{"id":2098,"date":"2018-02-07T16:06:57","date_gmt":"2018-02-07T13:06:57","guid":{"rendered":"http:\/\/polymerjournal.kiev.ua\/en\/?page_id=2098"},"modified":"2018-02-07T16:06:57","modified_gmt":"2018-02-07T13:06:57","slug":"2014-4-10","status":"publish","type":"page","link":"http:\/\/polymerjournal.kiev.ua\/en\/2014-4-10\/","title":{"rendered":"2014 (4) 10"},"content":{"rendered":"<p><strong>Sens<\/strong><strong>\u043e<\/strong><strong>r system based on molecular imprinted polymers with catalytic properties to determination <em>o<\/em>-hydroxyphenol in the environment<\/strong><\/p>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong><em>T.<\/em><\/strong><strong><em>\u0410<\/em><\/strong><strong><em>. Sergeyeva<\/em><\/strong><strong><em>1<\/em><\/strong><strong><em>, L.A. Gorbach<\/em><\/strong><strong><em>2<\/em><\/strong><strong><em>, <\/em><\/strong><strong><em>\u041e<\/em><\/strong><strong><em>.D. Lutsyk<\/em><\/strong><strong><em>2 <\/em><\/strong><strong><em>, <\/em><\/strong><strong><em>\u041e<\/em><\/strong><strong><em>.O. Brovko<\/em><\/strong><strong><em>2<\/em><\/strong><strong><em>, L.M. Sergeeva<\/em><\/strong><strong><em>2<\/em><\/strong><strong><em>, G.V. Elska<\/em><\/strong><strong><em>1<\/em><\/strong><\/p>\n<p>&nbsp;<\/p>\n<p>1Institute of Molecular Biology and Genetics NAS of Ukraine<\/p>\n<p>150, Zabolotnogo str., Kyiv, 03680, Ukraine<\/p>\n<p>2Institute of Macromolecular Chemistry NAS of Ukraine<\/p>\n<p>48, Kharkivske shose, Kyiv, 02160, Ukraine<\/p>\n<p>&nbsp;<\/p>\n<p>Polym. J., 2014, <strong>36<\/strong>, no. 4: 406-412.<\/p>\n<p>&nbsp;<\/p>\n<p>Section: Synthesis polymers.<\/p>\n<p>&nbsp;<\/p>\n<p>Language: Ukrainian.<\/p>\n<p>&nbsp;<\/p>\n<p>Abstract:<\/p>\n<p><em>Organic polymers-biomimicks, containing catalytic sites in their structure, which mimic mushroom tyrosinase active sites, that are capable of highly-selective recognition of o-hydroxyphenols were synthesized according to the technique of molecular imprinting. Biosensor devices for o-hydroxyphenols detection in environmental samples were developed on their basis. The methodology of calibration of the laboratory prototype of the biosensor based on tyrosinase mimicks for the detection of\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0o-hydroxyphenols in natural and waste waters was developed. Comparison of data of the biosensor analysis and traditional HPLC method was made. Real samples of river water were analyzed as for\u00a0\u00a0\u00a0\u00a0\u00a0 o-hydroxyphenol content using developed biosensor. The protocol for the determination of\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 o-hydroxyphenol concentration in real samples was worked out. As compared to traditional analytical methods of o-hydroxyphenol detection the proposed biosensor method is more effective from the point of view of simplicity of operation, as well as cost and size of equipment.<\/em><\/p>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong>Keywords: <\/strong>molecular imprinted polymers, binding sites, portable biosensors<strong>, <\/strong><em>o<\/em>-hydroxyphenols.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u041b\u0456\u0442\u0435\u0440\u0430\u0442\u0443\u0440\u0430<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p>1. Dangerouns Properties of Industrial Materials \/ Ed. By N.J. Sax. \u2013 New York: VNR Company, 1984. &#8211; 3124 p.