SERS, fluorescence, absorption, and luminescence detection with flow-through multi-hole capillaries
View Patent ↗3-dimensional surface-enhanced Raman scattering (SERS), as well as absorption/fluorescence/luminescence detection is carried out using a platform based on nanoparticle-functionalized flow-through multi-hole capillaries for rapid analyte detection. The configuration provides an increased active area and fluidic channels for efficient sample delivery, and also confines and transmits light for a large signal accumulation. Using a capillary consisting of thousands of micron-sized holes adsorbed with gold nanoparticles, a detection limit better than 100 fM is achieved.
1. A method of detecting an analyte bound to a surface by use of absorption, luminescence, or fluorescence spectroscopy comprising exciting the analyte with electromagnetic radiation and detecting the absorption, luminescence, or fluorescence, wherein the surface onto which the analyte is bound is the interior surface of a micro-/nanofluidic channel in a multi-hole capillary, wherein the multi-hole capillary provides a plurality of micro-/nanofluidic channels for flow-through analyte delivery, wherein the micro-/nanofluidic channels are characterized by a dimension of 100 nm-200 microns, and wherein the multi-hole capillary does not have a photonic crystal structure.
2. The method of claim 1 , wherein the multi-hole capillary is made of fused silica glass or borosilicate glass.
3. The method of claim 1 , comprising exciting in the transverse configuration and detecting in the transverse configuration.
4. The method of claim 1 , comprising exciting in the transverse configuration and detecting in the longitudinal configuration.
5. The method of claim 1 , comprising exciting in the longitudinal configuration and detecting in the transverse configuration.
6. The method of claim 1 , comprising exciting in the longitudinal configuration and detecting in the longitudinal configuration.
7. The method of claim 1 , wherein the dimension is 1-5 microns.
8. The method of claim 1 , wherein the analyte is bound to the surface as part of an antibody complex.
9. A method of detecting an analyte by use of absorption, luminescence, or fluorescence spectroscopy comprising exciting the analyte with electromagnetic radiation or causing the analyte to luminescence, and detecting the luminescence, absorption, or fluorescence, wherein the analyte is a substrate of an enzyme attached to an antibody attached to the interior surface of a micro-/nanofluidic channel in a multi-hole capillary, wherein the multi-hole capillary provides a plurality of micro-/nanofluidic channels for flow-through analyte delivery, wherein the micro-/nanofluidic channels are characterized by a dimension of 10 nm-200 microns, and wherein the multi-hole capillary does not have a photonic crystal structure.
10. The method of claim 1 , wherein the multi-hole capillary is made of glass and contains 10-300,000 micro-/nanofluidic channels.
11. The method of claim 1 , wherein the multi-hole capillary is made of glass and contains 200-300,000 micro-/nanofluidic channels.
12. The method of claim 1 , wherein the multi-hole capillary is made of glass and contains 1000-300,000 micro-/nanofluidic channels.
13. The method of claim 1 , wherein the multi-hole capillary is made of glass and contains 1000-20,000 micro-/nanofluidic channels.
14. The method of claim 1 , wherein the multi-hole capillary is made of glass and contains 1000-10,000 micro-/nanofluidic channels.
15. The method of claim 1 , wherein the dimension of the channels is 100 nm-20 microns.