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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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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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.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202006481</identifier><identifier>PMID: 32869436</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Angewandte Chemie International Edition, 2020-12, Vol.59 (51), p.23162-23168</ispartof><rights>2020 Wiley‐VCH GmbH</rights><rights>2020 Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4501-178cf67d51af3d361576f1bcb21332ab892474cb0e6677b945fe977581454bed3</citedby><cites>FETCH-LOGICAL-c4501-178cf67d51af3d361576f1bcb21332ab892474cb0e6677b945fe977581454bed3</cites><orcidid>0000-0001-5591-4326 ; 0000-0001-5414-7401</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.202006481$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.202006481$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32869436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikhail, Ibraam E.</creatorcontrib><creatorcontrib>Tehranirokh, Masoomeh</creatorcontrib><creatorcontrib>Gooley, Andrew A.</creatorcontrib><creatorcontrib>Guijt, Rosanne M.</creatorcontrib><creatorcontrib>Breadmore, Michael C.</creatorcontrib><title>In‐Syringe Electrokinetic Protein Removal from Biological Samples prior to Electrospray Ionization Mass Spectrometry</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><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.</description><subject>Acetaminophen - blood</subject><subject>Atenolol</subject><subject>Atenolol - blood</subject><subject>bioanalysis</subject><subject>Biological properties</subject><subject>Biological samples</subject><subject>Blood Proteins - chemistry</subject><subject>Blood Proteins - isolation & purification</subject><subject>Chlorpheniramine - blood</subject><subject>Clomipramine</subject><subject>Clomipramine - blood</subject><subject>Dilution</subject><subject>Drugs</subject><subject>electrokinetic extraction</subject><subject>Electrokinetics</subject><subject>electrospray ionization-mass spectrometry</subject><subject>Humans</subject><subject>in-syringe protein removal</subject><subject>Ionization</subject><subject>Ions</subject><subject>Kinetics</subject><subject>Linearity</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Naproxen</subject><subject>Naproxen - blood</subject><subject>Paracetamol</subject><subject>Pharmaceuticals</subject><subject>Pindolol</subject><subject>Pindolol - blood</subject><subject>Proteins</subject><subject>Sample preparation</subject><subject>Serum proteins</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Syringes</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAQxy1ERR9w5YgsceklW7-dHEu1LSv1JRbOkeOdVC6JHexsq_TUj8Bn5JPgdvuQuHAYzYzmN3_N6I_QR0pmlBB2YLyDGSOMECVK-gbtUMlowbXmb3MtOC90Kek22k3pOvNlSdQ7tM1ZqSrB1Q66Wfg_97-XU3T-CvC8AzvG8NN5GJ3FlzGM4Dz-Bn24MR1uY-jxFxe6cOVs7pemHzpIeIguRDyG5_00RDPhRfDuzowueHxmUsLL4XHYwxin92irNV2CD095D_04nn8_-lqcXpwsjg5PCyskoQXVpW2VXklqWr7iikqtWtrYhlHOmWnKigktbENAKa2bSsgWKq1lSYUUDaz4Htrf6A4x_FpDGuveJQtdZzyEdaqZ4JVispIio5__Qa_DOvp8XaaUVjkYz9RsQ9n8ZorQ1vn53sSppqR-cKR-cKR-cSQvfHqSXTc9rF7wZwsyUG2AW9fB9B-5-vB8MX8V_wuQ4pmX</recordid><startdate>20201214</startdate><enddate>20201214</enddate><creator>Mikhail, Ibraam E.</creator><creator>Tehranirokh, Masoomeh</creator><creator>Gooley, Andrew A.</creator><creator>Guijt, Rosanne M.</creator><creator>Breadmore, Michael C.</creator><general>Wiley Subscription Services, Inc</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>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5591-4326</orcidid><orcidid>https://orcid.org/0000-0001-5414-7401</orcidid></search><sort><creationdate>20201214</creationdate><title>In‐Syringe Electrokinetic Protein Removal from Biological Samples prior to Electrospray Ionization Mass Spectrometry</title><author>Mikhail, Ibraam E. ; 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 & 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 & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikhail, Ibraam E.</au><au>Tehranirokh, Masoomeh</au><au>Gooley, Andrew A.</au><au>Guijt, Rosanne M.</au><au>Breadmore, Michael C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In‐Syringe Electrokinetic Protein Removal from Biological Samples prior to Electrospray Ionization Mass Spectrometry</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2020-12-14</date><risdate>2020</risdate><volume>59</volume><issue>51</issue><spage>23162</spage><epage>23168</epage><pages>23162-23168</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>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.</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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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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