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On-line SPE–CE for the determination of insulin derivatives in biological fluids
An on-line SPE–CE system is described for the determination of insulin derivatives in urine, serum and plasma. By combining techniques based on different separation mechanisms, in this case reversed-phase SPE and CE, a more selective sample clean-up is obtained. The described on-line SPE–CE procedur...
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Published in: | Journal of pharmaceutical and biomedical analysis 2003-10, Vol.33 (3), p.451-462 |
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container_title | Journal of pharmaceutical and biomedical analysis |
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creator | Visser, N.F.C van Harmelen, M Lingeman, H Irth, H |
description | An on-line SPE–CE system is described for the determination of insulin derivatives in urine, serum and plasma. By combining techniques based on different separation mechanisms, in this case reversed-phase SPE and CE, a more selective sample clean-up is obtained. The described on-line SPE–CE procedure is able to desalt and clean biological samples, resulting in more repeatable electrophoretic results as well as a good linearity for urine, serum and plasma samples spiked with insulin derivatives, thus proving the elimination of detrimental effects caused by the sample matrix. The on-line SPE–CE system was linear for urine, serum and plasma samples spiked with insulin derivatives between 5 and 80 mg/l. The repeatability in migration time was below 1% relative standard deviation (R.S.D.). The repeatability of the peak was better ( |
doi_str_mv | 10.1016/S0731-7085(03)00292-9 |
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By combining techniques based on different separation mechanisms, in this case reversed-phase SPE and CE, a more selective sample clean-up is obtained. The described on-line SPE–CE procedure is able to desalt and clean biological samples, resulting in more repeatable electrophoretic results as well as a good linearity for urine, serum and plasma samples spiked with insulin derivatives, thus proving the elimination of detrimental effects caused by the sample matrix. The on-line SPE–CE system was linear for urine, serum and plasma samples spiked with insulin derivatives between 5 and 80 mg/l. The repeatability in migration time was below 1% relative standard deviation (R.S.D.). The repeatability of the peak was better (<2.4% R.S.D.) when no off-line precipitation reaction (<6.2% R.S.D.) was used, proving the beneficial characteristics of on-line sample pretreatment procedures over off-line sample pretreatment procedures which are prone to sample losses and contamination.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/S0731-7085(03)00292-9</identifier><identifier>PMID: 14550864</identifier><identifier>CODEN: JPBADA</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Analysis ; Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Body Fluids - chemistry ; Cattle ; Electrophoresis, Capillary - methods ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Humans ; Insulin ; Insulin - analysis ; Insulin - genetics ; Medical sciences ; Molecular Sequence Data ; On-line ; Pharmacology. 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By combining techniques based on different separation mechanisms, in this case reversed-phase SPE and CE, a more selective sample clean-up is obtained. The described on-line SPE–CE procedure is able to desalt and clean biological samples, resulting in more repeatable electrophoretic results as well as a good linearity for urine, serum and plasma samples spiked with insulin derivatives, thus proving the elimination of detrimental effects caused by the sample matrix. The on-line SPE–CE system was linear for urine, serum and plasma samples spiked with insulin derivatives between 5 and 80 mg/l. The repeatability in migration time was below 1% relative standard deviation (R.S.D.). The repeatability of the peak was better (<2.4% R.S.D.) when no off-line precipitation reaction (<6.2% R.S.D.) was used, proving the beneficial characteristics of on-line sample pretreatment procedures over off-line sample pretreatment procedures which are prone to sample losses and contamination.