Simultaneous bioanalysis and pharmacokinetic interaction study of acebrophylline, levocetirizine and pranlukast in Sprague–Dawley rats
Autor: | Pinaki Sengupta, Manish Kumar Sharma, Rajeswari Rathod, Priyanka Lohar, Amit Kumar Sahu |
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Rok vydání: | 2019 |
Předmět: |
Male
Analyte Bioanalysis Clinical Biochemistry 030226 pharmacology & pharmacy 01 natural sciences Biochemistry Levocetirizine Pranlukast Analytical Chemistry Rats Sprague-Dawley 03 medical and health sciences 0302 clinical medicine Theophylline Pharmacokinetics Limit of Detection Drug Discovery medicine Sprague dawley rats Animals Molecular Biology Chromatography High Pressure Liquid Pharmacology Chromatography Chemistry 010401 analytical chemistry Reproducibility of Results General Medicine Acebrophylline Cetirizine Rats 0104 chemical sciences Ambroxol Chromones Linear Models Pharmacokinetic interaction medicine.drug |
Zdroj: | Biomedical Chromatography. 33 |
ISSN: | 1099-0801 0269-3879 |
DOI: | 10.1002/bmc.4672 |
Popis: | The combination of acebrophylline (ABP), levocetirizine (LCZ) and pranlukast (PRN) is used to treat allergic rhinitis, asthma, hay-fever and other conditions where patients experience difficulty in breathing. This study was carried out with the aim of developing and validating a reverse-phase high-performance liquid chromatographic bioanalytical method to simultaneously quantitate ABP, LCZ and PRN in rat plasma. The objective also includes determination of the pharmacokinetic interaction of these three drugs after administration via the oral route after individual and combination treatment in rat. Optimum resolution between the analytes was observed with a C18 Kinetex column (250 mm × 4.6 mm × 5 μm). The chromatography was performed in a gradient elution mode with a 1 mL/min flow rate. The calibration curves were linear over the concentration range of 100-1600 ng/mL. The intra- and inter-day precision and accuracy were found to be within acceptable limits as specified in US Food and Drug Administration guideline for bioanalytical method validation. The analytes were stable on the bench-top (8 h), after three freeze-thaw cycles, in the autosampler (8 h) and as a dry extract (-80°C for 48 h). The statistical results of the pharmacokinetic study in Sprague-Dawley rats showed a significant change in pharmacokinetic parameters for PRN upon co-administration of the three drugs. |
Databáze: | OpenAIRE |
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