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Simultaneous determination of antiepileptic drugs and their two active metabolites by HPLC

✍ Scribed by Lucie Budakova; Hana Brozmanova; Milan Grundmann; Jan Fischer


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
677 KB
Volume
31
Category
Article
ISSN
1615-9306

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✦ Synopsis


Abstract

An HPLC procedure for the determination of lamotrigine (LAM) simultaneously with other antiepileptic drugs, primidone (PD), phenobarbital (PB), phenytoin (DPH), carbamazepine (CMZ), and two active metabolites 2‐phenyl‐2‐ethyl‐malonamide (PEMA) and 10,11‐dihydro‐10,11‐epoxycarbamazepine (EPO) was developed and validated. The method involves an ordinary RP system and a liquid–liquid extraction. The mobile phase consisting of water/ACN/methanol/triethylamine in the ratio 72 : 23 : 5 : 0.1 with pH 7.0 was selected as the best one after the assays testing both pH and triethylamine contents. UV detection was carried out at a wavelength of 220 nm and the whole analysis took 15 min. The method was linear in the range of 0.5–25 mg/L for PEMA and LAM; 1.25–25 mg/L for PD and CMZ; 0.625–12.5 mg/L for EPO; 1.5–60 mg/L for PB; and 1.25–50 mg/L for DPH, respectively. Within‐day CV% and between‐day CV% were within 10%. The developed HPLC method can be used for routine therapeutic drug monitoring both in children and adults.


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Redox labeling of two antiepileptic drug
✍ Anne-Line Bordes; Bernd Schöllhorn; Benoît Limoges; Chantal Degrand 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 104 KB

Two different cationic redox labels, i.e. a ferroceneammonium ion and a cobaltocenium ion, were covalently attached to two antiepileptics, phenytoin and phenobarbital, respectively. The two labeled drugs possess distinct standard redox potentials of 0.39 V for the phenytoin derivative and Ϫ 0.92 V f