Liquid chromatography-tandem mass spectrometry
Template:Infobox laboratory technique
Liquid chromatography-tandem mass spectrometry (LC-MS/MS) is an advanced analytical technique that combines liquid chromatography (LC) and tandem mass spectrometry (MS/MS) to identify and quantify chemicals in complex mixtures. This method is widely used in various fields such as biomedical research, environmental science, and forensic science due to its high sensitivity and specificity.
Overview[edit | edit source]
LC-MS/MS involves two main components: liquid chromatography and tandem mass spectrometry. Liquid chromatography separates mixtures with multiple components, and mass spectrometry provides structural and quantitative information about the molecules. Tandem mass spectrometry, or MS/MS, involves multiple rounds of mass spectrometry, usually separated by some form of fragmentation of the analyte molecules. This process allows for more detailed analysis and identification of compounds.
Applications[edit | edit source]
LC-MS/MS is utilized in a variety of applications:
- In pharmacokinetics, to analyze drug metabolism and movement through the body.
- In proteomics, to identify proteins in complex biological samples and understand protein functions.
- In food safety, to detect contaminants such as pesticides or toxins.
- In environmental monitoring, to track pollution levels and detect hazardous substances in soil and water.
Advantages[edit | edit source]
The primary advantages of LC-MS/MS include:
- High sensitivity and specificity, allowing detection of low-abundance compounds in complex matrices.
- The ability to analyze a wide range of substances, including large biomolecules and small organic compounds.
- Rapid analysis times compared to other methods like gas chromatography.
Challenges[edit | edit source]
Despite its advantages, LC-MS/MS faces several challenges:
- The complexity of the equipment and the need for highly trained personnel.
- High operational and maintenance costs.
- Potential issues with matrix effects, where other compounds in the sample can interfere with the detection of the target analytes.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD