WO2010079630A1 - Analyzer - Google Patents

Analyzer Download PDF

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Publication number
WO2010079630A1
WO2010079630A1 PCT/JP2009/055507 JP2009055507W WO2010079630A1 WO 2010079630 A1 WO2010079630 A1 WO 2010079630A1 JP 2009055507 W JP2009055507 W JP 2009055507W WO 2010079630 A1 WO2010079630 A1 WO 2010079630A1
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WO
WIPO (PCT)
Prior art keywords
sample
analysis
blank
type
reagent
Prior art date
Application number
PCT/JP2009/055507
Other languages
French (fr)
Japanese (ja)
Inventor
修 野澤
Original Assignee
オリンパス株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by オリンパス株式会社 filed Critical オリンパス株式会社
Publication of WO2010079630A1 publication Critical patent/WO2010079630A1/en

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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/00584Control arrangements for automatic analysers
    • G01N35/00594Quality control, including calibration or testing of components of the analyser
    • G01N35/00613Quality control
    • G01N35/00663Quality control of consumables
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/00584Control arrangements for automatic analysers
    • G01N35/00594Quality control, including calibration or testing of components of the analyser
    • G01N35/00613Quality control
    • G01N35/00663Quality control of consumables
    • G01N2035/00673Quality control of consumables of reagents

Definitions

  • the present invention relates to an analyzer for analyzing a sample by mixing a sample and a reagent of a type corresponding to the analysis item of the sample, and measuring the absorbance of the mixed solution of the sample and the reagent.
  • a reagent blank analysis is performed every predetermined period and a blank sample (when the target component concentration in the sample is 0) Analyze the sample by determining the absorbance (reagent blank value) at the measurement wavelength of the sample and reagent mixture, and using this reagent blank value as a correction value to set the calibration curve used to calculate the absorbance of the sample and reagent mixture Analysis accuracy is maintained.
  • Patent Document 1 describes an analyzer that automatically performs a reagent blank analysis at an arbitrarily determined time.
  • reagent blank analysis is performed by using one type of blank sample.
  • the present invention has been made in view of the above, and provides an analyzer capable of performing a reagent blank analysis using an optimal blank sample for each analysis item without increasing the time spent for reagent blank analysis.
  • the purpose is to do.
  • an analyzer mixes a sample and a reagent of a type corresponding to an analysis item of the sample, and provides a mixture of the sample and the reagent.
  • blank sample information storage for storing blank sample information in which the analysis item is associated with a type of blank sample to be used for reagent blank analysis of the analysis item.
  • Extraction means for extracting based on the sample information, collation means for collating the analysis item extracted by the extraction means and the analysis item accepted by the acceptance means, and analysis items matched by the collation of the collation means, Reagent blank analysis according to each analysis item is determined according to the analysis order determined by the determination means for determining the analysis order of the reagent blank analysis so that at least the analysis items using the same type of blank sample are continuous. And a control means for performing control.
  • an analyzer mixes a sample and a reagent of a type corresponding to the analysis item of the sample, and provides a mixture of the sample and the reagent.
  • blank sample information storage for storing blank sample information in which the analysis item is associated with the type of blank sample to be used for the reagent blank analysis of the analysis item.
  • Extraction means for extracting based on rank sample information, collation means for collating the type of blank sample extracted by the extraction means with the type of blank sample obtained by the acquisition means, and a blank matched by the collation of the collation means
  • Determination means for determining the analysis order of the reagent blanks corresponding to each analysis item with respect to the analysis items suitable for the type of sample so that the analysis items using at least the same type of blank sample are continuous, and the determination means
  • Control means for performing control to execute reagent blank analysis in accordance with the determined analysis order.
  • the acquisition unit stores holding position information that associates the type of the blank sample with the holding position of the sample container determined for each type of the blank sample.
  • the type of the blank sample stored in each of the plurality of sample containers held by the holding means is obtained.
  • the analyzer outputs information in which the type of the blank sample and the holding position are associated with each other based on the holding position information stored in the holding position information storage means in the above invention.
  • An output means is provided.
  • the blank sample information storage unit stores the amount of the blank sample used as the blank sample information together with the type of the blank sample for each analysis item
  • the reception unit Comprises calculating means for calculating the amount used for each type of blank sample necessary for the reagent blank analysis according to the analysis item received based on the blank sample information stored in the blank sample information storage means, and the output means The use amount for each type of the blank sample calculated by the calculation means is output.
