气相色谱-质谱法测定人血清中的拉莫三嗪、卡马西平和环氧卡马西平。

J Hallbach, H Vogel, W G Guder
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引用次数: 23

摘要

描述了一种测定人血清中抗癫痫药拉莫三嗪、卡马西平和环氧卡马西平(活性代谢物)含量的方法。在难治性癫痫中,卡马西平和拉莫三嗪的联合治疗最近发展成为一种现代治疗概念。本文的目的是对这些物质进行治疗药物监测。采用快速沉淀法提取血清,采用气相色谱-质谱(GC-MS)分析。采用气相色谱-质谱法对拉莫三嗪进行了测定。本文首次发表了纯拉莫三嗪的参考谱。建立了一个新的质谱库,以支持人类血清中抗癫痫药物的鉴定。在特定离子监测模式(SIM)下,检测限低于治疗范围,回收率高于90%。通过GC-MS或市售的高效液相色谱(HPLC)方法(用于拉莫三嗪)和荧光偏振免疫分析法(FPIA)(用于卡马西平)从加标血清样品中获得的结果进行比较,结果显示两种方法之间的差异不超过10%,并证明了新方法的准确性。此外,在接受抗惊厥治疗的患者样本中,这些抗癫痫药物的定量测定显示,卡马西平和拉莫三嗪的线性相关性很强,r2 = 0.961, r2 = 0.964。在总共46个结果中,只有两个结果的差异超过10%。我们的血清拉莫三嗪定量方法似乎具有高度特异性,能够测量单次治疗患者的拉莫三嗪,以及卡马西平或卡马西平环氧化物的附加治疗。未发现其他共给药药物的干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of lamotrigine, carbamazepine and carbamazepine epoxide in human serum by gas chromatography mass spectrometry.

A method for the identification and quantification of the antiepileptics lamotrigine, carbamazepine and carbamazepine epoxide (active metabolite) in human serum is described. In refractory epilepsy the combination of carbamazepine and lamotrigine was recently developed to a modern therapeutic concept. The goal of this paper is therapeutic drug monitoring (TDM) of these substances. Serum was extracted with a quick precipitation method using a modified commercial extraction-kit and analysed by gas chromatography mass spectrometry (GC-MS). A gas-chromatographic temperature-pressure programme was developed that allowed the determination of lamotrigine by gas chromatography mass spectrometry. A reference spectrum of pure lamotrigine is herewith published for the first time. A new mass spectra library was created to support the identification of the antiepileptics in human serum. In the Specified Ions Monitoring mode (SIM) a detection limit below the therapeutic range and recoveries above 90% were obtained. Comparison of results obtained by GC-MS or a commercially available high performance liquid chromatographic (HPLC) method (for lamotrigine) and a fluorescence polarisation immunoassay (FPIA) (for carbamazepine) from spiked serum samples showed disagreement of no more than 10% between the methods and demonstrated the accuracy of the new method. In addition, quantitative determinations of these antiepileptics in samples from patients under anticonvulsive therapy showed a strong linear correlation with r2 = 0.961 for carbamazepine and r2 = 0.964 for lamotrigine. Only two from a total of 46 results differed by more than 10%. Our method for quantifying lamotrigine in serum seems to be highly specific and capable of measuring lamotrigine in patients on single therapy, as well as on add-on therapy with carbamazepine or carbamazepine epoxide. No interference from other coadministered drugs was detected.

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