Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry
This paper reports a new analytical method for the analysis of 18 amino acids in natural waters using solid-phase extraction (SPE) followed by liquid chromatography-electrospray tandem mass spectrometry (LC–MS/MS) operated in multiple reaction monitoring mode. Two different preconcentration methods,...
| Main Authors: | , , , , , |
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| Format: | Journal Article |
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Elsevier BV
2014
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| Online Access: | http://hdl.handle.net/20.500.11937/44212 |
| _version_ | 1848756933315526656 |
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| author | How, Zuo tong Busetti, Francesco Linge, Kathryn Kristiana, Ina Joll, Cynthia Charrois, Jeffrey |
| author_facet | How, Zuo tong Busetti, Francesco Linge, Kathryn Kristiana, Ina Joll, Cynthia Charrois, Jeffrey |
| author_sort | How, Zuo tong |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | This paper reports a new analytical method for the analysis of 18 amino acids in natural waters using solid-phase extraction (SPE) followed by liquid chromatography-electrospray tandem mass spectrometry (LC–MS/MS) operated in multiple reaction monitoring mode. Two different preconcentration methods, solid-phase extraction and concentration under reduced pressure, were tested in development of this method. Although concentration under reduced pressure provided better recoveries and method limits of detection for amino acids in ultrapure water, SPE was a more suitable extraction method for real samples due to the lower matrix effects for this method. Even though the strong cation exchange resin used in SPE method introduced exogenous matrix interferences into the sample extracts (inorganic salt originating from the acid–base reaction during the elution step), the SPE method still incorporates a broad sample clean-up and minimised endogenous matrix effects by reducing interferences originating from real water samples. The method limits of quantification (MLQ) for the SPE LC–MS/MS method in ultrapure water ranged from 0.1 to 100 μg L−1 as N for the different amino acids. The MLQs of the early eluting amino acids were limited by the presence of matrix interfering species, such as inorganic salts in natural water samples. The SPE LC–MS/MS method was successfully applied to the analysis of amino acids in 3 different drinking water source waters: the average total free amino acid content in these waters was found to be 19 μg L−1 as N, while among the 18 amino acids analysed, the most abundant amino acids were found to be tyrosine, leucine and isoleucine. |
| first_indexed | 2025-11-14T09:20:04Z |
| format | Journal Article |
| id | curtin-20.500.11937-44212 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T09:20:04Z |
| publishDate | 2014 |
| publisher | Elsevier BV |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-442122019-02-19T05:35:12Z Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry How, Zuo tong Busetti, Francesco Linge, Kathryn Kristiana, Ina Joll, Cynthia Charrois, Jeffrey amino acids liquid chromatography-mass spectrometry (LC-MS) disinfection by-products solid-phase extraction (SPE) This paper reports a new analytical method for the analysis of 18 amino acids in natural waters using solid-phase extraction (SPE) followed by liquid chromatography-electrospray tandem mass spectrometry (LC–MS/MS) operated in multiple reaction monitoring mode. Two different preconcentration methods, solid-phase extraction and concentration under reduced pressure, were tested in development of this method. Although concentration under reduced pressure provided better recoveries and method limits of detection for amino acids in ultrapure water, SPE was a more suitable extraction method for real samples due to the lower matrix effects for this method. Even though the strong cation exchange resin used in SPE method introduced exogenous matrix interferences into the sample extracts (inorganic salt originating from the acid–base reaction during the elution step), the SPE method still incorporates a broad sample clean-up and minimised endogenous matrix effects by reducing interferences originating from real water samples. The method limits of quantification (MLQ) for the SPE LC–MS/MS method in ultrapure water ranged from 0.1 to 100 μg L−1 as N for the different amino acids. The MLQs of the early eluting amino acids were limited by the presence of matrix interfering species, such as inorganic salts in natural water samples. The SPE LC–MS/MS method was successfully applied to the analysis of amino acids in 3 different drinking water source waters: the average total free amino acid content in these waters was found to be 19 μg L−1 as N, while among the 18 amino acids analysed, the most abundant amino acids were found to be tyrosine, leucine and isoleucine. 2014 Journal Article http://hdl.handle.net/20.500.11937/44212 10.1016/j.chroma.2014.10.040 Elsevier BV fulltext |
| spellingShingle | amino acids liquid chromatography-mass spectrometry (LC-MS) disinfection by-products solid-phase extraction (SPE) How, Zuo tong Busetti, Francesco Linge, Kathryn Kristiana, Ina Joll, Cynthia Charrois, Jeffrey Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title | Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title_full | Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title_fullStr | Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title_full_unstemmed | Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title_short | Analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| title_sort | analysis of free amino acids in natural waters by liquid chromatography-tandem mass spectrometry |
| topic | amino acids liquid chromatography-mass spectrometry (LC-MS) disinfection by-products solid-phase extraction (SPE) |
| url | http://hdl.handle.net/20.500.11937/44212 |