Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry
•Stir membrane device is adapted to solid–liquid–liquid extraction.•This combination is used to the isolation of parabens from lyophilized human milk.•The extracted analytes are finally determined by UHPLC-MS/MS.•Limits of detection were in the low ng mL−1 range with precision better than 8%.•Recove...
Gespeichert in:
Veröffentlicht in: | Journal of Chromatography A 2014-08, Vol.1354, p.26-33 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 33 |
---|---|
container_issue | |
container_start_page | 26 |
container_title | Journal of Chromatography A |
container_volume | 1354 |
creator | Rodríguez-Gómez, Rocío Roldán-Pijuán, Mercedes Lucena, Rafael Cárdenas, Soledad Zafra-Gómez, Alberto Ballesteros, Oscar Navalón, Alberto Valcárcel, Miguel |
description | •Stir membrane device is adapted to solid–liquid–liquid extraction.•This combination is used to the isolation of parabens from lyophilized human milk.•The extracted analytes are finally determined by UHPLC-MS/MS.•Limits of detection were in the low ng mL−1 range with precision better than 8%.•Recoveries varied between 91 and 106% indicating the applicability of the proposal.
In this article, stir-membrane solid–liquid–liquid microextraction (SM-SLLME) is tailored for the analysis of solid matrices and it has been evaluated for the determination of parabens in l breast milk samples. A three-phase microextraction mode was used for the extraction of the target compounds taking advantage of their acid–base properties. The unit allows the simultaneous extraction of the target compounds from the solid sample to an organic media and the subsequent transference of the analytes to an aqueous acceptor phase. The method includes the identification and quantification of the analytes by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). All the variables involved in the extraction procedure have been accurately studied and optimized. The analytes were detected and quantified using a triple quadrupole mass spectrometer (QqQ). The selection of two specific fragmentation transitions for each compound allowed simultaneous quantification and identification. The method has been analytically characterized on the basis of its linearity, sensitivity and precision. Limits of detection ranged from 0.1 to 0.2ngmL−1 with precision better than 8%, (expressed as relative standard deviation). Relative recoveries were in the range from 91 to 106% which demonstrated the applicability of the stir-membrane solid–liquid–liquid microextraction for the proposed analytical problem. Moreover, the method has been satisfactorily applied for the determination of parabens in lyophilized breast milk samples from 10 randomly selected individuals. |
doi_str_mv | 10.1016/j.chroma.2014.05.071 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1800427196</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021967314008565</els_id><sourcerecordid>1654665070</sourcerecordid><originalsourceid>FETCH-LOGICAL-c557t-9409ec763baddbe5314909121eb78f433c50d9c680b4a951adf9d665803a410b3</originalsourceid><addsrcrecordid>eNqFkkuO1DAQhiMEYpqBGyDkDRKbNOU4jpMNEhrxkkZiAawtPyoTN3GSsR1E77gD5-EynAQPaR4rWNmyv_qr_P8uiocU9hRo8_SwN0OYvdpXQOs98D0IeqvY0VawkgnR3i52ABUtu0aws-JejAcAKkBUd4uzqu4Yr5pmV3x7l1woPXod1IQkzqOz3798Hd31-teGeGfCjJ9TUCa5eSL9HEgakFhMGLyb1M_TuSeLCkrjFImbyLB6NREdUMWUFcaPJCq_jBiJPpJ1zGJkcFcDWTBkvcwaJKd-29PSfBXUMhzLpCaLnngVI4kLmpRvMYXj_eJOr8aID07refHh5Yv3F6_Ly7ev3lw8vywN5yKVXQ0dGtEwrazVyBmtO-hoRVGLtq8ZMxxsZ5oWdK06TpXtO9s0vAWmagqanRdPNt0lzNcrxiS9iwbHMXs2r1HSFqCuBO2a_6MNr7M0CMhovaHZ2xgD9nIJzqtwlBTkTcbyIDcj5E3GErjMGeeyR6cOq_Zofxf9CjUDj0-AikaNfU7WuPiHa3n-HpRl7tnGYbbuk8Mgo3GYU7AuZI-lnd2_J_kBWh3OIA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1654665070</pqid></control><display><type>article</type><title>Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Rodríguez-Gómez, Rocío ; Roldán-Pijuán, Mercedes ; Lucena, Rafael ; Cárdenas, Soledad ; Zafra-Gómez, Alberto ; Ballesteros, Oscar ; Navalón, Alberto ; Valcárcel, Miguel</creator><creatorcontrib>Rodríguez-Gómez, Rocío ; Roldán-Pijuán, Mercedes ; Lucena, Rafael ; Cárdenas, Soledad ; Zafra-Gómez, Alberto ; Ballesteros, Oscar ; Navalón, Alberto ; Valcárcel, Miguel</creatorcontrib><description>•Stir membrane device is adapted to solid–liquid–liquid extraction.•This combination is used to the isolation of parabens from lyophilized human milk.•The extracted analytes are finally determined by UHPLC-MS/MS.•Limits of detection were in the low ng mL−1 range with precision better than 8%.•Recoveries varied between 91 and 106% indicating the applicability of the proposal.
