Direct light differential measurement system
US-2024423517-A1 · Dec 26, 2024 · US
US2017356887A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017356887-A1 |
| Application number | US-201715617790-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 8, 2017 |
| Priority date | Jun 10, 2016 |
| Publication date | Dec 14, 2017 |
| Grant date | — |
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A minimum peak is determined from analysis results, a correction wavelength at which an S/N ratio of the minimum peak is greatest is determined, and the determined correction wavelength is used to execute correction of the minimum peak. A plurality of detector output value correction method are registered in a processor, correction method is selected from default correction method or from among a plurality of preset correction methods according to an object to perform correction.
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What is claimed is: 1 . A method for correcting detector output value of a liquid chromatograph, the method comprising: selecting an analysis condition for using a liquid chromatograph, the analysis condition being selected from preset recipes that are registered in advance according to an examination object, the analysis condition being a condition to be set with respect to devices included in the liquid chromatograph such as a pump, an auto sampler, a column oven, and a detector, starting analysis according to the analysis condition that is selected in the previous step, measuring a characteristic of a sample using the detector, the characteristic including at least one of an absorbency and a fluorescence amount, and storing and displaying a signal strength of the detector indicating the characteristic of the sample in relation to time as analysis results; obtaining a chromatogram; recognizing peaks included in the chromatogram; determining a most minute peak of the signal strength of the analysis results in peaks which are recognized as a correction target peak; determining correction candidate wavelengths with respect to the correction target peak; performing a correction process on detector output value fluctuation based on correction method which is selected from among a plurality of preset correction methods; and outputting the analysis conditions, the correction condition, and corrected results of the characteristic of the sample. 2 . The method of claim 1 further comprising: selecting one wavelength of a correction wavelength at which an S/N ratio, which is a ratio between a detector output signal of the correction target peak and a detector output signal in the correction wavelength, is greatest and correcting the detector output signal of the correction target peak. 3 . The method of claim 1 further comprising: selecting one of a correction wavelength at which reproducibility of an S/N ratio is most favorable and correcting a detector output signal of the correction target peak. 4 . The method of claim 1 further comprising: selecting a plurality of correction wavelengths at which reproducibility of an S/N ratio is most favorable and correcting a detector output signal of the correction target peak using an average value of the detector output values in the plurality of selected wavelengths. 5 . The method of claim 1 further comprising: selecting each correction wavelength such that an S/N ratio of the correction target peak of each measurement target component is greatest and correcting a detector output signal of each of the correction target peaks. 6 . The method of claim 1 further comprising: selecting a plurality of correction wavelengths at which reproducibility of an S/N ratio of the correction target peak of each measurement target component is most favorable and correcting a detector output signal of the correction target peak using an average value of the detector output values in the plurality of selected wavelengths. 7 . The method of claim 1 further comprising: registering absorption wavelengths of a mobile phase which is used in liquid chromatography in advance as a database; selecting correction wavelength from the database in accordance with the mobile phase being selected; and correcting a detector output signal of the correction target peak using the selected correction wavelength. 8 . A liquid chromatograph comprising: a pump that pumps a mobile phase; an auto sampler that injects a sample; a column oven that maintains a column that separates components at a constant temperature; a detector that detects separated components; a processor that selects a recipe during measurement from analysis conditions which are preset in advance, selects detector output value correction process method which is registered, and examines analysis results; a data storage that stores the analysis results and examination results; and a display unit that displays the analysis conditions, the analysis results, and the examination results, wherein the processor operates to perform a process comprising: selecting analysis conditions from a recipe which is registered in advance according to an examination object; performing analysis according to the selected analysis conditions; measuring a characteristic of a sample, the characteristic including at least one of an absorbency and a fluorescence amount; determining a signal strength of the detector such as the absorbency or the fluorescence amount of the sample as analysis results; recognizing peaks included in the chromatogram; setting a minimum peak from among the recognized peaks as a correction target peak; selecting a correction candidate wavelength for the correction target peak; selecting detector output value correction method which is registered in advance; and performing a correction process based on the selected detector output value correction method. 9 . A liquid chromatograph comprising: a pump that pumps a mobile phase; an auto sampler that injects a sample; a column oven that maintains a column that separates components at a constant temperature; a detector that detects separated components; a processor that selects a recipe during measurement from analysis conditions which are preset in advance, selects detector output value correction process method which is registered, and examines analysis results; a data storage that stores the analysis results and examination results; and a display unit that displays the analysis conditions, the analysis results, and the examination results, wherein the processor operates to perform a process comprising: selecting analysis conditions from a recipe which is registered in advance according to an examination object; performing analysis according to the selected analysis conditions; measuring a characteristic of a sample, the characteristic including at least one of an absorbency and a fluorescence amount; determining a signal strength of the detector such as the absorbency or the fluorescence amount of the sample as analysis results; recognizing peaks included in the chromatogram; setting a plurality of peaks from among the recognized peaks as a correction target peaks; selecting a plurality of correction candidate wavelengths for the correction target peaks; selecting detector output value correction method which is registered in advance; and performing a correction process based on the selected detector output value correction method.
with comparison of measurements at specific and non-specific wavelengths (dual wavelength spectrometry G01J3/427) · CPC title
of fluid composition, e.g. gradient (G01N30/36 takes precedence) · CPC title
Construction of the column · CPC title
Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title
Liquid chromatography · CPC title
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