Immobilization of Enzymes through One-Pot Chemical Preoxidation and Electropolymerization of Dithiols in Enzyme-Containing Aqueous Suspensions To Develop Biosensors with Improved Performance
A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be...
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Published in | Analytical chemistry (Washington) Vol. 80; no. 15; pp. 5829 - 5838 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Washington, DC
American Chemical Society
01.08.2008
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Abstract | A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K3Fe(CN)6 or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K3Fe(CN)6, yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV−vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. |
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AbstractList | A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K3Fe(CN)6 or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K3Fe(CN)6, yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV−vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of ... or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding ..., yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV-vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. (ProQuest: ... denotes formulae/symbols omitted.) A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K3Fe(CN)6 or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K3Fe(CN)6, yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV-vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications.A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K3Fe(CN)6 or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K3Fe(CN)6, yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV-vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6- hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K sub(3)Fe(CN) sub(6) or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K sub(3)Fe(CN) sub(6), yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4- benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV-vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed as a universal strategy for high-activity and high-load immobilization of enzymes to construct amperometric biosensors, which was proven to be effective for the monomer of 1,4-benzenedithiol (BDT), 1,6-hexanedithiol, o-phenylenediamine, o-aminophenol or pyrrole, the preoxidant of K3Fe(CN)6 or p-benzoquinone, and the enzyme of glucose oxidase (GOx) or alkaline phosphatase (AP) to develop GOx-based glucose biosensors or AP-based disodium phenyl phosphate biosensors. As a case examined in detail, a well-dispersed aqueous suspension of the poorly soluble BDT was obtained through its dispersion assisted by ultrasonication and coexisting GOx, which was then subject to chemical preoxidation through adding K3Fe(CN)6, yielding many composites of insoluble BDT oligomers with lots of high-activity enzyme molecules entrapped. Some insoluble composites were then electrochemically codeposited with poly(1,4-benzenedithiol) on an Au electrode, yielding an enzyme film with high-load and high-activity enzyme immobilized. The glucose biosensor prepared here from the CPEM protocol showed much better performance than that from the preoxidant-free conventional electropolymerization (CEP) protocol, with a detection sensitivity increase by a factor of 32 in this case. The GOx-based and AP-based first-generation biosensors developed from the present CPEM protocol all exhibited notably improved performance compared with the analogues from the preoxidant-free CEP protocol. The electrochemical quartz crystal microbalance (EQCM) technique was used to investigate various electrode modification processes. The values of quantity and enzymatic specific activity (ESA) of the