Morpho Detection, Inc.

Ge Homeland Protection, Inc.

General Electric Company

Michael Craig Burrell

Frank John Mondello

Tracy Lynn Paxon

Christopher Montalbano

Gregory Anthony Montalbano

Aaron Klein

William Scott Sutherland

Yuan-Hsiang Lee

Matthew David Butts

Christopher Michael Byrne

Andrew David Pris

Steven James Stoessel

Kathryn Ann Shaffer

Patrick Ronald Engel

A method for increasing a spectroscopic signal in a biological assay is provided. The method includes forming a suspension of magnetically attractable particles. The method also includes introducing a first magnetic field at a first location to draw the magnetically attractable particles towards the first location and form a first agglomeration. The method also includes removing the first magnetic field. The method further includes introducing a second magnetic field at a second location to draw the first agglomeration towards the second location and form a second agglomeration. The method further includes focusing an excitation source on the second agglomeration formed at the second location.

System and method for increasing spectroscopic signal

A portable substance identification system and method are configured to identify at least one detection target faster and with greater accuracy than is possible using prior substance identification systems and/or prior substance identification techniques. An embodiment of the portable substance identification system includes a portable substance identification device containing a Raman spectrometer, and a collection stem that includes a dry collector. One or more reservoirs for a liquid medium and/or a reagent can be formed in a cartridge that is configured to couple with a portable substance identification device. The cartridge has a chamber in which the reagent, liquid medium, and a detection target picked up by the dry collector are mixed. A magnet, positioned at a slant angle, can be used to form at least one pellet of aggregated magnetic particles within a pellet forming area of the chamber. The pellet is formed to maximize its surface area.

System and method for improved biodetection

Portable substance identification system and method are configured to identify at least one detection target faster and with greater accuracy than is possible using prior substance identification systems and/or prior substance identification techniques. An embodiment of the portable substance identification system includes a portable substance identification device containing a Raman spectrometer, and a collection stem that includes a collector. One or more reservoirs for a liquid medium and/or at least one reagent can be formed in the collection stem. The cartridge can include a chamber in which the reagents, liquid medium, and at least one detection target picked up by the collector are mixed. A magnet, positioned at a slant angle, can be used to form at least one pellet of aggregated magnetic particles within a pellet forming area of the chamber. The pellet is formed to maximize its surface area.

A lateral flow device is disclosed. The lateral flow device includes a substrate having a flow path and a detection zone disposed along the flow path. The detection zone includes an immobilized target-binding moiety directed against a target of a Raman-active complex. Also disclosed is a method of conducting a lateral flow assay and detection system. The method includes i) defining a flow path having a detection zone; ii) flowing a sample down the flow path; and iii) immobilizing a Raman-active complex if present, at the detection zone. The sample includes a Raman-active complex or a Raman-active tag.

Raman-active lateral flow device and methods of detection

Methods for amplifying the Raman signal of primary SERS nanoparticles are provided. One method generally includes binding secondary SERS particles to the primary SERS nanoparticles after binding of the primary SERS nanoparticles. In another method, secondary SERS nanoparticles are brought in close proximity to the primary SERS nanoparticles, wherein the secondary nanoparticles are free of a reporter molecule or have a reporter molecule different from that of the primary SERS nanoparticles.

Methods for amplifying the Raman signal of surface enhanced Raman scattering nanoparticles

A method for treating a cellulose-containing substrate is provided in the present invention, the method comprising contacting a silicone composition comprising at least one polysiloxane or silicone resin containing at least one functional group comprising at least one dialkylacetal group, at least one anhydride group, at least one reactive group, or combinations thereof with the cellulose-containing substrate; and curing the silicone composition on the cellulose-containing substrate at a temperature in a range between about 25&deg; C. and about 200&deg; C. A further embodiment of the present invention includes a formulation containing the aforementioned silicone composition.

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Clifton Park, NY, United States of America

Michael Craig Burrell