Recent Advances in Molecularly Imprinted-Polymer-Based Biosensors

A special issue of Biosensors (ISSN 2079-6374). This special issue belongs to the section "Biosensors and Healthcare".

Deadline for manuscript submissions: 31 May 2026 | Viewed by 1887

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CIQUP/IMS, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Rua do Campo Alegre, S/N, 4169-007 Porto, Portugal
Interests: electrochemistry; analytical chemistry; screen-printed electrodes (SPEs); electrochemical biosensors; amperometric; proteins
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CIQUP/IMS - Chemistry Research Center, Faculty of Sciences, University of Porto, Rua do Campo Alegre 1021, 4169-007 Porto, Portugal
Interests: supercapacitors; carbon nanomaterials; ionic liquids; energy storage; nanopesticides; environmental safety; cytotoxicity; ecotoxicity; food allergens
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Institute of Molecular Sciences, Departamento de Química e Bioquímica, Universidade do Porto, Porto, Portugal
Interests: sol-gel; molecular imprinting; selective photocatalys; artificial receptors; molecular recognition

Special Issue Information

Dear Colleagues,

Molecularly imprinted polymers (MIPs) have attracted significant attention for sensing applications due to their distinct advantages, including simplicity, cost-effectiveness, ease of preparation, long-term stability, and remarkable selectivity and sensitivity. Over the past decade, molecular imprinting (MI) technology has experienced substantial advancements, largely driven by breakthroughs in nanotechnology. These advancements have enabled the production of nanosized MIP materials, such as MIP nanoparticles and thin films, with enhanced target affinity and faster binding kinetics.

These biomimetic materials are typically obtained in high yields through established techniques, including radical polymerization, sol–gel synthesis, the surface imprinting of core–shell and metal nanoparticles, and greener approaches like electrochemical polymerization.

The synergistic integration of MI technology with sensor development is well established, particularly in electrochemical and optical sensing platforms. MIPs serving as synthetic receptors have been widely employed for detecting a broad spectrum of analytes, ranging from small molecules (e.g., drugs, pesticides, hormones) and peptides to large biomolecules like proteins, pathogens, and even whole cells.

The practical applications of MIP-based high-performance electrochemical (bio)sensors span diverse fields, including environmental monitoring, food quality and safety control, drug analysis, precision agriculture, biomedical applications, and advanced healthcare, using wearable, portable, or implantable systems.

Despite these achievements, several challenges remain unresolved. Notably, there is a need to improve the performance of MIP-based sensors in complex biological or environmental matrices and to develop robust systems capable of multi-analyte detection within a single sample. Addressing these issues will further expand the potential of MIP-based sensors in real-world applications.

Dr. José Ribeiro
Dr. Carlos Pereira
Dr. Manuel A. Azenha
Guest Editors

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Keywords

  • molecularly imprinted polymers (MIPs)
  • imprinted materials
  • molecular recognition
  • biomimetic devices
  • electrochemical sensing
  • optical sensing
  • food quality and safety
  • environmental monitoring
  • disease biomarkers
  • biomedical applications
  • health monitoring

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Published Papers (2 papers)

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Research

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13 pages, 1667 KB  
Article
Development of an Electrochemical Sensor Based on Molecularly Imprinted Polymer Using Functionalized Gold Nanoparticles for Caffeine Quantification
by Sergio Espinoza-Torres, Astrid Choquehuanca-Azaña, Marcos Rufino, Eleilton da Silva and Lucio Angnes
Biosensors 2025, 15(10), 704; https://doi.org/10.3390/bios15100704 (registering DOI) - 18 Oct 2025
Abstract
Caffeine is a natural alkaloid consumed primarily for its stimulant and metabolic effects. Some everyday products, such as coffee, tea, soft drinks, sports supplements, and even pain relievers, contain caffeine. However, excessive caffeine consumption, greater than 400 mg per day, can cause adverse [...] Read more.
Caffeine is a natural alkaloid consumed primarily for its stimulant and metabolic effects. Some everyday products, such as coffee, tea, soft drinks, sports supplements, and even pain relievers, contain caffeine. However, excessive caffeine consumption, greater than 400 mg per day, can cause adverse effects. Therefore, this work presents an electrochemical sensor based on a molecularly imprinted polymer (MIP) electropolymerized on gold nanoparticles functionalized with p-aminothiophenol (AuNPs-pATP) for caffeine quantification. AuNPs-pATP synthesized show a spherical morphology with an average diameter of 2.54 nm. Stages of MIP formation were monitored by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) using a potassium ferrocyanide redox probe, where the following were observed: (i) an increase in conductivity upon modification of the GCE with AuNPs-pATP, (ii) the blocking of active sites during the electropolymerization step, and (iii) the release of specific cavities upon template removal, revealing consistent differences between the MIP and the control polymer (NIP). SEM images revealed three-dimensional spherical cavities on MIP surface, while the NIP showed a more compact rough surface. Caffeine quantification was performed using square wave voltammetry (SWV) with LOD of 0.195 µmol L−1 and LOQ of 0.592 µmol L−1. Interference studies indicated high selectivity and a high density of caffeine-specific binding sites in the MIP. Additionally, MIP sensor demonstrated reusability, good reproducibility, and stability, as well as promising results for analysis in soft drink and sports supplement samples. Full article
(This article belongs to the Special Issue Recent Advances in Molecularly Imprinted-Polymer-Based Biosensors)

Review

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40 pages, 8156 KB  
Review
Advances in the Direct Nanoscale Integration of Molecularly Imprinted Polymers (MIPs) with Transducers for the Development of High-Performance Nanosensors
by Ibrar Muhammad Asif, Tiziano Di Giulio, Francesco Gagliani, Cosimino Malitesta and Elisabetta Mazzotta
Biosensors 2025, 15(8), 509; https://doi.org/10.3390/bios15080509 - 6 Aug 2025
Cited by 1 | Viewed by 1511
Abstract
Molecularly imprinted polymers (MIPs) have emerged as robust, cost-effective analogues of bioreceptors, offering high selectivity and stability. When applied in sensors, one key step is the integration of MIPs with the transducer, which critically affects sensor performance. Demanding challenges come when such integration [...] Read more.
Molecularly imprinted polymers (MIPs) have emerged as robust, cost-effective analogues of bioreceptors, offering high selectivity and stability. When applied in sensors, one key step is the integration of MIPs with the transducer, which critically affects sensor performance. Demanding challenges come when such integration involves nanoscaling processes, meaning that the transducer is nanostructured or the MIP itself is nanosized on a bulk transducer. In both cases, the integration results in the development of nanosensors, with advantages arising from the nanoscale, such as a high MIP surface-to-volume ratio, with surface-located, easily accessible binding sites, fast binding kinetics, and, thus, a rapid sensor response. Major advantages come also from nanostructured transducers, with nanoscale geometry enabling highly sensitive signal generation processes, not allowed on their bulk counterparts. In this review, we discuss advances in imprinting technologies, focusing on techniques that, enabling the nanoscale control of MIP synthesis, are conveniently applied to directly integrate MIPs with nanosensors in a one-step process. Two main approaches are reviewed, consisting in MIP nanostructuring on bulk transducers and in the direct growth of MIPs on nanotransducers, highlighting how different strategies achieve good conformity at the nanoscale and address spatial complexity to ensure stable and accurate signal acquisition. Finally, we consider future directions in MIP-based nanosensor development. Full article
(This article belongs to the Special Issue Recent Advances in Molecularly Imprinted-Polymer-Based Biosensors)
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