Loading…
Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium
•Evaluation of the enantioselective biodegradation of ofloxacin and levofloxacin by an activated sludge consortium.•Enantiomerization was observed in the biodegradation of the isolated (S)-enantiomer with formation of the (R) enantiomer.•Enantioselectivity and enantiomerization during the biodegrada...
Saved in:
Published in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1029-1030, p.174-183 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553 |
---|---|
cites | cdi_FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553 |
container_end_page | 183 |
container_issue | |
container_start_page | 174 |
container_title | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences |
container_volume | 1029-1030 |
creator | Maia, Alexandra S. Castro, Paula M.L. Tiritan, Maria Elizabeth |
description | •Evaluation of the enantioselective biodegradation of ofloxacin and levofloxacin by an activated sludge consortium.•Enantiomerization was observed in the biodegradation of the isolated (S)-enantiomer with formation of the (R) enantiomer.•Enantioselectivity and enantiomerization during the biodegradation were confirmed by exact mass spectrometry.
Ofloxacin is a chiral fluoroquinolone commercialized as racemate and as its enantiomerically pure form levofloxacin. This work presents an integrated liquid chromatography (LC) method with fluorescence detection (FD) and exact mass spectrometry (EMS) developed to assess the enantiomeric biodegradation of ofloxacin and levofloxacin in laboratory-scale microcosms. The optimized enantioseparation conditions were achieved using a macrocyclic antibiotic ristocetin A-bonded CSP (150×2.1mm i.d.; particle size 5μm) under reversed-phase elution mode. The method was validated using a mineral salts medium as matrix and presented selectivity and linearity over a concentration range from 5μgL−1 (quantification limit) to 350μgL−1 for each enantiomer. The method was successfully applied to evaluate biodegradation of ofloxacin enantiomers at 250μgL−1 by an activated sludge inoculum. Ofloxacin (racemic mixture) and (S)-enantiomer (levofloxacin) were degraded up to 58 and 52%, respectively. An additional degradable carbon source, acetate, enhanced biodegradation up to 23%. (S)-enantiomer presented the highest extent of degradation (66.8%) when ofloxacin was supplied along with acetate. Results indicated slightly higher biodegradation extents for the (S)-enantiomer when supplementation was done with ofloxacin. Degradation occurred faster in the first 3days and proceeded slowly until the end of the assays. The chromatographic results from LC-FD suggested the formation of the (R)-enantiomer during levofloxacin biodegradation which was confirmed by LC–MS with a LTQ Orbitrap XL. |
doi_str_mv | 10.1016/j.jchromb.2016.06.026 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808374003</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1570023216304135</els_id><sourcerecordid>1808374003</sourcerecordid><originalsourceid>FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553</originalsourceid><addsrcrecordid>eNqFUMuKFDEUDaI4D_0EJUs31eZRqVS5EWdwdGDAjYK7kM69NZ2mKulJUoO99ctNT7duhQPJTc6Dewh5w9mKM9693662bpPivF6JOq5YheiekXPea9lI3f18Xu9Ks4YJKc7IRc5bxrhmWr4kZ0K3Ug69OCe_b0PB-2QLAp38w-KBPtnaEuvrbrOnM5ZNBOoDxWBD8THjhK74R6S5LOAxf6BXPsLBBWz9DzSOFVP8ZV1VrffUBmoPiqeUPC1wj9TFkGMqfplfkRejnTK-Pp2X5MfN5-_XX5u7b19urz_dNU4OojQwuLYHza1wIB0o1Y6tHde2E7yO42gZG1ulkPNBg26BD04xUEIPzkqrlLwk746-uxQfFszFzD47nCYbMC7Z8J71UreMyUpVR6pLMeeEo9klP9u0N5yZQ_1ma071m0P9hlWIrureniKW9YzwT_W370r4eCRgXfTRYzLZeQwOwadaqoHo_xPxB-HHnTc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1808374003</pqid></control><display><type>article</type><title>Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Maia, Alexandra S. ; Castro, Paula M.L. ; Tiritan, Maria Elizabeth</creator><creatorcontrib>Maia, Alexandra S. ; Castro, Paula M.L. ; Tiritan, Maria Elizabeth</creatorcontrib><description>•Evaluation of the enantioselective biodegradation of ofloxacin and levofloxacin by an activated sludge consortium.•Enantiomerization was observed in the biodegradation of the isolated (S)-enantiomer with formation of the (R) enantiomer.•Enantioselectivity and enantiomerization during the biodegradation were confirmed by exact mass spectrometry.
