Ultrasensitive SERS flow detector
The invention provides an apparatus and methods for label-free, chemical specific detection in flow for high throughput characterization of analytes in applications such as flow injection analysis, electrophoresis, and chromatography. A surface-enhanced Raman scattering (SERS) flow detector capable of ultrasensitive optical detection on the millisecond time scale has been developed. The device employs hydrodynamic focusing to improve SERS detection in a flow channel where a sheath flow confines analyte molecules eluted from a capillary over a planar SERS-active substrate. Increased analyte interactions with the SERS substrate significantly improve detection sensitivity. Raman experiments at different sheath flow rates showed increased sensitivity compared with the modeling predictions, indicating increased adsorption. At low analyte concentrations, rapid analyte desorption is observed, enabling repeated and high-throughput SERS detection. The flow detector offers substantial advantages over conventional SERS-based assays such as minimal sample volumes and high detection efficiency.
1. An apparatus for performing surface-enhanced Raman scattering (SERS) comprising:
a Raman microscope,
a flow cell,
a first pumping apparatus configured for supplying a sheath fluid at flow rate (A) to the flow cell,
a second pumping apparatus to pump a sample fluid solution,
a narrow-bore capillary leading from the second pumping apparatus to the flow cell, and
a detector for detecting light scattered by an analyte dissolved in the sample fluid solution,
wherein the second pumping apparatus is configured to transport an analyte in solution through the capillary to the flow cell at flow rate (B) that is one-tenth or less than the volumetric velocity of (A), wherein the flow cell comprises:
an inlet port for the sheath fluid and an outlet port to drain fluids,
a planar noble metal SERS-active substrate,
the capillary that connects the second pumping apparatus to the SERS-active substrate of the flow cell, wherein the end of the capillary terminates at an analyte analysis zone accessible to a laser,
a flow channel extending from the end of the capillary and through the analyte analysis zone for analysis by a laser, and which concurrently defines a flow path between the inlet port and the outlet port, and
a flow cell cover through which a laser can be directed, which flow cell cover seals the flow cell to prevent fluid from escaping the flow cell except through the outlet port;
wherein the end of the capillary is directed toward the surface of the SERS-active substrate and the flow cell is configured to perform hydrodynamic focusing on an analyte dissolved in the sample fluid solution, wherein the volumetric velocities of (A) and (B) confine the width of the sample fluid solution exiting the capillary to a longitudinal stream, parallel to the plane of the SERS-active substrate surface at a width about or less than the thickness of the capillary's outer diameter, and confine the analytes in solution normal to the surface of the SERS-active substrate, thereby increasing adsorption of the analytes and providing a detection volume in close proximity to said surface.
2. The apparatus of claim 1 wherein the SERS-active substrate comprises a thin film of silver metal or gold metal.
3. The apparatus of claim 1 wherein the capillary leading to the flow cell is a fused silica capillary.
4. The apparatus of claim 1 wherein the capillary has an outer diameter of about 40 μm to about 300 μm.
5. The apparatus of claim 1 wherein the capillary has an outer diameter of about 50 μm to about 150 μm.
6. The apparatus of claim 1 wherein the capillary has an inner diameter of about 4 μm to about 100 μm.
7. The apparatus of claim 1 wherein the capillary has an inner diameter of about 10 μm to about 50 μm.
8. The apparatus of claim 1 wherein the Raman microscope includes a single longitudinal mode laser with a wavelength between about 632 nm and about 670 nm.
9. The apparatus of claim 1 wherein the sample capillary is connected to a direct output of a chemical separation for repeated analysis.
10. A method of detecting or characterizing an analyte in solution using the surface-enhanced Raman scattering (SERS) flow detector of claim 1 , the method comprising:
contacting an analyte solution and a SERS-active substrate using hydrodynamic focusing to co-locate the analyte on the SERS-active substrate;
wherein the hydrodynamic focusing comprises passing a sheath fluid over the analyte in solution, wherein the ratio of the sheath flow rate (A) to the capillary flow rate (B) is at least 10(A):1(B), thereby increasing the adsorption of analytes in the detection area of the SERS-active substrate;
conducting laser excitation of the analyte on the SERS-active substrate; and
detecting light scattered by the analyte in solution;
wherein the hydrodynamic focusing on the analyte solution confines the analyte at the SERS substrate, thereby increasing the frequency of interactions between the analyte and nanostructures of the SERS-active substrate, and improves the limit of detection for SERS detection.
11. The method of claim 10 wherein the ratio of the sheath flow rate (A) to the capillary flow rate (B) is about 10(A):1(B) to about 70(A):1(B).
12. The method of claim 10 wherein the ratio of the sheath flow rate (A) to the capillary flow rate (B) is about 12(A):1(B) to about 50(A):1(B).
13. The method of claim 10 wherein the ratio of the sheath flow rate (A) to the capillary flow rate (B) is about 25(A):1(B) to about 45(A):1(B).
14. The method of claim 10 wherein the sheath flow rate is about 50 μL/min to about 360 μL/min.
15. The method of claim 10 wherein the sheath flow rate is about 150 μL/min to about 200 μL/min.
16. The method of claim 10 wherein the range of particle size detection of the flow detector is about 3000 nm to about 50 nm.
17. The method of claim 10 wherein the lower detection limit of the flow detector for solutions is about 100 picomolar.
18. The method of claim 10 wherein the signal of the Raman spectra collected is enhanced by about 10 6 to about 10 8 compared to a corresponding spontaneous Raman analysis that does not employ hydrodynamic focusing and SERS.
19. The method of claim 10 wherein the signal of the Raman spectra collected is enhanced by about 10 3 to 10 4 compared to a corresponding SERS analysis that does not employ hydrodynamic focusing.
20. The method of claim 10 wherein the SERS-active substrate comprises a thin film of silver metal and the surface of the substrate resists fouling and lacks a memory effect of the analyte.