Published February 2019 | Version v1
Journal article

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

  • 1. Shimadzu Scientific Instrument Company, Beijing, 100020 (China)
  • 2. Shimadzu (Asia Pacific) Pte Ltd, 118264 (Singapore)
  • 3. Key Lab of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023 (China)

Description

Highlights: • A RP1-WAX-RP2-MS method was developed for impurity identification. • It can be used to identify impurity both in hydrophobic drug and hydrophilic drug. • Compare to RP-RP method, it was more effective for removing ion-pairing reagent. • Trapping column and its mobile phase were studied. • Ion-exchange capacity and target compound range were systematically investigated. -- 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.

Additional details

Identifiers

DOI
10.1016/j.aca.2018.10.031;
PII
S0003267018312613;

Publishing Information

Journal Title
Analytica Chimica Acta
Journal Volume
1049
Journal Page Range
p. 105-114
ISSN
0003-2670
CODEN
ACACAM

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Copyright
Copyright (c) 2018 Elsevier B.V. All rights reserved.