Effect of piperine on the steady-state pharmacokinetics of phenytoin in patients with epilepsy

التفاصيل البيبلوغرافية
العنوان: Effect of piperine on the steady-state pharmacokinetics of phenytoin in patients with epilepsy
المؤلفون: Smita Pattanaik, Debasish Hota, Sudesh Prabhakar, Parampreet S Kharbanda, Promila Pandhi
المصدر: Phytotherapy Research. 20:683-686
بيانات النشر: Wiley, 2006.
سنة النشر: 2006
مصطلحات موضوعية: Adult, Male, Phenytoin, Polyunsaturated Alkamides, medicine.medical_treatment, Biological Availability, Pharmacology, chemistry.chemical_compound, Alkaloids, Piperidines, Pharmacokinetics, Humans, Medicine, Drug Interactions, Benzodioxoles, Epilepsy, Dose-Response Relationship, Drug, business.industry, Alkaloid, Venous blood, Middle Aged, Bioavailability, Dose–response relationship, Anticonvulsant, chemistry, Area Under Curve, Piperine, Anticonvulsants, Female, business, Piper, medicine.drug
الوصف: Piperine, the active principle of Piper longum, Piper nigrum and Zingiber officinalis, has been reported to enhance the oral bioavailability of phenytoin in human volunteers. The objective of this study was to explore the effect of a single dose of piperine in patients with uncontrolled epilepsy on the steady-state pharmacokinetics of phenytoin. Two groups of 10 patients each receiving either a 150 mg or 200 mg twice daily dose of phenytoin were selected. Twelve hours after the night dose, venous blood samples were collected at 0, 0.5, 1, 2, 4, 6, 9, 12 h after administration of phenytoin. On the next study day, piperine 20 mg was administered along with phenytoin and samples were collected similarly. The mean plasma drug concentrations at different time points and the pharmacokinetic parameters before and after piperine administration were compared by Student's t-test. Piperine increased significantly the mean plasma concentration of phenytoin at most of the time points in both dose groups. There was a significant increase in AUC((0-12h)) (p < 0.01), C(max) (p < 0.001) and K(a) (p < 0.05) whereas the changes in K(el) and t(max) were not significant. The results showed that piperine enhanced the bioavailability of phenytoin significantly, possibly by increasing the absorption.
تدمد: 1099-1573
0951-418X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa95c5f9e57203e4db4ba44469f8eb0Test
https://doi.org/10.1002/ptr.1937Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....aaa95c5f9e57203e4db4ba44469f8eb0
قاعدة البيانات: OpenAIRE