The increasing need for compact, selective, ultrasensitive, fast and affordable optical biosensors in the medical and environmental sectors gave rise to new technological solutions, especially regarding sensors based on optical microresonators. If their surfaces are functionalized, these biosensors can provide a selective detection of low concentrations of biomolecules. However, two common optical interrogation methods – spectral scanning and intensity variation – cannot provide the same sensitivity as the method using phase detection of the guided modes nor the opto-geometrical parameters (propagation loss, effective refractive index, coupling coefficient), needed for the modeling of the sensor response. To get this information, we proposed to use the Phase Sensitive-Optical Low Coherence Interferometer (PS-OLCI) as a new alternative technical solution for interrogation and characterization of microresonators. The first part of this thesis is dedicated to the conception and fabrication of single mode microresonators with a quality factor higher than 20 000 in water. This work was validated by the manufacture of polymer microresonators with a quality factor up to 38 200, using UV photolithography and Reactive Ion Etching (RIE) processes. The second part of this work covers the adaptation of PS-OLCI setup, initially developed at Laboratoire national de métrologie et d'essais (LNE), to interrogate optical telecommunication devices, for the characterization of optical microresonators. The results, obtained through the analysis of spatial and spectral performances of various microresonators, showed that the PS-OLCI setup is not only an interrogation and characterization tool but also a real support tool for designing optical microresonators. The performed modelling of the PS-OLCI and microresonator association response, validated by the fitting of the experimental data, demonstrated the relation between PS-OLCI measurements and Fresnel integrals. The last part of this work is dedicated to label free biosensing experiments using PS-OLCI setup associated to an optofluidic component, made of polymer optical microresonators and polymer microfluidic circuit, to detect biological species. The glucose molecule was chosen to demonstrate the homogeneous sensing experiments in aqueous solution. The obtained detection limits are around 50 µg/ml when we exploited intensity and around 2 µg/ml when we exploited the PS-OLCI measurements phase. These results demonstrate the high sensitivity of the proposed biosensor as well as the value of the optical phase measurement, hence the interest of PS-OLCI set up. To address the problem of sensor selectivity in homogeneous sensing method, surface sensing experiences were performed. The first step of this method was the functionalization of the sensor surface, by binding adequate recognition molecular sites to the sensor surface in order to immobilize target molecules. Proteins were then chosen to perform this very same type of experiences. The preliminary results in the 0.02 pg/mm2 range clearly show that our sensors is ten times more sensitive than Surface Plasmon Resonance, which is actually considered among the most successful label free sensing methods. These first results, which can be improved, demonstrate that the sensors based on optical microresonators are promising candidates for the detection of low concentrations of biomolecules for biochemical investigation.