Ofloxacin is a chiral fluoroquinolone commercialized as racemate and as its enantiomerically pure form levofloxacin. This work presents an integrated liquid chromatography (LC) method with fluorescence detection (FD) and exact mass spectrometry (EMS) developed to assess the enantiomeric biodegradation of ofloxacin and levofloxacin in laboratory-scale microcosms. The optimized enantioseparation conditions were achieved using a macrocyclic antibiotic ristocetin A-bonded CSP (150×2.1mm i.d.; particle size 5μm) under reversed-phase elution mode. The method was validated using a mineral salts medium as matrix and presented selectivity and linearity over a concentration range from 5μgL−1 (quantification limit) to 350μgL−1 for each enantiomer. The method was successfully applied to evaluate biodegradation of ofloxacin enantiomers at 250μgL−1 by an activated sludge inoculum. Ofloxacin (racemic mixture) and (S)-enantiomer (levofloxacin) were degraded up to 58 and 52%, respectively. An additional degradable carbon source, acetate, enhanced biodegradation up to 23%. (S)-enantiomer presented the highest extent of degradation (66.8%) when ofloxacin was supplied along with acetate. Results indicated slightly higher biodegradation extents for the (S)-enantiomer when supplementation was done with ofloxacin. Degradation occurred faster in the first 3days and proceeded slowly until the end of the assays. The chromatographic results from LC-FD suggested the formation of the (R)-enantiomer during levofloxacin biodegradation which was confirmed by LC–MS with a LTQ Orbitrap XL.</description><identifier>ISSN: 1570-0232</identifier><identifier>EISSN: 1873-376X</identifier><identifier>DOI: 10.1016/j.jchromb.2016.06.026</identifier><identifier>PMID: 27433982</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Activated sludge ; Anti-Infective Agents - isolation & purification ; Biodegradation ; Biodegradation, Environmental ; Chromatography, Liquid - methods ; Enantioselectivity ; Levofloxacin ; Levofloxacin - isolation & purification ; Limit of Detection ; Macrocyclic antibiotic-based stationary phases ; Ofloxacin ; Sewage - analysis ; Sewage - microbiology ; Stereoisomerism ; Tandem Mass Spectrometry - methods ; Water Pollutants, Chemical - isolation & purification</subject><ispartof>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1029-1030, p.174-183</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553</citedby><cites>FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553</cites><orcidid>0000-0003-3320-730X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27433982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maia, Alexandra S.</creatorcontrib><creatorcontrib>Castro, Paula M.L.</creatorcontrib><creatorcontrib>Tiritan, Maria Elizabeth</creatorcontrib><title>Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium</title><title>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>•Evaluation of the enantioselective biodegradation of ofloxacin and levofloxacin by an activated sludge consortium.•Enantiomerization was observed in the biodegradation of the isolated (S)-enantiomer with formation of the (R) enantiomer.•Enantioselectivity and enantiomerization during the biodegradation were confirmed by exact mass spectrometry.
