Pressure-assisted introduction of urine samples into a short capillary for electrophoretic separation with contactless conductivity and UV spectrometry detection
A computer‐controlled hydrodynamic sample introduction method has been proposed for short‐capillary electrophoresis. In the method, the BGE flushes sample from the loop of a six‐way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the elec...
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Veröffentlicht in: | Electrophoresis 2015-08, Vol.36 (16), p.1962-1968 |
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container_issue | 16 |
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container_title | Electrophoresis |
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creator | Makrlíková, Anna Opekar, František Tůma, Petr |
description | A computer‐controlled hydrodynamic sample introduction method has been proposed for short‐capillary electrophoresis. In the method, the BGE flushes sample from the loop of a six‐way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the electrolyte stream at the time when the sample zone is at the capillary, leading to injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. This way of sample introduction does not involve movement of the capillary and both of its ends remain constantly in the solution during both sample injection and separation. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. The new sample introduction method was tested in the determination of ammonia, creatinine, uric acid, and hippuric acid in human urine. The determination was performed in a capillary with an overall length of 10.5 cm, in two BGEs with compositions 50 mM MES + 5 mM NaOH (pH 5.1) and 1 M acetic acid + 1.5 mM crown ether 18‐crown‐6 (pH 2.4). A dual contactless conductivity/UV spectrometric detector was used for the detection. |
doi_str_mv | 10.1002/elps.201400613 |
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In the method, the BGE flushes sample from the loop of a six‐way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the electrolyte stream at the time when the sample zone is at the capillary, leading to injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. This way of sample introduction does not involve movement of the capillary and both of its ends remain constantly in the solution during both sample injection and separation. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. The new sample introduction method was tested in the determination of ammonia, creatinine, uric acid, and hippuric acid in human urine. The determination was performed in a capillary with an overall length of 10.5 cm, in two BGEs with compositions 50 mM MES + 5 mM NaOH (pH 5.1) and 1 M acetic acid + 1.5 mM crown ether 18‐crown‐6 (pH 2.4). A dual contactless conductivity/UV spectrometric detector was used for the detection.</description><identifier>ISSN: 0173-0835</identifier><identifier>EISSN: 1522-2683</identifier><identifier>DOI: 10.1002/elps.201400613</identifier><identifier>PMID: 25752683</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Acetic acid ; Ammonia ; Ammonium Compounds - urine ; Capillarity ; Capillary flow ; Capillary pressure ; Cations - urine ; Creatinine ; Creatinine - urine ; Crown ethers ; Electric Conductivity ; Electrolytes ; Electrophoresis ; Electrophoresis, Capillary - instrumentation ; Electrophoresis, Capillary - methods ; Equipment Design ; Hippuric acid ; Human urine ; Humans ; Hydrodynamic sampling ; Limit of Detection ; Linear Models ; Pressure ; Reproducibility of Results ; Scientific apparatus & instruments ; Separation ; Short capillary separation ; Sodium hydroxide ; Spectrometry ; Spectrophotometry, Ultraviolet ; Spectroscopy ; Uric acid ; Urinalysis - instrumentation ; Urinalysis - methods ; Urine</subject><ispartof>Electrophoresis, 2015-08, Vol.36 (16), p.1962-1968</ispartof><rights>2015 WILEY‐VCH Verlag GmbH & Co. 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KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4724-eabe4d62d2a5783e9ab275afab62c1e0c2aaf90901df8d32c50f77764d4268cd3</citedby><cites>FETCH-LOGICAL-c4724-eabe4d62d2a5783e9ab275afab62c1e0c2aaf90901df8d32c50f77764d4268cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Felps.201400613$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Felps.201400613$$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/25752683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Makrlíková, Anna</creatorcontrib><creatorcontrib>Opekar, František</creatorcontrib><creatorcontrib>Tůma, Petr</creatorcontrib><title>Pressure-assisted introduction of urine samples into a short capillary for electrophoretic separation with contactless conductivity and UV spectrometry detection</title><title>Electrophoresis</title><addtitle>ELECTROPHORESIS</addtitle><description>A computer‐controlled hydrodynamic sample introduction method has been proposed for short‐capillary electrophoresis. In the method, the BGE flushes sample from the loop of a six‐way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the electrolyte stream at the time when the sample zone is at the capillary, leading to injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. This way of sample introduction does not involve movement of the capillary and both of its ends remain constantly in the solution during both sample injection and separation. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. The new sample introduction method was tested in the determination of ammonia, creatinine, uric acid, and hippuric acid in human urine. The determination was performed in a capillary with an overall length of 10.5 cm, in two BGEs with compositions 50 mM MES + 5 mM NaOH (pH 5.1) and 1 M acetic acid + 1.5 mM crown ether 18‐crown‐6 (pH 2.4). A dual contactless conductivity/UV spectrometric detector was used for the detection.