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Evaluation of chiral separation based on bovine serum albumin–conjugated carbon nanotubes as stationary phase in capillary electrochromatography
In this work, we utilized adsorbed BSA and multiwalled carbon nanoparticles (BSA/MWCNTs) as a stationary phase in open tubular (OT) capillary for separation of chiral drugs. (3‐Aminopropyl)triethoxysilane was used to assist fabrication of BSA/MWCNTs‐coated OT column by covalent bonding. Incorporatio...
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Published in: | Electrophoresis 2020-07, Vol.41 (13-14), p.1253-1260 |
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description | In this work, we utilized adsorbed BSA and multiwalled carbon nanoparticles (BSA/MWCNTs) as a stationary phase in open tubular (OT) capillary for separation of chiral drugs. (3‐Aminopropyl)triethoxysilane was used to assist fabrication of BSA/MWCNTs‐coated OT column by covalent bonding. Incorporation of MWCNTs nanomaterials into a polymer matrix could increase the phase ratio and take advantage of the easy preparation of an open tubular CEC column. SEM was carried out to characterize the BSA/MWCNTs OT columns. The electrochromatographic performance of the OT columns was evaluated by separation of ketoprofen, ibuprofen, uniconazole, and hesperidin. The effects of MWCNTs concentration, background solution pH and concentration, and applied voltage on separation were investigated. Chiral separations of ketoprofen, ibuprofen, uniconazole, and hesperidin were achieved using the BSA/MWCNTs‐coated OT column with resolutions of 24.20, 12.81, 1.50, and 1.85, respectively. Their optimas were found in the 30 mM phosphate buffers at pH 5.0, 6.5, 7.0, and 6.5, respectively. In addition, the columns demonstrated good repeatability and stability with the run‐to‐run, day‐to‐day, and batch‐to‐batch RSDs of migration times less than 3.5%. |
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(3‐Aminopropyl)triethoxysilane was used to assist fabrication of BSA/MWCNTs‐coated OT column by covalent bonding. Incorporation of MWCNTs nanomaterials into a polymer matrix could increase the phase ratio and take advantage of the easy preparation of an open tubular CEC column. SEM was carried out to characterize the BSA/MWCNTs OT columns. The electrochromatographic performance of the OT columns was evaluated by separation of ketoprofen, ibuprofen, uniconazole, and hesperidin. The effects of MWCNTs concentration, background solution pH and concentration, and applied voltage on separation were investigated. Chiral separations of ketoprofen, ibuprofen, uniconazole, and hesperidin were achieved using the BSA/MWCNTs‐coated OT column with resolutions of 24.20, 12.81, 1.50, and 1.85, respectively. Their optimas were found in the 30 mM phosphate buffers at pH 5.0, 6.5, 7.0, and 6.5, respectively. In addition, the columns demonstrated good repeatability and stability with the run‐to‐run, day‐to‐day, and batch‐to‐batch RSDs of migration times less than 3.5%.</description><identifier>ISSN: 0173-0835</identifier><identifier>EISSN: 1522-2683</identifier><identifier>DOI: 10.1002/elps.202000003</identifier><identifier>PMID: 32350876</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Bovine serum albumin ; Capillary Electrochromatography - instrumentation ; Capillary Electrochromatography - methods ; Electrochromatography ; Enantioseparation ; Ibuprofen ; Ketoprofen ; Multi wall carbon nanotubes ; Multiwalled carbon nanotubes ; Nanomaterials ; Nanoparticles ; Nanotubes, Carbon - chemistry ; Nonsteroidal anti-inflammatory drugs ; Open‐tubular capillary electrochromatography ; Pharmaceutical Preparations - analysis ; Pharmaceutical Preparations - chemistry ; Pharmaceutical Preparations - isolation & purification ; Phase ratio ; Protein Stability ; Reproducibility of Results ; Separation ; Serum albumin ; Serum Albumin, Bovine - chemistry ; Stereoisomerism</subject><ispartof>Electrophoresis, 2020-07, Vol.41 (13-14), p.1253-1260</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4715-7bd3b46f04ecefa4db6ed2f2103ed9a76c5b184726df00f649668d33f9a392003</citedby><cites>FETCH-LOGICAL-c4715-7bd3b46f04ecefa4db6ed2f2103ed9a76c5b184726df00f649668d33f9a392003</cites><orcidid>0000-0001-7332-4186</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32350876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bai, Qiufang</creatorcontrib><creatorcontrib>Zhang, Chenning</creatorcontrib><creatorcontrib>Zhao, Yanyan</creatorcontrib><creatorcontrib>Wang, Chao</creatorcontrib><creatorcontrib>Maihemuti, Mairewaniguli</creatorcontrib><creatorcontrib>Sun, Chengpeng</creatorcontrib><creatorcontrib>Qi, Yan</creatorcontrib><creatorcontrib>Peng, Jinyong</creatorcontrib><creatorcontrib>Guo, Xingjie</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Fang, Linlin</creatorcontrib><title>Evaluation