  • the acquisition unit is provided in the sample container, and the identification unit is configured to record the identification information for identifying the type of the blank sample in the sample container.
  • the type of the blank sample is acquired by reading information.
  • the blank sample information storage means for storing the blank sample information in which the analysis item of the sample and the type of the blank sample to be used for the reagent blank analysis of the analysis item are associated, and the target of the reagent blank analysis
  • Each of the plurality of sample containers held by the holding means accommodates an analysis apparatus including a receiving means for receiving the analysis item and a holding means for holding the plurality of sample containers in which the blank samples are accommodated.
  • the type of the blank sample is acquired, the analysis item that matches the type of the acquired blank sample is extracted based on the blank sample information, the extracted analysis item and the analysis item received by the reception unit are verified, and verification is performed.
  • the optimal blank sample can be selected for each analysis item without increasing the time spent on the reagent blank analysis.
  • the used reagent blank analysis can be performed.
  • FIG. 1 is a schematic diagram showing the configuration of the analyzer according to the first embodiment of the present invention.
  • FIG. 2 is a diagram showing blank sample information stored in the blank sample information storage unit shown in FIG.
  • FIG. 3 is a diagram showing the holding position information stored in the holding position information storage unit shown in FIG.
  • FIG. 4 is a flowchart showing the procedure of the reagent blank analysis process by the analyzer shown in FIG.
  • FIG. 5 is a diagram showing a reception menu screen output by the output unit shown in FIG.
  • FIG. 6 is a diagram illustrating a holding position information screen output by the output unit illustrated in FIG.
  • FIG. 7 is a diagram illustrating analysis items extracted by the extraction unit illustrated in FIG. 1.
  • FIG. 1 is a schematic diagram showing the configuration of the analyzer according to the first embodiment of the present invention.
  • FIG. 2 is a diagram showing blank sample information stored in the blank sample information storage unit shown in FIG.
  • FIG. 3 is a diagram showing the holding position information stored in the holding position information storage unit shown
  • FIG. 8 is a diagram illustrating analysis items that are matched by the collation performed by the collation unit illustrated in FIG. 1.
  • FIG. 9 is a schematic diagram showing the configuration of the analyzer according to the second embodiment of the present invention.
  • FIG. 10 is a flowchart showing the procedure of the reagent blank analysis process by the analyzer shown in FIG.
  • FIG. 11 is a diagram showing types of blank samples extracted by the extraction unit shown in FIG.
  • FIG. 12 is a diagram showing a usage amount display screen output by the output unit shown in FIG.
  • FIG. 13 is a diagram illustrating types of blank samples that are matched by collation performed by the collation unit illustrated in FIG. 9.
  • FIG. 14 is a schematic diagram showing the configuration of the analyzer according to the third embodiment of the present invention.
  • FIG. 15 is a flowchart showing a procedure of reagent blank analysis processing by the analyzer shown in FIG.
  • FIG. 16 is a diagram showing information in which the code number recorded on the sample container identification label shown in FIG. 14 is
  • FIG. 1 is a schematic diagram showing the configuration of the analyzer according to the first embodiment of the present invention.
  • the analysis device 1 includes a measurement unit 10 and a control device 30.
  • the measurement unit 10 dispenses a sample such as a specimen and a reagent into the reaction container 11c, and optically measures the reaction occurring in the reaction container 11c.
  • the control device 30 controls the entire analyzer 1 including the measurement unit 10 and analyzes measurement data in the measurement unit 10.
  • the analysis apparatus 1 automatically performs biochemical analysis of a plurality of samples sequentially in cooperation with each other.
  • the measurement unit 10 includes a sample supply unit 11, a sample holding unit 12, a reaction tank 13, a reagent storage 14, a sample dispensing mechanism 15, a reagent dispensing mechanism 16, a stirring unit 17, a photometric unit 18, a washing unit 19, and a container presence / absence A detection unit 20 is included.
  • the sample supply unit 11 transports the first sample container 11a to the sample suction position by transporting the rack 11b holding the first sample container 11a containing a sample such as a general specimen.
  • the sample in the first sample container 11a conveyed to the sample suction position is dispensed by the sample dispensing mechanism 15 into the reaction container 11c conveyed to the sample dispensing position.
  • the sample holding unit 12 can be rotated clockwise or counterclockwise about a vertical line passing through the center of the sample holding unit 12 as a rotation axis by driving a driving mechanism (not shown) under the control of the control device 30.
