Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers

Molecularly imprinted polymers (MIPs) have proven to be particularly effective chemical probes for the molecular recognition of proteins, DNA, and viruses. Here, we started from a filamentous bacteriophage to synthesize a multi-functionalized MIP for detecting the acidic pharmaceutic clofibric acid...

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Main Authors: In-Hyuk Baek, Hyung-Seop Han, Seungyun Baik, Volkhard Helms, Youngjun Kim
Format: Article
Language:English
Published: MDPI AG 2018-09-01
Series:Polymers
Subjects:
Online Access:http://www.mdpi.com/2073-4360/10/9/974
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spelling doaj-a01803175f3a4693aa6dba53319cadb72020-11-25T00:48:54ZengMDPI AGPolymers2073-43602018-09-0110997410.3390/polym10090974polym10090974Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted PolymersIn-Hyuk Baek0Hyung-Seop Han1Seungyun Baik2Volkhard Helms3Youngjun Kim4Environmental Safety Group, Korea Institute of Science & Technology Europe GmbH, 66123 Saarbrücken, GermanyNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, B4495 Oxford, UKEnvironmental Safety Group, Korea Institute of Science & Technology Europe GmbH, 66123 Saarbrücken, GermanyCenter for Bioinformatics, Saarland University, 66123 Saarbrücken, GermanyEnvironmental Safety Group, Korea Institute of Science & Technology Europe GmbH, 66123 Saarbrücken, GermanyMolecularly imprinted polymers (MIPs) have proven to be particularly effective chemical probes for the molecular recognition of proteins, DNA, and viruses. Here, we started from a filamentous bacteriophage to synthesize a multi-functionalized MIP for detecting the acidic pharmaceutic clofibric acid (CA) as a chemical pollutant. Adsorption and quartz crystal microbalance with dissipation monitoring experiments showed that the phage-functionalized MIP had a good binding affinity for CA, compared with the non-imprinted polymer and MIP. In addition, the reusability of the phage-functionalized MIP was demonstrated for at least five repeated cycles, without significant loss in the binding activity. The results indicate that the exposed amino acids of the phage, together with the polymer matrix, create functional binding cavities that provide higher affinity to acidic pharmaceutical compounds.http://www.mdpi.com/2073-4360/10/9/974molecularly imprinted polymerpolypyrrolefilamentous bacteriophageclofibric acidself-assemblyviruselectrochemical polymerizationmicrobalance sensor
collection DOAJ
language English
format Article
sources DOAJ
author In-Hyuk Baek
Hyung-Seop Han
Seungyun Baik
Volkhard Helms
Youngjun Kim
spellingShingle In-Hyuk Baek
Hyung-Seop Han
Seungyun Baik
Volkhard Helms
Youngjun Kim
Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
Polymers
molecularly imprinted polymer
polypyrrole
filamentous bacteriophage
clofibric acid
self-assembly
virus
electrochemical polymerization
microbalance sensor
author_facet In-Hyuk Baek
Hyung-Seop Han
Seungyun Baik
Volkhard Helms
Youngjun Kim
author_sort In-Hyuk Baek
title Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
title_short Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
title_full Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
title_fullStr Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
title_full_unstemmed Detection of Acidic Pharmaceutical Compounds Using Virus-Based Molecularly Imprinted Polymers
title_sort detection of acidic pharmaceutical compounds using virus-based molecularly imprinted polymers
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2018-09-01
description Molecularly imprinted polymers (MIPs) have proven to be particularly effective chemical probes for the molecular recognition of proteins, DNA, and viruses. Here, we started from a filamentous bacteriophage to synthesize a multi-functionalized MIP for detecting the acidic pharmaceutic clofibric acid (CA) as a chemical pollutant. Adsorption and quartz crystal microbalance with dissipation monitoring experiments showed that the phage-functionalized MIP had a good binding affinity for CA, compared with the non-imprinted polymer and MIP. In addition, the reusability of the phage-functionalized MIP was demonstrated for at least five repeated cycles, without significant loss in the binding activity. The results indicate that the exposed amino acids of the phage, together with the polymer matrix, create functional binding cavities that provide higher affinity to acidic pharmaceutical compounds.
topic molecularly imprinted polymer
polypyrrole
filamentous bacteriophage
clofibric acid
self-assembly
virus
electrochemical polymerization
microbalance sensor
url http://www.mdpi.com/2073-4360/10/9/974
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