of chiral separation based on bovine serum albumin–conjugated carbon nanotubes as stationary phase in capillary electrochromatography</title><title>Electrophoresis</title><addtitle>Electrophoresis</addtitle><description>In this work, we utilized adsorbed BSA and multiwalled carbon nanoparticles (BSA/MWCNTs) as a stationary phase in open tubular (OT) capillary for separation of chiral drugs. (3‐Aminopropyl)triethoxysilane was used to assist fabrication of BSA/MWCNTs‐coated OT column by covalent bonding. Incorporation of MWCNTs nanomaterials into a polymer matrix could increase the phase ratio and take advantage of the easy preparation of an open tubular CEC column. SEM was carried out to characterize the BSA/MWCNTs OT columns. The electrochromatographic performance of the OT columns was evaluated by separation of ketoprofen, ibuprofen, uniconazole, and hesperidin. The effects of MWCNTs concentration, background solution pH and concentration, and applied voltage on separation were investigated. Chiral separations of ketoprofen, ibuprofen, uniconazole, and hesperidin were achieved using the BSA/MWCNTs‐coated OT column with resolutions of 24.20, 12.81, 1.50, and 1.85, respectively. Their optimas were found in the 30 mM phosphate buffers at pH 5.0, 6.5, 7.0, and 6.5, respectively. In addition, the columns demonstrated good repeatability and stability with the run‐to‐run, day‐to‐day, and batch‐to‐batch RSDs of migration times less than 3.5%.</description><subject>Bovine serum albumin</subject><subject>Capillary Electrochromatography - instrumentation</subject><subject>Capillary Electrochromatography - methods</subject><subject>Electrochromatography</subject><subject>Enantioseparation</subject><subject>Ibuprofen</subject><subject>Ketoprofen</subject><subject>Multi wall carbon nanotubes</subject><subject>Multiwalled carbon nanotubes</subject><subject>Nanomaterials</subject><subject>Nanoparticles</subject><subject>Nanotubes, Carbon - chemistry</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Open‐tubular capillary electrochromatography</subject><subject>Pharmaceutical Preparations - analysis</subject><subject>Pharmaceutical Preparations - chemistry</subject><subject>Pharmaceutical Preparations - isolation & purification</subject><subject>Phase ratio</subject><subject>Protein Stability</subject><subject>Reproducibility of Results</subject><subject>Separation</subject><subject>Serum albumin</subject><subject>Serum Albumin, Bovine - chemistry</subject><subject>Stereoisomerism</subject><issn>0173-0835</issn><issn>1522-2683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkc1O3DAUha0KVAbabZfIEusM_ouTLCs0hUojFal0HV079kxGTpzaCWh2fQZ4wz5JHQZmW29s3fv53KtzEPpCyZISwq6NG-KSEUbmwz-gBc0Zy5gs-QlaEFrwjJQ8P0PnMe4SISohPqIzznhOykIu0PPqEdwEY-t77C3W2zaAw9EMEA5FBdE0eH74x7Y3qRWmDoNTU9f2f_-8aN_vpg2MCdIQVAJ76P04KRMxRBzHVxkIezxskxRu-8QNrXNzyTijx-D1NvgORr8JMGz3n9CpBRfN57f7Av36tnq4ucvWP26_33xdZ1oUNM8K1XAlpCXCaGNBNEqahllGCTdNBYXUuaKlKJhsLCFWikrKsuHcVsCr5Be_QFcH3SH435OJY73zU-jTyJoJxosy2VclanmgdPAxBmPrIbRdWr6mpJ4jqOcI6mME6cPlm-ykOtMc8XfPEyAOwFPrzP4_cvVqff-zoFXO_wF8u5b_</recordid><startdate>202007</startdate><enddate>202007</enddate><creator>Bai, Qiufang</creator><creator>Zhang, Chenning</creator><creator>Zhao, Yanyan</creator><creator>Wang, Chao</creator><creator>Maihemuti, Mairewaniguli</creator><creator>Sun, Chengpeng</creator><creator>Qi, Yan</creator><creator>Peng, Jinyong</creator><creator>Guo, Xingjie</creator><creator>Zhang, Zhen</creator><creator>Fang, Linlin</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>7U5</scope><scope>8FD</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-7332-4186</orcidid></search><sort><creationdate>202007</creationdate><title>Evaluation of chiral separation based on bovine serum albumin–conjugated carbon nanotubes as stationary phase in capillary electrochromatography</title><author>Bai, Qiufang ; Zhang, Chenning ; Zhao, Yanyan ; Wang, Chao ; Maihemuti, Mairewaniguli ; Sun, Chengpeng ; Qi, Yan ; Peng, Jinyong ; Guo, Xingjie ; Zhang, Zhen ; Fang, Linlin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4715-7bd3b46f04ecefa4db6ed2f2103ed9a76c5b184726df00f649668d33f9a392003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bovine serum albumin</topic><topic>Capillary