Reusable Solid-Phase Microextraction Coating for Direct Immersion Whole-Blood Analysis and Extracted Blood Spot Sampling Coupled with Liquid Chromatography–Tandem Mass Spectrometry and Direct Analysis in Real Time–Tandem Mass Spectrometry

Three different biocompatible polymers were tested and evaluated in order to improve the whole-blood biocompatibility of previously developed C18–polyacrylonitrile (C18–PAN) thin-film solid-phase microextraction (SPME) coating. Among all methods of modification, UV-dried thin PAN-over C18–PAN provid...

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Veröffentlicht in:Analytical chemistry (Washington) 2012-10, Vol.84 (19), p.8301-8309
Hauptverfasser: Mirnaghi, Fatemeh S, Pawliszyn, Janusz
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Pawliszyn, Janusz
description Three different biocompatible polymers were tested and evaluated in order to improve the whole-blood biocompatibility of previously developed C18–polyacrylonitrile (C18–PAN) thin-film solid-phase microextraction (SPME) coating. Among all methods of modification, UV-dried thin PAN-over C18–PAN provided the best results. This coating presented reusable properties and reproducible extraction efficiency for at least 30 direct extractions of diazepam from whole blood [relative standard deviation (RSD) = 12% using external calibration and 4% using isotope dilution calibration]. The amount of absolute recovery for direct immersion analysis and based on the free concentration of diazepam in blood matrix was about 4.8% (desorption efficiency = 98%). The limit of quantitation (LOQ) for the developed solid-phase microextraction liquid chromatography–tandem mass spectrometry (SPME-LC–MS/MS) method for direct whole-blood analysis was 0.5 ng/mL. The optimized modification of the coating was then used for an extracted blood spot (EBS) sampling approach, a new sampling method which is introduced to address the limitations of dried blood spot sampling. EBS was evaluated using LC–MS/MS and direct analysis in real time (DART)–MS/MS, where, for a 5 μL blood spot, LOQs of 0.2 and 1 μg/mL, respectively, were achieved for extraction of diazepam.
doi_str_mv 10.1021/ac3018229
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Chem</addtitle><date>2012-10-02</date><risdate>2012</risdate><volume>84</volume><issue>19</issue><spage>8301</spage><epage>8309</epage><pages>8301-8309</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>Three different biocompatible polymers were tested and evaluated in order to improve the whole-blood biocompatibility of previously developed C18–polyacrylonitrile (C18–PAN) thin-film solid-phase microextraction (SPME) coating. Among all methods of modification, UV-dried thin PAN-over C18–PAN provided the best results. This coating presented reusable properties and reproducible extraction efficiency for at least 30 direct extractions of diazepam from whole blood [relative standard deviation (RSD) = 12% using external calibration and 4% using isotope dilution calibration]. The amount of absolute recovery for direct immersion analysis and based on the free concentration of diazepam in blood matrix was about 4.8% (desorption efficiency = 98%). The limit of quantitation (LOQ) for the developed solid-phase microextraction liquid chromatography–tandem mass spectrometry (SPME-LC–MS/MS) method for direct whole-blood analysis was 0.5 ng/mL. The optimized modification of the coating was then used for an extracted blood spot (EBS) sampling approach, a new sampling method which is introduced to address the limitations of dried blood spot sampling. EBS was evaluated using LC–MS/MS and direct analysis in real time (DART)–MS/MS, where, for a 5 μL blood spot, LOQs of 0.2 and 1 μg/mL, respectively, were achieved for extraction of diazepam.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>22928515</pmid><doi>10.1021/ac3018229</doi><tpages>9</tpages></addata></record>
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source MEDLINE; ACS Publications
subjects Analytical chemistry
Biocompatible Materials - chemistry
Biopolymers
Blood Chemical Analysis - instrumentation
Blood tests
Chemistry
Chromatographic methods and physical methods associated with chromatography
Chromatography
Chromatography, Liquid - instrumentation
Diazepam - analogs & derivatives
Diazepam - blood
Exact sciences and technology
Humans
Mass spectrometry
Other chromatographic methods
Sensitivity and Specificity
Solid Phase Microextraction - instrumentation
Spectrometric and optical methods
Tandem Mass Spectrometry - instrumentation
Thin film coatings
Time Factors
title Reusable Solid-Phase Microextraction Coating for Direct Immersion Whole-Blood Analysis and Extracted Blood Spot Sampling Coupled with Liquid Chromatography–Tandem Mass Spectrometry and Direct Analysis in Real Time–Tandem Mass Spectrometry
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