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Published on: February 16, 2018
Molecularly imprinted polymers for histamine recognition in aqueous environment
Foteini A Trikka1, Keiichi Yoshimatsu, Lei Ye
1Laboratory of Biochemistry, Department of Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Amino Acids
|April 25, 2012
Summary
This study developed molecularly imprinted polymers (MIPs) for histamine detection. These novel MIPs demonstrate specific binding capabilities for histamine, offering potential for future analytical applications.
Area of Science:
- Polymer Science
- Analytical Chemistry
- Biochemistry
Background:
- Histamine is a crucial biogenic amine with significant roles in physiological and pathological processes.
- Developing selective recognition materials for histamine is essential for diagnostics and monitoring.
- Molecularly imprinted polymers (MIPs) offer a promising platform for creating tailored recognition sites.
Purpose of the Study:
- To develop and characterize molecularly imprinted polymers (MIPs) for selective histamine recognition.
- To investigate the binding affinity and selectivity of histamine MIPs in various media and conditions.
- To elucidate the imprinting and recognition mechanisms underlying histamine binding to MIPs.
Main Methods:
- Synthesis of molecularly imprinted polymers (MIPs) using methacrylic acid as the functional monomer.
- Evaluation of binding affinity and selectivity against histamine and structurally related compounds in organic and aqueous media.
- Utilisation of Nuclear Magnetic Resonance (NMR) and UV spectroscopy to investigate imprinting and recognition properties.
Main Results:
- Histamine MIPs exhibited significantly higher binding affinity for histamine compared to ranitidine and fluoxetine in organic media.
- In aqueous media, MIPs demonstrated specific recognition of histamine over L-histidine and higher affinity for histamine compared to other analogues.
- Spectroscopic analyses indicated strong specific interactions between the functional monomer and histamine, driving the recognition mechanism.
Conclusions:
- The developed histamine MIPs show excellent selectivity and affinity for histamine.
- The study elucidates the imprinting and recognition mechanisms, highlighting the role of specific monomer-analyte interactions.
- These histamine MIPs hold potential for future applications in histamine detection and analysis.