  • the predetermined second sample container 12a is transferred to the sample suction position by the sample dispensing mechanism 15.
  • the reaction tank 13 has a heat insulating member (not shown) and a wheel 13a.
  • the wheel 13a holds a plurality of reaction vessels 11c and rotates by a drive mechanism (not shown) to transfer the reaction vessels 11c in the circumferential direction.
  • the reaction tank 13 is covered with a disk-shaped lid (not shown), and a heat insulation tank that keeps the internal temperature at a human body temperature is provided along with a heat insulation member (not shown) disposed on the inside and outside in the radial direction of the wheel 13a. It is composed.
  • the reagent storage 14 detachably stores a plurality of reagent containers 14a in which reagents to be dispensed in the reaction container 11c are stored.
  • the reagent storage 14 can be rotated clockwise or counterclockwise about a vertical line passing through the center of the reagent storage 14 as a rotation axis by driving a drive mechanism (not shown) under the control of the control device 30.
  • the predetermined reagent container 14a is transferred to the reagent suction position by the reagent dispensing mechanism 16.
  • the sample dispensing mechanism 15 has an arm 15b to which a nozzle 15a for sucking and discharging a sample is attached at the tip.
  • the arm 15b freely moves up and down in the vertical direction and rotates around a vertical line passing through its base end as a central axis.
  • the sample dispensing mechanism 15 has an intake / exhaust mechanism using an intake / exhaust syringe or a piezoelectric element.
  • the sample dispensing mechanism 15 sucks the sample from the first sample container 11a transferred to the sample suction position of the sample supply unit 11 by the nozzle 15a, rotates the arm 15b counterclockwise in the drawing, The sample is discharged into the reaction container 11c conveyed to the sample discharge position.
  • the reagent dispensing mechanism 16 has an arm 16b to which a nozzle 16a for sucking and discharging the reagent is attached to the tip.
  • the arm 16b freely moves up and down in the vertical direction and rotates around the vertical line passing through its base end as a central axis.
  • the reagent dispensing mechanism 16 has an intake / exhaust mechanism using an unillustrated intake / exhaust syringe or piezoelectric element.
  • the reagent dispensing mechanism 16 sucks the reagent in the reagent container 14a transferred to a predetermined position on the reagent storage 14 by the nozzle 16a, rotates the arm 16b clockwise in the drawing, and moves the arm 16b to the predetermined position on the reaction tank 13.
  • the reagent is discharged into the transported reaction container 11c.
  • the stirring unit 17 stirs the mixed solution of the reagent and the sample dispensed in the reaction vessel 11c to promote the reaction between the sample and the reagent.
  • the photometry unit 18 irradiates the reaction vessel 11c, which has been transferred to a predetermined measurement position, with measurement light from the light source 18a, disperses the light transmitted through the mixture of the sample and the reagent in the reaction vessel 11c, and uses the light receiving element 18b. By measuring the intensity of each wavelength light, the absorbance at a wavelength peculiar to the mixed solution of the sample to be analyzed and the reagent is measured.
  • the cleaning unit 19 performs cleaning by sucking and discharging the mixed solution in the reaction vessel 11c that has been measured by the photometry unit 18 by using a nozzle (not shown) and injecting and sucking cleaning liquid such as detergent and cleaning water. .
  • the container presence / absence detection unit 20 is disposed in the vicinity of the sample holding unit 12.
  • the container presence / absence detection unit 20 detects the presence / absence of the second sample container 12a at the holding position Pv as detection means.
  • the container presence / absence detection unit 20 is realized by, for example, an optical sensor that optically detects the presence / absence of the second sample container 12a.
  • the container presence / absence detection unit 20 outputs a detection signal to the control device 30 when detecting the second sample container 12a.
  • the control device 30 includes a control unit 31, an input unit 32, an analysis unit 33, an output unit 34, a storage unit 35, an acquisition unit 36, an extraction unit 37, a collation unit 38, and a determination unit 39.
  • the control unit 31 is realized by a CPU or the like, and controls processing and operation of each unit of the analyzer 1.
  • the control unit 31 performs predetermined input / output control on information input / output to / from each of these components, and performs predetermined information processing on this information.
  • the input unit 32 is realized by a keyboard, a mouse, or the like, and can input various information such as the number of samples or analysis items.
  • the input unit 32 receives input of analysis items corresponding to reagent blank analysis as receiving means.
