In‐Syringe Electrokinetic Protein Removal from Biological Samples prior to Electrospray Ionization Mass Spectrometry

Here, an electrokinetic extraction (EkE) syringe is presented allowing for on‐line electrokinetic removal of serum proteins before ESI‐MS. The proposed concept is demonstrated by the determination of pharmaceuticals from human serum within minutes, with sample preparation limited to a 5× dilution of...

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Veröffentlicht in:Angewandte Chemie International Edition 2020-12, Vol.59 (51), p.23162-23168
Hauptverfasser: Mikhail, Ibraam E., Tehranirokh, Masoomeh, Gooley, Andrew A., Guijt, Rosanne M., Breadmore, Michael C.
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container_end_page 23168
container_issue 51
container_start_page 23162
container_title Angewandte Chemie International Edition
container_volume 59
creator Mikhail, Ibraam E.
Tehranirokh, Masoomeh
Gooley, Andrew A.
Guijt, Rosanne M.
Breadmore, Michael C.
description Here, an electrokinetic extraction (EkE) syringe is presented allowing for on‐line electrokinetic removal of serum proteins before ESI‐MS. The proposed concept is demonstrated by the determination of pharmaceuticals from human serum within minutes, with sample preparation limited to a 5× dilution of the sample in the background electrolyte (BGE) and application of voltage, both of which can be performed in‐syringe. Signal enhancements of 3.6–32 fold relative to direct infusion of diluted serum and up to 10.8 fold enhancement, were obtained for basic and acidic pharmaceuticals, respectively. Linear correlations for the basic drugs by EkE‐ESI‐MS/MS were achieved, covering the necessary clinical range with LOQs of 5.3, 7.8, 6.1, and 17.8 ng mL−1 for clomipramine, chlorphenamine, pindolol, and atenolol, respectively. For the acidic drugs, the EkE‐ESI‐MS LOQs were 3.1 μg mL−1 and 2.9 μg mL−1 for naproxen and paracetamol, respectively. The EkE‐ESI‐MS and EkE‐ESI‐MS/MS methods showed good accuracy (%found of 81 % to 120 %), precision (≤20 %), and linearity (r>0.997) for all the studied drugs in spiked serum samples. In‐syringe electrokinetic protein removal is introduced and hyphenated with electrospray ionization mass spectrometry (ESI‐MS) for the direct analysis of biological samples. The novel approach can simplify the bioanalytical workflow, minimize the use of organic solvent to few microliters, and allow the whole analysis—in‐syringe sample preparation and online ESI‐MS determination—to be accomplished in less than five minutes.
doi_str_mv 10.1002/anie.202006481
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Tehranirokh, Masoomeh ; Gooley, Andrew A. ; Guijt, Rosanne M. ; Breadmore, Michael C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4501-178cf67d51af3d361576f1bcb21332ab892474cb0e6677b945fe977581454bed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetaminophen - blood</topic><topic>Atenolol</topic><topic>Atenolol - blood</topic><topic>bioanalysis</topic><topic>Biological properties</topic><topic>Biological samples</topic><topic>Blood Proteins - chemistry</topic><topic>Blood Proteins - isolation &amp; purification</topic><topic>Chlorpheniramine - blood</topic><topic>Clomipramine</topic><topic>Clomipramine - blood</topic><topic>Dilution</topic><topic>Drugs</topic><topic>electrokinetic extraction</topic><topic>Electrokinetics</topic><topic>electrospray ionization-mass spectrometry</topic><topic>Humans</topic><topic>in-syringe protein removal</topic><topic>Ionization</topic><topic>Ions</topic><topic>Kinetics</topic><topic>Linearity</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Naproxen</topic><topic>Naproxen - blood</topic><topic>Paracetamol</topic><topic>Pharmaceuticals</topic><topic>Pindolol</topic><topic>Pindolol - blood</topic><topic>Proteins</topic><topic>Sample preparation</topic><topic>Serum proteins</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Syringes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikhail, Ibraam E.</creatorcontrib><creatorcontrib>Tehranirokh, Masoomeh</creatorcontrib><creatorcontrib>Gooley, Andrew A.</creatorcontrib><creatorcontrib>Guijt, Rosanne M.</creatorcontrib><creatorcontrib>Breadmore, Michael C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; 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The proposed concept is demonstrated by the determination of pharmaceuticals from human serum within minutes, with sample preparation limited to a 5× dilution of the sample in the background electrolyte (BGE) and application of voltage, both of which can be performed in‐syringe. Signal enhancements of 3.6–32 fold relative to direct infusion of diluted serum and up to 10.8 fold enhancement, were obtained for basic and acidic pharmaceuticals, respectively. Linear correlations for the basic drugs by EkE‐ESI‐MS/MS were achieved, covering the necessary clinical range with LOQs of 5.3, 7.8, 6.1, and 17.8 ng mL−1 for clomipramine, chlorphenamine, pindolol, and atenolol, respectively. For the acidic drugs, the EkE‐ESI‐MS LOQs were 3.1 μg mL−1 and 2.9 μg mL−1 for naproxen and paracetamol, respectively. The EkE‐ESI‐MS and EkE‐ESI‐MS/MS methods showed good accuracy (%found of 81 % to 120 %), precision (≤20 %), and linearity (r&gt;0.997) for all the studied drugs in spiked serum samples. In‐syringe electrokinetic protein removal is introduced and hyphenated with electrospray ionization mass spectrometry (ESI‐MS) for the direct analysis of biological samples. The novel approach can simplify the bioanalytical workflow, minimize the use of organic solvent to few microliters, and allow the whole analysis—in‐syringe sample preparation and online ESI‐MS determination—to be accomplished in less than five minutes.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32869436</pmid><doi>10.1002/anie.202006481</doi><tpages>7</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-5591-4326</orcidid><orcidid>https://orcid.org/0000-0001-5414-7401</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Acetaminophen - blood
Atenolol
Atenolol - blood
bioanalysis
Biological properties
Biological samples
Blood Proteins - chemistry
Blood Proteins - isolation & purification
Chlorpheniramine - blood
Clomipramine
Clomipramine - blood
Dilution
Drugs
electrokinetic extraction
Electrokinetics
electrospray ionization-mass spectrometry
Humans
in-syringe protein removal
Ionization
Ions
Kinetics
Linearity
Mass spectrometry
Mass spectroscopy
Naproxen
Naproxen - blood
Paracetamol
Pharmaceuticals
Pindolol
Pindolol - blood
Proteins
Sample preparation
Serum proteins
Spectrometry, Mass, Electrospray Ionization
Syringes
title In‐Syringe Electrokinetic Protein Removal from Biological Samples prior to Electrospray Ionization Mass Spectrometry
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