Development and validation of an HPLC method for determination of carbamazepine in human plasma and applications to a therapeutic drug monitoring study

被引:1
作者
Dural, Emrah [1 ]
Cetin, Suleyman [1 ]
Bolayir, Asli [2 ]
Cigdem, Burhanettin [2 ]
机构
[1] Sivas Cumhuriyet Univ, Fac Pharm, Dept Pharmaceut Toxicol, Sivas, Turkey
[2] Sivas Cumhuriyet Univ, Fac Med, Dept Neurol, Sivas, Turkey
来源
ISTANBUL JOURNAL OF PHARMACY | 2020年 / 50卷 / 01期
关键词
Carbamazepine; plasma; therapeutic drug monitoring; validation; high-performance liquid chromatography; ultraviolet detection; PERFORMANCE LIQUID-CHROMATOGRAPHY; SOLID-PHASE EXTRACTION; 6 ANTIEPILEPTIC DRUGS; POLYMORPHIC FORMS; PACKED SORBENT; UV METHOD; PHARMACOKINETICS; CARBAMAZEPINE-10,11-EPOXIDE; METABOLITES; SERUM;
D O I
10.26650/IstanbulJPharm.2019.0054
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and Aims: Carbamazepine (CBZ) is an antiepileptic drug, which is prescribed as a first-line drug for the treatment of partial and generalized tonic-clonic epileptic seizures. The aim of this study was to develop and validate a simple, fast and reliable HPLC method for the determination of carbamazepine in human plasma. Methods: Chlorpromazine (CPR) was used as an internal standard. The separation was conducted with a C18 reverse-phase column (150x3.9 mm, 5 mu m) at 30 degrees C, using a mobile phase prepared with 20 mM KH2PO4, acetonitrile and methanol (6:3:1, v/v/v) by isocratic elution. Results: The method was linear between 0.5 and 40 mu g/mL, determined by 10 individual calibration points. Total run time was <= 5 mins. Accuracy (RE%) values were determined between (-5.6) and 3.6%, and precision was determined at <= 4.2%. Limit of detection (LOD) was 0.04 mu g/mL. The robustness test results of the method showed good values. Plasma CBZ of (n=30) those receiving CBZ quantities ranging from 0.2 to 1.2 g/day were measured with this method, and following analyses of their concentrations were found to be between 0.1 and 11.4 mu g/mL (6.2 +/- 2.4 mu g/mL). While all plasma sample analyses were applied properly, it was observed that 16 (53.3%) of the plasma samples had CBZ lower than the recommended range. In addition to that, female patient plasma-CBZ levels were found significantly higher than male plasma contents (p<0.05). Conclusion: This method was found suitable for the analysis of plasma samples collected during the therapeutic drug monitoring (TDM) of patients treated with CBZ.
引用
收藏
页码:6 / 15
页数:10
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