Cargando…
An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry
We developed two independent approaches for separation and quantitation of 24 oxygenated polycyclic aromatic hydrocarbons (OPAHs) using both liquid chromatography-atmospheric pressure chemical ionization/mass spectrometry (LC-APCI/MS) and gas chromatography-electron impact/mass spectrometry (GC-EI/M...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824841/ https://www.ncbi.nlm.nih.gov/pubmed/24005604 http://dx.doi.org/10.1007/s00216-013-7319-x |
_version_ | 1782290749070508032 |
---|---|
author | O’Connell, Steven G. Haigh, Theodore Wilson, Glenn Anderson, Kim A. |
author_facet | O’Connell, Steven G. Haigh, Theodore Wilson, Glenn Anderson, Kim A. |
author_sort | O’Connell, Steven G. |
collection | PubMed |
description | We developed two independent approaches for separation and quantitation of 24 oxygenated polycyclic aromatic hydrocarbons (OPAHs) using both liquid chromatography-atmospheric pressure chemical ionization/mass spectrometry (LC-APCI/MS) and gas chromatography-electron impact/mass spectrometry (GC-EI/MS). Building on previous OPAH research, we examined laboratory stability of OPAHs, improved existing method parameters, and compared quantification strategies using standard addition and an internal standard on an environmental sample. Of 24 OPAHs targeted in this research, 19 compounds are shared between methods, with 3 uniquely quantitated by GC-EI/MS and 2 by LC-APCI/MS. Using calibration standards, all GC-EI/MS OPAHs were within 15 % of the true value and had less than 15 % relative standard deviations (RSDs) for interday variability. Similarly, all LC-APCI/MS OPAHs were within 20 % of the true value and had less than 15 % RSDs for interday variability. Instrument limits of detection ranged from 0.18 to 36 ng mL(−1) on the GC-EI/MS and 2.6 to 26 ng mL(−1) on the LC-APCI/MS. Four standard reference materials were analyzed with each method, and we report some compounds not previously published in these materials, such as perinaphthenone and xanthone. Finally, an environmental passive sampling extract from Portland Harbor Superfund, OR was analyzed by each method using both internal standard and standard addition to compensate for potential matrix effects. Internal standard quantitation resulted in increased precision with similar accuracy to standard addition for most OPAHs using 2-fluoro-fluorenone-(13)C as an internal standard. Overall, this work improves upon OPAH analytical methods and provides some considerations and strategies for OPAHs as focus continues to expand on this emerging chemical class. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-013-7319-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3824841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-38248412013-11-21 An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry O’Connell, Steven G. Haigh, Theodore Wilson, Glenn Anderson, Kim A. Anal Bioanal Chem Research Paper We developed two independent approaches for separation and quantitation of 24 oxygenated polycyclic aromatic hydrocarbons (OPAHs) using both liquid chromatography-atmospheric pressure chemical ionization/mass spectrometry (LC-APCI/MS) and gas chromatography-electron impact/mass spectrometry (GC-EI/MS). Building on previous OPAH research, we examined laboratory stability of OPAHs, improved existing method parameters, and compared quantification strategies using standard addition and an internal standard on an environmental sample. Of 24 OPAHs targeted in this research, 19 compounds are shared between methods, with 3 uniquely quantitated by GC-EI/MS and 2 by LC-APCI/MS. Using calibration standards, all GC-EI/MS OPAHs were within 15 % of the true value and had less than 15 % relative standard deviations (RSDs) for interday variability. Similarly, all LC-APCI/MS OPAHs were within 20 % of the true value and had less than 15 % RSDs for interday variability. Instrument limits of detection ranged from 0.18 to 36 ng mL(−1) on the GC-EI/MS and 2.6 to 26 ng mL(−1) on the LC-APCI/MS. Four standard reference materials were analyzed with each method, and we report some compounds not previously published in these materials, such as perinaphthenone and xanthone. Finally, an environmental passive sampling extract from Portland Harbor Superfund, OR was analyzed by each method using both internal standard and standard addition to compensate for potential matrix effects. Internal standard quantitation resulted in increased precision with similar accuracy to standard addition for most OPAHs using 2-fluoro-fluorenone-(13)C as an internal standard. Overall, this work improves upon OPAH analytical methods and provides some considerations and strategies for OPAHs as focus continues to expand on this emerging chemical class. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-013-7319-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-09-05 2013 /pmc/articles/PMC3824841/ /pubmed/24005604 http://dx.doi.org/10.1007/s00216-013-7319-x Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Research Paper O’Connell, Steven G. Haigh, Theodore Wilson, Glenn Anderson, Kim A. An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title | An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title_full | An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title_fullStr | An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title_full_unstemmed | An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title_short | An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry |
title_sort | analytical investigation of 24 oxygenated-pahs (opahs) using liquid and gas chromatography–mass spectrometry |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824841/ https://www.ncbi.nlm.nih.gov/pubmed/24005604 http://dx.doi.org/10.1007/s00216-013-7319-x |
work_keys_str_mv | AT oconnellsteveng ananalyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT haightheodore ananalyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT wilsonglenn ananalyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT andersonkima ananalyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT oconnellsteveng analyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT haightheodore analyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT wilsonglenn analyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry AT andersonkima analyticalinvestigationof24oxygenatedpahsopahsusingliquidandgaschromatographymassspectrometry |