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UHPLC-MS/MS method for the determination of the cyclic depsipeptide mycotoxins beauvericin and enniatins in in vitro transdermal experiments
•We developed a high-throughput bioanalytical UHPLC-MS/MS method for BEA and ENNs.•Significant adsorption to glass occurs, depending on solvent composition.•BEA and ENNs are chemically stable under in vitro transdermal test conditions. Currently, dermal exposure data of cyclic depsipeptide mycotoxin...
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Published in: | Journal of pharmaceutical and biomedical analysis 2014-11, Vol.100, p.50-57 |
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creator | Taevernier, Lien Veryser, Lieselotte Vandercruyssen, Kirsten D’Hondt, Matthias Vansteelandt, Stijn De Saeger, Sarah De Spiegeleer, Bart |
description | •We developed a high-throughput bioanalytical UHPLC-MS/MS method for BEA and ENNs.•Significant adsorption to glass occurs, depending on solvent composition.•BEA and ENNs are chemically stable under in vitro transdermal test conditions.
Currently, dermal exposure data of cyclic depsipeptide mycotoxins beauvericin and enniatins are completely absent with a lack of local skin and systemic kinetics, despite their widespread skin contact and intrinsic hazard. Therefore a sensitive and specific bioanalytical high-throughput UHPLC-MS/MS method was developed for the quantitative and simultaneous determination of cyclic depsipeptide mycotoxins beauvericin and enniatins (A, A1, B, B1, D, E, C/F) in human skin Franz diffusion cell samples. The limits of detection ranged between 10 and 17pg/ml, while the total run time was only 4.5min. There was no significant effect of endogenous skin compounds on the mycotoxin MS signal observed, and the accuracy (0.68–24.68% bias) and precision (0.57–10.70% RSD) were considered acceptable for our purposes. Moreover, it was demonstrated that these cyclic depsipeptides are stable for at least 7 days when formulated in different organic or aqueous mixtures. Finally, adsorption to glass did occur: at least 50% ethanol or acetonitrile is required to prevent significant adsorption effects, which could be as high as 45%. |
doi_str_mv | 10.1016/j.jpba.2014.07.021 |
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Currently, dermal exposure data of cyclic depsipeptide mycotoxins beauvericin and enniatins are completely absent with a lack of local skin and systemic kinetics, despite their widespread skin contact and intrinsic hazard. Therefore a sensitive and specific bioanalytical high-throughput UHPLC-MS/MS method was developed for the quantitative and simultaneous determination of cyclic depsipeptide mycotoxins beauvericin and enniatins (A, A1, B, B1, D, E, C/F) in human skin Franz diffusion cell samples. The limits of detection ranged between 10 and 17pg/ml, while the total run time was only 4.5min. There was no significant effect of endogenous skin compounds on the mycotoxin MS signal observed, and the accuracy (0.68–24.68% bias) and precision (0.57–10.70% RSD) were considered acceptable for our purposes. Moreover, it was demonstrated that these cyclic depsipeptides are stable for at least 7 days when formulated in different organic or aqueous mixtures. Finally, adsorption to glass did occur: at least 50% ethanol or acetonitrile is required to prevent significant adsorption effects, which could be as high as 45%.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2014.07.021</identifier><identifier>PMID: 25128875</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Adsorption ; Beauvericin ; Bioanalytical UHPLC-MS/MS method ; Calibration ; Chromatography, High Pressure Liquid - methods ; Chromatography, High Pressure Liquid - standards ; Depsipeptides - chemistry ; Depsipeptides - metabolism ; Diffusion Chambers, Culture ; Drug Stability ; Enniatins ; Glass - chemistry ; High-Throughput Screening Assays - methods ; High-Throughput Screening Assays - standards ; Humans ; Kinetics ; Limit of Detection ; Linear Models ; Permeability ; Reference Standards ; Skin - metabolism ; Skin Absorption ; Spectrometry, Mass, Electrospray Ionization - standards ; Tandem Mass Spectrometry - standards ; Transdermal Franz diffusion cell</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2014-11, Vol.100, p.50-57</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-3b0d9c6455bc555bf1ff4242e6eb48075fbb86ba0b1111d4e34e087e3442b4e3</citedby><cites>FETCH-LOGICAL-c356t-3b0d9c6455bc555bf1ff4242e6eb48075fbb86ba0b1111d4e34e087e3442b4e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25128875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Taevernier, Lien</creatorcontrib><creatorcontrib>Veryser, Lieselotte</creatorcontrib><creatorcontrib>Vandercruyssen, Kirsten</creatorcontrib><creatorcontrib>D’Hondt, Matthias</creatorcontrib><creatorcontrib>Vansteelandt, Stijn</creatorcontrib><creatorcontrib>De Saeger, Sarah</creatorcontrib><creatorcontrib>De Spiegeleer, Bart</creatorcontrib><title>UHPLC-MS/MS method for the determination of the cyclic depsipeptide mycotoxins beauvericin and enniatins in in vitro transdermal experiments</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>•We developed a high-throughput bioanalytical UHPLC-MS/MS method for BEA and ENNs.•Significant adsorption to glass occurs, depending on solvent composition.•BEA and ENNs are chemically stable under in vitro transdermal test conditions.
