Small footprint liquid chromatography-mass spectrometry for pharmaceutical reaction monitoring and automated process analysis

被引:12
|
作者
Hemida, Mohamed [1 ,2 ]
Haddad, Paul R. [1 ,2 ]
Lam, Shing C. [1 ,3 ]
Coates, Lewellwyn J. [1 ,3 ]
Riley, Frank [4 ]
Diaz, Angel [4 ]
Gooley, Andrew A. [1 ,3 ]
Wirth, Hans-Juergen [1 ,3 ]
Guinness, Steven [4 ]
Sekulic, Sonja [4 ]
Paull, Brett [1 ,2 ]
机构
[1] Univ Tasmania, Sch Nat Sci, ARC Training Ctr Portable Analyt Separat Technol, Private Bag 75, Hobart, Tas 7001, Australia
[2] Univ Tasmania, Australian Ctr Res Separat Sci ACROSS, Sch Nat Sci, Private Bag 75, Hobart, Tas 7001, Australia
[3] Trajan Sci & Med, 7 Argent Pl, Victoria 3134, Australia
[4] Pfizer Worldwide Res & Dev, Eastern Point Rd, Groton, CT 06340 USA
基金
澳大利亚研究理事会;
关键词
Miniaturization; Capillary liquid chromatography; Absorbance detectors; Portable mass spectrometry; Process analytical technologies; ANALYTICAL TECHNOLOGY PAT; HPLC; SPECTROSCOPY; MINIATURE; TOOL; NMR;
D O I
10.1016/j.chroma.2021.462545
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liquid chromatography (LC) has broad applicability in the pharmaceutical industry, from the early stages of drug discovery to reaction monitoring and process control. However, small footprint, truly portable LC systems have not yet been demonstrated and fully evaluated practically for on-line, in-line or at-line pharmaceutical analysis. Herein, a portable, briefcase-sized capillary LC fitted with a miniature multi-deep UV-LED detector has been developed and interfaced with a portable mass spectrometer for on-site pharmaceutical analysis. With this configuration, the combined small footprint portable LC-UV/MS system was utilized for the determination of small molecule pharmaceuticals and reaction monitoring. The LC-UV/MS system was interfaced directly with a process sample cart and applied to automated pharmaceutical analysis, as well as also being benchmarked against a commercial process UPLC system (Waters PATROL system). The portable system gave low detection limits (similar to 3 ppb), a wide dynamic range (up to 200 ppm) and was used to confirm the identity of reaction impurities and for studying the kinetics of synthesis. The developed platform showed robust performance for automated process analysis, with less than 5.0% relative standard deviation (RSD) on sample-to-sample reproducibility, and less than 2% carryover between samples. The system has been shown to significantly increase throughput by providing near real-time analysis and to improve understanding of synthetic processes. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:10
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