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Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology
The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) sys...
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Published in: | Water research (Oxford) 2010-01, Vol.44 (1), p.243-255 |
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description | The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed. |
doi_str_mv | 10.1016/j.watres.2009.09.018 |
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A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed.</description><identifier>ISSN: 0043-1354</identifier><identifier>EISSN: 1879-2448</identifier><identifier>DOI: 10.1016/j.watres.2009.09.018</identifier><identifier>PMID: 19800649</identifier><identifier>CODEN: WATRAG</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Acidic pharmaceuticals ; Anti-Inflammatory Agents, Non-Steroidal - analysis ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Applied sciences ; Bromides ; By-products ; Byproducts ; Chlorination ; Chromatography, Liquid ; Degradation ; Diclofenac ; Diclofenac - analysis ; Diclofenac - chemistry ; drinking water ; drugs ; Environmental fate ; Exact sciences and technology ; Halogenation ; Hydrogen-Ion Concentration ; indomethacine ; Kinetics ; liquid chromatography ; Liquid chromatography–mass spectrometry (LC–MS) ; Mass Spectrometry ; methodology ; Molecular Structure ; Naproxen ; Naproxen - analysis ; Naproxen - chemistry ; Non-steroidal anti-inflammatory drugs (NSAIDs) ; Other industrial wastes. Sewage sludge ; Pharmaceuticals ; Pollution ; Salicylic acid ; Salicylic Acid - analysis ; Salicylic Acid - chemistry ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Tandem Mass Spectrometry ; Time-of-flight (TOF) ; Wastes ; wastewater ; Water Pollutants, Chemical - analysis ; Water Pollutants, Chemical - chemistry ; Water Supply - analysis ; Water treatment and pollution</subject><ispartof>Water research (Oxford), 2010-01, Vol.44 (1), p.243-255</ispartof><rights>2009 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c547t-c4d327eb45107bb3bf2917a92015281e716b2c3b39cf6e41b748fddcd89cd44f3</citedby><cites>FETCH-LOGICAL-c547t-c4d327eb45107bb3bf2917a92015281e716b2c3b39cf6e41b748fddcd89cd44f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,4010,27904,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22289109$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19800649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quintana, José Benito</creatorcontrib><creatorcontrib>Rodil, Rosario</creatorcontrib><creatorcontrib>López-Mahía, Purificación</creatorcontrib><creatorcontrib>Muniategui-Lorenzo, Soledad</creatorcontrib><creatorcontrib>Prada-Rodríguez, Darío</creatorcontrib><title>Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology</title><title>Water research (Oxford)</title><addtitle>Water Res</addtitle><description>The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed.</description><subject>Acidic pharmaceuticals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - analysis</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Applied sciences</subject><subject>Bromides</subject><subject>By-products</subject><subject>Byproducts</subject><subject>Chlorination</subject><subject>Chromatography, Liquid</subject><subject>Degradation</subject><subject>Diclofenac</subject><subject>Diclofenac - analysis</subject><subject>Diclofenac - chemistry</subject><subject>drinking water</subject><subject>drugs</subject><subject>Environmental fate</subject><subject>Exact sciences and technology</subject><subject>Halogenation</subject><subject>Hydrogen-Ion Concentration</subject><subject>indomethacine</subject><subject>Kinetics</subject><subject>liquid chromatography</subject><subject>Liquid chromatography–mass spectrometry (LC–MS)</subject><subject>Mass Spectrometry</subject><subject>methodology</subject><subject>Molecular Structure</subject><subject>Naproxen</subject><subject>Naproxen - analysis</subject><subject>Naproxen - chemistry</subject><subject>Non-steroidal anti-inflammatory drugs (NSAIDs)</subject><subject>Other industrial wastes. Sewage sludge</subject><subject>Pharmaceuticals</subject><subject>Pollution</subject><subject>Salicylic acid</subject><subject>Salicylic Acid - analysis</subject><subject>Salicylic Acid - chemistry</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Tandem Mass Spectrometry</subject><subject>Time-of-flight (TOF)</subject><subject>Wastes</subject><subject>wastewater</subject><subject>Water Pollutants, Chemical - analysis</subject><subject>Water Pollutants, Chemical - chemistry</subject><subject>Water Supply - analysis</subject><subject>Water treatment and pollution</subject><issn>0043-1354</issn><issn>1879-2448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkV-L1DAUxYso7rj6DUTzIvrSMTfJNM2LIIt_FhZ80H0OaXLbydA2Y9KuzoPf3dQO-rbChUDu796cnFMUz4FugUL19rD9YaaIacsoVduloH5QbKCWqmRC1A-LDaWCl8B34qJ4ktKBUsoYV4-LC1A1pZVQm-LX9XiHafKdmfzYkWmPxO77EP2YL8JIQkuM9c5bctybOBiL8-St6RMxoyPNqTzG4GY7kTbk7p8R4x0urUwQ_HnE6AccJ9MTh8l3Ixlw2gcX-tCdnhaP2rwLn53Py-L244dvV5_Lmy-frq_e35R2J-RUWuE4k9iIHVDZNLxpmQJpFKOwYzWghKphljdc2bZCAY0UdeucdbWyToiWXxav171Z7fc5_1cPPlnsezNimJOWXEDFs2mZfHMvCZJn56iq4f8oqyrJJQeVUbGiNoaUIrb6mF0x8aSB6iVNfdBrmnpJUy8Fi5gX5xfmZkD3b-gcXwZenQGTcihtNKP16S_HGKsV0IV7uXKtCdp0MTO3X7N7nIJkUNEqE-9WAnMMdx6jTtbjaNH5iHbSLvj7tf4GNf_KpA</recordid><startdate>201001</startdate><enddate>201001</enddate><creator>Quintana, José