  • the analysis unit 33 obtains the concentration of the detection target in the sample based on the measurement result measured by the photometry unit 18, and performs component analysis of the sample.
  • the output unit 34 is realized by a display panel, a printer, or the like, and outputs various types of information such as sample analysis data and alarms as output means.
  • the output unit 34 can output information that assists the input of analysis items corresponding to the reagent blank analysis by the input unit 32.
  • the storage unit 35 includes a blank sample information storage unit 35a and a holding position information storage unit 35b.
  • the blank sample information storage unit 35a stores, as blank sample information storage means, blank sample information in which sample analysis items are associated with types of blank samples to be used for reagent blank analysis of the analysis items.
  • FIG. 11 is a diagram showing a blank sample information table 35a-1 in which n is a natural number). In the blank sample information table 35a-1, for example, indicates that the blank sample type B 1 is, it is associated as blank sample to be used for the reagent blank analysis of analysis items A 1.
  • the holding position information storage unit 35b stores, as holding position information storage means, holding position information that associates the type of blank sample with the holding position of the second sample container 12a determined for each type.
  • Figure 3 is a diagram showing a holding position P 1 ⁇ P n, the holding position P 1 ⁇ type B 1 ⁇ holding position information table 35b-1 that the B n in correspondence of the blank sample to be retained in the P n .
  • Holding position information table 35b-1 indicates that it should retain the blank sample type B 1 in the holding position P 1.
  • the blank sample may be held at the holding position P 1, and the blank sample may be held at the holding position P 3 without holding the blank sample at the holding position P 2 .
  • the storage unit 35 includes a hard disk that magnetically stores information, and a memory that electrically reads various programs related to this process from the hard disk when the analyzer 1 executes the process.
  • the storage unit 35 stores analysis data of the sample including the absorbance and the like that have been subjected to arithmetic processing.
  • the acquisition unit 36 acquires the type of blank sample accommodated in each of the plurality of second sample containers 12a held by the sample holding unit 12 as an acquisition unit.
  • the acquisition unit 36 uses each of the plurality of second sample containers 12a held by the sample holding unit 12 by using the holding position information stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20.
  • the type of the blank sample accommodated by is acquired.
  • the extraction unit 37 extracts analysis items that match the type of blank sample acquired by the acquisition unit 36 based on the blank sample information stored in the blank sample information storage unit 35a.
  • the collation unit 38 collates the analysis item extracted by the extraction unit 37 and the analysis item received by the input unit 32.
  • the determination unit 39 determines the analysis order of the reagent blank analysis corresponding to each analysis item for the analysis items matched by the verification of the verification unit 38 so that the analysis items using at least the same type of blank sample are continuous. .
  • the reagent dispensing mechanism 16 dispenses a reagent from the reagent container 14a to the reaction container 11c with respect to the plurality of reaction containers 11c that are sequentially transported, and the sample dispensing mechanism. 15 dispenses a predetermined amount of sample from the first sample container 11a to the reaction container 11c.
  • the photometry unit 18 measures the absorbance of the mixed solution of the reagent and the sample.
  • the analysis unit 33 performs an operation for analyzing the measurement result of the photometry unit 18 and automatically performs a component analysis of the sample.
  • the cleaning unit 19 cleans and dries the reaction vessel 11 c that has been measured by the photometry unit 18.
  • the analyzer 1 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S101).
  • the reception of the analysis item corresponding to the reagent blank analysis is performed via the input unit 32 using the reception menu screen output by the output unit 34, for example.
  • FIG. 5 is a display example of a reception menu screen for receiving an analysis item corresponding to the reagent blank analysis output by the output unit 34.
  • Operator selects a reception menu analysis item A 1 ⁇ A predetermined analysis item from m on the screen 34a through the input unit 32, by registering, receiving the analysis item corresponding to the reagent blank analysis is performed .
  • the operator selects each analysis item button 34 a-3, 34 a-4, 34 a-5 on the reception menu screen 34 a via a mouse or the like.
  • the analysis items A 1 , A 3 , A 4 are accepted by selecting the registration button 34a-1.
  • the case where the analysis item is received using the reception menu screen 34a output by the output unit 34 is illustrated, but the code assigned to each analysis item may be input via the keyboard. Good.
  • step S101 When an analysis item corresponding to the reagent blank analysis is received in step S101 (step S101: Yes), the output unit 34 outputs a holding position information screen (step S102).
