Method for Measuring Fibroblast Growth Factor-23 and Reagent Therefor
US-2024402163-A1 · Dec 5, 2024 · US
US9500644B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9500644-B2 |
| Application number | US-201113032316-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2011 |
| Priority date | Feb 23, 2010 |
| Publication date | Nov 22, 2016 |
| Grant date | Nov 22, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Particle populations and assays are provided which have varying amounts of magnetic material and varying particle concentrations among different subsets of particles. In particular, the particle populations and assays include at least two particle sets with distinct sums of particles which are inversely related to the magnetic material concentration comprising each of the particles within the two particle sets, respectively. A method for processing an assay having such particle sets includes routing the assay in proximity to an imaging plane within a static imaging optical analysis system and generating a magnetic field in proximity to the imaging plane. The magnetic field is sufficient to attract and immobilize a ratio of particles from the at least two discrete particle sets that is different from the ratio of particles comprising the at least two discrete particle sets in the assay as the assay is introduced into the static imaging optical analysis system.
Opening claim text (preview).
What is claimed is: 1. A method, comprising: introducing an assay into a static imaging optical analysis system, wherein the assay comprises (i) one or more analytes of interest, and (ii) at least two discrete particle sets distinguishable at least by their distinct concentrations of particles within the assay and the discrete ranges of magnetic material coupled to the particles of the respective particle sets; routing the assay in proximity to an, imaging plane within the static imaging optical analysis system; generating a magnetic field in proximity to the imaging plane that is sufficient to attract and immobilize a ratio of particles from the at least two discrete particle sets that is different from the ratio of particles comprising the at least two discrete particle sets in the assay as the assay is introduced into the static imaging optical analysis system; imaging the particles immobilized on the imaging plane; and analyzing one or more images produced from the step of imaging to determine the presence, absence and/or concentrations of the one or more analytes of interest within the assay. 2. The method of claim 1 , wherein the distinct concentrations of particles of the at least two discrete particle sets are inversely related to the amount of magnetic material coupled to the particles of the at least two discrete particle sets. 3. The method of claim 1 , wherein the number of immobilized particles on the imaging plane from each of the two discrete particle sets is sufficient such that the data collected for each of the two discrete particle sets during the step of analyzing is statistically significant. 4. The method of claim 1 , wherein the at least two discrete particle sets are further distinguishable by different reactants coupled to the particles of the respective particle sets, wherein the different reactants are reactive with different analytes of interest within the assay, and wherein concentrations of the different analytes of interest within the assay are inversely related to the amount of magnetic material coupled to the particles of the at least two discrete particle sets. 5. The method of claim 1 , where in the particles in the particle sets are encoded with fluorescent labels such that one set of particles can be distinguished from another set of particles based on different emission spectra and/or different emission intensities. 6. The method of claim 5 , wherein each of the particles in the particle sets are are encoded with two different fluorescent labels. 7. A method for imaging a population of magnetic particles comprising: introducing a population of magnetic particles into a static imaging optical analysis system, wherein the population of magnetic particles comprises a first particle set and a second particle set, wherein the average amount of magnetic material in particles of the first particle set is greater than the average amount of magnetic material in particles of the second particle set, and the sum of particles in the first particle set is less than the sum of particles in the second particle set; generating a magnetic field in proximity to an imaging plane in the static imaging optical analysis system that is sufficient to attract and immobilize particles from the first and second particle sets such that the ratio of particles of the first particle set to particles of the second particle set immobilized on the imaging plane is greater than the ratio of particles of the first particle set to particles of the second particle set in the population of magnetic particles introduced into the static imaging optical analysis system; and imaging the particles immobilized on the imaging plane. 8. The method of claim 7 , wherein the sum of particles in the first particle set is less than one-tenth the sum of particles in the second particle set when the population of magnetic particles is introduced into the static imaging optical analysis system. 9. The method of claim 7 , wherein the ratio of particles of the first particle set to particles of the second particle set immobilized on the imaging plane is about 1:1. 10. The method of claim 7 , wherein each particle of the first particle set contains at least one order of magnitude more magnetic material than each particle of the second particle set. 11. The method of claim 7 , where in the particles in the first and second particle sets are encoded with fluorescent labels such that the first set of particles can be distinguished from the second set of particles based on different emission spectra and/or different emission intensities. 12. A method for multiplex detection of analytes comprising: obtaining a population of magnetic particles comprising a first particle set and a second particle set, wherein the average amount of magnetic material in particles of the first particle set is greater than the average amount of magnetic material in particles of the second particle set, the sum of particles in the first particle set is less than the sum of particles in the second particle set, and the particles of the first particle set comprise a first reagent configured to react with a first reagent of interest and the particles of the second particle set comprise a second reagent configured to react with a second reagent of interest; combining the population of magnetic particles with a sample comprising the first and second reagents under conditions suitable for the first and second reagents to react with the first and second analytes, respectively, wherein the amount of the first analyte in the sample is lower than the amount of the second analyte in the sample; introducing the population of magnetic particles into a static imaging optical analysis system; generating a magnetic field in proximity to an imaging plane in the static imaging optical analysis system that is sufficient to attract and immobilize particles from the first and second particle sets such that the ratio of particles of the first particle set to particles of the second particle set immobilized on the imaging plane is greater than the ratio of particles of the first particle set to particles of the second particle set in the population of magnetic particles introduced into the static imaging optical analysis system; imaging the particles immobilized on the imaging plane; and detecting the presence or absence of the first and second analytes on the particles. 13. The method of claim 12 , wherein the ratio of particles of the first particle set to particles of the second particle set is less than 1:10 when the population of magnetic particles is introduced into the static imaging optical analysis system. 14. The method of claim 12 , wherein the ratio of particles of the first particle set to particles of the second particle set immobilized on the imaging plane is about 1:1. 15. The method of claim 12 , wherein each particle of the first particle set contains at least one order of magnitude more magnetic material than each particle of the second particle set. 16. The method of claim 12 , where in the particles in the first and second particle sets are encoded with fluorescent labels such that the first set of particles can be distinguished from the second set of particles based on different emission spectra and/or different emission intensities.
Coated nanoparticles, e.g. nanoparticles coated with organic surfactant · CPC title
Modification of conditions of immunological binding reaction, e.g. use of more than one type of particle, use of chemical agents to improve binding, choice of incubation time or application of magnetic field during binding reaction · CPC title
Nanomagnetism, e.g. magnetoimpedance, anisotropic magnetoresistance, giant magnetoresistance or tunneling magnetoresistance · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.