Abstract: Techniques for detecting a presence of an analyte and determining a concentration of analytes are provided. An analyte may be provided on an LSPR-active surface. The LSPR-active surface may comprise sensitivity enhancing labels. The analyte may induce a local change near the LSPR-active surface. The LSPR-active surface may be imaged with an imaging device for images before, during, or after a reaction takes place. Local regions of interest within the images may be analyzed to detect the local changes.

Abstract: Systems, methods, and devices related to detecting a presence of an analyte and/or determining a concentration of analytes are provided. An analyte may be provided on an LSPR-active surface. The LSPR-active surface may comprise sensitivity enhancing labels. The analyte may induce a local change near the LSPR-active surface. The LSPR-active surface may be imaged with an imaging device for images before, during, or after a reaction takes place. Local regions of interest within the images may be analyzed to detect the local changes.

Abstract: Systems, methods, and devices related to detecting a presence of an analyte and/or determining a concentration of analytes are provided. An analyte may be provided on an LSPR-active surface. The LSPR-active surface may comprise sensitivity enhancing labels. The analyte may induce a local change near the LSPR-active surface. The LSPR-active surface may be imaged with an imaging device for images before, during, or after a reaction takes place. Local regions of interest within the images may be analyzed to detect the local changes.

Abstract: Compositions, methods, devices, and systems are described for performing single-step, homogenous, localized surface plasmon resonance (LSPR)-based plasmonic assays having exceptional assay sensitivity and extremely low limits of detection (LODs). Ag/Au core/shell nanoparticles are described, which may be used with LSPR sensors to develop single-step, homogeneous, LSPR-based assays.

Abstract: Sensor chips and devices that incorporate localized surface plasmon resonance (LSPR) sensors are described which are suitable for use in near-patient and point-of-care diagnostic testing. In some embodiments, LSPR sensors are integrated with microfabricated fluidics and other system components to create compact, portable bench-top or hand-held diagnostic testing systems. In some embodiments, all components are packaged in compact, portable wearable devices.

Abstract: Systems, methods, and devices related to detecting a presence of an analyte and/or determining a concentration of analytes are provided. An analyte may be provided on an LSPR-active surface. The LSPR-active surface may comprise sensitivity enhancing labels. The analyte may induce a local change near the LSPR-active surface. The LSPR-active surface may be imaged with an imaging device for images before, during, or after a reaction takes place. Local regions of interest within the images may be analyzed to detect the local changes.

Abstract: The present invention provides a method of detecting changes in the refractive index at the surface of a localized surface plasmon resonance (LSPR) detection system. The method includes generating an insoluble product from an enzymatic substrate using an immobilized enzyme, wherein the insoluble product accumulates at a LSPR supporting surface. The method also includes detecting changes in the reflected or transmitted light of the surface arising from the presence of the insoluble product using LSPR.

Abstract: The present invention provides a method of detecting changes in the refractive index at the surface of a localized surface plasmon resonance (LSPR) detection system. The method includes generating an insoluble product from an enzymatic substrate using an immobilized enzyme, wherein the insoluble product accumulates at a LSPR supporting surface. The method also includes detecting changes in the reflected or transmitted light of the surface arising from the presence of the insoluble product using LSPR.

Abstract: The present invention provides a method of preparing a silica layer on a surface, the method comprising contacting the surface with a first alkoxysilane and a first base, such that a first siloxane layer is formed on the surface; and contacting the first siloxane layer with a combination of a binding alkoxysilane, a growth limiting alkoxysilane and a second base, such that a second siloxane layer forms on top of the first siloxane layer, wherein the silica layer is prepared at a temperature of less than 100° C., and wherein the growth limiting alkoxysilane limits the thickness of the silica layer to less than 100 nm, thereby preparing the silica layer.

Abstract: The present invention provides signal peptide-semiconductor nanocrystal-peptide conjugates and methods for using the conjugates in methods for imaging live cells and subcellular trafficking processes.