Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure

A rapid, sensitive, accurate and specific ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC–MS/MS) method for the detection of N-nitrosodiethanolamine (NDELA), a highly toxic contaminant in cosmetic raw materials and products was developed and validated. Systematized...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Talanta (Oxford) 2015-05, Vol.137, p.109-119
Hauptverfasser: Joo, Kyung-Mi, Shin, Mi-Sook, Jung, Ji-hee, Kim, Boo-Min, Lee, John-Whan, Jeong, Hye-Jin, Lim, Kyung-Min
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 119
container_issue
container_start_page 109
container_title Talanta (Oxford)
container_volume 137
creator Joo, Kyung-Mi
Shin, Mi-Sook
Jung, Ji-hee
Kim, Boo-Min
Lee, John-Whan
Jeong, Hye-Jin
Lim, Kyung-Min
description A rapid, sensitive, accurate and specific ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC–MS/MS) method for the detection of N-nitrosodiethanolamine (NDELA), a highly toxic contaminant in cosmetic raw materials and products was developed and validated. Systematized sample preparation steps were developed according to product types. Various SPE cartridges and columns were examined to establish the condition of SPE and chromatographic separation for NDELA. Sample cleanup steps consisting of solvent and liquid–liquid extraction tailored to the various sample matrix types were established prior to mixed mode SPE (Bond Elut AccuCAT). Chromatographic separation was achieved within 7min on a porous graphitic carbon (PGC) column using a gradient elution with the mobile phase of 1mM ammonium acetate containing 0.1% acetic acid and methanol. NDELA was monitored using an electrospray positive ionization mass spectrometry in the multiple reaction monitoring (MRM) mode (m/z 134.9>103.7(quantifier) and 73.7(qualifier ion)) with d8-NDELA (m/z 143.1>111.0) as internal standard. The standard curves were linear over the concentration range of 1–100ng/mL with a correlation coefficient higher than 0.99. The limit of detection (LOD) and the limit of quantification (LOQ) was 10 and 20μg/kg, respectively (0.5 and 1ng/mL in standard solution). The intra- and inter-day precisions were estimated to be below 11.1% and accuracies were within the range of 90.8–115.8%. The validated method was successfully applied to the analysis of real samples including raw materials, skin care, make-up, shampoos and hair products. [Display omitted] •Here, we established a systemic sample pre-cleanup procedure for the analysis of NDELA in cosmetics.•We identified that mixed mode SPE (Bond Elut AccuCAT) and PGC column display a good performance among 6 SPE and 5 columns.•With this method, we successfully quantitated NDELA in various real cosmetic products.
doi_str_mv 10.1016/j.talanta.2015.01.019
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1677913623</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0039914015000387</els_id><sourcerecordid>1677913623</sourcerecordid><originalsourceid>FETCH-LOGICAL-c468t-7ffcef9d2812d0845b9eef4b5dc41a694c42d498271bae4fb45728e380ae8e9e3</originalsourceid><addsrcrecordid>eNqFUc1u1DAQjhAVXQqPAPKRA9nacX5PqNqWH2lVONCz5diTjVdxHGwHujfegTfkBXgFJuzSa6WRPNb3zXwz8yXJK0bXjLLycr-OcpBjlOuMsmJNGUbzJFmxuuIpLyr-NFlRypu0YTk9T56HsKeUZpzyZ8l5VlQVLRlfJX-uIYK3ZpTRuJG4jtymo4neBacNxF6ObpAIw1tye32zvSJmJMoFC9EozHcekDbGQOSoyeSdnhV-2gOx5h40sU4DCW4wCPYyAIH76KX6p7VU3H3Zbn7__BUxB0usDIGECRTqo4I_kB8m9mRy3s2B7LycerPoKulbt8wxzHYksUd415NwCBEswkHaaQCcBlI1gBznaZlMgZ49vEjOOjkEeHl6L5K79zdfNx_T7ecPnzZX21TlZR3TqusUdI3OapZpWudF2wB0eVtolTNZNrnKM503dVaxVkLetXlRZTXwmkqooQF-kbw59kXlbzOEKKwJCga0DHAZwcqqahgvM47U4khVePXgoROTN1b6g2BULF6LvTh5LRavBWUYDda9PknMrQX9UPXfXCS8OxIAF_1uwIug0Cw8hPF4Y6GdeUTiLzIzxpw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1677913623</pqid></control><display><type>article</type><title>Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Joo, Kyung-Mi ; Shin, Mi-Sook ; Jung, Ji-hee ; Kim, Boo-Min ; Lee, John-Whan ; Jeong, Hye-Jin ; Lim, Kyung-Min</creator><creatorcontrib>Joo, Kyung-Mi ; Shin, Mi-Sook ; Jung, Ji-hee ; Kim, Boo-Min ; Lee, John-Whan ; Jeong, Hye-Jin ; Lim, Kyung-Min</creatorcontrib><description>A rapid, sensitive, accurate and specific ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC–MS/MS) method for the detection of N-nitrosodiethanolamine (NDELA), a highly toxic contaminant in cosmetic raw materials and products was developed and validated. Systematized sample preparation steps were developed according to product types. Various SPE cartridges and columns were examined to establish the condition of SPE and chromatographic separation for NDELA. Sample cleanup steps consisting of solvent and liquid–liquid extraction tailored to the various sample matrix types were established prior to mixed mode SPE (Bond Elut AccuCAT). Chromatographic separation was achieved within 7min on a porous graphitic carbon (PGC) column using a gradient elution with the mobile phase of 1mM ammonium acetate containing 0.1% acetic acid and methanol. NDELA was monitored using an electrospray positive ionization mass spectrometry in the multiple reaction monitoring (MRM) mode (m/z 134.9&gt;103.7(quantifier) and 73.7(qualifier ion)) with d8-NDELA (m/z 143.1&gt;111.0) as internal standard. The standard curves were linear over the concentration range of 1–100ng/mL with a correlation coefficient higher than 0.99. The limit of detection (LOD) and the limit of quantification (LOQ) was 10 and 20μg/kg, respectively (0.5 and 1ng/mL in standard solution). The intra- and inter-day precisions were estimated to be below 11.1% and accuracies were within the range of 90.8–115.8%. The validated method was successfully applied to the analysis of real samples including raw materials, skin care, make-up, shampoos and hair products. [Display omitted] •Here, we established a systemic sample pre-cleanup procedure for the analysis of NDELA in cosmetics.•We identified that mixed mode SPE (Bond Elut AccuCAT) and PGC column display a good performance among 6 SPE and 5 columns.•With this method, we successfully quantitated NDELA in various real cosmetic products.</description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2015.01.019</identifier><identifier>PMID: 25770613</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Analytic Sample Preparation Methods ; Carbon ; Chromatography, High Pressure Liquid - instrumentation ; Chromatography, High Pressure Liquid - methods ; Cosmetics ; Cosmetics - chemistry ; Diethylnitrosamine - analogs &amp; derivatives ; Diethylnitrosamine - analysis ; Diethylnitrosamine - chemistry ; Diethylnitrosamine - isolation &amp; purification ; Extraction ; Graphite - chemistry ; Ingredients ; Limit of Detection ; Linear Models ; Mass spectrometry ; Mixed mode solid phase extraction ; N-nitrosodiethanolamine (NDELA) ; Porosity ; Porous graphitic carbon (PGC) column ; Reproducibility of Results ; Solid Phase Extraction - instrumentation ; Solid Phase Extraction - methods ; Solid phases ; Tandem Mass Spectrometry - instrumentation ; Tandem Mass Spectrometry - methods ; UPLC–MS/MS</subject><ispartof>Talanta (Oxford), 2015-05, Vol.137, p.109-119</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-7ffcef9d2812d0845b9eef4b5dc41a694c42d498271bae4fb45728e380ae8e9e3</citedby><cites>FETCH-LOGICAL-c468t-7ffcef9d2812d0845b9eef4b5dc41a694c42d498271bae4fb45728e380ae8e9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.talanta.2015.01.