Apparatus for sensitive fluorescence optical measurement of biological parameters in freely behaving animals
US-2024426754-A1 · Dec 26, 2024 · US
US9134235B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9134235-B2 |
| Application number | US-201113817356-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 27, 2011 |
| Priority date | Aug 17, 2010 |
| Publication date | Sep 15, 2015 |
| Grant date | Sep 15, 2015 |
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[Object] It is an object of the invention to provide a sensor area which can suppress a decrease in assay signal and an increase in assay blank in an SPFS measurement. [Solution] An SPFS sensor chip of the invention includes a purification area and a sensor area arranged upstream and downstream, respectively, relative to each other along a flow direction in a channel for surface plasmon-field enhanced fluorescence spectroscopy [SPFS].
Opening claim text (preview).
The invention claimed is: 1. An SPFS sensor chip, comprising a purification area and a sensor area arranged upstream and downstream, respectively, relative to each other along a flow direction in a channel for surface plasmon-field enhanced fluorescence spectroscopy [SPFS], wherein the purification area includes a sample purification area and a labeled antibody purification area, wherein the channel is in such a form that the sample purification area and the labeled antibody purification area define respective branches and merge with each other to lead to the sensor area, and wherein the labeled antibody purification area comprises: a transparent support; a metal membrane formed on one surface of the transparent support; a self-assembled monolayer [SAM] formed on the surface of the metal membrane opposite to the transparent support; a hydrophilic polymer layer formed on the surface of the SAM opposite to the metal membrane; and a bioactive substance immobilized on the surface of the hydrophilic polymer layer opposite to the SAM. 2. The SPFS sensor chip according to claim 1 , wherein the sensor area comprises: a transparent support; a metal membrane formed on one surface of the transparent support; a self-assembled monolayer [SAM] formed on the surface of the metal membrane opposite to the transparent support; a hydrophilic polymer layer formed on the surface of the SAM opposite to the metal membrane; and a bioactive substance immobilized on the surface of the hydrophilic polymer layer opposite to the SAM. 3. The SPFS sensor chip according to claim 1 , wherein the purification area comprises: a transparent support; a metal membrane formed on one surface of the transparent support; a self-assembled monolayer [SAM] formed on the surface of the metal membrane opposite to the transparent support; and a hydrophilic polymer layer formed on the surface of the SAM opposite to the metal membrane; and the sensor area comprises: a transparent support; a metal membrane formed on one surface of the transparent support; a SAM formed on the surface of the metal membrane opposite to the transparent support; a hydrophilic polymer layer formed on the surface of the SAM opposite to the metal membrane; and a bioactive substance immobilized on the surface of the hydrophilic polymer layer opposite to the SAM; and further wherein a hydrophilic polymer forming the purification area layer in the sensor substrate, and a hydrophilic polymer forming the sensor area in the plasmon excitation sensor are different from each other. 4. The SPFS sensor chip according to claim 1 , wherein the purification area is arranged in the entirety of a channel portion upstream from the sensor area. 5. An SPFS sensor chip, comprising a purification area and a sensor area arranged upstream and downstream, respectively, relative to each other along a flow direction in a channel for surface plasmon-field enhanced fluorescence spectroscopy [SPFS], wherein the purification area comprises a sample purification area and a labeled antibody purification area, wherein the channel is in such a form that the sample purification area and the labeled antibody purification area define respective branches and merge with each other to lead to the sensor area, and wherein the sample purification area comprises a transparent support; a metal membrane formed on one surface of the transparent support; a self-assembled monolayer [SAM] formed on the surface of the metal membrane opposite to the transparent support; and a hydrophilic polymer layer formed on the surface of the SAM opposite to the metal membrane. 6. The SPFS sensor chip according to claim 2 , wherein the bioactive substance in the labeled antibody purification area is the same as the bioactive substance in the sensor area.
Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding · CPC title
using evanescent coupling or surface plasmon coupling for the excitation of fluorescence · CPC title
Atomic fluorescence; Laser induced fluorescence · CPC title
involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings · CPC title
Flow-through cuvettes (G01N21/09 takes precedence; handling fluid samples G01N1/10) · CPC title
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