Ofloxacin is a chiral fluoroquinolone commercialized as racemate and as its enantiomerically pure form levofloxacin. This work presents an integrated liquid chromatography (LC) method with fluorescence detection (FD) and exact mass spectrometry (EMS) developed to assess the enantiomeric biodegradation of ofloxacin and levofloxacin in laboratory-scale microcosms. The optimized enantioseparation conditions were achieved using a macrocyclic antibiotic ristocetin A-bonded CSP (150×2.1mm i.d.; particle size 5μm) under reversed-phase elution mode. The method was validated using a mineral salts medium as matrix and presented selectivity and linearity over a concentration range from 5μgL−1 (quantification limit) to 350μgL−1 for each enantiomer. The method was successfully applied to evaluate biodegradation of ofloxacin enantiomers at 250μgL−1 by an activated sludge inoculum. Ofloxacin (racemic mixture) and (S)-enantiomer (levofloxacin) were degraded up to 58 and 52%, respectively. An additional degradable carbon source, acetate, enhanced biodegradation up to 23%. (S)-enantiomer presented the highest extent of degradation (66.8%) when ofloxacin was supplied along with acetate. Results indicated slightly higher biodegradation extents for the (S)-enantiomer when supplementation was done with ofloxacin. Degradation occurred faster in the first 3days and proceeded slowly until the end of the assays. The chromatographic results from LC-FD suggested the formation of the (R)-enantiomer during levofloxacin biodegradation which was confirmed by LC–MS with a LTQ Orbitrap XL.</description><subject>Activated sludge</subject><subject>Anti-Infective Agents - isolation & purification</subject><subject>Biodegradation</subject><subject>Biodegradation, Environmental</subject><subject>Chromatography, Liquid - methods</subject><subject>Enantioselectivity</subject><subject>Levofloxacin</subject><subject>Levofloxacin - isolation & purification</subject><subject>Limit of Detection</subject><subject>Macrocyclic antibiotic-based stationary phases</subject><subject>Ofloxacin</subject><subject>Sewage - analysis</subject><subject>Sewage - microbiology</subject><subject>Stereoisomerism</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Water Pollutants, Chemical - isolation & purification</subject><issn>1570-0232</issn><issn>1873-376X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFUMuKFDEUDaI4D_0EJUs31eZRqVS5EWdwdGDAjYK7kM69NZ2mKulJUoO99ctNT7duhQPJTc6Dewh5w9mKM9693662bpPivF6JOq5YheiekXPea9lI3f18Xu9Ks4YJKc7IRc5bxrhmWr4kZ0K3Ug69OCe_b0PB-2QLAp38w-KBPtnaEuvrbrOnM5ZNBOoDxWBD8THjhK74R6S5LOAxf6BXPsLBBWz9DzSOFVP8ZV1VrffUBmoPiqeUPC1wj9TFkGMqfplfkRejnTK-Pp2X5MfN5-_XX5u7b19urz_dNU4OojQwuLYHza1wIB0o1Y6tHde2E7yO42gZG1ulkPNBg26BD04xUEIPzkqrlLwk746-uxQfFszFzD47nCYbMC7Z8J71UreMyUpVR6pLMeeEo9klP9u0N5yZQ_1ma071m0P9hlWIrureniKW9YzwT_W370r4eCRgXfTRYzLZeQwOwadaqoHo_xPxB-HHnTc</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Maia, Alexandra S.</creator><creator>Castro, Paula M.L.</creator><creator>Tiritan, Maria Elizabeth</creator><general>Elsevier B.V</general><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>7X8</scope><orcidid>https://orcid.org/0000-0003-3320-730X</orcidid></search><sort><creationdate>20160901</creationdate><title>Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium</title><author>Maia, Alexandra S. ; Castro, Paula M.L. ; Tiritan, Maria Elizabeth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Activated sludge</topic><topic>Anti-Infective Agents - isolation & purification</topic><topic>Biodegradation</topic><topic>Biodegradation, Environmental</topic><topic>Chromatography, Liquid - methods</topic><topic>Enantioselectivity</topic><topic>Levofloxacin</topic><topic>Levofloxacin - isolation & purification</topic><topic>Limit of Detection</topic><topic>Macrocyclic antibiotic-based stationary phases</topic><topic>Ofloxacin</topic><topic>Sewage - analysis</topic><topic>Sewage - microbiology</topic><topic>Stereoisomerism</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Water Pollutants, Chemical - isolation & purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maia, Alexandra S.</creatorcontrib><creatorcontrib>Castro, Paula M.L.</creatorcontrib><creatorcontrib>Tiritan, Maria Elizabeth</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maia, Alexandra S.</au><au>Castro, Paula M.L.</au><au>Tiritan, Maria Elizabeth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium</atitle><jtitle>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</jtitle><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>1029-1030</volume><spage>174</spage><epage>183</epage><pages>174-183</pages><issn>1570-0232</issn><eissn>1873-376X</eissn><abstract>•Evaluation of the enantioselective biodegradation of ofloxacin and levofloxacin by an activated sludge consortium.•Enantiomerization was observed in the biodegradation of the isolated (S)-enantiomer with formation of the (R) enantiomer.•Enantioselectivity and enantiomerization during the biodegradation were confirmed by exact mass spectrometry.