</description><subject>Amino Acid Sequence</subject><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Fluids - chemistry</subject><subject>Cattle</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - analysis</subject><subject>Insulin - genetics</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>On-line</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasma</subject><subject>Serum</subject><subject>SPE</subject><subject>Technology, Pharmaceutical - methods</subject><subject>Urine</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KxDAQgIMouv48gtKLoodq0rRNchJZ1h8QFH_AW0iTiUa6jSbtgjffwTf0SYzuokcnh4HJNzPJh9A2wYcEk_roFjNKcoZ5tY_pAcaFKHKxhEaEM5oXdfmwjEa_yBpaj_EZY1wRUa6iNVJWFeZ1OUI3V13eug6y2-vJ5_vHeJJZH7L-CTIDPYSp61TvfJd5m7kuDglNF8HNUnUGMdWyxvnWPzqt2sy2gzNxE61Y1UbYWuQNdH86uRuf55dXZxfjk8tcU0H6nFGLudFaCMWpbTjjDSemYLUGazRUSqmmUA0UxtYFMcSykgMTmNbADRGWbqC9-dyX4F8HiL2cuqihbVUHfoiSVemkSGA1B3XwMQaw8iW4qQpvkmD5LVP-yJTfpiSm8kemFKlvZ7FgaKZg_roW9hKwuwBUTP-3QXXaxT-uKhlndZG44zkHScfMQZBRO-g0GBdA99J4989TvgDIXpKy</recordid><startdate>20031015</startdate><enddate>20031015</enddate><creator>Visser, N.F.C</creator><creator>van Harmelen, M</creator><creator>Lingeman, H</creator><creator>Irth, H</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20031015</creationdate><title>On-line SPE–CE for the determination of insulin derivatives in biological fluids</title><author>Visser, N.F.C ; van Harmelen, M ; Lingeman, H ; Irth, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-73f08dcc99a83fb878b81d276cefdce5aaab2abe2df621d1f748e79036e8d19f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Amino Acid Sequence</topic><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Body Fluids - chemistry</topic><topic>Cattle</topic><topic>Electrophoresis, Capillary - methods</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Insulin</topic><topic>Insulin - analysis</topic><topic>Insulin - genetics</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>On-line</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasma</topic><topic>Serum</topic><topic>SPE</topic><topic>Technology, Pharmaceutical - methods</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Visser, N.F.C</creatorcontrib><creatorcontrib>van Harmelen, M</creatorcontrib><creatorcontrib>Lingeman, H</creatorcontrib><creatorcontrib>Irth, H</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>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Visser, N.F.C</au><au>van Harmelen, M</au><au>Lingeman, H</au><au>Irth, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>On-line SPE–CE for the determination of insulin derivatives in biological fluids</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2003-10-15</date><risdate>2003</risdate><volume>33</volume><issue>3</issue><spage>451</spage><epage>462</epage><pages>451-462</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>An on-line SPE–CE system is described for the determination of insulin derivatives in urine, serum and plasma. By combining techniques based on different separation mechanisms, in this case reversed-phase SPE and CE, a more selective sample clean-up is obtained. The described on-line SPE–CE procedure is able to desalt and clean biological samples, resulting in more repeatable electrophoretic results as well as a good linearity for urine, serum and plasma samples spiked with insulin derivatives, thus proving the elimination of detrimental effects caused by the sample matrix. The on-line SPE–CE system was linear for urine, serum and plasma samples spiked with insulin derivatives between 5 and 80 mg/l. The repeatability in migration time was below 1% relative standard deviation (R.S.D.). The repeatability of the peak was better (<2.4% R.S.D.) when no off-line precipitation reaction (<6.2% R.S.D.) was used, proving the beneficial characteristics of on-line sample pretreatment procedures over off-line sample pretreatment procedures which are prone to sample losses and contamination.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>14550864</pmid><doi>10.1016/S0731-7085(03)00292-9</doi><tpages>12</tpages></addata></record> |
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subjects | Amino Acid Sequence Analysis Analytical, structural and metabolic biochemistry Animals Biological and medical sciences Body Fluids - chemistry Cattle Electrophoresis, Capillary - methods Fundamental and applied biological sciences. Psychology General pharmacology Humans Insulin Insulin - analysis Insulin - genetics Medical sciences Molecular Sequence Data On-line Pharmacology. Drug treatments Plasma Serum SPE Technology, Pharmaceutical - methods Urine |
title | On-line SPE–CE for the determination of insulin derivatives in biological fluids |
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