A novel HPLC-DAD method for simultaneous determination of febuxostat and diclofenac in biological samples: Pharmacokinetic outcomes
| dc.contributor.author | El-Yazbi, Fawzy A. | |
| dc.contributor.author | Amin, Omayma Abdel Razak | |
| dc.contributor.author | El-Kimary, Eman I. | |
| dc.contributor.author | Khamis, Essam F. | |
| dc.contributor.author | Younis, Sameh E. | |
| dc.contributor.author | ElKhatib, Mohammed A.W. | |
| dc.contributor.author | El-Yazbi, Ahmed F. | |
| dc.contributor.department | Pharmacology and Toxicology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:39:37Z | |
| dc.date.available | 2025-01-24T11:39:37Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Aim: To develop a simple HPLC-DAD method for simultaneous determination of febuxostat (FEB) and diclofenac (DIC) in biological samples to assess pharmacokinetic outcomes of their coadministration. Methodology & results: Sample preparation was performed by liquid-liquid extraction. Drugs analysis was done on C18 column using methanol-formic acid pH 2.1 (76:24, v/v) as mobile phase and time-programmed UV detection. Lower limits of quantitation for FEB and DIC were 10 and 20 ng/ml, respectively. Baseline pharmacokinetics were similar to published data on either drug alone. Coadministration led to more than twofold increase in FEB C max and AUC together with a reduced hepatic uptake in rats. Conclusion: DIC interfered with initial distribution and terminal clearance of FEB potentially due to reduced FEB hepatic uptake. © 2018 Newlands Press. | |
| dc.identifier.doi | https://doi.org/10.4155/bio-2018-0219 | |
| dc.identifier.eid | 2-s2.0-85058491865 | |
| dc.identifier.pmid | 30475064 | |
| dc.identifier.uri | http://hdl.handle.net/10938/29299 | |
| dc.language.iso | en | |
| dc.publisher | Future Medicine Ltd. | |
| dc.relation.ispartof | Bioanalysis | |
| dc.source | Scopus | |
| dc.subject | Diclofenac | |
| dc.subject | Febuxostat | |
| dc.subject | Hplc-dad | |
| dc.subject | Human plasma | |
| dc.subject | Liver uptake | |
| dc.subject | Pharmacokinetics | |
| dc.subject | Adult | |
| dc.subject | Animals | |
| dc.subject | Area under curve | |
| dc.subject | Calibration | |
| dc.subject | Chromatography, high pressure liquid | |
| dc.subject | Cross-over studies | |
| dc.subject | Healthy volunteers | |
| dc.subject | Humans | |
| dc.subject | Liquid-liquid extraction | |
| dc.subject | Liver | |
| dc.subject | Male | |
| dc.subject | Rats | |
| dc.subject | Rats, sprague-dawley | |
| dc.subject | Reproducibility of results | |
| dc.subject | Sensitivity and specificity | |
| dc.subject | Tissue distribution | |
| dc.subject | Area under the curve | |
| dc.subject | Article | |
| dc.subject | Diode array detector | |
| dc.subject | Drug clearance | |
| dc.subject | Drug determination | |
| dc.subject | Drug distribution | |
| dc.subject | Drug uptake | |
| dc.subject | High performance liquid chromatography | |
| dc.subject | Human | |
| dc.subject | Human experiment | |
| dc.subject | Limit of detection | |
| dc.subject | Limit of quantitation | |
| dc.subject | Liquid liquid extraction | |
| dc.subject | Maximum concentration | |
| dc.subject | Nonhuman | |
| dc.subject | Normal human | |
| dc.subject | Rat | |
| dc.subject | Animal | |
| dc.subject | Blood | |
| dc.subject | Crossover procedure | |
| dc.subject | Metabolism | |
| dc.subject | Reproducibility | |
| dc.subject | Sprague dawley rat | |
| dc.title | A novel HPLC-DAD method for simultaneous determination of febuxostat and diclofenac in biological samples: Pharmacokinetic outcomes | |
| dc.type | Article |
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