</description><subject>Acetic acid</subject><subject>Ammonia</subject><subject>Ammonium Compounds - urine</subject><subject>Capillarity</subject><subject>Capillary flow</subject><subject>Capillary pressure</subject><subject>Cations - urine</subject><subject>Creatinine</subject><subject>Creatinine - urine</subject><subject>Crown ethers</subject><subject>Electric Conductivity</subject><subject>Electrolytes</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Capillary - instrumentation</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Equipment Design</subject><subject>Hippuric acid</subject><subject>Human urine</subject><subject>Humans</subject><subject>Hydrodynamic sampling</subject><subject>Limit of Detection</subject><subject>Linear Models</subject><subject>Pressure</subject><subject>Reproducibility of Results</subject><subject>Scientific apparatus & instruments</subject><subject>Separation</subject><subject>Short capillary separation</subject><subject>Sodium hydroxide</subject><subject>Spectrometry</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Spectroscopy</subject><subject>Uric acid</subject><subject>Urinalysis - instrumentation</subject><subject>Urinalysis - methods</subject><subject>Urine</subject><issn>0173-0835</issn><issn>1522-2683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk9vEzEQxS0EomnhyhFZ4sJlg9d_1psjqkpAiqAoFFAulmPPqi67663tpc3H4ZviTUoOXOBkS_N7zzPzjNCLksxLQugbaIc4p6TkhFQle4RmpaC0oFXNHqMZKSUrSM3ECTqN8YYQwhecP0UnVEgxMTP06zJAjGOAQsfoYgKLXZ-Ct6NJzvfYN3gMrgccdTe0EKeqxxrHax8SNnpwbavDDjc-YGjBZOmQS5CcwREGHfTe5s6la2x8n7RJ2SVO9_0TP13aYd1bfPUVx2Gv7yBlQwsJ9i08Q08a3UZ4_nCeoat3F1_O3xerT8sP529XheGS8gL0FritqKVayJrBQm-pFLrR24qaEoihWjcLsiClbWrLqBGkkVJW3PK8CWPZGXp98B2Cvx0hJtW5aCCP14Mfo8q7JCWltOL_gRIhmajrOqOv_kJv_Bj6PIiiObEciRCT4fxAmeBjDNCoIbgu71WVRE05qylndcw5C14-2I7bDuwR_xNsBvgBuHMt7P5hpy5Wl-vcxtRIcZBNX-H-KNPhh6okk0J9-7hU3-V6ufm83qgN-w3MDsfn</recordid><startdate>201508</startdate><enddate>201508</enddate><creator>Makrlíková, Anna</creator><creator>Opekar, František</creator><creator>Tůma, Petr</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>201508</creationdate><title>Pressure-assisted introduction of urine samples into a short capillary for electrophoretic separation with contactless conductivity and UV spectrometry detection</title><author>Makrlíková, Anna ; Opekar, František ; Tůma, Petr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4724-eabe4d62d2a5783e9ab275afab62c1e0c2aaf90901df8d32c50f77764d4268cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acetic acid</topic><topic>Ammonia</topic><topic>Ammonium Compounds - urine</topic><topic>Capillarity</topic><topic>Capillary flow</topic><topic>Capillary pressure</topic><topic>Cations - urine</topic><topic>Creatinine</topic><topic>Creatinine - urine</topic><topic>Crown ethers</topic><topic>Electric Conductivity</topic><topic>Electrolytes</topic><topic>Electrophoresis</topic><topic>Electrophoresis, Capillary - instrumentation</topic><topic>Electrophoresis, Capillary - methods</topic><topic>Equipment Design</topic><topic>Hippuric acid</topic><topic>Human urine</topic><topic>Humans</topic><topic>Hydrodynamic sampling</topic><topic>Limit of Detection</topic><topic>Linear Models</topic><topic>Pressure</topic><topic>Reproducibility of Results</topic><topic>Scientific apparatus & instruments</topic><topic>Separation</topic><topic>Short capillary separation</topic><topic>Sodium hydroxide</topic><topic>Spectrometry</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Spectroscopy</topic><topic>Uric acid</topic><topic>Urinalysis - instrumentation</topic><topic>Urinalysis - methods</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Makrlíková, Anna</creatorcontrib><creatorcontrib>Opekar, František</creatorcontrib><creatorcontrib>Tůma, Petr</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Electrophoresis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Makrlíková, Anna</au><au>Opekar, František</au><au>Tůma, Petr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pressure-assisted introduction of urine samples into a short capillary for electrophoretic separation with contactless conductivity and UV spectrometry detection</atitle><jtitle>Electrophoresis</jtitle><addtitle>ELECTROPHORESIS</addtitle><date>2015-08</date><risdate>2015</risdate><volume>36</volume><issue>16</issue><spage>1962</spage><epage>1968</epage><pages>1962-1968</pages><issn>0173-0835</issn><eissn>1522-2683</eissn><abstract>A computer‐controlled hydrodynamic sample introduction method has been proposed for short‐capillary electrophoresis. In the method, the BGE flushes sample from the loop of a six‐way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the electrolyte stream at the time when the sample zone is at the capillary, leading to injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. This way of sample introduction does not involve movement of the capillary and both of its ends remain constantly in the solution during both sample injection and separation. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. The new sample introduction method was tested in the determination of ammonia, creatinine, uric acid, and hippuric acid in human urine. The determination was performed in a capillary with an overall length of 10.5 cm, in two BGEs with compositions 50 mM MES + 5 mM NaOH (pH 5.1) and 1 M acetic acid + 1.5 mM crown ether 18‐crown‐6 (pH 2.4). A dual contactless conductivity/UV spectrometric detector was used for the detection.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>25752683</pmid><doi>10.1002/elps.201400613</doi><tpages>7</tpages></addata></record> |
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subjects | Acetic acid Ammonia Ammonium Compounds - urine Capillarity Capillary flow Capillary pressure Cations - urine Creatinine Creatinine - urine Crown ethers Electric Conductivity Electrolytes Electrophoresis Electrophoresis, Capillary - instrumentation Electrophoresis, Capillary - methods Equipment Design Hippuric acid Human urine Humans Hydrodynamic sampling Limit of Detection Linear Models Pressure Reproducibility of Results Scientific apparatus & instruments Separation Short capillary separation Sodium hydroxide Spectrometry Spectrophotometry, Ultraviolet Spectroscopy Uric acid Urinalysis - instrumentation Urinalysis - methods Urine |
title | Pressure-assisted introduction of urine samples into a short capillary for electrophoretic separation with contactless conductivity and UV spectrometry detection |
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