Electrochromatography - instrumentation</topic><topic>Capillary Electrochromatography - methods</topic><topic>Electrochromatography</topic><topic>Enantioseparation</topic><topic>Ibuprofen</topic><topic>Ketoprofen</topic><topic>Multi wall carbon nanotubes</topic><topic>Multiwalled carbon nanotubes</topic><topic>Nanomaterials</topic><topic>Nanoparticles</topic><topic>Nanotubes, Carbon - chemistry</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Open‐tubular capillary electrochromatography</topic><topic>Pharmaceutical Preparations - analysis</topic><topic>Pharmaceutical Preparations - chemistry</topic><topic>Pharmaceutical Preparations - isolation & purification</topic><topic>Phase ratio</topic><topic>Protein Stability</topic><topic>Reproducibility of Results</topic><topic>Separation</topic><topic>Serum albumin</topic><topic>Serum Albumin, Bovine - chemistry</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bai, Qiufang</creatorcontrib><creatorcontrib>Zhang, Chenning</creatorcontrib><creatorcontrib>Zhao, Yanyan</creatorcontrib><creatorcontrib>Wang, Chao</creatorcontrib><creatorcontrib>Maihemuti, Mairewaniguli</creatorcontrib><creatorcontrib>Sun, Chengpeng</creatorcontrib><creatorcontrib>Qi, Yan</creatorcontrib><creatorcontrib>Peng, Jinyong</creatorcontrib><creatorcontrib>Guo, Xingjie</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Fang, Linlin</creatorcontrib><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><jtitle>Electrophoresis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bai, Qiufang</au><au>Zhang, Chenning</au><au>Zhao, Yanyan</au><au>Wang, Chao</au><au>Maihemuti, Mairewaniguli</au><au>Sun, Chengpeng</au><au>Qi, Yan</au><au>Peng, Jinyong</au><au>Guo, Xingjie</au><au>Zhang, Zhen</au><au>Fang, Linlin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of chiral separation based on bovine serum albumin–conjugated carbon nanotubes as stationary phase in capillary electrochromatography</atitle><jtitle>Electrophoresis</jtitle><addtitle>Electrophoresis</addtitle><date>2020-07</date><risdate>2020</risdate><volume>41</volume><issue>13-14</issue><spage>1253</spage><epage>1260</epage><pages>1253-1260</pages><issn>0173-0835</issn><eissn>1522-2683</eissn><abstract>In this work, we utilized adsorbed BSA and multiwalled carbon nanoparticles (BSA/MWCNTs) as a stationary phase in open tubular (OT) capillary for separation of chiral drugs. (3‐Aminopropyl)triethoxysilane was used to assist fabrication of BSA/MWCNTs‐coated OT column by covalent bonding. Incorporation of MWCNTs nanomaterials into a polymer matrix could increase the phase ratio and take advantage of the easy preparation of an open tubular CEC column. SEM was carried out to characterize the BSA/MWCNTs OT columns. The electrochromatographic performance of the OT columns was evaluated by separation of ketoprofen, ibuprofen, uniconazole, and hesperidin. The effects of MWCNTs concentration, background solution pH and concentration, and applied voltage on separation were investigated. Chiral separations of ketoprofen, ibuprofen, uniconazole, and hesperidin were achieved using the BSA/MWCNTs‐coated OT column with resolutions of 24.20, 12.81, 1.50, and 1.85, respectively. Their optimas were found in the 30 mM phosphate buffers at pH 5.0, 6.5, 7.0, and 6.5, respectively. In addition, the columns demonstrated good repeatability and stability with the run‐to‐run, day‐to‐day, and batch‐to‐batch RSDs of migration times less than 3.5%.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32350876</pmid><doi>10.1002/elps.202000003</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7332-4186</orcidid></addata></record> |
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subjects | Bovine serum albumin Capillary Electrochromatography - instrumentation Capillary Electrochromatography - methods Electrochromatography Enantioseparation Ibuprofen Ketoprofen Multi wall carbon nanotubes Multiwalled carbon nanotubes Nanomaterials Nanoparticles Nanotubes, Carbon - chemistry Nonsteroidal anti-inflammatory drugs Open‐tubular capillary electrochromatography Pharmaceutical Preparations - analysis Pharmaceutical Preparations - chemistry Pharmaceutical Preparations - isolation & purification Phase ratio Protein Stability Reproducibility of Results Separation Serum albumin Serum Albumin, Bovine - chemistry Stereoisomerism |
title | Evaluation of chiral separation based on bovine serum albumin–conjugated carbon nanotubes as stationary phase in capillary electrochromatography |
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