Capillary electrophoresis with dual C4D/UV detection for simultaneously determining major metal cations and whey proteins in milk
A reliable and simple CE method with dual C4D and UV detection modes for simultaneous determination of major metal cations and whey proteins in milk samples was developed. Sample pretreatment comprised dilution, acidification to pH 4.55 with 10 mM AcOH and centrifugation. The complete separation of...
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Veröffentlicht in: | Analytical methods 2021-02, Vol.13 (6), p.801-808 |
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description | A reliable and simple CE method with dual C4D and UV detection modes for simultaneous determination of major metal cations and whey proteins in milk samples was developed. Sample pretreatment comprised dilution, acidification to pH 4.55 with 10 mM AcOH and centrifugation. The complete separation of metal cations K+, Ca2+, Na+, and Mg2+ and whey proteins α-Lac, and β-Lg could be achieved respectively within 10 min and 20 min in a simple BGE composed of 1.0 M AcOH, 12 mM l-His and 2 mM 18-crown-6 with pH 2.74 at a voltage/current of +15 kV/12.5 μA. The samples were injected hydrodynamically by a pressure of 50 mbar for 5 s, the excitation voltage and excitation frequency of the C4D detector were 80 V and 1000 kHz, respectively and the detection wavelength of UV detection was set at 200 nm. In cation analysis, the range of the detection limit was 0.05–0.10 mg L−1 for C4D detection and 0.10–0.50 mg L−1 for UV detection, respectively, and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.37–0.55% and 0.46–0.79% for the relative migration time, and 2.51–4.12% and 3.65–4.91% for the peak area, respectively. In whey protein analysis, the detection limits of β-Lg and α-Lac analysis were 5 mg L−1 and 3 mg L−1, respectively and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.29–0.31% and 0.43–0.48% for the migration time and 2.89–3.25% and 3.29–4.18% for the peak area, respectively. The content of four major metal cations and two whey proteins in various types of milk samples was obtained. The results indicated that the content of metal cations varied little in milk samples of different brands and prices, while the content of whey proteins, as thermosensitive active proteins, varied greatly among different heat-treated milk samples. |
doi_str_mv | 10.1039/d0ay02092c |
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Sample pretreatment comprised dilution, acidification to pH 4.55 with 10 mM AcOH and centrifugation. The complete separation of metal cations K+, Ca2+, Na+, and Mg2+ and whey proteins α-Lac, and β-Lg could be achieved respectively within 10 min and 20 min in a simple BGE composed of 1.0 M AcOH, 12 mM l-His and 2 mM 18-crown-6 with pH 2.74 at a voltage/current of +15 kV/12.5 μA. The samples were injected hydrodynamically by a pressure of 50 mbar for 5 s, the excitation voltage and excitation frequency of the C4D detector were 80 V and 1000 kHz, respectively and the detection wavelength of UV detection was set at 200 nm. In cation analysis, the range of the detection limit was 0.05–0.10 mg L−1 for C4D detection and 0.10–0.50 mg L−1 for UV detection, respectively, and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.37–0.55% and 0.46–0.79% for the relative migration time, and 2.51–4.12% and 3.65–4.91% for the peak area, respectively. In whey protein analysis, the detection limits of β-Lg and α-Lac analysis were 5 mg L−1 and 3 mg L−1, respectively and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.29–0.31% and 0.43–0.48% for the migration time and 2.89–3.25% and 3.29–4.18% for the peak area, respectively. The content of four major metal cations and two whey proteins in various types of milk samples was obtained. The results indicated that the content of metal cations varied little in milk samples of different brands and prices, while the content of whey proteins, as thermosensitive active proteins, varied greatly among different heat-treated milk samples.