immobilized enzymes were evaluated through the EQCM and the conventional UV-vis spectrophotometric method, given that the CPEM protocol notably improved the quantity and the ESA of immobilized enzymes as compared with the preoxidant-free CEP protocol. The proposed CPEM protocol may be interesting in a number of fields, including biosensing, biocatalysis, biofuel cells, bioaffinity chromatography, and biomaterials, and the successful electropolymerization of dithiols in aqueous suspensions (two-phase electropolymerization) may open a new avenue for many monomers that are poorly soluble in neutral aqueous solutions to in situ immobilize biomolecules for bioapplications. |
Author | Xu, Xiahong Zhang, Youyu Xie, Qingji Fu, Yingchun Chen, Chao Zhou, Qingmei Zou, Can Tan, Liang Tang, Hao Yao, Shouzhuo |
Author_xml | – sequence: 1 givenname: Yingchun surname: Fu fullname: Fu, Yingchun – sequence: 2 givenname: Chao surname: Chen fullname: Chen, Chao – sequence: 3 givenname: Qingji surname: Xie fullname: Xie, Qingji email: xieqj@hunnu.edu.cn – sequence: 4 givenname: Xiahong surname: Xu fullname: Xu, Xiahong – sequence: 5 givenname: Can surname: Zou fullname: Zou, Can – sequence: 6 givenname: Qingmei surname: Zhou fullname: Zhou, Qingmei – sequence: 7 givenname: Liang surname: Tan fullname: Tan, Liang – sequence: 8 givenname: Hao surname: Tang fullname: Tang, Hao – sequence: 9 givenname: Youyu surname: Zhang fullname: Zhang, Youyu – sequence: 10 givenname: Shouzhuo surname: Yao fullname: Yao, Shouzhuo |
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Cites_doi | 10.1021/ja050390v 10.1002/adma.19960080306 10.1016/j.bios.2007.03.028 10.1021/ja012680r 10.1021/cm980729v 10.1021/bp070256+ 10.1002/pat.474 10.1021/ac048686r 10.1149/1.2044006 10.1021/ac9901788 10.1021/ja980397v 10.1016/j.bej.2004.09.011 10.1002/(SICI)1521-3773(20000403)39:7<1180::AID-ANIE1180>3.0.CO;2-E 10.1021/ac0518194 10.1016/j.snb.2004.04.100 10.1016/j.aca.2005.10.009 10.1021/j100668a024 10.1021/ac980125a 10.1021/la0205248 10.1016/0302-4598(92)80051-H 10.1002/elan.1140091803 10.1149/1.1391831 10.1021/ja00256a040 10.1021/jp971502a 10.1021/ac950431d 10.1016/j.jelechem.2007.01.016 10.1021/ac052143f 10.1002/app.22455 10.1021/bp049623x 10.1007/BF01337937 10.1016/S0956-5663(99)00024-X 10.1002/anie.200500828 10.1016/j.snb.2006.05.017 10.1021/ac00081a031 10.1021/la062901c 10.1016/j.bios.2006.12.004 10.1016/j.electacta.2006.02.023 10.1016/0925-4005(90)80268-5 10.1021/ja071946c 10.1002/elan.200603552 10.1021/cr00014a006 |
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Keywords | Performance evaluation Phosphates Alkaline phosphatase Glucose oxidase Electrochemical method In situ Phosphoric monoester hydrolases Immobilization Esterases Benzoquinone Biofuel Oligomer Electrochemical polymerization Aminophenols Specific activity Enzymatic activity Amperometry Enzyme Enzyme electrode Chromatography Sensitivity Biosensor Hydrolases Oxidoreductases Aqueous solution Spectrophotometry Immobilized enzyme Quartz microbalance Ultraviolet visible spectrometry |
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Notes | ark:/67375/TPS-QL1P8NTH-P istex:2983F78436FD85B582C6658373E2D94494CF038A The spelling of p-benzenequinone was changed to p-benzoquinone, and there were errors in the LDR values in Table 1. This manuscript was first published ASAP on July 2, 2008; the corrected version was published ASAP July 12, 2008. Additional information as noted in text. This material is available free of charge via the Internet at http://pubs.acs.org. SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