Benito</creator><creator>Rodil, Rosario</creator><creator>López-Mahía, Purificación</creator><creator>Muniategui-Lorenzo, Soledad</creator><creator>Prada-Rodríguez, Darío</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>7ST</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>SOI</scope><scope>7SU</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope><scope>7X8</scope></search><sort><creationdate>201001</creationdate><title>Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology</title><author>Quintana, José Benito ; Rodil, Rosario ; López-Mahía, Purificación ; Muniategui-Lorenzo, Soledad ; Prada-Rodríguez, Darío</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c547t-c4d327eb45107bb3bf2917a92015281e716b2c3b39cf6e41b748fddcd89cd44f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acidic pharmaceuticals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - analysis</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Applied sciences</topic><topic>Bromides</topic><topic>By-products</topic><topic>Byproducts</topic><topic>Chlorination</topic><topic>Chromatography, Liquid</topic><topic>Degradation</topic><topic>Diclofenac</topic><topic>Diclofenac - analysis</topic><topic>Diclofenac - chemistry</topic><topic>drinking water</topic><topic>drugs</topic><topic>Environmental fate</topic><topic>Exact sciences and technology</topic><topic>Halogenation</topic><topic>Hydrogen-Ion Concentration</topic><topic>indomethacine</topic><topic>Kinetics</topic><topic>liquid chromatography</topic><topic>Liquid chromatography–mass spectrometry (LC–MS)</topic><topic>Mass Spectrometry</topic><topic>methodology</topic><topic>Molecular Structure</topic><topic>Naproxen</topic><topic>Naproxen - analysis</topic><topic>Naproxen - chemistry</topic><topic>Non-steroidal anti-inflammatory drugs (NSAIDs)</topic><topic>Other industrial wastes. Sewage sludge</topic><topic>Pharmaceuticals</topic><topic>Pollution</topic><topic>Salicylic acid</topic><topic>Salicylic Acid - analysis</topic><topic>Salicylic Acid - chemistry</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Tandem Mass Spectrometry</topic><topic>Time-of-flight (TOF)</topic><topic>Wastes</topic><topic>wastewater</topic><topic>Water Pollutants, Chemical - analysis</topic><topic>Water Pollutants, Chemical - chemistry</topic><topic>Water Supply - analysis</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quintana, José Benito</creatorcontrib><creatorcontrib>Rodil, Rosario</creatorcontrib><creatorcontrib>López-Mahía, Purificación</creatorcontrib><creatorcontrib>Muniategui-Lorenzo, Soledad</creatorcontrib><creatorcontrib>Prada-Rodríguez, Darío</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Environment 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><collection>Environment Abstracts</collection><collection>Environmental Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Water research (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quintana, José Benito</au><au>Rodil, Rosario</au><au>López-Mahía, Purificación</au><au>Muniategui-Lorenzo, Soledad</au><au>Prada-Rodríguez, Darío</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology</atitle><jtitle>Water research (Oxford)</jtitle><addtitle>Water Res</addtitle><date>2010-01</date><risdate>2010</risdate><volume>44</volume><issue>1</issue><spage>243</spage><epage>255</epage><pages>243-255</pages><issn>0043-1354</issn><eissn>1879-2448</eissn><coden>WATRAG</coden><abstract>The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>19800649</pmid><doi>10.1016/j.watres.2009.09.018</doi><tpages>13</tpages></addata></record> |
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subjects | Acidic pharmaceuticals Anti-Inflammatory Agents, Non-Steroidal - analysis Anti-Inflammatory Agents, Non-Steroidal - chemistry Applied sciences Bromides By-products Byproducts Chlorination Chromatography, Liquid Degradation Diclofenac Diclofenac - analysis Diclofenac - chemistry drinking water drugs Environmental fate Exact sciences and technology Halogenation Hydrogen-Ion Concentration indomethacine Kinetics liquid chromatography Liquid chromatography–mass spectrometry (LC–MS) Mass Spectrometry methodology Molecular Structure Naproxen Naproxen - analysis Naproxen - chemistry Non-steroidal anti-inflammatory drugs (NSAIDs) Other industrial wastes. Sewage sludge Pharmaceuticals Pollution Salicylic acid Salicylic Acid - analysis Salicylic Acid - chemistry Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Tandem Mass Spectrometry Time-of-flight (TOF) Wastes wastewater Water Pollutants, Chemical - analysis Water Pollutants, Chemical - chemistry Water Supply - analysis Water treatment and pollution |
title | Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology |
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