In this article, stir-membrane solid–liquid–liquid microextraction (SM-SLLME) is tailored for the analysis of solid matrices and it has been evaluated for the determination of parabens in l breast milk samples. A three-phase microextraction mode was used for the extraction of the target compounds taking advantage of their acid–base properties. The unit allows the simultaneous extraction of the target compounds from the solid sample to an organic media and the subsequent transference of the analytes to an aqueous acceptor phase. The method includes the identification and quantification of the analytes by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). All the variables involved in the extraction procedure have been accurately studied and optimized. The analytes were detected and quantified using a triple quadrupole mass spectrometer (QqQ). The selection of two specific fragmentation transitions for each compound allowed simultaneous quantification and identification. The method has been analytically characterized on the basis of its linearity, sensitivity and precision. Limits of detection ranged from 0.1 to 0.2ngmL−1 with precision better than 8%, (expressed as relative standard deviation). Relative recoveries were in the range from 91 to 106% which demonstrated the applicability of the stir-membrane solid–liquid–liquid microextraction for the proposed analytical problem. Moreover, the method has been satisfactorily applied for the determination of parabens in lyophilized breast milk samples from 10 randomly selected individuals.</description><identifier>ISSN: 0021-9673</identifier><identifier>EISSN: 1873-3778</identifier><identifier>DOI: 10.1016/j.chroma.2014.05.071</identifier><identifier>PMID: 24935266</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analytical chemistry ; Biological and medical sciences ; Breast ; Calibration ; Chemical and industrial products toxicology. Toxic occupational diseases ; Chromatography ; Chromatography, High Pressure Liquid - methods ; Delivery. Postpartum. Lactation ; Extraction ; Gynecology. Andrology. Obstetrics ; Humans ; Liquid Phase Microextraction - methods ; Liquids ; Lyophilized human milk samples ; Mass spectrometry ; Maternal, fetal and perinatal monitoring ; Mathematical analysis ; Medical sciences ; Milk ; Milk, Human - chemistry ; Parabens ; Solid Phase Microextraction - methods ; Solvents - chemistry ; Stir-membrane solid–liquid–liquid microextraction ; Tandem Mass Spectrometry - methods ; Toxicology ; UHPLC-MS/MS ; Various organic compounds</subject><ispartof>Journal of Chromatography A, 2014-08, Vol.1354, p.26-33</ispartof><rights>2014 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-9409ec763baddbe5314909121eb78f433c50d9c680b4a951adf9d665803a410b3</citedby><cites>FETCH-LOGICAL-c557t-9409ec763baddbe5314909121eb78f433c50d9c680b4a951adf9d665803a410b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chroma.2014.05.071$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28577813$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24935266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodríguez-Gómez, Rocío</creatorcontrib><creatorcontrib>Roldán-Pijuán, Mercedes</creatorcontrib><creatorcontrib>Lucena, Rafael</creatorcontrib><creatorcontrib>Cárdenas, Soledad</creatorcontrib><creatorcontrib>Zafra-Gómez, Alberto</creatorcontrib><creatorcontrib>Ballesteros, Oscar</creatorcontrib><creatorcontrib>Navalón, Alberto</creatorcontrib><creatorcontrib>Valcárcel, Miguel</creatorcontrib><title>Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>•Stir membrane device is adapted to solid–liquid–liquid extraction.•This combination is used to the isolation of parabens from lyophilized human milk.•The extracted analytes are finally determined by UHPLC-MS/MS.•Limits of detection were in the low ng mL−1 range with precision better than 8%.•Recoveries varied between 91 and 106% indicating the applicability of the proposal.