Currently, dermal exposure data of cyclic depsipeptide mycotoxins beauvericin and enniatins are completely absent with a lack of local skin and systemic kinetics, despite their widespread skin contact and intrinsic hazard. Therefore a sensitive and specific bioanalytical high-throughput UHPLC-MS/MS method was developed for the quantitative and simultaneous determination of cyclic depsipeptide mycotoxins beauvericin and enniatins (A, A1, B, B1, D, E, C/F) in human skin Franz diffusion cell samples. The limits of detection ranged between 10 and 17pg/ml, while the total run time was only 4.5min. There was no significant effect of endogenous skin compounds on the mycotoxin MS signal observed, and the accuracy (0.68–24.68% bias) and precision (0.57–10.70% RSD) were considered acceptable for our purposes. Moreover, it was demonstrated that these cyclic depsipeptides are stable for at least 7 days when formulated in different organic or aqueous mixtures. Finally, adsorption to glass did occur: at least 50% ethanol or acetonitrile is required to prevent significant adsorption effects, which could be as high as 45%.</description><subject>Adsorption</subject><subject>Beauvericin</subject><subject>Bioanalytical UHPLC-MS/MS method</subject><subject>Calibration</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Chromatography, High Pressure Liquid - standards</subject><subject>Depsipeptides - chemistry</subject><subject>Depsipeptides - metabolism</subject><subject>Diffusion Chambers, Culture</subject><subject>Drug Stability</subject><subject>Enniatins</subject><subject>Glass - chemistry</subject><subject>High-Throughput Screening Assays - methods</subject><subject>High-Throughput Screening Assays - standards</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Limit of Detection</subject><subject>Linear Models</subject><subject>Permeability</subject><subject>Reference Standards</subject><subject>Skin - metabolism</subject><subject>Skin Absorption</subject><subject>Spectrometry, Mass, Electrospray Ionization - standards</subject><subject>Tandem Mass Spectrometry - standards</subject><subject>Transdermal Franz diffusion cell</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9UV1rFDEUDaLYtfoHfJA8-jLTJJNMpuCLLNUWtii0gm8hH3dolplkTLJL9z_4o826rY-GSy733nMONzkIvaekpYT2F9t2uxjdMkJ5S2RLGH2BVnSQXcN6_vMlWhHZ0UaSQZyhNzlvCSGCXvLX6IwJyoZBihX6_eP6-2bd3N5d3N7hGcpDdHiMCZcHwA4KpNkHXXwMOI5_m_ZgJ2_rbMl-gaV4B3g-2Fjiow8ZG9C7PSRvfcA6OAwh-Mqvk9qosfclRVySDtlVcT1heFwqfoZQ8lv0atRThndP-Rzdf7m6X183m29fb9afN43tRF-azhB3aXsuhLGiXiMdR844gx4MH4gUozFDbzQxtB7HoeNABlkTZ6ZW5-jjSXZJ8dcOclGzzxamSQeIu6yo6PuBCSlJhbIT1KaYc4JRLXVXnQ6KEnU0QW3V0QR1NEERqaoJlfThSX9nZnD_KM-_XgGfTgCoj9x7SCpbD8GC8wlsUS76_-n_ARnJmwk</recordid><startdate>20141101</startdate><enddate>20141101</enddate><creator>Taevernier, Lien</creator><creator>Veryser, Lieselotte</creator><creator>Vandercruyssen, Kirsten</creator><creator>D’Hondt, Matthias</creator><creator>Vansteelandt, Stijn</creator><creator>De Saeger, Sarah</creator><creator>De Spiegeleer, Bart</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></search><sort><creationdate>20141101</creationdate><title>UHPLC-MS/MS method for the determination of the cyclic depsipeptide mycotoxins beauvericin and enniatins in in vitro transdermal experiments</title><author>Taevernier, Lien ; Veryser, Lieselotte ; Vandercruyssen, Kirsten ; D’Hondt, Matthias ; Vansteelandt, Stijn ; De Saeger, Sarah ; De Spiegeleer, Bart</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-3b0d9c6455bc555bf1ff4242e6eb48075fbb86ba0b1111d4e34e087e3442b4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adsorption</topic><topic>Beauvericin</topic><topic>Bioanalytical UHPLC-MS/MS method</topic><topic>Calibration</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Chromatography, High Pressure Liquid - standards</topic><topic>Depsipeptides - chemistry</topic><topic>Depsipeptides - metabolism</topic><topic>Diffusion Chambers, Culture</topic><topic>Drug Stability</topic><topic>Enniatins</topic><topic>Glass - chemistry</topic><topic>High-Throughput Screening Assays - methods</topic><topic>High-Throughput Screening Assays - standards</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Limit of Detection</topic><topic>Linear Models</topic><topic>Permeability</topic><topic>Reference Standards</topic><topic>Skin - metabolism</topic><topic>Skin Absorption</topic><topic>Spectrometry, Mass, Electrospray Ionization - standards</topic><topic>Tandem Mass Spectrometry - standards</topic><topic>Transdermal Franz diffusion cell</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Taevernier, Lien</creatorcontrib><creatorcontrib>Veryser, Lieselotte</creatorcontrib><creatorcontrib>Vandercruyssen, Kirsten</creatorcontrib><creatorcontrib>D’Hondt, Matthias</creatorcontrib><creatorcontrib>Vansteelandt, Stijn</creatorcontrib><creatorcontrib>De Saeger, Sarah</creatorcontrib><creatorcontrib>De Spiegeleer, Bart</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 pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Taevernier, Lien</au><au>Veryser, Lieselotte</au><au>Vandercruyssen, Kirsten</au><au>D’Hondt, Matthias</au><au>Vansteelandt, Stijn</au><au>De Saeger, Sarah</au><au>De Spiegeleer, Bart</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>UHPLC-MS/MS method for the determination of the cyclic depsipeptide mycotoxins beauvericin and enniatins in in vitro transdermal experiments</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2014-11-01</date><risdate>2014</risdate><volume>100</volume><spage>50</spage><epage>57</epage><pages>50-57</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><abstract>•We developed a high-throughput bioanalytical UHPLC-MS/MS method for BEA and ENNs.•Significant adsorption to glass occurs, depending on solvent composition.•BEA and ENNs are chemically stable under in vitro transdermal test conditions.
Currently, dermal exposure data of cyclic depsipeptide mycotoxins beauvericin and enniatins are completely absent with a lack of local skin and systemic kinetics, despite their widespread skin contact and intrinsic hazard. Therefore a sensitive and specific bioanalytical high-throughput UHPLC-MS/MS method was developed for the quantitative and simultaneous determination of cyclic depsipeptide mycotoxins beauvericin and enniatins (A, A1, B, B1, D, E, C/F) in human skin Franz diffusion cell samples. The limits of detection ranged between 10 and 17pg/ml, while the total run time was only 4.5min. There was no significant effect of endogenous skin compounds on the mycotoxin MS signal observed, and the accuracy (0.68–24.68% bias) and precision (0.57–10.70% RSD) were considered acceptable for our purposes. Moreover, it was demonstrated that these cyclic depsipeptides are stable for at least 7 days when formulated in different organic or aqueous mixtures. Finally, adsorption to glass did occur: at least 50% ethanol or acetonitrile is required to prevent significant adsorption effects, which could be as high as 45%.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>25128875</pmid><doi>10.1016/j.jpba.2014.07.021</doi><tpages>8</tpages></addata></record> |
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subjects | Adsorption Beauvericin Bioanalytical UHPLC-MS/MS method Calibration Chromatography, High Pressure Liquid - methods Chromatography, High Pressure Liquid - standards Depsipeptides - chemistry Depsipeptides - metabolism Diffusion Chambers, Culture Drug Stability Enniatins Glass - chemistry High-Throughput Screening Assays - methods High-Throughput Screening Assays - standards Humans Kinetics Limit of Detection Linear Models Permeability Reference Standards Skin - metabolism Skin Absorption Spectrometry, Mass, Electrospray Ionization - standards Tandem Mass Spectrometry - standards Transdermal Franz diffusion cell |
title | UHPLC-MS/MS method for the determination of the cyclic depsipeptide mycotoxins beauvericin and enniatins in in vitro transdermal experiments |
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