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一种新颖的二维液相色谱-质谱法,用于直接从含有离子对试剂的流动相的 HPLC 洗脱液中鉴定药物杂质。

A novel two-dimensional liquid chromatography - Mass spectrometry method for direct drug impurity identification from HPLC eluent containing ion-pairing reagent in mobile phases.

机构信息

Shimadzu Scientific Instrument Company, Beijing, 100020, China.

Shimadzu (Asia Pacific) Pte Ltd, 118264, Singapore.

出版信息

Anal Chim Acta. 2019 Feb 21;1049:105-114. doi: 10.1016/j.aca.2018.10.031. Epub 2018 Oct 23.

Abstract

In this study, a novel two dimensional liquid chromatography - mass spectrometry (2D-LC-MS) method with use of a weak anion exchange column between the 1st DLC RP column and the 2nd DLC RP column (RP1-WAX-RP2) was developed and applied to identify drug impurities from MS incompatible mobile phases containing sodium 1-octanesulfonate and non-volatile buffer. The 1st DLC conditions follow exactly the original standard HPLC method recorded in Chinese Pharmacopeia (ChP), European Pharmacopeia (EP) or US Pharmacopeia (USP). An impurity fraction was collected with a built-in sample loop (100 μL) and transferred to the WAX column where 1-octanesulfonate and phosphate were trapped and removed. While, the impurity and other cations were eluted to the 2nd D column (RP2) for separation and identification by connected IT-TOF MS. Methods were programmed and applied to identify impurities in two generic drugs, sulpiride (hydrophilic drug with logP 0.57) and dobutamine (hydrophobic drug with logP 3.6). The results indicate that the methods based on RP1-WAX-RP2 column configuration offer a feasible solution for direct impurity identification in generic drug product or API without needs of off-line desalting from the MS incompatible mobile phases containing ion-pairing reagent and non-volatile buffer.

摘要

本研究开发了一种新型二维液相色谱 - 质谱(2D-LC-MS)方法,在第一 DLC RP 柱和第二 DLC RP 柱(RP1-WAX-RP2)之间使用弱阴离子交换柱,用于从含有 1-辛烷磺酸钠和非挥发性缓冲剂的 MS 不兼容流动相鉴定药物杂质。第一 DLC 条件完全遵循中国药典(ChP)、欧洲药典(EP)或美国药典(USP)中记录的原始标准 HPLC 方法。杂质部分用内置进样环(100µL)收集,并转移到 WAX 柱上,在该柱上 1-辛烷磺酸盐和磷酸盐被捕获并去除。同时,杂质和其他阳离子被洗脱至第二 D 柱(RP2),通过连接的 IT-TOF MS 进行分离和鉴定。方法进行编程并应用于两种仿制药(舒必利[亲水性药物,logP 0.57]和多巴酚丁胺[疏水性药物,logP 3.6])中杂质的鉴定。结果表明,基于 RP1-WAX-RP2 柱配置的方法为直接从含有离子对试剂和非挥发性缓冲剂的 MS 不兼容流动相中对仿制药产品或原料药中的杂质进行鉴定提供了一种可行的解决方案,而无需进行离线脱盐。

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