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Pre-Equilibrium Solid-Phase Microextraction of Free Analyte in Complex Samples: Correction for Mass Transfer Variation from Protein Binding and Matrix Tortuosity
The accurate measurement of free analyte concentrations within complex sample matrixes by pre-equilibrium solid-phase microextraction (SPME) has proven challenging due to variations in mass uptake kinetics. For the first time, the effects of the sample binding matrix and tortuosity on the kinetics o...
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Published in: | Analytical chemistry (Washington) 2011-05, Vol.83 (9), p.3365-3370 |
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creator | Zhang, Xu Oakes, Ken D Hoque, Md Ehsanul Luong, Di Metcalfe, Chris D Pawliszyn, Janusz Servos, Mark R |
description | The accurate measurement of free analyte concentrations within complex sample matrixes by pre-equilibrium solid-phase microextraction (SPME) has proven challenging due to variations in mass uptake kinetics. For the first time, the effects of the sample binding matrix and tortuosity on the kinetics of analyte extraction (from the sample to the SPME fiber) are demonstrated to be quantitatively symmetrical with those of the desorption of preloaded deuterated standards (from the fiber to the sample matrix). Consequently, kinetic calibration methods can be employed to correct for variation in SPME sampling kinetics, facilitating the application of pre-equilibrium SPME within complex sample systems. This approach was applied ex vivo to measure pharmaceuticals in fish muscle tissues, with results consistent with those obtained from equilibrium SPME and microdialysis. The developed method has the inherent advantages of being more accurate, precise, and reproducible, thus providing the framework for applications where rapid measurement of free analyte concentrations (within complicated sample matrixes such as biological tissues, sediment, and surface water) are required. |
doi_str_mv | 10.1021/ac2004899 |
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For the first time, the effects of the sample binding matrix and tortuosity on the kinetics of analyte extraction (from the sample to the SPME fiber) are demonstrated to be quantitatively symmetrical with those of the desorption of preloaded deuterated standards (from the fiber to the sample matrix). Consequently, kinetic calibration methods can be employed to correct for variation in SPME sampling kinetics, facilitating the application of pre-equilibrium SPME within complex sample systems. This approach was applied ex vivo to measure pharmaceuticals in fish muscle tissues, with results consistent with those obtained from equilibrium SPME and microdialysis. The developed method has the inherent advantages of being more accurate, precise, and reproducible, thus providing the framework for applications where rapid measurement of free analyte concentrations (within complicated sample matrixes such as biological tissues, sediment, and surface water) are required.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac2004899</identifier><identifier>PMID: 21456585</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Absorption ; Analytical chemistry ; Animals ; Binding sites ; Cattle ; Chemical compounds ; Chemistry ; Environmental Pollutants - analysis ; Environmental Pollutants - chemistry ; Environmental Pollutants - isolation & purification ; Exact sciences and technology ; Extraction processes ; Fishes ; Muscles - chemistry ; Protein Binding ; Proteins ; Reaction kinetics ; Serum Albumin, Bovine - chemistry ; Solid Phase Microextraction - methods ; Tissues</subject><ispartof>Analytical chemistry (Washington), 2011-05, Vol.83 (9), p.3365-3370</ispartof><rights>Copyright © 2011 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><rights>Copyright American Chemical Society May 1, 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a371t-52f1d2859327e0f317fca798a999b2617f86167057b6d17839f5b9b10a9049983</citedby><cites>FETCH-LOGICAL-a371t-52f1d2859327e0f317fca798a999b2617f86167057b6d17839f5b9b10a9049983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24121874$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21456585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xu</creatorcontrib><creatorcontrib>Oakes, Ken D</creatorcontrib><creatorcontrib>Hoque, Md Ehsanul</creatorcontrib><creatorcontrib>Luong, Di</creatorcontrib><creatorcontrib>Metcalfe, Chris D</creatorcontrib><creatorcontrib>Pawliszyn, Janusz</creatorcontrib><creatorcontrib>Servos, Mark