Liquid chromatography–mass spectrometry
Analytical chemistry technique / From Wikipedia, the free encyclopedia
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Liquid chromatography–mass spectrometry (LC–MS) is an analytical chemistry technique that combines the physical separation capabilities of liquid chromatography (or HPLC) with the mass analysis capabilities of mass spectrometry (MS). Coupled chromatography – MS systems are popular in chemical analysis because the individual capabilities of each technique are enhanced synergistically. While liquid chromatography separates mixtures with multiple components, mass spectrometry provides spectral information that may help to identify (or confirm the suspected identity of) each separated component.[1] MS is not only sensitive, but provides selective detection, relieving the need for complete chromatographic separation.[2] LC–MS is also appropriate for metabolomics because of its good coverage of a wide range of chemicals.[3] This tandem technique can be used to analyze biochemical, organic, and inorganic compounds commonly found in complex samples of environmental and biological origin. Therefore, LC–MS may be applied in a wide range of sectors including biotechnology, environment monitoring, food processing, and pharmaceutical, agrochemical, and cosmetic industries.[4][5] Since the early 2000s, LC–MS (or more specifically LC–MS–MS) has also begun to be used in clinical applications.[6]
Acronym | LCMS |
---|---|
Classification | Chromatography Mass spectrometry |
Analytes | organic molecules biomolecules |
Manufacturers | Agilent Bruker PerkinElmer SCIEX Shimadzu Scientific Thermo Fisher Scientific Waters Corporation |
Other techniques | |
Related | Gas chromatography–mass spectrometry |
In addition to the liquid chromatography and mass spectrometry devices, an LC–MS system contains an interface that efficiently transfers the separated components from the LC column into the MS ion source.[5][7] The interface is necessary because the LC and MS devices are fundamentally incompatible. While the mobile phase in a LC system is a pressurized liquid, the MS analyzers commonly operate under high vacuum. Thus, it is not possible to directly pump the eluate from the LC column into the MS source. Overall, the interface is a mechanically simple part of the LC–MS system that transfers the maximum amount of analyte, removes a significant portion of the mobile phase used in LC and preserves the chemical identity of the chromatography products (chemically inert). As a requirement, the interface should not interfere with the ionizing efficiency and vacuum conditions of the MS system.[5] Nowadays, most extensively applied LC–MS interfaces are based on atmospheric pressure ionization (API) strategies like electrospray ionization (ESI), atmospheric-pressure chemical ionization (APCI), and atmospheric pressure photoionization (APPI). These interfaces became available in the 1990s after a two decade long research and development process.[8][7]