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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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 |
work_keys_str_mv |
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1725254353436016640 |