Hartman interferometer: versatile integrated optic sensor for label-free, real-time quantification of nucleic acids, proteins, and pathogens
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TL;DR: The Hartman interferometer addresses the challenge of creating a simple, low-cost configuration for multianalyte testing by relying on linearly polarized light and a planar waveguide format, thereby avoiding the problems associated with circular polarization and channel waveguides.
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Abstract: The Hartman interferometer, a proprietary integrated optic sensor, provides a basis for a broad range of biomedical diagnostics, including antibody-based and gene probe-based assays. As with other evanescent-wave optical sensors, the interferometer measures the refractive index change resulting from biomolecular binding on a waveguide surface. The exciting promise of evanescent-wave sensors lies, in general, in their potential to be used as label-free, real-time transducers that can operate in a true mix-and-read fashion and provide fast, quantitative results. One of the major issues facing their development, however, is creating a simple, low-cost configuration for multianalyte testing. The Hartman interferometer addresses this challenge by relying on linearly polarized light and a planar waveguide format, thereby avoiding the problems associated with circular polarization and channel waveguides. We report preliminary experiments that demonstrate the applicability of this sensor configuration to detection of a wide range of protein, nucleic acid, and pathogen analytes.
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Citations
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Optical biosensors: an exhaustive and comprehensive review.
Chen Chen,Junsheng Wang +1 more
TL;DR: The state of the art optical biosensor technologies, including those based on surface plasmon resonance (SPR), optical waveguides, optical resonators, photonic crystals, and optical fibers, are presented.
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Quantitative and simultaneous detection of four foodborne bacterial pathogens with a multi-channel SPR sensor.
TL;DR: The quantitative and simultaneous detection of four species of bacteria, Escherichia coli O157:H7, Salmonella choleraesuis serotype typhimurium, Listeria monocytogenes, and Campylobacter jejuni, using an eight-channel surface plasmon resonance (SPR) sensor based on wavelength division multiplexing is reported.
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TL;DR: In this paper, a theory of the sensor sensitivities is developed; conditions for the waveguide parameters in order to obtain high sensitivities are derived; and it is shown that effects (1) and (2) can be distinguished by measurements of the effective index changes of both the TE0 and the TM0 modes.
664
The resonant mirror: a novel optical biosensor for direct sensing of biomolecular interactions Part I: Principle of operation and associated instrumentation
TL;DR: The Resonant Mirror biosensor as discussed by the authors is a new design of optical sensor, aimed at combining the improved sensitivity of waveguide sensors with the simplicity of fabrication and ease of use associated with surface plasmon sensors.
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The Resonant Mirror: a novel optical biosensor for direct sensing of biomolecular interactions
P.E. Buckle,R.J. Davies,C.H. Maule,J O Molloy,D Pollard-Knight,J.M. Cronin,R. Cush,W.J. Stewart,Nicholas J. Goddard,Christopher R. Lowe +9 more
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TL;DR: The Resonant Mirror biosensor as mentioned in this paper uses the evanescent wave associated with a dielectric resonant structure to probe reactions occurring in a sensing layer, deposited within a few hundred nanometers of the device surface.
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The resonant mirror: a novel optical sensor for direct sensing of biomolecular interactions part II: applications
P.E. Buckle,R.J. Davies,T. Kinning,D. Yeung,Paul R. Edwards,D Pollard-Knight,Christopher R. Lowe +6 more
TL;DR: The broader applicability of the RM to studies on molecular interaction studies was demonstrated in an assay for the proteolytic enzyme trypsin and the specific inhibition of enzyme activity by α1-anti-trypsin.
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Optical Biosensor for Monitoring Microbial Cells
TL;DR: The potential of a new optical biosensor, the resonant mirror, for detecting whole cells is demonstrated and the sensitivity of the technique was increased a 1000-fold by using a human IgG-colloidal gold conjugate in a sandwich assay format.
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