In this article, stir-membrane solid–liquid–liquid microextraction (SM-SLLME) is tailored for the analysis of solid matrices and it has been evaluated for the determination of parabens in l breast milk samples. A three-phase microextraction mode was used for the extraction of the target compounds taking advantage of their acid–base properties. The unit allows the simultaneous extraction of the target compounds from the solid sample to an organic media and the subsequent transference of the analytes to an aqueous acceptor phase. The method includes the identification and quantification of the analytes by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). All the variables involved in the extraction procedure have been accurately studied and optimized. The analytes were detected and quantified using a triple quadrupole mass spectrometer (QqQ). The selection of two specific fragmentation transitions for each compound allowed simultaneous quantification and identification. The method has been analytically characterized on the basis of its linearity, sensitivity and precision. Limits of detection ranged from 0.1 to 0.2ngmL−1 with precision better than 8%, (expressed as relative standard deviation). Relative recoveries were in the range from 91 to 106% which demonstrated the applicability of the stir-membrane solid–liquid–liquid microextraction for the proposed analytical problem. Moreover, the method has been satisfactorily applied for the determination of parabens in lyophilized breast milk samples from 10 randomly selected individuals.</description><subject>Analytical chemistry</subject><subject>Biological and medical sciences</subject><subject>Breast</subject><subject>Calibration</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Delivery. Postpartum. Lactation</subject><subject>Extraction</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Liquid Phase Microextraction - methods</subject><subject>Liquids</subject><subject>Lyophilized human milk samples</subject><subject>Mass spectrometry</subject><subject>Maternal, fetal and perinatal monitoring</subject><subject>Mathematical analysis</subject><subject>Medical sciences</subject><subject>Milk</subject><subject>Milk, Human - chemistry</subject><subject>Parabens</subject><subject>Solid Phase Microextraction - methods</subject><subject>Solvents - chemistry</subject><subject>Stir-membrane solid–liquid–liquid microextraction</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Toxicology</subject><subject>UHPLC-MS/MS</subject><subject>Various organic compounds</subject><issn>0021-9673</issn><issn>1873-3778</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkkuO1DAQhiMEYpqBGyDkDRKbNOU4jpMNEhrxkkZiAawtPyoTN3GSsR1E77gD5-EynAQPaR4rWNmyv_qr_P8uiocU9hRo8_SwN0OYvdpXQOs98D0IeqvY0VawkgnR3i52ABUtu0aws-JejAcAKkBUd4uzqu4Yr5pmV3x7l1woPXod1IQkzqOz3798Hd31-teGeGfCjJ9TUCa5eSL9HEgakFhMGLyb1M_TuSeLCkrjFImbyLB6NREdUMWUFcaPJCq_jBiJPpJ1zGJkcFcDWTBkvcwaJKd-29PSfBXUMhzLpCaLnngVI4kLmpRvMYXj_eJOr8aID07refHh5Yv3F6_Ly7ev3lw8vywN5yKVXQ0dGtEwrazVyBmtO-hoRVGLtq8ZMxxsZ5oWdK06TpXtO9s0vAWmagqanRdPNt0lzNcrxiS9iwbHMXs2r1HSFqCuBO2a_6MNr7M0CMhovaHZ2xgD9nIJzqtwlBTkTcbyIDcj5E3GErjMGeeyR6cOq_Zofxf9CjUDj0-AikaNfU7WuPiHa3n-HpRl7tnGYbbuk8Mgo3GYU7AuZI-lnd2_J_kBWh3OIA</recordid><startdate>20140808</startdate><enddate>20140808</enddate><creator>Rodríguez-Gómez, Rocío</creator><creator>Roldán-Pijuán, Mercedes</creator><creator>Lucena, Rafael</creator><creator>Cárdenas, Soledad</creator><creator>Zafra-Gómez, Alberto</creator><creator>Ballesteros, Oscar</creator><creator>Navalón, Alberto</creator><creator>Valcárcel, Miguel</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20140808</creationdate><title>Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry</title><author>Rodríguez-Gómez, Rocío ; Roldán-Pijuán, Mercedes ; Lucena, Rafael ; Cárdenas, Soledad ; Zafra-Gómez, Alberto ; Ballesteros, Oscar ; Navalón, Alberto ; Valcárcel, Miguel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c557t-9409ec763baddbe5314909121eb78f433c50d9c680b4a951adf9d665803a410b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical chemistry</topic><topic>Biological and medical sciences</topic><topic>Breast</topic><topic>Calibration</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Chromatography</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Delivery. Postpartum. Lactation</topic><topic>Extraction</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Liquid Phase Microextraction - methods</topic><topic>Liquids</topic><topic>Lyophilized human milk samples</topic><topic>Mass spectrometry</topic><topic>Maternal, fetal and perinatal monitoring</topic><topic>Mathematical analysis</topic><topic>Medical sciences</topic><topic>Milk</topic><topic>Milk, Human - chemistry</topic><topic>Parabens</topic><topic>Solid Phase Microextraction - methods</topic><topic>Solvents - chemistry</topic><topic>Stir-membrane solid–liquid–liquid microextraction</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Toxicology</topic><topic>UHPLC-MS/MS</topic><topic>Various organic compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodríguez-Gómez, Rocío</creatorcontrib><creatorcontrib>Roldán-Pijuán, Mercedes</creatorcontrib><creatorcontrib>Lucena, Rafael</creatorcontrib><creatorcontrib>Cárdenas, Soledad</creatorcontrib><creatorcontrib>Zafra-Gómez, Alberto</creatorcontrib><creatorcontrib>Ballesteros, Oscar</creatorcontrib><creatorcontrib>Navalón, Alberto</creatorcontrib><creatorcontrib>Valcárcel, Miguel</creatorcontrib><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>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>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodríguez-Gómez, Rocío</au><au>Roldán-Pijuán, Mercedes</au><au>Lucena, Rafael</au><au>Cárdenas, Soledad</au><au>Zafra-Gómez, Alberto</au><au>Ballesteros, Oscar</au><au>Navalón, Alberto</au><au>Valcárcel, Miguel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>2014-08-08</date><risdate>2014</risdate><volume>1354</volume><spage>26</spage><epage>33</epage><pages>26-33</pages><issn>0021-9673</issn><eissn>1873-3778</eissn><coden>JOCRAM</coden><abstract>•Stir membrane device is adapted to solid–liquid–liquid extraction.•This combination is used to the isolation of parabens from lyophilized human milk.•The extracted analytes are finally determined by UHPLC-MS/MS.•Limits of detection were in the low ng mL−1 range with precision better than 8%.•Recoveries varied between 91 and 106% indicating the applicability of the proposal.
