Treatment of hemophilia with fitusiran
US-2024027478-A1 · Jan 25, 2024 · US
US2016299158A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016299158-A1 |
| Application number | US-201615094565-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 8, 2016 |
| Priority date | Jun 1, 2012 |
| Publication date | Oct 13, 2016 |
| Grant date | — |
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The method is provided for characterizing agglomeration of particles in a liquid containing an analyte, including introducing liquid into a fluid chamber; mixing the liquid with a bifunctional reagent, lighting the fluid chamber using an excitation light beam extending through the fluid chamber in a longitudinal direction (X); acquiring at least one image using a matrix photodetector, each image including pixels (I n (x,y), x,y representing the coordinates of a pixel of an image, the image (I(x,y)) being formed by radiation transmitted by the lighted fluid chamber; and calculating from at least one acquired image (I(x,y)), at least one indicator (Ind 2 ) characterizing the particle agglomeration. The photodetector can be positioned less than 1 cm from the fluid chamber, and during the calculation step, the calculated indicator (Ind 2 ) is representative of the intensity of the pixels of the image. The method advantageously allows for charactering the agglomeration of particles in a liquid.
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What is claimed is: 1 . A method for characterizing an agglomeration of particles being contained in a liquid, the liquid including an analyte, the method comprising the following steps: a) introducing the liquid into a fluid chamber; b) mixing the liquid with a bifunctional reagent capable of creating an agglomeration of said particles within said liquid, due to said analyte, said bifunctional reagent being able to bond with both a particle and an analyte within said liquid; c) lighting the fluid chamber using an excitation light beam emitted by a light source, the light beam extending through the fluid chamber in a longitudinal direction (X); d) acquiring at least one image using a matrix photodetector, each image including pixels (I n (x,y), x,y representing the coordinates of a pixel of an image, the image (I(x,y)) being formed by radiation transmitted by the lighted fluid chamber; and e) calculating, from said at least one acquired image (I(x,y)), at least one indicator (Ind 2 ) characterizing the agglomeration of the particles; wherein: during the acquisition step, the photodetector is positioned at a distance smaller than 1 cm from the fluid chamber in the longitudinal direction; during the calculation step, the calculated indicator (Ind 2 ) is representative of the intensity of the pixels of said image; and the method further comprises estimating a quantity of said analyte from said indicator. 2 . The method according to claim 1 , wherein the particles comprise red blood cells. 3 . The method according to claim 1 , wherein the fluid chamber includes several fluid circulation channels, and wherein, during the calculation step, an indicator is calculated for each of the channels. 4 . The method according to claim 1 , wherein the indicator represents the distribution of intensity of the pixels in each acquired image. 5 . The method according to claim 1 , wherein the indicator represents the segmentation of each acquired image into different areas, each area including pixels of comparable intensity. 6 . The method according to claim 1 , wherein there is no magnifying lens between the fluid chamber and the matrix photodetector. 7 . The method according to claim 1 , wherein the light source is a light emitting diode. 8 . The method according to claim 1 , wherein the fluid chamber has a thickness ranging from 20 μm to 1000 μm. 9 . A method for characterizing an agglomeration of particles being contained in a liquid, the liquid including an analyte, the method comprising the following steps: a) introducing the liquid into a fluid chamber; b) mixing the liquid with a reagent capable of creating an agglomeration of said particles within said liquid, due to said analyte; c) lighting the fluid chamber using an excitation light beam emitted by a light source, the light beam extending through the fluid chamber in a longitudinal direction (X); d) acquiring at least one image using a matrix photodetector, each image including pixels (I n (x,y), x,y representing the coordinates of a pixel of an image, the image (I(x,y)) being formed by radiation transmitted by the lighted fluid chamber; and e) calculating, from said at least one acquired image (I(x,y)), at least one indicator (Ind 2 ) characterizing the agglomeration of the particles; wherein: during the acquisition step, the photodetector is positioned at a distance smaller than 1 cm from the fluid chamber in the longitudinal direction; during the calculation step, the calculated indicator (Ind 2 ) is representative of the intensity of the pixels of said image; and the method further comprises determining a quantity or a presence of said analyte from said indicator. 10 . The method according to claim 9 , wherein the particles comprise red blood cells. 11 . The method according to claim 9 , wherein the fluid chamber includes several fluid circulation channels, and wherein, during the calculation step, an indicator is calculated for each of the channels. 12 . The method according to claim 9 , wherein the indicator represents the distribution of intensity of the pixels in each acquired image. 13 . The method according to claim 9 , wherein the indicator represents the segmentation of each acquired image into different areas, each area including pixels of comparable intensity. 14 . The method according to claim 9 , wherein there is no magnifying lens between the fluid chamber and the matrix photodetector. 15 . The method according to claim 9 , wherein the light source is a light emitting diode. 16 . The method according to claim 9 , wherein the fluid chamber has a thickness ranging from 20 μm to 1000 μm. 17 . The method according to claim 9 , wherein the liquid is blood, the reagent comprises an antibody, and the analyte comprises an antigen, the method further including deriving a blood group from the calculated indicator.
Monitoring flocculation or agglomeration · CPC title
by observing the effect on a chemical indicator · CPC title
Optical arrangements · CPC title
Particle shape · CPC title
involving blood coagulating time {or factors, or their receptors} · CPC title
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