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References | McMahon C. P. (ref17/cit17) 2005; 77 Tatsuma T. (ref26/cit26) 1997; 101 Nien P. C. (ref14/cit14) 2006; 18 Deng C. Y. (ref19/cit19) 2006; 557 Bergmeyer H. (ref42/cit42) 1963 Ryabov A. D. (ref15/cit15) 1999; 11 Willner I. (ref2/cit2) 2000; 39 Li M. R. (ref23/cit23) 2006; 51 Schuhmann W. (ref6/cit6) 1990; 1 Li J. (ref20/cit20) 2007; 22 Sauerbrey G. (ref34/cit34) 1959; 155 Potyrailo R. A. (ref3/cit3) 2006; 45 Hiller M. (ref7/cit7) 1996; 8 Su Y. H. (ref32/cit32) 2008; 24 Raitman O. A. (ref9/cit9) 2002; 124 Cosnier S. (ref25/cit25) 1997; 9 Njagi J. (ref24/cit24) 2007; 23 Zhang Z. N. (ref22/cit22) 1996; 68 Georganopoulou D. G. (ref38/cit38) 2003; 19 Cosnier S. (ref1/cit1) 1999; 14 Naoi K. (ref27/cit27) 1995; 142 Willner I. (ref16/cit16) 1992; 29 Buttry D. A. (ref33/cit33) 1992; 92 Hana K. (ref41/cit41) 2005; 22 Cosnier S. (ref13/cit13) 1999; 71 Ferreira L. F. P. (ref40/cit40) 2005; 21 Borole D. D. (ref8/cit8) 2004; 15 McMahon C. P. (ref18/cit18) 2006; 78 Haddour N. (ref4/cit4) 2005; 127 Fu Y. C. (ref28/cit28) 2007; 603 Bartlett P. N. (ref11/cit11) 1994; 66 Houk J. (ref36/cit36) 1987; 109 Yu L. (ref35/cit35) 1999; 146 Chohan R. K. (ref37/cit37) 1972; 76 Cosnier S. (ref12/cit12) 1998; 70 Mano N. (ref10/cit10) 2007; 129 Deng C. Y. (ref31/cit31) 2007; 122 Ma M. M. (ref5/cit5) 2005; 98 Jena B. K. (ref29/cit29) 2006; 78 Emori E. (ref39/cit39) 1998; 120 Pan D. W. (ref21/cit21) 2005; 104 Pandey P. (ref30/cit30) 2007; 23 |
References_xml | – volume: 127 start-page: 5752 year: 2005 ident: ref4/cit4 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja050390v – volume: 8 start-page: 219 year: 1996 ident: ref7/cit7 publication-title: Adv. Mater. doi: 10.1002/adma.19960080306 – volume: 23 start-page: 168 year: 2007 ident: ref24/cit24 publication-title: Biosens. Bioelectron. doi: 10.1016/j.bios.2007.03.028 – volume: 124 start-page: 6487 year: 2002 ident: ref9/cit9 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja012680r – volume: 11 start-page: 600 year: 1999 ident: ref15/cit15 publication-title: Chem. Mater. doi: 10.1021/cm980729v – volume: 24 start-page: 262 year: 2008 ident: ref32/cit32 publication-title: Biotechnol. Prog. doi: 10.1021/bp070256+ – volume: 15 start-page: 306 year: 2004 ident: ref8/cit8 publication-title: Polym. Adv. Technol. doi: 10.1002/pat.474 – volume: 77 start-page: 1196 year: 2005 ident: ref17/cit17 publication-title: Anal. Chem. doi: 10.1021/ac048686r – volume: 142 start-page: 354 year: 1995 ident: ref27/cit27 publication-title: J. Electrochem. Soc. doi: 10.1149/1.2044006 – volume: 71 start-page: 3692 year: 1999 ident: ref13/cit13 publication-title: Anal. Chem. doi: 10.1021/ac9901788 – volume: 120 start-page: 4043 year: 1998 ident: ref39/cit39 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja980397v – volume: 22 start-page: 161 year: 2005 ident: ref41/cit41 publication-title: Biochem. Eng. J. doi: 10.1016/j.bej.2004.09.011 – volume: 39 start-page: 1180 year: 2000 ident: ref2/cit2 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/(SICI)1521-3773(20000403)39:7<1180::AID-ANIE1180>3.0.CO;2-E – volume: 78 start-page: 2352 year: 2006 ident: ref18/cit18 publication-title: Anal. Chem. doi: 10.1021/ac0518194 – volume: 104 start-page: 68 year: 2005 ident: ref21/cit21 publication-title: Sens. Actuators, B doi: 10.1016/j.snb.2004.04.100 – volume: 557 start-page: 85 year: 2006 ident: ref19/cit19 publication-title: Anal. Chim. Acta doi: 10.1016/j.aca.2005.10.009 – volume: 76 start-page: 3641 year: 1972 ident: ref37/cit37 publication-title: J. Phys. Chem. doi: 10.1021/j100668a024 – volume: 70 start-page: 3952 year: 1998 ident: ref12/cit12 publication-title: Anal. Chem. doi: 10.1021/ac980125a – volume: 19 start-page: 4977 year: 2003 ident: ref38/cit38 publication-title: Langmuir doi: 10.1021/la0205248 – volume: 29 start-page: 29 year: 1992 ident: ref16/cit16 publication-title: Bioelectrochem. Bioenerg. doi: 10.1016/0302-4598(92)80051-H – volume: 9 start-page: 1387 year: 1997 ident: ref25/cit25 publication-title: Electroanalysis doi: 10.1002/elan.1140091803 – volume: 146 start-page: 1712 year: 1999 ident: ref35/cit35 publication-title: J. Electrochem. Soc. doi: 10.1149/1.1391831 – volume: 109 start-page: 6825 year: 1987 ident: ref36/cit36 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00256a040 – volume-title: Methods of Enzymatic Analysis year: 1963 ident: ref42/cit42 – volume: 101 start-page: 7556 year: 1997 ident: ref26/cit26 publication-title: J. Phys. Chem. B doi: 10.1021/jp971502a – volume: 68 start-page: 1632 year: 1996 ident: ref22/cit22 publication-title: Anal. Chem. doi: 10.1021/ac950431d – volume: 603 start-page: 96 year: 2007 ident: ref28/cit28 publication-title: J. Electroanal. Chem. doi: 10.1016/j.jelechem.2007.01.016 – volume: 78 start-page: 6332 year: 2006 ident: ref29/cit29 publication-title: Anal. Chem. doi: 10.1021/ac052143f – volume: 98 start-page: 2550 year: 2005 ident: ref5/cit5 publication-title: J. Appl. Polym. Sci. doi: 10.1002/app.22455 – volume: 21 start-page: 868 year: 2005 ident: ref40/cit40 publication-title: Biotechnol. Prog. doi: 10.1021/bp049623x – volume: 155 start-page: 206 year: 1959 ident: ref34/cit34 publication-title: Z. Phys. doi: 10.1007/BF01337937 – volume: 14 start-page: 443 year: 1999 ident: ref1/cit1 publication-title: Biosens. Bioelectron. doi: 10.1016/S0956-5663(99)00024-X – volume: 45 start-page: 702 year: 2006 ident: ref3/cit3 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200500828 – volume: 122 start-page: 148 year: 2007 ident: ref31/cit31 publication-title: Sens. Actuators, B doi: 10.1016/j.snb.2006.05.017 – volume: 66 start-page: 1552 year: 1994 ident: ref11/cit11 publication-title: Anal. Chem. doi: 10.1021/ac00081a031 – volume: 23 start-page: 3333 year: 2007 ident: ref30/cit30 publication-title: Langmuir doi: 10.1021/la062901c – volume: 22 start-page: 2898 year: 2007 ident: ref20/cit20 publication-title: Biosens. Bioelectron. doi: 10.1016/j.bios.2006.12.004 – volume: 51 start-page: 5478 year: 2006 ident: ref23/cit23 publication-title: Electrochim. Acta doi: 10.1016/j.electacta.2006.02.023 – volume: 1 start-page: 537 year: 1990 ident: ref6/cit6 publication-title: Sens. Actuators, B doi: 10.1016/0925-4005(90)80268-5 – volume: 129 start-page: 7006 year: 2007 ident: ref10/cit10 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja071946c – volume: 18 start-page: 1408 year: 2006 ident: ref14/cit14 publication-title: Electroanalysis doi: 10.1002/elan.200603552 – volume: 92 start-page: 1355 year: 1992 ident: ref33/cit33 publication-title: Chem. Rev. doi: 10.1021/cr00014a006 |
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Snippet | A protocol of one-pot chemical preoxidation and electropolymerization of monomers (CPEM) in enzyme-containing aqueous suspensions (or solutions) was proposed... |
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SubjectTerms | Alkaline Phosphatase Analytical chemistry Aqueous solutions Biofuels Biological and medical sciences Biomaterials Biosensing Techniques - methods Biosensors Biotechnology Chemistry Electrochemical methods Electrochemistry Electrochemistry - methods Electrodes Enzymes Enzymes, Immobilized - chemical synthesis Enzymes, Immobilized - chemistry Exact sciences and technology Fundamental and applied biological sciences. Psychology Glucose Glucose - analysis Glucose Oxidase Methods. Procedures. Technologies Organophosphates - analysis Oxidation Polymers - chemical synthesis Spectrometric and optical methods Suspensions Toluene - analogs & derivatives Toluene - chemistry Various methods and equipments |
Title | Immobilization of Enzymes through One-Pot Chemical Preoxidation and Electropolymerization of Dithiols in Enzyme-Containing Aqueous Suspensions To Develop Biosensors with Improved Performance |
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