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25770613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joo, Kyung-Mi</creatorcontrib><creatorcontrib>Shin, Mi-Sook</creatorcontrib><creatorcontrib>Jung, Ji-hee</creatorcontrib><creatorcontrib>Kim, Boo-Min</creatorcontrib><creatorcontrib>Lee, John-Whan</creatorcontrib><creatorcontrib>Jeong, Hye-Jin</creatorcontrib><creatorcontrib>Lim, Kyung-Min</creatorcontrib><title>Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description>A rapid, sensitive, accurate and specific ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC–MS/MS) method for the detection of N-nitrosodiethanolamine (NDELA), a highly toxic contaminant in cosmetic raw materials and products was developed and validated. Systematized sample preparation steps were developed according to product types. Various SPE cartridges and columns were examined to establish the condition of SPE and chromatographic separation for NDELA. Sample cleanup steps consisting of solvent and liquid–liquid extraction tailored to the various sample matrix types were established prior to mixed mode SPE (Bond Elut AccuCAT). Chromatographic separation was achieved within 7min on a porous graphitic carbon (PGC) column using a gradient elution with the mobile phase of 1mM ammonium acetate containing 0.1% acetic acid and methanol. NDELA was monitored using an electrospray positive ionization mass spectrometry in the multiple reaction monitoring (MRM) mode (m/z 134.9&gt;103.7(quantifier) and 73.7(qualifier ion)) with d8-NDELA (m/z 143.1&gt;111.0) as internal standard. The standard curves were linear over the concentration range of 1–100ng/mL with a correlation coefficient higher than 0.99. The limit of detection (LOD) and the limit of quantification (LOQ) was 10 and 20μg/kg, respectively (0.5 and 1ng/mL in standard solution). The intra- and inter-day precisions were estimated to be below 11.1% and accuracies were within the range of 90.8–115.8%. The validated method was successfully applied to the analysis of real samples including raw materials, skin care, make-up, shampoos and hair products. [Display omitted] •Here, we established a systemic sample pre-cleanup procedure for the analysis of NDELA in cosmetics.•We identified that mixed mode SPE (Bond Elut AccuCAT) and PGC column display a good performance among 6 SPE and 5 columns.•With this method, we successfully quantitated NDELA in various real cosmetic products.</description><subject>Analytic Sample Preparation Methods</subject><subject>Carbon</subject><subject>Chromatography, High Pressure Liquid - instrumentation</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Cosmetics</subject><subject>Cosmetics - chemistry</subject><subject>Diethylnitrosamine - analogs &amp; derivatives</subject><subject>Diethylnitrosamine - analysis</subject><subject>Diethylnitrosamine - chemistry</subject><subject>Diethylnitrosamine - isolation &amp; purification</subject><subject>Extraction</subject><subject>Graphite - chemistry</subject><subject>Ingredients</subject><subject>Limit of Detection</subject><subject>Linear Models</subject><subject>Mass spectrometry</subject><subject>Mixed mode solid phase extraction</subject><subject>N-nitrosodiethanolamine (NDELA)</subject><subject>Porosity</subject><subject>Porous graphitic carbon (PGC) column</subject><subject>Reproducibility of Results</subject><subject>Solid Phase Extraction - instrumentation</subject><subject>Solid Phase Extraction - methods</subject><subject>Solid phases</subject><subject>Tandem Mass Spectrometry - instrumentation</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>UPLC–MS/MS</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUc1u1DAQjhAVXQqPAPKRA9nacX5PqNqWH2lVONCz5diTjVdxHGwHujfegTfkBXgFJuzSa6WRPNb3zXwz8yXJK0bXjLLycr-OcpBjlOuMsmJNGUbzJFmxuuIpLyr-NFlRypu0YTk9T56HsKeUZpzyZ8l5VlQVLRlfJX-uIYK3ZpTRuJG4jtymo4neBacNxF6ObpAIw1tye32zvSJmJMoFC9EozHcekDbGQOSoyeSdnhV-2gOx5h40sU4DCW4wCPYyAIH76KX6p7VU3H3Zbn7__BUxB0usDIGECRTqo4I_kB8m9mRy3s2B7LycerPoKulbt8wxzHYksUd415NwCBEswkHaaQCcBlI1gBznaZlMgZ49vEjOOjkEeHl6L5K79zdfNx_T7ecPnzZX21TlZR3TqusUdI3OapZpWudF2wB0eVtolTNZNrnKM503dVaxVkLetXlRZTXwmkqooQF-kbw59kXlbzOEKKwJCga0DHAZwcqqahgvM47U4khVePXgoROTN1b6g2BULF6LvTh5LRavBWUYDda9PknMrQX9UPXfXCS8OxIAF_1uwIug0Cw8hPF4Y6GdeUTiLzIzxpw</recordid><startdate>20150515</startdate><enddate>20150515</enddate><creator>Joo, Kyung-Mi</creator><creator>Shin, Mi-Sook</creator><creator>Jung, Ji-hee</creator><creator>Kim, Boo-Min</creator><creator>Lee, John-Whan</creator><creator>Jeong, Hye-Jin</creator><creator>Lim, Kyung-Min</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>7QQ</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20150515</creationdate><title>Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure</title><author>Joo, Kyung-Mi ; Shin, Mi-Sook ; Jung, Ji-hee ; Kim, Boo-Min ; Lee, John-Whan ; Jeong, Hye-Jin ; Lim, Kyung-Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-7ffcef9d2812d0845b9eef4b5dc41a694c42d498271bae4fb45728e380ae8e9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Analytic Sample Preparation Methods</topic><topic>Carbon</topic><topic>Chromatography, High Pressure Liquid - instrumentation</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Cosmetics</topic><topic>Cosmetics - chemistry</topic><topic>Diethylnitrosamine - analogs &amp; derivatives</topic><topic>Diethylnitrosamine - analysis</topic><topic>Diethylnitrosamine - chemistry</topic><topic>Diethylnitrosamine - isolation &amp; purification</topic><topic>Extraction</topic><topic>Graphite - chemistry</topic><topic>Ingredients</topic><topic>Limit of Detection</topic><topic>Linear Models</topic><topic>Mass spectrometry</topic><topic>Mixed mode solid phase extraction</topic><topic>N-nitrosodiethanolamine (NDELA)</topic><topic>Porosity</topic><topic>Porous graphitic carbon (PGC) column</topic><topic>Reproducibility of Results</topic><topic>Solid Phase Extraction - instrumentation</topic><topic>Solid Phase Extraction - methods</topic><topic>Solid phases</topic><topic>Tandem Mass Spectrometry - instrumentation</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>UPLC–MS/MS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joo, Kyung-Mi</creatorcontrib><creatorcontrib>Shin, Mi-Sook</creatorcontrib><creatorcontrib>Jung, Ji-hee</creatorcontrib><creatorcontrib>Kim, Boo-Min</creatorcontrib><creatorcontrib>Lee, John-Whan</creatorcontrib><creatorcontrib>Jeong, Hye-Jin</creatorcontrib><creatorcontrib>Lim, Kyung-Min</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joo, Kyung-Mi</au><au>Shin, Mi-Sook</au><au>Jung, Ji-hee</au><au>Kim, Boo-Min</au><au>Lee, John-Whan</au><au>Jeong, Hye-Jin</au><au>Lim, Kyung-Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2015-05-15</date><risdate>2015</risdate><volume>137</volume><spage>109</spage><epage>119</epage><pages>109-119</pages><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract>A rapid, sensitive, accurate and specific ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC–MS/MS) method for the detection of N-nitrosodiethanolamine (NDELA), a highly toxic contaminant in cosmetic raw materials and products was developed and validated. Systematized sample preparation steps were developed according to product types. Various SPE cartridges and columns were examined to establish the condition