Ofloxacin is a chiral fluoroquinolone commercialized as racemate and as its enantiomerically pure form levofloxacin. This work presents an integrated liquid chromatography (LC) method with fluorescence detection (FD) and exact mass spectrometry (EMS) developed to assess the enantiomeric biodegradation of ofloxacin and levofloxacin in laboratory-scale microcosms. The optimized enantioseparation conditions were achieved using a macrocyclic antibiotic ristocetin A-bonded CSP (150×2.1mm i.d.; particle size 5μm) under reversed-phase elution mode. The method was validated using a mineral salts medium as matrix and presented selectivity and linearity over a concentration range from 5μgL−1 (quantification limit) to 350μgL−1 for each enantiomer. The method was successfully applied to evaluate biodegradation of ofloxacin enantiomers at 250μgL−1 by an activated sludge inoculum. Ofloxacin (racemic mixture) and (S)-enantiomer (levofloxacin) were degraded up to 58 and 52%, respectively. An additional degradable carbon source, acetate, enhanced biodegradation up to 23%. (S)-enantiomer presented the highest extent of degradation (66.8%) when ofloxacin was supplied along with acetate. Results indicated slightly higher biodegradation extents for the (S)-enantiomer when supplementation was done with ofloxacin. Degradation occurred faster in the first 3days and proceeded slowly until the end of the assays. The chromatographic results from LC-FD suggested the formation of the (R)-enantiomer during levofloxacin biodegradation which was confirmed by LC–MS with a LTQ Orbitrap XL.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27433982</pmid><doi>10.1016/j.jchromb.2016.06.026</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3320-730X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1570-0232 |
ispartof | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1029-1030, p.174-183 |
issn | 1570-0232 1873-376X |
language | eng |
recordid | cdi_proquest_miscellaneous_1808374003 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Activated sludge Anti-Infective Agents - isolation & purification Biodegradation Biodegradation, Environmental Chromatography, Liquid - methods Enantioselectivity Levofloxacin Levofloxacin - isolation & purification Limit of Detection Macrocyclic antibiotic-based stationary phases Ofloxacin Sewage - analysis Sewage - microbiology Stereoisomerism Tandem Mass Spectrometry - methods Water Pollutants, Chemical - isolation & purification |
title | Integrated liquid chromatography method in enantioselective studies: Biodegradation of ofloxacin by an activated sludge consortium |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T16%3A07%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Integrated%20liquid%20chromatography%20method%20in%20enantioselective%20studies:%20Biodegradation%20of%20ofloxacin%20by%20an%20activated%20sludge%20consortium&rft.jtitle=Journal%20of%20chromatography.%20B,%20Analytical%20technologies%20in%20the%20biomedical%20and%20life%20sciences&rft.au=Maia,%20Alexandra%20S.&rft.date=2016-09-01&rft.volume=1029-1030&rft.spage=174&rft.epage=183&rft.pages=174-183&rft.issn=1570-0232&rft.eissn=1873-376X&rft_id=info:doi/10.1016/j.jchromb.2016.06.026&rft_dat=%3Cproquest_cross%3E1808374003%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c392t-d9c48d71a2cd3cd554f4afba6213cdffa00f455e1197d74d19c50d5279ca3a553%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1808374003&rft_id=info:pmid/27433982&rfr_iscdi=true |