<br \/>\n2. \u0424\u0438\u0442\u043e\u0442\u043e\u043a\u0441\u0438\u0447\u043d\u043e\u0441\u0442\u044c \u043e\u0440\u0433\u0430\u043d\u0438\u0447\u0435\u0441\u043a\u0438\u0445 \u0438 \u043d\u0435\u043e\u0440\u0433\u0430\u043d\u0438\u0447\u0435\u0441\u043a\u0438\u0445 \u0437\u0430\u0433\u0440\u044f\u0437\u043d\u0438\u0442\u0435\u043b\u0435\u0439: \u043f\u0440\u043e\u0431\u043b\u0435\u043c\u044b \u043f\u0440\u043e\u043c\u044b\u0448\u043b\u0435\u043d\u043d\u043e\u0439 \u0431\u043e\u0442\u0430\u043d\u0438\u043a\u0438 \/ \u041f\u043e\u0434 \u043e\u0431\u0449. \u0440\u0435\u0434.: \u0415. \u041d. \u041a\u043e\u043d\u0434\u0440\u0430\u0442\u044e\u043a \u0410\u041d \u0423\u043a\u0440\u0430\u0438\u043d\u0441\u043a\u043e\u0439 \u0421\u0421\u0420, \u0414\u043e\u043d\u0435\u0446\u043a\u0438\u0439 \u0431\u043e\u0442\u0430\u043d\u0438\u0447\u0435\u0441\u043a\u0438\u0439 \u0441\u0430\u0434 . \u2013 \u041a\u0438\u0435\u0432 : \u041d\u0430\u0443\u043a. \u0434\u0443\u043c\u043a\u0430, 1986. \u2013 215 \u0441.<br \/>\n3. Xie T.M., Hulthe B., Folestad S. \/\/ Chemosphere. &#8211; 1984. &#8211; 13, \u2116 3. &#8211; P. 445-459.<br \/>\n4. Moldoveanu S.C., Kise M. \/\/ J. of Chromatography. Part A. \u2013 2007. &#8211; 1141, N1. &#8211; P. 90-97.<br \/>\n5. Nagaraja P., Vasantha R.A., Sunitha K.R. \/\/ Talanta. \u2013 2001. \u2013 55, N 6. &#8211; P. 1039-1046.<br \/>\n6. Yue X., Pang S., Han P., Zhang C., Wang J., Zhang L. \/\/ Electrochemistry Communications. \u2013 2013. \u2013 Vol. 34. \u2013 P. 356\u2013359.<br \/>\n7. Handbook of biosensors and Biochips \/ Lowe C., Weetall H., Cullen D., Karube I.-New York.: John Willey and Sons Inc., 2007. \u2013 1500 p.<br \/>\n8. Cooper J., Cass T. Biosensors. Practical approach. 2nd Edition. &#8211; Oxford: Oxford University Press, 2004. \u2013 251 p.<br \/>\n9. \u0421\u0435\u0440\u0433\u0435\u0454\u0432\u0430 \u0422.\u0410., \u0421\u043b\u0456\u043d\u0447\u0435\u043d\u043a\u043e \u041e.\u0410., \u0411\u0440\u043e\u0432\u043a\u043e \u041e.\u041e., \u041f\u0456\u043b\u0435\u0446\u044c\u043a\u0438\u0439 \u0421.\u0410., \u0404\u043b\u044c\u0441\u044c\u043a\u0430 \u0413.\u0412. \/\/ \u0423\u043a\u0440. \u0431\u0456\u043e\u0445\u0456\u043c. \u0436\u0443\u0440\u043d. \u2013 2009. \u2013 81, \u2116 1. \u2013 \u0421. 20\u201330.<br \/>\n10. Mayer A.M. \/\/ Phytochemistry. \u2013 2006. \u2013 67, \u2116 21. \u2013 P. 2318\u20132331.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Sens\u043er system based on molecular imprinted polymers with catalytic properties to determination o-hydroxyphenol in the environment \u00a0 T.\u0410. Sergeyeva1, L.A. Gorbach2, \u041e.D. Lutsyk2 , \u041e.O. Brovko2, L.M. Sergeeva2, G.V. Elska1 &nbsp; 1Institute of Molecular Biology and Genetics NAS of Ukraine 150, Zabolotnogo str., Kyiv, 03680, Ukraine 2Institute of Macromolecular Chemistry NAS of Ukraine 48, Kharkivske [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"acf":[],"_links":{"self":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/2098"}],"collection":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/comments?post=2098"}],"version-history":[{"count":1,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/2098\/revisions"}],"predecessor-version":[{"id":2099,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/2098\/revisions\/2099"}],"wp:attachment":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/media?parent=2098"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}