Development and Bioanalytical Validation of RP-HPLC Method for the Simultaneous Determination of Perampanel and Carbamazepine in Human Plasma for Therapeutic Drug Monitoring

被引:6
作者
Hassan, Said A. H. [1 ]
Helmy, Aya A. [2 ]
Weshahy, Soheir F. [1 ]
Youssef, Nadia A. [2 ]
El-Zeany, Badr [1 ]
机构
[1] Cairo Univ, Fac Pharm, Analyt Chem Dept, Kasr El-Aini St, Cairo 11562, Egypt
[2] Egyptian Drug Author EDA, Pharmaceut Chem Dept, Giza, Egypt
关键词
bio-analytical validation; carbamazepine; EMA; HPLC; perampanel; therapeutic drug monitoring; PERFORMANCE LIQUID-CHROMATOGRAPHY; ANTIEPILEPTIC DRUGS; PARTIAL-ONSET; SERUM; PHARMACOKINETICS; IMPACT;
D O I
10.1134/S1061934823050076
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Common antiepileptic drugs have complex pharmacokinetic characteristics leading to fluctuation in their plasma levels at the same therapeutic doses. Therefore, antiepileptic drugs turn out to be among the most common medications for which therapeutic drug monitoring (TDM) is crucial. Indeed, TDM provides a realistic approach to adjust drug doses in epilepsy care based on plasma concentrations to optimize its clinical outcome. Perampanel (PER) is an antiepileptic drug used for the treatment of primary generalized tonic-clonic seizures in combination with other drugs, such as carbamazepine (CAR). Drug-drug pharmacokinetic interactions are very common in this combination, which makes TDM of PER essential. A selective, accurate, and precise bioanalytical method has been developed for the simultaneous determination of PER and CAR in human plasma for the purpose of TDM. Liquid-liquid extraction using ethyl acetate was applied for sample preparation, and diazepam (DZP) was the internal standard. The adopted method could successfully determine PER and CAR within their c(max) levels as the linearity range was 0.2-10 mu g/mL for PER and 5-100 mu g/mL for CAR. The chromatographic separation was achieved on a C8 column using acetonitrile, aqueous 0.1% glacial acetic acid (75 : 25, v/v) as a mobile phase in isocratic elution at a flow rate of 0.8 mL/min and an UV detection at 225 nm. The adopted method was validated according to EMA guidelines, and the results were within the acceptance criteria.
引用
收藏
页码:622 / 627
页数:6
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