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    • 1. 发明专利
    • DISEASE STATE DIAGNOSING DEVICE
    • JPS5663255A
    • 1981-05-29
    • JP14061379
    • 1979-10-30
    • HITACHI LTD
    • MIYAGI HIROYUKITAKADA YOSHITADAMIURA JIYUNKICHITAKI MAMORU
    • G01N30/86G01N33/50G06F17/00
    • PURPOSE:To secure an effective application for the diagnosis of the disease state, by integrating the chromatogram of the organism liquid with every peak and then showing the relation between the integrated value and the holding time in a 2- dimensional diagram or into the 2-dimensional matrix. CONSTITUTION:The components in the organism liquid are separated and detected via the liquid or gas chromatograph, and an integration is given to peaks of the chromatograph individually. Based on this data, a 2-dimensional diagram or a matrix is produced for the relation between the holding time and the peak area (integrated vaue). The data of a subject are compared with the data showing the upper and lower limits of a healthy person which is filed previously to give a study whether the data of the subject is within the healthy region or not. If the subject is within the healthy region, the data with no fault are delivered to stop the operation of decision. But in case some component exceed the healthy region, the data of the subject are compared with the data of patients field according to the states of disease. Thus the corresponding or approximate data are looked for and obtained, and then the name of the corresponding disease or an approximate disease is delivered.
    • 6. 发明专利
    • LIQUID CHROMATOGRAPH
    • JPS5661632A
    • 1981-05-27
    • JP13812979
    • 1979-10-25
    • HITACHI LTD
    • MIURA JIYUNKICHITAKI MAMORUMIYAGI HIROYUKITAKADA YOSHITADA
    • G01N21/27G01N21/31G01N30/74
    • PURPOSE:To permit a liquid chromatograph to automatically analyze a living body fluid by adding to it memories and the like for storing two kinds of data: the hold time and the ratio of the detection signals at specific two wavelengths. CONSTITUTION:Successively connected to a photometer 8 are memories 10a and 10b, display 11, data processor 12, retriever 13, disk memory 14 and printer 15, which are controlled by a microcomputer 18 having a control interface 16, magnetic card 17 and input key panel 19. Thus, the outputs from a plurality of photoactive elements are stored in the memory 10a at specific time intervals, before being processed in the data processor 12 to obtain the hold time of the eluted constituent and the absorbance at each wavelength during the time as well as compute each ratio of the absorbances at two wavelengths, and each pair of the value and the hold time is stored in the memory 10b. The content is taken out for the retriever 13 to retrieve the forecast data on the analytical object filed in the disk memory 14, and the content is printed on the printer 15.
    • 9. 发明专利
    • LIQUID CHROMATOGRAPH
    • JPS5663256A
    • 1981-05-29
    • JP13902979
    • 1979-10-26
    • HITACHI LTD
    • MIURA JIYUNKICHITAKI MAMORUMIYAGI HIROYUKITAKADA YOSHITADA
    • G01N30/88G01N30/86
    • PURPOSE:To increase the accuracy of reproduction for the analysis data, by obtaining both the holding time and the column efficiency for one of the identified uric acid, hippuric acid and indole acetic acid each and then displaying them with every execution of analysis. CONSTITUTION:The three components, the uric acid, hippuric acid and indole acetic acid, are contained in a high probability in any kind of urine. Thus if both the holding time and the peak duration are obtained for either one of the above three components, the monitor is possible for the state of the separation column 5. Based on the holding time and the peak duration, the column efficiency is obtained via the data processor 12 and with every execution of analysis and then displayed on the display unit 11. The initial value of both the holding time and the column efficiency each is written into the magnetic card 17 through the input key panel 19 and under the condition of each column and separation. And in case the column efficiency of every execution of analysis shifts to the initial value and by an amount over the fixed range, the microcomputer 18 stops the operation of the liquid sending pump 3 via the control interface 16.
    • 10. 发明专利
    • ANALYSIS METHOD FOR URINE COMPOSING MATERIAL
    • JPS55103462A
    • 1980-08-07
    • JP1046179
    • 1979-02-02
    • HITACHI LTD
    • MIURA JIYUNKICHITAKI MAMORUMIYAGI HIROYUKITAKADA YOSHITADA
    • G01N33/493G01N30/34G01N30/88G01N33/50
    • PURPOSE:To increase both the detection accuracy and the detection wavelength region as well as reduce the analysis time by giving the stepped or continuous change to the density of the elution aqueous solution containing the chloride and acetonitrile. CONSTITUTION:In the analysis of the gradient elution ion exchange chromatography for the urine composing materials of various kinds of organic acid such as the urine composing material, the organism related materials, the nucleic acid or the like, the sample is led via pump 2 to isolation column 4 which is balanced previously by the water to be absorbed to the anion exchange resion for the component elements. Then gradient unit 8 is actuated to give change to the density of the chloride and acetonitrile in the elution aqueous solution from 0.001M-3.0M and from 0.1 capacity % to 30 capacity % each along with lapse of the analysis time for the aqueous solution mentioned above composed of acetonitrile and the chloride composed of the potassium chloride of low and high density in tanks 1A and 1B each, and then the aqueous solution is supplied to column 4. The urine composing materials absorbed into the resion mentioned above are isolated into each component and then detected by ultraviolet ray absorption meter 5, and then the output signals are recorded 6 in accordance with the amount of each component.