R</creatorcontrib><title>Pre-Equilibrium Solid-Phase Microextraction of Free Analyte in Complex Samples: Correction for Mass Transfer Variation from Protein Binding and Matrix Tortuosity</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>The accurate measurement of free analyte concentrations within complex sample matrixes by pre-equilibrium solid-phase microextraction (SPME) has proven challenging due to variations in mass uptake kinetics. For the first time, the effects of the sample binding matrix and tortuosity on the kinetics of analyte extraction (from the sample to the SPME fiber) are demonstrated to be quantitatively symmetrical with those of the desorption of preloaded deuterated standards (from the fiber to the sample matrix). Consequently, kinetic calibration methods can be employed to correct for variation in SPME sampling kinetics, facilitating the application of pre-equilibrium SPME within complex sample systems. This approach was applied ex vivo to measure pharmaceuticals in fish muscle tissues, with results consistent with those obtained from equilibrium SPME and microdialysis. 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Oakes, Ken D ; Hoque, Md Ehsanul ; Luong, Di ; Metcalfe, Chris D ; Pawliszyn, Janusz ; Servos, Mark R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a371t-52f1d2859327e0f317fca798a999b2617f86167057b6d17839f5b9b10a9049983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Absorption</topic><topic>Analytical chemistry</topic><topic>Animals</topic><topic>Binding sites</topic><topic>Cattle</topic><topic>Chemical compounds</topic><topic>Chemistry</topic><topic>Environmental Pollutants - analysis</topic><topic>Environmental Pollutants - chemistry</topic><topic>Environmental Pollutants - isolation & purification</topic><topic>Exact sciences and technology</topic><topic>Extraction processes</topic><topic>Fishes</topic><topic>Muscles - chemistry</topic><topic>Protein Binding</topic><topic>Proteins</topic><topic>Reaction kinetics</topic><topic>Serum Albumin, Bovine - chemistry</topic><topic>Solid Phase Microextraction - methods</topic><topic>Tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xu</creatorcontrib><creatorcontrib>Oakes, Ken D</creatorcontrib><creatorcontrib>Hoque, Md Ehsanul</creatorcontrib><creatorcontrib>Luong, Di</creatorcontrib><creatorcontrib>Metcalfe, Chris D</creatorcontrib><creatorcontrib>Pawliszyn, Janusz</creatorcontrib><creatorcontrib>Servos, Mark R</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>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xu</au><au>Oakes, Ken D</au><au>Hoque, Md Ehsanul</au><au>Luong, Di</au><au>Metcalfe, Chris D</au><au>Pawliszyn, Janusz</au><au>Servos, Mark R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pre-Equilibrium Solid-Phase Microextraction of Free Analyte in Complex Samples: Correction for Mass Transfer Variation from Protein Binding and Matrix Tortuosity</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2011-05-01</date><risdate>2011</risdate><volume>83</volume><issue>9</issue><spage>3365</spage><epage>3370</epage><pages>3365-3370</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>The accurate measurement of free analyte concentrations within complex sample matrixes by pre-equilibrium solid-phase microextraction (SPME) has proven challenging due to variations in mass uptake kinetics. For the first time, the effects of the sample binding matrix and tortuosity on the kinetics of analyte extraction (from the sample to the SPME fiber) are demonstrated to be quantitatively symmetrical with those of the desorption of preloaded deuterated standards (from the fiber to the sample matrix). Consequently, kinetic calibration methods can be employed to correct for variation in SPME sampling kinetics, facilitating the application of pre-equilibrium SPME within complex sample systems. 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subjects | Absorption Analytical chemistry Animals Binding sites Cattle Chemical compounds Chemistry Environmental Pollutants - analysis Environmental Pollutants - chemistry Environmental Pollutants - isolation & purification Exact sciences and technology Extraction processes Fishes Muscles - chemistry Protein Binding Proteins Reaction kinetics Serum Albumin, Bovine - chemistry Solid Phase Microextraction - methods Tissues |
title | Pre-Equilibrium Solid-Phase Microextraction of Free Analyte in Complex Samples: Correction for Mass Transfer Variation from Protein Binding and Matrix Tortuosity |
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