Polymer capable of specific binding to Cu2+-2,2'-dipyridyl complex was prepared by molecular imprinting technology. The binding specificity of the polymer to the template (Cu2+-2, 2'-dipyridyl complex) was investigated by cyclic voltammetric scanning using the carbon paste electrode modified by polymer particles in phosphate buffer solution. Factors that influence rebinding of the imprinted polymer were explored. The results demonstrated that cyclic voltammetry was an efficient approach to explore interactions between template and imprinted polymers. Copyright (C) 2002 John Wiley Sons, Ltd.Biochemistry & Molecular BiologyBiophysicsSCI(E)PubMed5ARTICLE4204-2081
Looking at the literature focused on molecularly imprinted polymers (MIPs) for protein, it soon beco...
This work demonstrated the possibility to integrate electrochemical molecularly imprinted polymers (...
Molecular imprinting is an attractive approach for designing selective materials because it allows t...
Polymer capable of specific binding to Cu-dipyridyl complex was prepared by molecular imprinting tec...
<p>Novel molecularly imprinted polymers (MIPs) were synthesized by the electrochemical polymerizatio...
A novel imprinting scheme, combining for the first time electropolymerization with metal-ion coordin...
WOS: 000318798000011In this study graphite electrodes modified by a thin DNA-imprinted polypyrrole l...
In this review, the applications of molecularly imprinted polymer (MIP) materials in the area of ele...
This critical review describes a class of polymers prepared by electrochemical polymerization that e...
Molecularly imprinted polymers (MIP's) have been applied in several areas of analytical chemistry, i...
Molecularly imprinted polymer (MIP) was synthesized by using the complex of o-phthalic acid-Cu(Ac)2 ...
The development of an electrosynthesized molecularly imprinted polymer (MIP) based on a metal comple...
Functional polymers that selectively recognize target compounds are developed by imprinting polymeri...
Molecular Imprinted Polymers (MIP) are synthetic polymers containing sites able to selectively recom...
The electrochemical synthesis of a metal complex based molecularly imprinted polymer (MIP) has been ...
Looking at the literature focused on molecularly imprinted polymers (MIPs) for protein, it soon beco...
This work demonstrated the possibility to integrate electrochemical molecularly imprinted polymers (...
Molecular imprinting is an attractive approach for designing selective materials because it allows t...
Polymer capable of specific binding to Cu-dipyridyl complex was prepared by molecular imprinting tec...
<p>Novel molecularly imprinted polymers (MIPs) were synthesized by the electrochemical polymerizatio...
A novel imprinting scheme, combining for the first time electropolymerization with metal-ion coordin...
WOS: 000318798000011In this study graphite electrodes modified by a thin DNA-imprinted polypyrrole l...
In this review, the applications of molecularly imprinted polymer (MIP) materials in the area of ele...
This critical review describes a class of polymers prepared by electrochemical polymerization that e...
Molecularly imprinted polymers (MIP's) have been applied in several areas of analytical chemistry, i...
Molecularly imprinted polymer (MIP) was synthesized by using the complex of o-phthalic acid-Cu(Ac)2 ...
The development of an electrosynthesized molecularly imprinted polymer (MIP) based on a metal comple...
Functional polymers that selectively recognize target compounds are developed by imprinting polymeri...
Molecular Imprinted Polymers (MIP) are synthetic polymers containing sites able to selectively recom...
The electrochemical synthesis of a metal complex based molecularly imprinted polymer (MIP) has been ...
Looking at the literature focused on molecularly imprinted polymers (MIPs) for protein, it soon beco...
This work demonstrated the possibility to integrate electrochemical molecularly imprinted polymers (...
Molecular imprinting is an attractive approach for designing selective materials because it allows t...