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High-performance liquid chromatography coupled to direct analysis in real time mass spectrometry: Investigations on gradient elution and influence of complex matrices on signal intensities
Direct analysis in real time (DART) time-of-flight mass spectrometry (TOF-MS) has been tested for its suitability as a detector for gradient elution HPLC. Thereby a strong dependency of signal intensity on the amount of organic solvent present in the eluent could be observed. Adding a make-up liquid...
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Published in: | Journal of Chromatography A 2011-08, Vol.1218 (31), p.5180-5186 |
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container_end_page | 5186 |
container_issue | 31 |
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container_title | Journal of Chromatography A |
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creator | Beißmann, Susanne Buchberger, Wolfgang Hertsens, Robert Klampfl, Christian W. |
description | Direct analysis in real time (DART) time-of-flight mass spectrometry (TOF-MS) has been tested for its suitability as a detector for gradient elution HPLC. Thereby a strong dependency of signal intensity on the amount of organic solvent present in the eluent could be observed. Adding a make-up liquid (iso-propanol) post-column to the HPLC effluent greatly enhanced detection limits for early eluting compounds. Limits of detection achieved employing this approach were in the range of 7–27
μg
L
−1 for the parabene test mixture and 15–87
μg
L
−1 for the pharmaceuticals. In further investigations DART ionization was compared to several other widely used atmospheric pressure ionization methods with respect to signal suppression phenomena occurring in when samples with problematic matrices are analyzed. For this purpose extracts from environmental and waste water samples were selected as model matrices which were subsequently spiked with a set of six substances commonly present in personal care products as well as six pharmaceuticals at concentration levels between 100
μg
L
−1 and 500
μg
L
−1 corresponding to 100
ng
L
−1 and 500
ng
L
−1 respectively in the original sample. With ionization suppression of less than 11% for most analytes investigated, DART ionization showed similar to even somewhat superior behavior compared to atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo ionization (APPI) for the Danube river water extract; for the more challenging matrix of the sewage plant effluent extract DART provided better results with ion suppression being less than 11% for 9 out of 12 analytes while values for APCI were lying between 20% and >90%. Electrospray ionization (ESI) was much more affected by suppression effects than DART with values between 26% and 80% for Danube river water; in combination with the sewage plant effluent matrix suppression >50% was observed for all analytes. |
doi_str_mv | 10.1016/j.chroma.2011.05.092 |
format | article |
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μg
L
−1 for the parabene test mixture and 15–87
μg
L
−1 for the pharmaceuticals. In further investigations DART ionization was compared to several other widely used atmospheric pressure ionization methods with respect to signal suppression phenomena occurring in when samples with problematic matrices are analyzed. For this purpose extracts from environmental and waste water samples were selected as model matrices which were subsequently spiked with a set of six substances commonly present in personal care products as well as six pharmaceuticals at concentration levels between 100
μg
L
−1 and 500
μg
L
−1 corresponding to 100
ng
L
−1 and 500
ng
L
−1 respectively in the original sample. With ionization suppression of less than 11% for most analytes investigated, DART ionization showed similar to even somewhat superior behavior compared to atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo ionization (APPI) for the Danube river water extract; for the more challenging matrix of the sewage plant effluent extract DART provided better results with ion suppression being less than 11% for 9 out of 12 analytes while values for APCI were lying between 20% and >90%. Electrospray ionization (ESI) was much more affected by suppression effects than DART with values between 26% and 80% for Danube river water; in combination with the sewage plant effluent matrix suppression >50% was observed for all analytes.</description><identifier>ISSN: 0021-9673</identifier><identifier>DOI: 10.1016/j.chroma.2011.05.092</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analysis methods ; Analytical chemistry ; Applied sciences ; Atmospheric pressure ; Barometric pressure ; Chemical industry and chemicals ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Cosmetics, toiletries ; Direct analysis in real time ; Effluents ; Elution ; Exact sciences and technology ; Freshwater ; HPLC ; Hyphenated methods ; Ionization ; Mathematical analysis ; Matrices ; Matrix methods ; Natural water pollution ; Other chromatographic methods ; Other wastewaters ; Pollution ; Washing products. Cosmetics and toiletries. Perfumes ; Wastewaters ; Water treatment and pollution</subject><ispartof>Journal of Chromatography A, 2011-08, Vol.1218 (31), p.5180-5186</ispartof><rights>2011 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-4749fb1e8da29de525ab2ed0403a6494d922de0412d113ab55c3ebd18364a6ea3</citedby><cites>FETCH-LOGICAL-c456t-4749fb1e8da29de525ab2ed0403a6494d922de0412d113ab55c3ebd18364a6ea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24340114$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Beißmann, Susanne</creatorcontrib><creatorcontrib>Buchberger, Wolfgang</creatorcontrib><creatorcontrib>Hertsens, Robert</creatorcontrib><creatorcontrib>Klampfl, Christian W.</creatorcontrib><title>High-performance liquid chromatography coupled to direct analysis in real time mass spectrometry: Investigations on gradient elution and influence of complex matrices on signal intensities</title><title>Journal of Chromatography A</title><description>Direct analysis in real time (DART) time-of-flight mass spectrometry (TOF-MS) has been tested for its suitability as a detector for gradient elution HPLC. Thereby a strong dependency of signal intensity on the amount of organic solvent present in the eluent could be observed. Adding a make-up liquid (iso-propanol) post-column to the HPLC effluent greatly enhanced detection limits for early eluting compounds. Limits of detection achieved employing this approach were in the range of 7–27
