Noble metal-containing compound detection by catalysis of optical dye reduction
US-2024377333-A1 · Nov 14, 2024 · US
US10203277B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10203277-B2 |
| Application number | US-201113641881-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 5, 2011 |
| Priority date | Apr 20, 2010 |
| Publication date | Feb 12, 2019 |
| Grant date | Feb 12, 2019 |
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.
There is provided a technique for automatically determining or predicting a line range specific to a sample that appears in a reaction curve in an automated analyzer for mixing a specimen and a reagent and measuring a change in a mixture of the specimen and the reagent with time. This invention approximates reaction curve data by a function and automatically determines a curve part at an early stage or a second stage of a reaction. The invention determines a line range not including a curve part for each sample and calculates a laboratory test value using absorbance data within the determined line range. This invention also automatically determines a start time of line at the early stage of the reaction on the basis of absorbance data obtained up to a point halfway through the reaction curve, predicts a line range on the basis of the end time of line and a planned end time of line, and calculates a predictive value on the basis of a result of the prediction.
Opening claim text (preview).
The invention claimed is: 1. An automated analyzer for mixing a specimen and a reagent and measuring a change in a mixture of the specimen and the reagent with time to reduce a number of reexaminations and shorten a measurement time of the mixture of the specimen and reagent, comprising: an absorption detection mechanism configured to detect degrees of absorption related to mixing of the specimen and the reagent and to output a reaction curve of the specimen and the reagent based on the detected degrees of absorption; a measurement point data acquisition unit which acquires a plurality of measurement point data from the reaction curve of the specimen and the reagent; a data processing unit which processes the measurement point data; a storage unit which stores a first approximation formula used by the data processing unit; an output unit which outputs a processing result from the data processing unit; and a measuring unit that utilizes the processing result to conduct the measuring of the change in the mixture of the specimen and the reagent with a reduced number of reexaminations and a shorten measurement time, wherein the data processing unit causes the first approximation formula stored in the storage unit, which approaches a straight line to approximate the plurality of measurement point data, calculates a straight line which is approached by second approximation formula that is obtained as a result of the approximation, sets a time when a difference between the straight line and the second approximation formula falls below a reference value or a difference between a slope of the straight line and a slope of the second approximation formula falls below a reference value as a start time of line, and determines a line range of the reaction curve, wherein the data processing unit calculates the second approximation formula using ones of the plurality of measurement point data which are acquired up to a predetermined time and estimates the line range of the reaction curve on the basis of the second approximation formula to shorten the measurement time thereof, wherein the data processing unit calculates the straight line which is approached by the second approximation formula, sets a time when a difference between the straight line and the second approximation formula falls below a reference value as a start time of line, wherein the data processing unit calculates a difference value between each of ones of the measurement point data after the start time of line and the straight line which is approached by the second approximation formula and determines, as an end time of line, a time when the difference value reaches a maximum, wherein the data processing unit calculates an abnormality as a result of it being determined that a number of absorbance data in line is smaller than the threshold value, wherein the data processing unit calculates the straight line and calculates a slope used for a laboratory test value conversion from the linear function as a result of it being determined that the number of absorbance data in line is not less than the threshold value to reduce the number of reexaminations, wherein the data processing unit outputs the calculated laboratory test value on a display screen. 2. The automated analyzer according to claim 1 , wherein the storage unit stores a reference range for the start time of line, and the data processing unit compares the reference range with an estimated value of the line range and determines on the basis of a result of the comparison whether the line range can be estimated. 3. The automated analyzer according to claim 1 , wherein the storage unit stores a reference value of the number of ones of the measurement point data which are to be included in the line range, and the data processing unit includes a process of counting the number of measurement point data included in the line range that is estimated through signal processing and a process of comparing the reference value with the counted number of measurement point data and determining whether the line range can be estimated. 4. The automated analyzer according to claim 1 , wherein the first approximation formula is one of the following Expressions 1 to 4: x=a*t+b+c *exp(− k*t ) (Expression 1) x=a*t+b+e /( t+d ) (Expression 2) x=a*t+b+w/{ exp( u*t )+ v} (Expression 3) x=a*t+b+p *log{1 +q* exp( r*t )} (Expression 4) where t represents a time, x represents absorbance, and a, b, c, d, e, k, p, q, r, u, v, and w are parameters. 5. The automated analyzer according to claim 1 , wherein the data processing unit calculates a straight line which is approached by the second approximation formula and determines a time when a difference between the straight line and the second approximation formula falls below a reference value as a start time of line. 6. The automated analyzer according to claim 1 , wherein the data processing unit calculates a difference value between each of ones of the measurement point data after the start time of line and the straight line which is approached by the second approximation formula and determines, as an end time of line, a time when the difference value reaches a maximum. 7. The automated analyzer according to claim 1 , wherein the data processing unit includes a process of sequentially calculating the second approximation formula using each of a determining, as the start time of line, a time when a change in at least one parameter of the sequentially calculated second approximation formula falls below a tolerance level. 8. The automated analyzer according to claim 1 , wherein the data processing unit includes a process of sequentially calculating the second approximation formula using each of a plurality of measurement point data which are acquired at respective times even after the start time of line is determined and a process of determining, as an end time of line, a time when a change above a threshold value in at least one parameter of the sequentially calculated second approximation formula is detected. 9. The automated analyzer according to claim 8 , wherein the one parameter is a parameter which gives a slope of a linear component defining the second approximation formula. 10. The automated analyzer according to claim 1 , wherein the storage unit stores a reference value of the number of ones of the measurement point data which are to be included in the line range, and the data processing unit includes a process of counting the number of measurement point data included in the line range that is determined through signal processing and a process of determining presence or absence of an abnormality related to the line range that is determined by comparing the reference value with the counted number of measurement point data. 11. The automated analyzer according to claim 1 , wherein the data processing unit includes a process of calculating an index of precision for the determined line range and a process of outputting the calculated index of precision to the output unit. 12. An automated analysis method for measuring a change in a mixture of a specimen and a reagent with time using an automated analyzer to reduce a number of reexaminations and shorten a measurement time of the mixture of the specimen and reagent, comprising: a process of detecting degrees of absorption related to mixing of the specimen and the reagent and generating a reaction curve of the specimen and the reagent based on the detected degrees of absorption; a process of acquiring a plurality of measurement point data from a reaction curve of the specimen and the reagent by the automated analyzer; a process
for following a reaction, e.g. for determining photometrically a reaction rate (photometric cinetic analysis) · CPC title
Separating and mixing arrangements · CPC title
Control arrangements for automatic analysers · CPC title
Calibration · CPC title
producing a change of colour · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.