Interferometric detection of mode splitting for whispering gallery mode
  biosensors

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Abstract

Sensors based on whispering gallery mode resonators can detect single nanoparticles and even single molecules. Particles attaching to the resonator induce a doublet in the transmission spectrum which provides a self-referenced detection signal. However, in practice this spectral feature is often obscured by the width of the resonance line which hides the doublet structure. This happens particularly in liquid environments that reduce the effective Q factor of the resonator. In this paper we demonstrate an interferometric set-up that allows the direct detection of the hidden doublet and thus provides a pathway for developing practical sensor applications.

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Whispering-gallery-mode biosensing: label-free detection down to single molecules.

Frank Vollmer, Stephen Arnold (2008)

Optical label-free detectors, such as the venerable surface plasmon resonance (SPR) sensor, are generally favored for their ability to obtain quantitative data on intermolecular binding. However, before the recent introduction of resonant microcavities that use whispering gallery mode (WGM) recirculation, sensitivity to single binding events had not materialized. Here we describe the enhancement mechanisms responsible for the extreme sensitivity of the WGM biosensor, review its current implementations and applications, and discuss its future possibilities.

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Label-free, single-molecule detection with optical microcavities.

Andrea M Armani, Rajan Kulkarni, Scott Fraser … (2007)

Current single-molecule detection techniques require labeling the target molecule. We report a highly specific and sensitive optical sensor based on an ultrahigh quality (Q) factor (Q > 10(8)) whispering-gallery microcavity. The silica surface is functionalized to bind the target molecule; binding is detected by a resonant wavelength shift. Single-molecule detection is confirmed by observation of single-molecule binding events that shift the resonant frequency, as well as by the statistics for these shifts over many binding events. These shifts result from a thermo-optic mechanism. Additionally, label-free, single-molecule detection of interleukin-2 was demonstrated in serum. These experiments demonstrate a dynamic range of 10(12) in concentration, establishing the microcavity as a sensitive and versatile detector.