Luminex Corporation

Other

Kurt D Hoffacker

Ananda G Lugade

Ewald Alois Terpetschnig

Leonid Davidovych Patsenker

Karri Lynn Michael-Ballard

Veronica D Thomason

Charles J Collins

Chuck Collins

Bruce Bernard

Ralph L McDade

Adam J Jenkins

Bruce J C Bernard

Bruce J-c Bernard

Leonid Patsenker

Ewald Terpetschnig

Ralph Mcdade

Anada G Lugade

Various methods for forming dyed microspheres are provided. One method includes activating a chemical structure coupled to a dye using heat or light to form a reaction intermediate in the presence of a microsphere. The reaction intermediate covalently attaches to a polymer of the microsphere thereby coupling the dye to the polymer and forming the dyed microsphere. Additional methods are provided for forming a dyed microsphere coupled to a molecule. These methods include dyeing the microspheres as described above in addition to synthesizing the molecule on an outer surface of the dyed microspheres. A population of dyed microspheres is also provided. Each of the dyed microspheres of the population includes a dye attached to a polymer of each of the dyed microspheres by a chemical structure. A coefficient of variation in dye characteristics of the population of dyed microspheres attributable to the dye is less than about 10%.

Methods for forming dyed microspheres and populations of dyed microspheres

The present invention relates to methods and systems for labeling, isolating, detecting, and/or enumerating a statistically significant number of biological cells, or other biological analytes of interest, present in a complex matrix sample. The isolation of a biological target of interest from a sample mixture is done by immunomagnetic separation. Upon introduction of the sample within an imaging chamber, the capture complex (biological target-magnetic capture agent) will be attracted by the magnetic field and will lay on the surface of the chamber in the focal plane of the imaging system.

Immunomagnetic capture and imaging of biological targets

The present invention relates to improved covalent coupling of two or more entities such as biomolecules, polymer compositions, organic/inorganic molecules/materials, and the like, including their combinations, through one or more novel reactive groups attached to linker groups of 2-1000 atoms length. The present invention also contemplates the use of bifunctional bridge molecules to link two or more entities, wherein the functional groups of the bridge molecules are the novel reactive groups of the present invention.

Functionalized compositions for improved immobilization

Various methods for altering surface characteristics of a microsphere are provided. One method includes coupling an enolic acid to the microsphere to modify the surface characteristics of the microsphere. The surface characteristics may include charge density and/or pKa. A reagent can be coupled to the microsphere via the enolic acid. The reagent may include a biomolecule. The modified surface characteristics may increase a stability of the reagent when the reagent is coupled to the microsphere. The modified surface characteristics may also improve performance of an assay carried out with the microsphere. Another embodiment relates to a microsphere that includes an enolic acid coupled to a polymer core of the microsphere such that the enolic acid modifies surface characteristics of the microsphere. A reagent can be coupled to the microsphere via the enolic acid.

Methods for altering surface characteristics of microspheres

A method for altering fluorescent emissions of particles includes setting the particles in motion and exposing the moving particles to light such that fluorescent intensities of the particles are lessened isotropically and substantially simultaneously. Another method includes measuring fluorescent emissions of particles, determining the measured fluorescent emissions do not collectively fit within a first predetermined range of fluorescent values, and exposing the particles to one or more incidents of light that are configured to cooperatively alter the fluorescent emissions of the particles to be within a second predetermined range of fluorescent values. An embodiment of an apparatus includes a vessel configured to contain a plurality of particles and a means for setting the particles in motion. The apparatus further includes an illumination subsystem configured to direct light toward the vessel and at a spectral window (i.e., wavelength or band of wavelengths) which is configured to isotropically and substantially simultaneously lessen the fluorescent emissions of each of the particles.

Methods and systems for altering fluorescent intensities of a plurality of particles

Various methods for forming dyed microspheres are provided. One method includes attaching a hydrophilic dye to chemical groups to form a bubble. The bubble includes the chemical groups surrounding the hydrophilic dye and an aqueous solution. The chemical groups are soluble in aqueous and organic solvents. The method also includes disposing the bubble and a microsphere to be dyed in a solvent such that the bubble is incorporated into the microsphere thereby dyeing the microsphere. Another method includes adsorbing a hydrophilic dye on a surface of a hydrophobic polymer core of a microsphere to be dyed thereby dyeing the microsphere. The method also includes attaching chemical groups to the hydrophilic dye. The chemical groups are soluble in aqueous and organic solvents. The chemical groups attached to the hydrophilic dye form an enclosure surrounding the hydrophilic dye and an aqueous solution.

Methods for forming dyed microspheres and populations of microspheres

The present invention relates to improved covalent coupling of two or more entities such as biomolecules, polymer compositions, organic/inorganic molecules/materials, and the like, including their combinations, through one or more novel reactive groups attached to linker groups of 2&#x2013;1000 atoms length. The present invention also contemplates the use of bifunctional bridge molecules to link two or more entities, wherein the functional groups of the bridge molecules are the novel reactive groups of the present invention.

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Austin, TX, United States of America

Kurt D Hoffacker