Clusters of microresonators for cavity mode optical sensing
A method for sensing a target object using optical mode excitations in microresonators, comprises: preparing at least one cluster including at least two microresonators; obtaining some first spectra of the cluster; adsorbing the target object on a surface of the cluster; obtaining some second spectra of the cluster; and sensing the target object by comparing a lineshape of the first spectra with a lineshape of the second spectra.
1. A method for sensing a target object using optical mode excitations in microresonators, comprising:
preparing at least one cluster including at least two microresonators;
obtaining at least one first spectrum of the cluster;
adsorbing the target object on a surface of the cluster;
obtaining at least one second spectrum of the cluster; and
sensing the target object by comparing a lineshape of the at least one first spectrum with a lineshape of the at least one second spectrum, wherein
the at least one first spectrum is collectively obtained from the microresonators included in the cluster, and
the at least one second spectrum is collectively obtained from the microresonators included in the cluster.
2. The method according to claim 1 , wherein
the cluster is deposited on a substrate.
3. The method according to claim 1 , wherein
the cluster is floated in a fluidic cell.
4. The method according to claim 1 , wherein
the type of a part of the microresonators in the cluster is different from the type of the other part of the microresonators in that cluster.
5. The method according to claim 1 , wherein
the at least one first spectrum of the cluster is obtained after introduction of a probe molecule to adsorb the target object on the surface of the cluster and passivation of non-specific binding sites on the surface of the cluster.
6. The method according to claim 1 , wherein
the target object is adsorbed on the surface of the cluster by exposing the cluster to an analyte containing the target object.
7. The method according to claim 1 , wherein
the target object is detected by determining a magnitude of a wavelength shift between the lineshape of the at least one first spectrum and the lineshape of the at least one second spectrum in at least a part of the measured range.
8. The method according to claim 1 , wherein
the at least one second spectrum corresponding to the at least one first spectrum is identified and an average peak shift between the lineshape of the at least one first spectrum and the lineshape of the at least one second spectrum is obtained based on an autocorrelation between the lineshape of the at least one first spectrum and the lineshape of the at least one second spectrum.
9. The method according to claim 1 ,
preparing a plurality of clusters;
obtaining the at least one first spectrum of each of the clusters;
adsorbing the target object on the surface of at least a part of the clusters;
obtaining the at least one second spectrum of each of the clusters; and
sensing the target object by comparing the lineshape of the at least one first spectrum prior to the change with the lineshape of the at least one second spectrum after the change.
10. The method according to claim 9 , wherein
the shape of a part of the clusters is different from the shape of the other part of the clusters.
11. The method according to claim 9 , wherein
the type of a part of the microresonators in at least one of the clusters is different from the type of the other part of the microresonators in that cluster.
12. The method according to claim 9 , wherein
a part of the clusters is separated from the other clusters.
13. The method according to claim 9 , wherein
a part of the clusters is functionalized in a different way from the other part of the clusters.
14. The method according to claim 9 , wherein
the at least one first spectrum and the at least one second spectrum are obtained by recording an image scan of the surface of the clusters at once or in a sequence of measurements.
15. A biosensor chip for sensing a target object using optical mode excitations in microresonators, comprising:
a substrate having a surface; and
at least one cluster including at least two microresonators disposed on the surface of the substrate, wherein,
all microparticles within the cluster are operated collectively.
16. The biosensor chip according to claim 15 , wherein,
a plurality of the clusters are disposed on the surface of the substrate, whereby, if a cluster out of this plurality is operated, all microparticles within that cluster are operated collectively.
17. The biosensor chip according to claim 15 , wherein,
the shape of a part of the clusters is different from the shape of the other part of the clusters.
18. The biosensor chip according to claim 15 , wherein,
the type of a part of the microresonators in at least one of the clusters is different from the type of the other part of the microresonators in that cluster, whereby all microparticles within the cluster are operated simultaneously.
19. The biosensor chip according to claim 16 , wherein, a part of the clusters is separated from the other clusters.
20. The biosensor chip according to claim 16 , wherein, a part of the clusters is functionalized in a different way to the other part of the clusters.