Nanoplasmonic platform for multiparametric and highthroughput biosensing
The advances in proteomics and genomics have led to discover a lot of biomarkers that can potentially be used as diagnostic and prognostic indicators of diseases. Simultaneously, a huge research effort has been invested in developing biosensors that could monitor the interaction of biological materi...
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Published in: | 18th Italian National Conference on Photonic Technologies (Fotonica 2016) |
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Main Authors: | , , , , , , , , |
Format: | Conference Proceeding |
Language: | English |
Published: |
Stevenage
The Institution of Engineering & Technology
06-06-2016
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Subjects: | |
Online Access: | Get full text |
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Summary: | The advances in proteomics and genomics have led to discover a lot of biomarkers that can potentially be used as diagnostic and prognostic indicators of diseases. Simultaneously, a huge research effort has been invested in developing biosensors that could monitor the interaction of biological materials. Such sensors are required to be fast, real time, label free and highly sensitive to the appropriate biomarker. One of the possible solutions is surface plasmon resonance imaging (iSPR) biosensor. Nevertheless, some important milestones still need to be reached for a successful application. Indeed, iSPR instruments commercially available have a poor sensitivity to low biomarker concentration and they are quite expensive. In this paper, we show a compact instrument, called Imaging NanoplasmonicsTM (iNPx), designed to overcome these limits. A nanostructured interface is introduced to increase the sensitivity of different immunoassay reactions and with the use of a very low volume of material. Then, as a proof of principle, we report an example of specific application for the monitoring of the interaction between some variants of FLAG peptides with the monoclonal antibody Anti-FLAG. The proposed platform allows extreme versatility for multiplexed diagnostic and/or food quality applications. |
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ISBN: | 9781785612688 1785612689 |
DOI: | 10.1049/cp.2016.0904 |