  • FIG. 6 is a display example of a holding position information screen that the output unit 34 outputs to the display panel based on the holding position information stored in the holding position information storage unit 35b.
  • the holding position information screen 34b shown in the figure is output, for example, by selecting the holding position button 34a-2 on the reception menu screen 34a.
  • Holding position information screen 34b is a holding position P 1, it indicates that it should retain the blank sample type B 1. Since the type of blank sample to be held for each holding position is determined in advance, the holding position information screen 34b need not be output.
  • step S101 step S101: No
  • the control unit 31 repeats this determination process.
  • step S103 determines whether or not the setting of the second sample container 12a to the sample holding unit 12 is completed. The determination in step S103 is performed based on, for example, whether or not a signal indicating completion of setting, that is, a signal indicating that reagent blank analysis is started is output from the input unit 32 to the control unit 31.
  • step S103 When the setting of the second sample container 12a to the sample holding unit 12 is completed in step S103 (step S103: Yes), the container presence / absence detection unit 20 performs the second operation at the holding positions P 1 to P n where the blank sample is held. The presence or absence of the sample container 12a is detected (step S104). This detection is performed while the sample holder 12 makes a round clockwise or counterclockwise with a vertical line passing through the center of the sample holder 12 as a rotation axis. On the other hand, when the setting of the second sample container 12a to the sample holding unit 12 is not completed (step S103: No), the output unit 34 repeats this determination process.
  • the acquiring unit 36 After detecting the presence or absence of the second sample container 12a at the holding positions P 1 to P n in step S104, the acquiring unit 36 acquires the type of blank sample in the second sample container 12a held by the sample holding unit 12. (Step S105). Specifically, the acquisition unit 36 obtains the holding position information of the second sample container 12a determined for each type of blank sample stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20. By using it, the type of the blank sample is acquired. For example, as when the container presence detector 20 detects that the second sample container 12a is in the holding position P 1, the blank sample B 1 corresponding to the holding position P 1 is accommodated in the second sample vessel 12a To do.
  • the extraction part 37 extracts the analysis item suitable for the kind of blank sample which the acquisition part 36 acquired (step S106).
  • the analysis item is extracted based on the blank sample information stored in the blank sample information storage unit 35a.
  • FIG. 7 is a diagram illustrating an example of analysis items extracted by the extraction unit 37.
  • FIG. 7 shows a case where the acquisition unit 36 acquires the types B 1 and B 2 of the blank sample.
  • the extraction unit 37 extracts the analysis item A 1 as an analysis item suitable for the type B 1 blank sample, and extracts the analysis items A 2 to A 5 as analysis items suitable for the type B 2 blank sample.
  • FIG. 8 is a diagram showing analysis items matched by collation by the collation unit 38 among the analysis items A 1 to A 5 extracted by the extraction unit 37 shown in FIG. Figure 8 is accepted analysis items in step S101 shows the case of A 1, A 3 and A 4, analysis item A 1, A 3 and that meet in the analysis item A 1 ⁇ A 5 shown in FIG. 7 and a 4, showing the correspondence between the type of the obtained blank sample.
  • control unit 31 determines whether or not it is possible to perform all of the reagent blank analysis of the received analysis items (step S108). This determination is made based on whether or not all the reagent blank analyzes of the received analysis items can be performed when the reagent blank analysis of the analysis items matched by the verification of the verification unit 38 is performed.
  • the determination unit 39 performs the reagent blank analysis corresponding to each analysis item with respect to the analysis item matched by the collation of the collation unit 38.
  • the analysis order is determined (step S109). This analysis order is determined so that analysis items using the same type of blank sample are continuous. As shown in FIG. 8, analysis item using the blank sample type B 2 be a A 3 and A 4, the reagent blank analysis of analysis items A 3 and A 4 determines the analysis order to continuously.
  • step S108 when it is not possible to perform all the reagent blank analysis of the reception analysis item (step S108: No), the output unit 34 outputs abnormality information indicating that the reagent blank analysis process is abnormal (step S110). Then, the control part 31 complete
  • control unit 31 After determining the analysis order of the reagent blank analysis of the reception analysis item in step S109, the control unit 31 causes the analyzer 1 to perform the reagent blank analysis of the reception analysis item according to the analysis order determined by the determination unit 39 (step S111). . Then, the control part 31 complete
  • a blank sample information storage unit 35a for storing blank sample information in which a sample analysis item is associated with a type of blank sample to be used for a reagent blank analysis of the analysis item, and a reagent blank analysis
  • the sample holding unit 12 holds the analyzer 1 including an input unit 32 that receives an analysis item that is a target of the sample and a sample holding unit 12 that holds a plurality of second sample containers 12a in which blank samples are stored.
