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Antonio Guerreiro

Researcher at University of Leicester

Publications -  89
Citations -  4027

Antonio Guerreiro is an academic researcher from University of Leicester. The author has contributed to research in topics: Molecularly imprinted polymer & Molecular imprinting. The author has an hindex of 32, co-authored 88 publications receiving 3337 citations. Previous affiliations of Antonio Guerreiro include University of Perpignan & Cranfield University.

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Solid-Phase Synthesis of Molecularly Imprinted Polymer Nanoparticles with a Reusable Template - "Plastic Antibodies".

TL;DR: This work reports a reusable solid-phase template approach (fully compatible with automation) for the synthesis of MIP nanoparticles and their precise manufacture using a prototype automated UV photochemical reactor and demonstrates the reliable re-use of molecular templates in the synthesisof MIPs for the first time.
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Solid-phase synthesis of molecularly imprinted nanoparticles

TL;DR: This work developed a method for the synthesis of MIP nanoparticles (nanoMIPs) using an innovative solid-phase approach, which relies on the covalent immobilization of the template molecules onto the surface of a solid support (glass beads).
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How to find effective functional monomers for effective molecularly imprinted polymers

TL;DR: This review covers work developed in understanding molecular imprinting mechanisms and presents different strategies utilised in optimising MIP design.
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Sensing and analysis of soluble phosphates in environmental samples: A review

TL;DR: Progress in the development of phosphate sensors, designed for use in a variety of disciplines, is highlighted and the need for long term stability, low maintenance, specificity and the capability of measuring total phosphorus concentrations down to at least 1 mg/l is considered, as required by legislation.
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Direct Replacement of Antibodies with Molecularly Imprinted Polymer Nanoparticles in ELISA—Development of a Novel Assay for Vancomycin

TL;DR: In these experiments, nanoMIPs have shown high affinity and minimal interference from blood plasma components and the lack of a requirement for cold chain logistics make them an attractive alternative to traditional antibodies used in ELISA.