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MIP-esterase/Tyrosinase Combinations for Paracetamol and Phenacetin

  • A new electrochemical MIP sensor for the most frequently used drug paracetamol (PAR) was prepared by electropolymerization of mixtures containing the template molecule and the functional monomers ophenylenediamine, resorcinol and aniline. The imprinting factor of 12 reflects the effective target binding to the MIP as compared with the non-imprinted electropolymer. Combination of the MIP with a nonspecific esterase allows the measurement of phenacetin - another analgesic drug. In the second approach the PAR containing sample solution was pretreated with tyrosinase in order to prevent electrochemical interferences by ascorbic acid and uric acid. Interference-free indication at a very low electrode potential without fouling of the electrode surface was achieved with the o-phenylenediamine: resorcinol-based MIP.

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Metadaten
Author details:Aysu YarmanORCiDGND, Frieder W. SchellerORCiDGND
DOI:https://doi.org/10.1002/elan.201600042
ISSN:1040-0397
ISSN:1521-4109
Title of parent work (English):Electroanalysis : an international journal devoted to fundamental and practical aspects of electroanalysis
Publisher:Wiley-VCH
Place of publishing:Weinheim
Publication type:Article
Language:English
Year of first publication:2016
Publication year:2016
Release date:2020/03/22
Tag:Electropolymerization; Esterase; Molecularly imprinted polymers; Paracetamol; Phenacetin; Tyrosinase
Volume:28
Number of pages:6
First page:2222
Last Page:2227
Funding institution:Deutsche Forschungsgemeinschaft (DFG) within the framework of the German Excellence Initiative [EXC 314]; BMBF in TERA-Sens [93719903]
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
Peer review:Referiert
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