In this article, stir-membrane solid–liquid–liquid microextraction (SM-SLLME) is tailored for the analysis of solid matrices and it has been evaluated for the determination of parabens in l breast milk samples. A three-phase microextraction mode was used for the extraction of the target compounds taking advantage of their acid–base properties. The unit allows the simultaneous extraction of the target compounds from the solid sample to an organic media and the subsequent transference of the analytes to an aqueous acceptor phase. The method includes the identification and quantification of the analytes by ultra high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). All the variables involved in the extraction procedure have been accurately studied and optimized. The analytes were detected and quantified using a triple quadrupole mass spectrometer (QqQ). The selection of two specific fragmentation transitions for each compound allowed simultaneous quantification and identification. The method has been analytically characterized on the basis of its linearity, sensitivity and precision. Limits of detection ranged from 0.1 to 0.2ngmL−1 with precision better than 8%, (expressed as relative standard deviation). Relative recoveries were in the range from 91 to 106% which demonstrated the applicability of the stir-membrane solid–liquid–liquid microextraction for the proposed analytical problem. Moreover, the method has been satisfactorily applied for the determination of parabens in lyophilized breast milk samples from 10 randomly selected individuals.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>24935266</pmid><doi>10.1016/j.chroma.2014.05.071</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9673 |
ispartof | Journal of Chromatography A, 2014-08, Vol.1354, p.26-33 |
issn | 0021-9673 1873-3778 |
language | eng |
recordid | cdi_proquest_miscellaneous_1800427196 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Analytical chemistry Biological and medical sciences Breast Calibration Chemical and industrial products toxicology. Toxic occupational diseases Chromatography Chromatography, High Pressure Liquid - methods Delivery. Postpartum. Lactation Extraction Gynecology. Andrology. Obstetrics Humans Liquid Phase Microextraction - methods Liquids Lyophilized human milk samples Mass spectrometry Maternal, fetal and perinatal monitoring Mathematical analysis Medical sciences Milk Milk, Human - chemistry Parabens Solid Phase Microextraction - methods Solvents - chemistry Stir-membrane solid–liquid–liquid microextraction Tandem Mass Spectrometry - methods Toxicology UHPLC-MS/MS Various organic compounds |
title | Stir-membrane solid–liquid–liquid microextraction for the determination of parabens in human breast milk samples by ultra high performance liquid chromatography-tandem mass spectrometry |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T06%3A59%3A54IST&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=Stir-membrane%20solid%E2%80%93liquid%E2%80%93liquid%20microextraction%20for%20the%20determination%20of%20parabens%20in%20human%20breast%20milk%20samples%20by%20ultra%20high%20performance%20liquid%20chromatography-tandem%20mass%20spectrometry&rft.jtitle=Journal%20of%20Chromatography%20A&rft.au=Rodr%C3%ADguez-G%C3%B3mez,%20Roc%C3%ADo&rft.date=2014-08-08&rft.volume=1354&rft.spage=26&rft.epage=33&rft.pages=26-33&rft.issn=0021-9673&rft.eissn=1873-3778&rft.coden=JOCRAM&rft_id=info:doi/10.1016/j.chroma.2014.05.071&rft_dat=%3Cproquest_cross%3E1654665070%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1654665070&rft_id=info:pmid/24935266&rft_els_id=S0021967314008565&rfr_iscdi=true |