  • the type of blank sample accommodated in each of the plurality of second sample containers 12a is acquired, analysis items that match the acquired type of blank sample are extracted based on the blank sample information, and the extracted analysis items and input unit 32 are provided.
  • the analysis order received is collated, and the analysis order of the reagent blank analysis according to each analysis item is set to at least the analysis item matched by the collation.
  • the analysis items that use different types of blank samples are determined to be continuous, and the reagent blank analysis is controlled according to the determined order of analysis, so there is no increase in the time spent on reagent blank analysis. Reagent blank analysis using an optimal blank sample can be performed.
  • the output unit 34 outputs information that associates the type of the blank sample with the holding position based on the holding position information stored in the holding position information storage unit 35b. The operator can reliably set the blank sample for each type in the sample holder 12.
  • FIG. 9 is a schematic diagram showing the configuration of the analyzer according to the second embodiment of the present invention.
  • the analysis device 2 illustrated in FIG. 9 includes a measurement unit 10 and a control device 50.
  • symbol is attached
  • the control unit 51 of the control device 50 includes an extraction unit 53, a collation unit 54, a determination unit 55, and a calculation unit 56.
  • the storage unit 52 includes a blank sample information storage unit 52a.
  • the extraction unit 53 extracts the type of blank sample that matches the analysis item received by the input unit 32 (hereinafter referred to as reception analysis item) based on the blank sample information described above.
  • the collation unit 54 collates the type of the blank sample extracted by the extraction unit 53 and the type of the blank sample acquired by the acquisition unit 36.
  • the determination unit 55 sets the analysis order of the reagent blanks according to each analysis item to the analysis item that uses at least the same type of blank sample. Decide to be continuous.
  • the calculation part 56 calculates the usage-amount for every kind of blank sample required for the reagent blank analysis according to a reception analysis item based on the blank sample information which the blank sample information storage part 52a memorize
  • the blank sample information storage unit 52a stores the amount of the blank sample used together with the type of the blank sample for each analysis item as blank sample information.
  • the analyzer 2 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S201).
  • the analysis item corresponding to the reagent blank analysis is received via the input unit 32 using the reception menu screen 34a output to the display panel by the output unit 34, for example, as in the first embodiment.
  • step S201 When the analysis item corresponding to the reagent blank analysis is received in step S201 (step S201: Yes), the extraction unit 53 stores the blank sample type that matches the received analysis item in the blank sample information storage unit 52a. Extraction is performed based on the sample information (step S202).
  • FIG. 11 is a diagram illustrating the types of blank samples extracted by the extraction unit 53. The case shown in FIG. 11, the extraction unit 53 extracts the type B 1 as a blank sample type conforming to the acceptance analysis item A 1, type B 2 as a blank kinds of samples conform to the accepted analysis item A 3 and A 4 To extract.
  • step S201 step S201: No
  • the control unit 51 repeats this determination process.
  • the calculation unit 56 calculates the usage amount of each blank sample type necessary for the reagent blank analysis according to the received analysis item (step S203). The calculation of the usage amount is performed based on the usage amount of the blank sample that the blank sample information storage unit 52a stores together with the type of the blank sample. Thereafter, the output unit 34 outputs the usage amount of the blank sample calculated by the calculation unit 56 (step S204).
  • FIG. 12 is a usage amount display screen 54a in which the usage amount calculated by the calculation unit 56 is further associated with the type of blank sample in association with the information that associates the type of blank sample with the holding positions P 1 to P n .
  • the usage amount display screen 54a indicates that 10 ⁇ L of the type B 1 blank sample should be held at the holding position P 1 , and indicates that 20 ⁇ L of the type B 2 blank sample should be held at the holding position P 2 . Since the type of blank sample for each holding position is determined in advance, the output unit 34 may output only information in which the amount used corresponds to the type of blank sample.
  • the control unit 51 determines whether or not the setting of the second sample container 12a to the sample holding unit 12 is completed (step S205).
  • the determination as to whether or not the setting of the second sample container 12a to the sample holding unit 12 has been completed is, for example, a signal indicating the completion of setting, that is, a signal indicating the start of reagent blank analysis, as in the first embodiment. Is performed depending on whether or not is output from the input unit 32 to the control unit 51.
