A one-dimensional photonic crystal (1DPC) based on a planar stack of dielectric layers is used as an optical transducer for biosensing, upon the coupling of TE-polarized Bloch Surface Waves (BSW). The structure is tailored with a polymeric layer providing a chemical functionality facilitating the covalent binding of orienting proteins needed for a subsequent grafting of antibodies in an immunoassay detection scheme. The polymeric layer is impregnated with Cy3 dye, in such a way that the photonic structure can exhibit an emissive behavior. The BSW-coupled fluorescence shift is used as a means for detecting refractive index variations occurring at the 1DPC surface, according to a label-free concept. The proposed working principle is successfully demonstrated in real-time tracking of protein G covalent binding on the 1DPC surface within a fluidic cell. © 2013 by the authors; licensee MDPI, Basel, Switzerland.
A fluorescent one-dimensional photonic crystal for label-free biosensing based on bloch surface waves / Francesca, F., Serena, R., Paola, R., Valeria, M., Fabrizio, G., Emiliano, D., Michelotti, F., Peter, M., Norbert, D., Lucia, N., Maria, A., Federico, B.. - In: SENSORS. - ISSN 1424-8220. - STAMPA. - 13:2(2013), pp. 2011-2022. [10.3390/s130202011]
A fluorescent one-dimensional photonic crystal for label-free biosensing based on bloch surface waves
MICHELOTTI, Francesco;
2013
Abstract
A one-dimensional photonic crystal (1DPC) based on a planar stack of dielectric layers is used as an optical transducer for biosensing, upon the coupling of TE-polarized Bloch Surface Waves (BSW). The structure is tailored with a polymeric layer providing a chemical functionality facilitating the covalent binding of orienting proteins needed for a subsequent grafting of antibodies in an immunoassay detection scheme. The polymeric layer is impregnated with Cy3 dye, in such a way that the photonic structure can exhibit an emissive behavior. The BSW-coupled fluorescence shift is used as a means for detecting refractive index variations occurring at the 1DPC surface, according to a label-free concept. The proposed working principle is successfully demonstrated in real-time tracking of protein G covalent binding on the 1DPC surface within a fluidic cell. © 2013 by the authors; licensee MDPI, Basel, Switzerland.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