</description><identifier>ISSN: 1759-9660</identifier><identifier>EISSN: 1759-9679</identifier><identifier>DOI: 10.1039/d0ay02092c</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Acidification ; Calcium ; Calcium ions ; Capillary electrophoresis ; Cations ; Centrifugation ; Detection limits ; Dilution ; Electric potential ; Electrophoresis ; Excitation ; Heat treatment ; Ions ; Magnesium ; Metal ions ; Milk ; pH effects ; Pretreatment ; Proteins ; Standard deviation ; Ultraviolet radiation ; Voltage ; Whey ; Whey protein</subject><ispartof>Analytical methods, 2021-02, Vol.13 (6), p.801-808</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Zhao, Jing</creatorcontrib><creatorcontrib>Xu, Zhongqi</creatorcontrib><title>Capillary electrophoresis with dual C4D/UV detection for simultaneously determining major metal cations and whey proteins in milk</title><title>Analytical methods</title><description>A reliable and simple CE method with dual C4D and UV detection modes for simultaneous determination of major metal cations and whey proteins in milk samples was developed. Sample pretreatment comprised dilution, acidification to pH 4.55 with 10 mM AcOH and centrifugation. The complete separation of metal cations K+, Ca2+, Na+, and Mg2+ and whey proteins α-Lac, and β-Lg could be achieved respectively within 10 min and 20 min in a simple BGE composed of 1.0 M AcOH, 12 mM l-His and 2 mM 18-crown-6 with pH 2.74 at a voltage/current of +15 kV/12.5 μA. The samples were injected hydrodynamically by a pressure of 50 mbar for 5 s, the excitation voltage and excitation frequency of the C4D detector were 80 V and 1000 kHz, respectively and the detection wavelength of UV detection was set at 200 nm. In cation analysis, the range of the detection limit was 0.05–0.10 mg L−1 for C4D detection and 0.10–0.50 mg L−1 for UV detection, respectively, and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.37–0.55% and 0.46–0.79% for the relative migration time, and 2.51–4.12% and 3.65–4.91% for the peak area, respectively. In whey protein analysis, the detection limits of β-Lg and α-Lac analysis were 5 mg L−1 and 3 mg L−1, respectively and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.29–0.31% and 0.43–0.48% for the migration time and 2.89–3.25% and 3.29–4.18% for the peak area, respectively. The content of four major metal cations and two whey proteins in various types of milk samples was obtained. The results indicated that the content of metal cations varied little in milk samples of different brands and prices, while the content of whey proteins, as thermosensitive active proteins, varied greatly among different heat-treated milk samples.</description><subject>Acidification</subject><subject>Calcium</subject><subject>Calcium ions</subject><subject>Capillary electrophoresis</subject><subject>Cations</subject><subject>Centrifugation</subject><subject>Detection limits</subject><subject>Dilution</subject><subject>Electric potential</subject><subject>Electrophoresis</subject><subject>Excitation</subject><subject>Heat treatment</subject><subject>Ions</subject><subject>Magnesium</subject><subject>Metal ions</subject><subject>Milk</subject><subject>pH effects</subject><subject>Pretreatment</subject><subject>Proteins</subject><subject>Standard deviation</subject><subject>Ultraviolet radiation</subject><subject>Voltage</subject><subject>Whey</subject><subject>Whey protein</subject><issn>1759-9660</issn><issn>1759-9679</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdj8tOwzAQRS0EEqWw4QsssWET6kfsxEsUnlIlNoVt5fhBXRwnxImqLPlz3IJYsJrRzLlz5wJwidENRlQsNJITIkgQdQRmuGAiE7wQx389R6fgLMYtQlxQjmfgq5Kd8172EzTeqKFvu03bm-gi3LlhA_UoPazyu8XrG9RmSIRrA7RtD6NrRj_IYNox-umw7BsXXHiHjdwmoDFD0iq5V0Qog4a7jZlg17eDcWniAmyc_zgHJ1b6aC5-6xysHu5X1VO2fHl8rm6XWccxygzGTOU1VRxzzTjVVhBmRSm0ocRSSQSjDBdE5ZrpWmvBjLR1YZUsibIa0Tm4_jmb_D9HE4d146IyKfohwZrkJcaIYbJHr_6h23bsQ3ouUQIJWjJU0m9F9XGk</recordid><startdate>20210214</startdate><enddate>20210214</enddate><creator>Zhao, Jing</creator><creator>Xu, Zhongqi</creator><general>Royal Society of Chemistry</general><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>L7M</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20210214</creationdate><title>Capillary