  • step S205 When the setting of the second sample container 12a to the sample holding unit 12 is completed in step S205 (step S205: Yes), the container presence / absence detection unit 20 performs the second operation at the holding positions P 1 to P n where the blank sample is held. The presence or absence of the sample container 12a is detected (step S206). This detection is performed while the sample holder 12 makes a round clockwise or counterclockwise with a vertical line passing through the center of the sample holder 12 as a rotation axis. On the other hand, when the setting of the second sample container 12a to the sample holding unit 12 is not completed (step S205: No), the output unit 34 repeats this determination process.
  • the acquisition unit 36 After detecting the presence or absence of the second sample container 12a at the holding positions P 1 to P n in step S206, the acquisition unit 36 acquires the type of blank sample in the second sample container 12a held by the sample holding unit 12. (Step S207).
  • the acquisition unit 36 uses the holding position information of the second sample container 12a determined for each type of blank sample stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20 to perform the second operation.
  • the type of blank sample in the sample container 12a is acquired.
  • FIG. 13 is a diagram illustrating the types of blank samples that are matched by the collation by the collation unit 54.
  • FIG. 13 shows a case where the acquisition unit 36 acquires only a blank sample of type B 1 in step S207, which matches among the types of blank samples B 1 and B 2 shown in FIG. 11 extracted by the extraction unit 53. the type B 1 of the blank sample, showing the correspondence between the reception analysis item.
  • the control unit 51 determines whether or not it is possible to perform all of the reagent blank analysis of the received analysis items (step S209). This determination is based on whether or not all the reagent blank analyzes of the reception analysis items can be performed when the reagent blank analysis of the analysis items matching the type of the blank sample matched by the verification of the verification unit 54 is performed. To be judged.
  • the determination unit 55 performs each analysis on the analysis item that matches the type of the blank sample matched by the collation of the collation unit 54. An analysis order of reagent blank analysis corresponding to the item is determined (step S210).
  • This analysis order is determined so that analysis items using at least the same type of blank sample are continuous.
  • the output unit 34 outputs abnormality information indicating that the reagent blank analysis process is abnormal (step S211). Then, the control part 51 complete
  • step S211 after determining the analysis order of the reagent blank analysis of the reception analysis item, the control unit 51 causes the analyzer 2 to execute the reagent blank analysis of the reception analysis item according to the analysis order determined by the determination unit 55 (step S212). ). Then, the control part 51 complete
  • the analysis device 2 acquires the type of blank sample stored in each of the plurality of second sample containers 12a held by the sample holding unit 12, and the analysis item received by the input unit 32
  • the blank sample type that conforms to the criteria is extracted based on the blank sample information, the extracted blank sample type is collated with the acquired blank sample type, , Because the reagent blank analysis order according to each analysis item is determined so that at least the analysis items using the same type of blank sample are continuous, and the reagent blank analysis is performed according to the determined analysis order, As in the first embodiment, a reagent using an optimal blank sample for each analysis item without increasing the time spent for reagent blank analysis It is possible to perform the rank analysis.
  • the calculation part 56 calculates based on the blank sample information which the blank sample information storage part 52a memorize
  • the output unit 34 outputs information in which the type of the blank sample is associated with the holding positions P 1 to P n and information in which the usage amount calculated by the calculation unit 56 is associated with the type of the blank sample. Therefore, the operator can reliably set the blank sample for each type in the sample holding unit 12 and can set the blank sample corresponding to the amount used.
  • the analysis apparatus 1 includes the calculation unit 56, and after the collation unit 38 collates the analysis item extracted by the extraction unit 37 with the received analysis item, the calculation unit 56 uses the reagent blank of the blank sample.
  • the usage amount in the analysis may be calculated, and the output unit 34 may output the usage amount calculated by the calculation unit 56 according to the type of the blank sample.
  • FIG. 14 is a schematic diagram showing the configuration of the analyzer according to the third embodiment of the present invention.
  • the analysis device 3 illustrated in FIG. 14 includes a measurement unit 60 and a control device 70.
  • symbol is attached
  • FIG. The measurement unit 60 includes a sample container identification label reading unit 61
  • the control unit 71 of the control device 70 includes a storage unit 72 and an acquisition unit 73 that do not include the holding position information storage unit 35b.
  • the blank sample is accommodated not in the second sample container 12a but in, for example, the first sample container 11a held in the rack 11b having five holding positions p 1 to p 5 .