μg
L
−1 for the parabene test mixture and 15–87
μg
L
−1 for the pharmaceuticals. In further investigations DART ionization was compared to several other widely used atmospheric pressure ionization methods with respect to signal suppression phenomena occurring in when samples with problematic matrices are analyzed. For this purpose extracts from environmental and waste water samples were selected as model matrices which were subsequently spiked with a set of six substances commonly present in personal care products as well as six pharmaceuticals at concentration levels between 100
μg
L
−1 and 500
μg
L
−1 corresponding to 100
ng
L
−1 and 500
ng
L
−1 respectively in the original sample. With ionization suppression of less than 11% for most analytes investigated, DART ionization showed similar to even somewhat superior behavior compared to atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo ionization (APPI) for the Danube river water extract; for the more challenging matrix of the sewage plant effluent extract DART provided better results with ion suppression being less than 11% for 9 out of 12 analytes while values for APCI were lying between 20% and >90%. Electrospray ionization (ESI) was much more affected by suppression effects than DART with values between 26% and 80% for Danube river water; in combination with the sewage plant effluent matrix suppression >50% was observed for all analytes.</description><subject>Analysis methods</subject><subject>Analytical chemistry</subject><subject>Applied sciences</subject><subject>Atmospheric pressure</subject><subject>Barometric pressure</subject><subject>Chemical industry and chemicals</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Cosmetics, toiletries</subject><subject>Direct analysis in real time</subject><subject>Effluents</subject><subject>Elution</subject><subject>Exact sciences and technology</subject><subject>Freshwater</subject><subject>HPLC</subject><subject>Hyphenated methods</subject><subject>Ionization</subject><subject>Mathematical analysis</subject><subject>Matrices</subject><subject>Matrix methods</subject><subject>Natural water pollution</subject><subject>Other chromatographic methods</subject><subject>Other wastewaters</subject><subject>Pollution</subject><subject>Washing products. Cosmetics and toiletries. 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Cosmetics and toiletries. Perfumes</topic><topic>Wastewaters</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beißmann, Susanne</creatorcontrib><creatorcontrib>Buchberger, Wolfgang</creatorcontrib><creatorcontrib>Hertsens, Robert</creatorcontrib><creatorcontrib>Klampfl, Christian W.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beißmann, Susanne</au><au>Buchberger, Wolfgang</au><au>Hertsens, Robert</au><au>Klampfl, Christian W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-performance liquid chromatography coupled to direct analysis in real time mass spectrometry: Investigations on gradient elution and influence of complex matrices on signal intensities</atitle><jtitle>Journal of Chromatography A</jtitle><date>2011-08-05</date><risdate>2011</risdate><volume>1218</volume><issue>31</issue><spage>5180</spage><epage>5186</epage><pages>5180-5186</pages><issn>0021-9673</issn><coden>JOCRAM</coden><abstract>Direct analysis in real time (DART) time-of-flight mass spectrometry (TOF-MS) has been tested for its suitability as a detector for gradient elution HPLC. Thereby a strong dependency of signal intensity on the amount of organic solvent present in the eluent could be observed. Adding a make-up liquid (iso-propanol) post-column to the HPLC effluent greatly enhanced detection limits for early eluting compounds. Limits of detection achieved employing this approach were in the range of 7–27
μg
L
−1 for the parabene test mixture and 15–87
μg
L
−1 for the pharmaceuticals. In further investigations DART ionization was compared to several other widely used atmospheric pressure ionization methods with respect to signal suppression phenomena occurring in when samples with problematic matrices are analyzed. For this purpose extracts from environmental and waste water samples were selected as model matrices which were subsequently spiked with a set of six substances commonly present in personal care products as well as six pharmaceuticals at concentration levels between 100
μg
L
−1 and 500
μg
L
−1 corresponding to 100
ng
L
−1 and 500
ng
L
−1 respectively in the original sample. With ionization suppression of less than 11% for most analytes investigated, DART ionization showed similar to even somewhat superior behavior compared to atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo ionization (APPI) for the Danube river water extract; for the more challenging matrix of the sewage plant effluent extract DART provided better results with ion suppression being less than 11% for 9 out of 12 analytes while values for APCI were lying between 20% and >90%. Electrospray ionization (ESI) was much more affected by suppression effects than DART with values between 26% and 80% for Danube river water; in combination with the sewage plant effluent matrix suppression >50% was observed for all analytes.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.chroma.2011.05.092</doi><tpages>7</tpages></addata></record> |
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source | Elsevier |
subjects | Analysis methods Analytical chemistry Applied sciences Atmospheric pressure Barometric pressure Chemical industry and chemicals Chemistry Chromatographic methods and physical methods associated with chromatography Cosmetics, toiletries Direct analysis in real time Effluents Elution Exact sciences and technology Freshwater HPLC Hyphenated methods Ionization Mathematical analysis Matrices Matrix methods Natural water pollution Other chromatographic methods Other wastewaters Pollution Washing products. Cosmetics and toiletries. Perfumes Wastewaters Water treatment and pollution |
title | High-performance liquid chromatography coupled to direct analysis in real time mass spectrometry: Investigations on gradient elution and influence of complex matrices on signal intensities |
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