Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
We propose a concept for enhancing the fluorescent detection signal of on-chip immunoassays by using three-dimensional 3 and 8 mu m size microtextured structures as substrates for the assay, which allows exploitation of a large number of fluorophores within the focal plane of an optical microscope for detection. Additionally, we demonstrate the use of 3 and 9.75 mu m dielectric microparticles, respectively, as in situ lenses on the 3 and 8 mu m microstructures, respectively, for further enhancement of the optical signal. In our model system, the fluorescent complex is formed on (3-aminopropyl)triethoxysilane microstructures and we use carboxyl-functionalized melamine microparticles as the in situ lenses. Mouse IgG diluted in phosphate-buffered saline is used as model target antigen and can be easily detected down to a concentration of 2 ng/mL thanks to these approaches. Also, we present a detailed two-dimensional numerical study of the light propagation through a dielectric microparticle using the finite element method, providing key insight into the signal amplification mechanism of a microlens, and point out its advantageous use in microfluidic assays.
Edoardo Charbon, Claudio Bruschini