Binding of Sulfonamide Antibiotics to CTABr Micelles Characterized Using 1H NMR Spectroscopy
Interactions of nine sulfonamide antibiotics (sulfadoxine, sulfathiazole, sulfamethoxazole, sulfamerazine, sulfadiazine, sulfamethazine, sulfacetamide, sulfaguanidine, and sulfanilamide) with cetyltrimethylamonium bromide (CTABr) micelles were examined using 1H NMR spectroscopy. Seven of the nine pr...
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Veröffentlicht in: | Langmuir 2016-08, Vol.32 (31), p.7814-7820 |
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creator | Sarker, Ashish K. Cashin, Patrick J. Balakrishnan, Vimal K. Exall, Kirsten Buncel, Erwin Brown, R. Stephen |
description | Interactions of nine sulfonamide antibiotics (sulfadoxine, sulfathiazole, sulfamethoxazole, sulfamerazine, sulfadiazine, sulfamethazine, sulfacetamide, sulfaguanidine, and sulfanilamide) with cetyltrimethylamonium bromide (CTABr) micelles were examined using 1H NMR spectroscopy. Seven of the nine provided a significant change in the 1H NMR chemical shift such that the magnitude and direction (upfield vs downfield) of the chemical shift could be used to propose a locus and orientation of the sulfonamide within the micelle structure. The magnitude of the chemical shift was used to estimate the binding constant for seven sulfonamides with CTABr micelles, providing values and an overall pattern consistent with previous studies of these sulfonamides. |
doi_str_mv | 10.1021/acs.langmuir.6b00947 |
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Stephen</creator><creatorcontrib>Sarker, Ashish K. ; Cashin, Patrick J. ; Balakrishnan, Vimal K. ; Exall, Kirsten ; Buncel, Erwin ; Brown, R. Stephen</creatorcontrib><description>Interactions of nine sulfonamide antibiotics (sulfadoxine, sulfathiazole, sulfamethoxazole, sulfamerazine, sulfadiazine, sulfamethazine, sulfacetamide, sulfaguanidine, and sulfanilamide) with cetyltrimethylamonium bromide (CTABr) micelles were examined using 1H NMR spectroscopy. Seven of the nine provided a significant change in the 1H NMR chemical shift such that the magnitude and direction (upfield vs downfield) of the chemical shift could be used to propose a locus and orientation of the sulfonamide within the micelle structure. The magnitude of the chemical shift was used to estimate the binding constant for seven sulfonamides with CTABr micelles, providing values and an overall pattern consistent with previous studies of these sulfonamides.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/acs.langmuir.6b00947</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>Interface Components: Nanops, Colloids, Emulsions, Surfactants, Proteins, Polymers</subject><ispartof>Langmuir, 2016-08, Vol.32 (31), p.7814-7820</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.langmuir.6b00947$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.langmuir.6b00947$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27075,27923,27924,56737,56787</link.rule.ids></links><search><creatorcontrib>Sarker, Ashish K.</creatorcontrib><creatorcontrib>Cashin, Patrick J.</creatorcontrib><creatorcontrib>Balakrishnan, Vimal K.</creatorcontrib><creatorcontrib>Exall, Kirsten</creatorcontrib><creatorcontrib>Buncel, Erwin</creatorcontrib><creatorcontrib>Brown, R. Stephen</creatorcontrib><title>Binding of Sulfonamide Antibiotics to CTABr Micelles Characterized Using 1H NMR Spectroscopy</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Interactions of nine sulfonamide antibiotics (sulfadoxine, sulfathiazole, sulfamethoxazole, sulfamerazine, sulfadiazine, sulfamethazine, sulfacetamide, sulfaguanidine, and sulfanilamide) with cetyltrimethylamonium bromide (CTABr) micelles were examined using 1H NMR spectroscopy. Seven of the nine provided a significant change in the 1H NMR chemical shift such that the magnitude and direction (upfield vs downfield) of the chemical shift could be used to propose a locus and orientation of the sulfonamide within the micelle structure. The magnitude of the chemical shift was used to estimate the binding constant for seven sulfonamides with CTABr micelles, providing values and an overall pattern consistent with previous studies of these sulfonamides.</description><subject>Interface Components: Nanops, Colloids, Emulsions, Surfactants, Proteins, Polymers</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqdj0FuwjAURK2qlUhbbsDiXyDpdxJIWULUig1dFNghWcZx4CNjI9tZtKdvIsEFuhppNDOax9iEY8Yx529ShcxIe7x05LPZAXFeVg8s4dMc0-l7Xj2yBKuySKtyVozYcwhn7DNFOU_Yfkm2IXsE18KmM62z8kKNhoWNdCAXSQWIDurtYulhTUobowPUJ-mlitrTr25gF4YBvoKv9TdsrlpF74Jy159X9tRKE_T4pi8MPz-29SrtD4uz67ztXcFRDBRiMO8U4kZR_KPyBy9pVO4</recordid><startdate>20160809</startdate><enddate>20160809</enddate><creator>Sarker, Ashish K.</creator><creator>Cashin, Patrick J.</creator><creator>Balakrishnan, Vimal K.</creator><creator>Exall, Kirsten</creator><creator>Buncel, Erwin</creator><creator>Brown, R. Stephen</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20160809</creationdate><title>Binding of Sulfonamide Antibiotics to CTABr Micelles Characterized Using 1H NMR Spectroscopy</title><author>Sarker, Ashish K. ; Cashin, Patrick J. ; Balakrishnan, Vimal K. ; Exall, Kirsten ; Buncel, Erwin ; Brown, R. Stephen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-acs_journals_10_1021_acs_langmuir_6b009473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Interface Components: Nanops, Colloids, Emulsions, Surfactants, Proteins, Polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarker, Ashish K.</creatorcontrib><creatorcontrib>Cashin, Patrick J.</creatorcontrib><creatorcontrib>Balakrishnan, Vimal K.</creatorcontrib><creatorcontrib>Exall, Kirsten</creatorcontrib><creatorcontrib>Buncel, Erwin</creatorcontrib><creatorcontrib>Brown, R. Stephen</creatorcontrib><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarker, Ashish K.</au><au>Cashin, Patrick J.</au><au>Balakrishnan, Vimal K.</au><au>Exall, Kirsten</au><au>Buncel, Erwin</au><au>Brown, R. Stephen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Binding of Sulfonamide Antibiotics to CTABr Micelles Characterized Using 1H NMR Spectroscopy</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2016-08-09</date><risdate>2016</risdate><volume>32</volume><issue>31</issue><spage>7814</spage><epage>7820</epage><pages>7814-7820</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><abstract>Interactions of nine sulfonamide antibiotics (sulfadoxine, sulfathiazole, sulfamethoxazole, sulfamerazine, sulfadiazine, sulfamethazine, sulfacetamide, sulfaguanidine, and sulfanilamide) with cetyltrimethylamonium bromide (CTABr) micelles were examined using 1H NMR spectroscopy. Seven of the nine provided a significant change in the 1H NMR chemical shift such that the magnitude and direction (upfield vs downfield) of the chemical shift could be used to propose a locus and orientation of the sulfonamide within the micelle structure. The magnitude of the chemical shift was used to estimate the binding constant for seven sulfonamides with CTABr micelles, providing values and an overall pattern consistent with previous studies of these sulfonamides.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.langmuir.6b00947</doi></addata></record> |
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title | Binding of Sulfonamide Antibiotics to CTABr Micelles Characterized Using 1H NMR Spectroscopy |
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