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基于环糊精的非水电动色谱法结合紫外和质谱检测:应用于胺碘酮的杂质分析

Cyclodextrin-based nonaqueous electrokinetic chromatography with UV and mass spectrometric detection: application to the impurity profiling of amiodarone.

作者信息

Mol Roelof, de Jong Gerhardus J, Somsen Govert W

机构信息

Biomedical Analysis, Utrecht University, Utrecht, The Netherlands.

出版信息

Electrophoresis. 2008 Sep;29(17):3575-81. doi: 10.1002/elps.200800074.

Abstract

The potential of nonaqueous electrokinetic chromatography (NAEKC) using cyclodextrins (CD) for the analysis of basic drugs and related compounds was evaluated. Both UV absorbance and mass spectrometric (MS) detection were employed. Addition of neutral CD to the NA background electrolyte did not significantly enhance the separation of a test mixture of basic drugs, and no change in selectivity was observed. In contrast, anionic single-isomer-sulfated CD strongly added to the selectivity of the NAEKC system inducing an improved resolution among the test compounds and increasing the migration time window. The applicability of the NAEKC system using anionic CD is demonstrated by the profiling of a sample of the drug amiodarone that had been stored for 1 year at room temperature. Amiodarone is poorly soluble in water. NAEKC-UV analysis indicated the presence of at least seven impurities in the amiodarone sample. In order to identify these compounds, the NAEKC system was coupled directly to electrospray ionization (ESI) ion-trap MS. The total of detected impurities increased to 12 due to the added sensitivity and selectivity of MS detection. Based on the acquired MS/MS data, three sample constituents could be identified as 'known' impurities (British Pharmacopoeia), whereas for three unknown impurities molecular structures could be proposed. Estimated limits of detection for amiodarone using the NAEKC method were 1 microg/mL with UV detection and 15 ng/mL with ESI-MS detection (full-scan). Based on relative responses, the impurity content of the stored drug substance was estimated to be 0.33 and 0.47% using NAEKC-UV and NAEKC-ESI-MS, respectively.

摘要

评估了使用环糊精(CD)的非水电动力学色谱法(NAEKC)分析碱性药物及相关化合物的潜力。采用了紫外吸光度检测和质谱(MS)检测。向非水背景电解质中添加中性CD并不能显著增强碱性药物测试混合物的分离效果,且未观察到选择性变化。相比之下,向NAEKC系统中强烈添加阴离子单异构体硫酸化CD会改变选择性,提高测试化合物之间的分离度,并增加迁移时间窗口。通过对在室温下储存1年的胺碘酮药物样品进行分析,证明了使用阴离子CD的NAEKC系统的适用性。胺碘酮在水中溶解度很差。NAEKC-UV分析表明胺碘酮样品中至少存在七种杂质。为了鉴定这些化合物,将NAEKC系统直接与电喷雾电离(ESI)离子阱质谱联用。由于MS检测的灵敏度和选择性提高,检测到的杂质总数增加到12种。根据获得的MS/MS数据,三种样品成分可鉴定为“已知”杂质(英国药典),而对于三种未知杂质,可提出分子结构。使用NAEKC方法,胺碘酮的紫外检测估计检测限为1μg/mL,ESI-MS检测(全扫描)为15 ng/mL。根据相对响应,使用NAEKC-UV和NAEKC-ESI-MS分别估计储存原料药的杂质含量为0.33%和0.47%。

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