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Journal Article

Plasmonic Nanomaterials for Colorimetric Biosensing: A Review.

MPS-Authors

Acunzo,  Adriano
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

Scardapane,  Emanuela
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

De Luca,  Maria
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

Marra,  Daniele
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

Velotta,  Raffaele
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Minopoli,  Antonio
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Acunzo, A., Scardapane, E., De Luca, M., Marra, D., Velotta, R., & Minopoli, A. (2022). Plasmonic Nanomaterials for Colorimetric Biosensing: A Review. Chemosensors, 10(4): 136. doi:10.3390/chemosensors10040136.


Cite as: https://hdl.handle.net/21.11116/0000-000B-0371-2
Abstract
In the last few decades, plasmonic colorimetric biosensors raised increasing interest in bioanalytics thanks to their cost-effectiveness, responsiveness, and simplicity as compared to conventional laboratory techniques. Potential high-throughput screening and easy-to-use assay procedures make them also suitable for realizing point of care devices. Nevertheless, several challenges such as fabrication complexity, laborious biofunctionalization, and poor sensitivity compromise their technological transfer from research laboratories to industry and, hence, still hamper their adoption on large-scale. However, newly-developing plasmonic colorimetric biosensors boast impressive sensing performance in terms of sensitivity, dynamic range, limit of detection, reliability, and specificity thereby continuously encouraging further researches. In this review, recently reported plasmonic colorimetric biosensors are discussed with a focus on the following categories: (i) on-platform-based (localized surface plasmon resonance, coupled plasmon resonance and surface lattice resonance); (ii) colloid aggregation-based (label-based and label free); (iii) colloid non-aggregation-based (nanozyme, etching-based and growth-based).