You have requested a machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Neither SPIE nor the owners and publishers of the content make, and they explicitly disclaim, any express or implied representations or warranties of any kind, including, without limitation, representations and warranties as to the functionality of the translation feature or the accuracy or completeness of the translations.
Translations are not retained in our system. Your use of this feature and the translations is subject to all use restrictions contained in the Terms and Conditions of Use of the SPIE website.
8 September 2004Development of a highly sensitive interferometric biosensor
For the measurement of biomolecular interactions such as immunoreactions it is often necessary to prepare reporter molecules to detect small biomolecules. In many cases fluorescence markers are used to detect the binding between molecules. These markers, however, can influence the examined reaction. A label-free optical detection method based on the principle of a Young interferometer offers an alternative solution. This technology allows real-time, kinetic analysis of antigene-antibody reactions or the detection of a specific analyte without elaborate sample preparation. Especially reactions where it is inconvenient or impossible to use markers can be detected with this method. In this paper, an interferometric device based on a planar waveguide as sensing element is presented. The system yields a high resolution with respect to surface mass coverage and a low sensitivity towards undesired external influences. Interferometric sensors theoretically have the highest detection limits among label-free bionsensors.
The alert did not successfully save. Please try again later.
Katrin Schmitt, Bernd Schirmer, Albrecht Brandenburg, "Development of a highly sensitive interferometric biosensor," Proc. SPIE 5461, Biophotonics New Frontier: From Genome to Proteome, (8 September 2004); https://doi.org/10.1117/12.554231