi et al. reported 8-benzoyl-2-(4-(methylsulfonyl)phenyl)quinoline-4-carboxylic acid (AZGH 102) as a novel compound with similar IC50 to celecoxib besides improved selectivity index (COX-1/COX-2 inhibitory potency) in comparison with celecoxib.
In this study the physicochemical properties of AZGH 102 such as solubility, log P and stability was evaluated and the pharmacokinetic characteristics of this compound following intravenous (10 mg/kg), and oral administration (20 mg/kg), to male and female Wistar rats were investigated.
As the data demonstrated the AZGH 102 classified as lipophil compound and had suitable stability. This derivative absorbs and distributes faster in female than male. The AUC 0-∞, absolute bioavailability, Cl and Vd were different in both sexes.
According to the obtained data the AZGH 102 has a sex dependent pharmacokinetic in Wistar rats.