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采用超高效液相色谱-质谱检测技术测定血浆中四种抗癫痫药物。

Determination of four antiepileptic drugs in plasma using ultra-performance liquid chromatography with mass detection technique.

作者信息

Hassib Sonia T, Hashem Hanaa M A, Mahrouse Marianne A, Mostafa Eman A

机构信息

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.

出版信息

Biomed Chromatogr. 2018 Aug;32(8):e4253. doi: 10.1002/bmc.4253. Epub 2018 May 16.

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.

摘要

癫痫持续状态(SE)被认为是第二常见的神经急症。其治疗管理采用序贯抗癫痫药物方案。地西泮(DIA)、咪达唑仑(MID)、苯妥英(PHT)和苯巴比妥(PB)是在SE管理中依次使用的四种不同类别的药物。开发并验证了一种灵敏、选择性好、准确且精密的方法,用于同时测定人血浆中的这四种抗癫痫药物。使用超高效液相色谱(UPLC)结合以卡马西平为内标(IS)的质谱检测实现了它们的分离和定量。对于前三种药物和内标,采用电喷雾电离在多反应监测模式下工作的UPLC-MS/MS,其跃迁如下:DIA为m/z 285 → 193;MID为m/z 326 → 291;PHT为m/z 253 → 182;内标为m/z 237 → 194、237 → 192。对于第四种药物(PB),使用PB的分子离子峰m/z 233 [M + H]进行定量。该方法在DIA和MID的浓度范围为5 - 500 ng/mL以及PHT和PB为0.25 - 20 μg/mL时呈线性。根据欧洲药品管理局的指南对所开发方法进行了生物分析验证。所开发的方法可应用于常规药物分析、治疗药物监测和生物等效性研究。

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