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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Determination of four antiepileptic drugs in plasma using ultra‐performance liquid chromatography with mass detection technique
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Determination of four antiepileptic drugs in plasma using ultra‐performance liquid chromatography with mass detection technique

机译:用大规模检测技术用超高效液相色谱法测定血浆中四种抗癫痫药物

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Abstract Status epilepticus (SE) is considered the second most frequent neurological emergency. Its therapeutic management is performed using sequential antiepileptic drug regimens. Diazepam (DIA), midazolam (MID), phenytoin (PHT) and phenobarbital (PB) are four drugs of different classes used sequentially in the management of SE. A sensitive, selective, accurate and precise method was developed and validated for simultaneous determination of the four antiepileptic drugs in human plasma. Their separation and quantification were achieved using ultra‐performance liquid chromatography (UPLC) with mass detection using carbamazepine as internal standard (IS). For the first three drugs and the IS, UPLC–MS/MS with electrospray ionization working in multiple reaction monitoring mode was used at the following transitions: m/z 285?→?193 for DIA; m/z 326?→?291 for MID; m/z 253?→?182 for PHT; and m/z 237?→?194, 237?→?192 for IS. For the fourth drug (PB), a molecular ion peak of PB [M?+?H] + at m/z 233 was used for its quantitation. The method was linear over concentration ranges 5–500?ng/mL for DIA and MID and 0.25–20?μg/mL for PHT and PB. Bioanalytical validation of the developed method was carried out according to European Medicines Agency guidelines. The developed method can be applied for routine drug analysis, therapeutic drug monitoring and bioequivalence studies.
机译:摘要状态癫痫(SE)被认为是第二次常见的神经系统紧急情况。其治疗性管理是使用顺序抗癫痫药物方案进行的。 Diazepam(Dia),咪达唑仑(中间),苯妥林(Pht)和苯巴比妥(PB)是在SE管理中依次使用的不同类别的四种药物。开发并验证了敏感,选择性,准确和精确的方法,同时测定人血浆中的四种抗癫痫药物。使用超级性液相色谱(UPLC)实现它们的分离和定量,所述超级性能液相色谱(UPLC)使用Carbamazepine作为内标(是)的质量检测。对于前三种药物和IS,在以下过渡时使用具有电喷雾电离的UPLC-MS / MS,在以下过渡:M / Z 285?→193用于直径; m / z 326?→291为中旬; m / z 253?→182为pht;和m / z 237?→194,237?→192 for。对于第四药物(PB),M / Z 233的Pb [M-+ + H] +的分子离子峰用于其定量。该方法在浓度范围内为5-500〜20μg/ ml,对于PHT和Pb,直径和中生和0.25-20Ωμg/ ml。根据欧洲药物代理指南,进行了开发方法的生物分析验证。开发方法可用于常规药物分析,治疗药物监测和生物等效性研究。

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