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High performance liquid chromatographic determination of YJC-10592, a new chemokine receptor 2 (CCR-2) antagonist, in biological samples
- Source :
- Journal of Pharmaceutical Investigation. 46:495-504
- Publication Year :
- 2016
- Publisher :
- Springer Science and Business Media LLC, 2016.
-
Abstract
- YJC-10592, a new chemokine receptor 2 (CCR-2) antagonist, was newly synthesized for the treatment of asthma and atopic dermatitis. To evaluate the pharmacokinetic characteristics of YJC-10592, a high-performance liquid chromatographic (HPLC) method was developed for the determination of YJC-10592 in rat plasma, urine, and tissue homogenates, using YJC-10450 as an internal standard. The mobile phase was a gradient of acetate buffer (50 mM, pH 3.0) in acetonitrile at a flow rate of 1.0 mL/min. Chromatograms were monitored by an ultraviolet detector at 230 nm. The retention times for YJC-10592 and the internal standard were 8.0 and 6.3 min, respectively, and the lower limits of quantification (LLOQ) for YJC-10592 in rat plasma and urine were 0.05 and 0.2 μg/mL, respectively. The intra- and inter-assay precisions (coefficients of variation, CVs) were generally low (below 11.4 %) for rat plasma and urine samples. The accuracies (relative errors) ranged from 94.2 to 108 %. No interferences from endogenous substances were found. YJC-10592 was stable in rat whole blood but unstable in the liver homogenate. An initial pharmacokinetic study was performed in Sprague–Dawley rats and demonstrated that YJC-10592 has a half-life of 86.8 min and wide tissue distribution. In summary, this HPLC method can be applied to future preclinical and clinical evaluation of YJC-10592.
- Subjects :
- 0301 basic medicine
Chromatography
Chemistry
Antagonist
Pharmaceutical Science
Endogeny
Urine
030226 pharmacology & pharmacy
High-performance liquid chromatography
03 medical and health sciences
Chemokine receptor
030104 developmental biology
0302 clinical medicine
Pharmacokinetics
Hplc method
Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Whole blood
Subjects
Details
- ISSN :
- 20936214 and 20935552
- Volume :
- 46
- Database :
- OpenAIRE
- Journal :
- Journal of Pharmaceutical Investigation
- Accession number :
- edsair.doi...........7548bfff14ae274f1d450aa1b2d2dc8c
- Full Text :
- https://doi.org/10.1007/s40005-016-0257-9