electrophoresis with dual C4D/UV detection for simultaneously determining major metal cations and whey proteins in milk</title><author>Zhao, Jing ; Xu, Zhongqi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p610-e115c4b3c616d563df925f989de32f3a29535172c4d5dbdd95eafb7fca82cfd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acidification</topic><topic>Calcium</topic><topic>Calcium ions</topic><topic>Capillary electrophoresis</topic><topic>Cations</topic><topic>Centrifugation</topic><topic>Detection limits</topic><topic>Dilution</topic><topic>Electric potential</topic><topic>Electrophoresis</topic><topic>Excitation</topic><topic>Heat treatment</topic><topic>Ions</topic><topic>Magnesium</topic><topic>Metal ions</topic><topic>Milk</topic><topic>pH effects</topic><topic>Pretreatment</topic><topic>Proteins</topic><topic>Standard deviation</topic><topic>Ultraviolet radiation</topic><topic>Voltage</topic><topic>Whey</topic><topic>Whey protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Jing</creatorcontrib><creatorcontrib>Xu, Zhongqi</creatorcontrib><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Jing</au><au>Xu, Zhongqi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Capillary electrophoresis with dual C4D/UV detection for simultaneously determining major metal cations and whey proteins in milk</atitle><jtitle>Analytical methods</jtitle><date>2021-02-14</date><risdate>2021</risdate><volume>13</volume><issue>6</issue><spage>801</spage><epage>808</epage><pages>801-808</pages><issn>1759-9660</issn><eissn>1759-9679</eissn><abstract>A reliable and simple CE method with dual C4D and UV detection modes for simultaneous determination of major metal cations and whey proteins in milk samples was developed. Sample pretreatment comprised dilution, acidification to pH 4.55 with 10 mM AcOH and centrifugation. The complete separation of metal cations K+, Ca2+, Na+, and Mg2+ and whey proteins α-Lac, and β-Lg could be achieved respectively within 10 min and 20 min in a simple BGE composed of 1.0 M AcOH, 12 mM l-His and 2 mM 18-crown-6 with pH 2.74 at a voltage/current of +15 kV/12.5 μA. The samples were injected hydrodynamically by a pressure of 50 mbar for 5 s, the excitation voltage and excitation frequency of the C4D detector were 80 V and 1000 kHz, respectively and the detection wavelength of UV detection was set at 200 nm. In cation analysis, the range of the detection limit was 0.05–0.10 mg L−1 for C4D detection and 0.10–0.50 mg L−1 for UV detection, respectively, and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.37–0.55% and 0.46–0.79% for the relative migration time, and 2.51–4.12% and 3.65–4.91% for the peak area, respectively. In whey protein analysis, the detection limits of β-Lg and α-Lac analysis were 5 mg L−1 and 3 mg L−1, respectively and the relative standard deviations (RSD%, n = 5) of intraday and interday analysis were 0.29–0.31% and 0.43–0.48% for the migration time and 2.89–3.25% and 3.29–4.18% for the peak area, respectively. The content of four major metal cations and two whey proteins in various types of milk samples was obtained. The results indicated that the content of metal cations varied little in milk samples of different brands and prices, while the content of whey proteins, as thermosensitive active proteins, varied greatly among different heat-treated milk samples.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d0ay02092c</doi><tpages>8</tpages></addata></record> |
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subjects | Acidification Calcium Calcium ions Capillary electrophoresis Cations Centrifugation Detection limits Dilution Electric potential Electrophoresis Excitation Heat treatment Ions Magnesium Metal ions Milk pH effects Pretreatment Proteins Standard deviation Ultraviolet radiation Voltage Whey Whey protein |
title | Capillary electrophoresis with dual C4D/UV detection for simultaneously determining major metal cations and whey proteins in milk |
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