of SPE and chromatographic separation for NDELA. Sample cleanup steps consisting of solvent and liquid–liquid extraction tailored to the various sample matrix types were established prior to mixed mode SPE (Bond Elut AccuCAT). Chromatographic separation was achieved within 7min on a porous graphitic carbon (PGC) column using a gradient elution with the mobile phase of 1mM ammonium acetate containing 0.1% acetic acid and methanol. NDELA was monitored using an electrospray positive ionization mass spectrometry in the multiple reaction monitoring (MRM) mode (m/z 134.9&gt;103.7(quantifier) and 73.7(qualifier ion)) with d8-NDELA (m/z 143.1&gt;111.0) as internal standard. The standard curves were linear over the concentration range of 1–100ng/mL with a correlation coefficient higher than 0.99. The limit of detection (LOD) and the limit of quantification (LOQ) was 10 and 20μg/kg, respectively (0.5 and 1ng/mL in standard solution). The intra- and inter-day precisions were estimated to be below 11.1% and accuracies were within the range of 90.8–115.8%. The validated method was successfully applied to the analysis of real samples including raw materials, skin care, make-up, shampoos and hair products. [Display omitted] •Here, we established a systemic sample pre-cleanup procedure for the analysis of NDELA in cosmetics.•We identified that mixed mode SPE (Bond Elut AccuCAT) and PGC column display a good performance among 6 SPE and 5 columns.•With this method, we successfully quantitated NDELA in various real cosmetic products.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25770613</pmid><doi>10.1016/j.talanta.2015.01.019</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0039-9140
ispartof Talanta (Oxford), 2015-05, Vol.137, p.109-119
issn 0039-9140
1873-3573
language eng
recordid cdi_proquest_miscellaneous_1677913623
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Analytic Sample Preparation Methods
Carbon
Chromatography, High Pressure Liquid - instrumentation
Chromatography, High Pressure Liquid - methods
Cosmetics
Cosmetics - chemistry
Diethylnitrosamine - analogs & derivatives
Diethylnitrosamine - analysis
Diethylnitrosamine - chemistry
Diethylnitrosamine - isolation & purification
Extraction
Graphite - chemistry
Ingredients
Limit of Detection
Linear Models
Mass spectrometry
Mixed mode solid phase extraction
N-nitrosodiethanolamine (NDELA)
Porosity
Porous graphitic carbon (PGC) column
Reproducibility of Results
Solid Phase Extraction - instrumentation
Solid Phase Extraction - methods
Solid phases
Tandem Mass Spectrometry - instrumentation
Tandem Mass Spectrometry - methods
UPLC–MS/MS
title Determination of N-nitrosodiethanolamine, NDELA in cosmetic ingredients and products by mixed mode solid phase extraction and UPLC–tandem mass spectrometry with porous graphitic carbon column through systemic sample pre-cleanup procedure
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T23%3A41%3A06IST&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=Determination%20of%20N-nitrosodiethanolamine,%20NDELA%20in%20cosmetic%20ingredients%20and%20products%20by%20mixed%20mode%20solid%20phase%20extraction%20and%20UPLC%E2%80%93tandem%20mass%20spectrometry%20with%20porous%20graphitic%20carbon%20column%20through%20systemic%20sample%20pre-cleanup%20procedure&rft.jtitle=Talanta%20(Oxford)&rft.au=Joo,%20Kyung-Mi&rft.date=2015-05-15&rft.volume=137&rft.spage=109&rft.epage=119&rft.pages=109-119&rft.issn=0039-9140&rft.eissn=1873-3573&rft_id=info:doi/10.1016/j.talanta.2015.01.019&rft_dat=%3Cproquest_cross%3E1677913623%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=1677913623&rft_id=info:pmid/25770613&rft_els_id=S0039914015000387&rfr_iscdi=true