  • the sample container identification label reading unit 61 is disposed in the vicinity of the sample supply unit 11.
  • the sample container identification label reading unit 61 is provided in the first sample container 11a, and reads and reads the identification information of the sample container identification label 11f in which the identification information for identifying the type of the blank sample in the first sample container 11a is recorded.
  • the identification information is output to the control device 70.
  • the sample container identification label 11f is realized by, for example, a barcode.
  • the sample container identification label reading unit 61 may use, for example, an apparatus that reads an information recording medium on which information for identifying the type of specimen in the first sample container 11a is recorded.
  • the acquisition unit 73 accommodates each of the plurality of first sample containers 11a held by the rack 11b based on the identification information recorded on the sample container identification label 11f output to the control device 70 by the sample container identification label reading unit 61.
  • the type of blank sample to be acquired is acquired.
  • the analyzer 3 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S301).
  • the analysis item corresponding to the reagent blank analysis is received through the input unit 32 using the reception menu screen 34a output to the display panel by the output unit 34, for example, as in the first and second embodiments.
  • step S301 determines whether or not the setting of the rack 11b to the sample supply unit 11 is completed (step S302). ). The determination in step S302 is performed based on, for example, whether a signal indicating completion of setting, that is, a signal indicating that reagent blank analysis is started is output from the input unit 32 to the control unit 71. On the other hand, when the analysis item corresponding to the reagent blank analysis is not received in step S301 (step S301: No), the control unit 71 repeats this determination process.
  • step S302 When the setting of the rack 11b to the sample supply unit 11 is completed in step S302 (step S302: Yes), the sample container identification label reading unit 61 applies the first sample container 11a at the holding positions p 1 to p 5 of the rack 11b.
  • the identification information of the provided sample container identification label 11f is read (step S303). This reading is performed while the rack 11 b is transported in the vicinity of the sample container identification label reading unit 61 by the sample supply unit 11.
  • step S302: No the control unit 71 repeats this determination process.
  • FIG. 16 shows an information table 72-1 in which code numbers as identification information recorded on the sample container identification label 11f are associated with the types of blank samples. Using the information table 72-1 stored in the storage unit 72, the acquisition unit 73 acquires the type of blank sample in the first sample container 11a from the code number read by the sample container identification label reading unit 61.
  • the analysis device 3 performs the same processing as the processing of steps S106 to S111 performed by the analysis device 1 (steps S305 to S310).
  • the analysis device 3 acquires the type of blank sample accommodated in each of the plurality of first sample containers 11a held by the rack 11b, and analyzes that match the acquired type of blank sample.
  • the items are extracted based on the blank sample information, the extracted analysis items and the analysis items received by the input unit 32 are collated, and the analysis order of the reagent blank analysis corresponding to each analysis item is performed on the analysis items matched by the collation. Is determined so that at least analysis items using the same type of blank sample are continuous, and the reagent blank analysis is performed in accordance with the determined analysis order.
  • the reagent It is possible to perform reagent blank analysis using an optimal blank sample for each analysis item without increasing the time spent for blank analysis. Rutotomoni, sample container identification label reader 61, so as to read each sample vessel identification label 11f the holding position p 1 ⁇ p 5 which records the code number identifying the blank type of sample in the first sample vessel 11a Therefore, even if the first sample container 11a is held at an arbitrary holding position in the rack 11b, the type of blank sample in the first sample container 11a can be acquired.
  • the analyzer according to the present invention is useful for a medical analyzer that automatically analyzes different analysis items for a specimen.

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Abstract

Provided is an analyzer which can perform analysis of a reagent blank by using an optimal blank sample for each item of analysis without increasing the time being spent for analysis of a reagent blank. The analyzer comprises a blank sample information storage section (35a) for storing correspondence information between an item of analysis and the kind of a blank sample to be used for analysis of a reagent blank, an acquisition section (36) for acquiring the kind of a blank sample in a second sample container (12a) held at a sample holding section (12) from information in a holding position information storage section (35b) and a detection result from a section (20) for detecting the presence/absence of a container, an extraction section (37) for extracting an item of analysis conforming to the kind thus acquired, a collation section (38) for collating the extracted item of analysis with an item of analysis received at an input section (32), a determination section (39) for determining the order of analysis of a reagent blank according to each item of analysis for an item of analysis matched by the collating such that analyses using the same kind of blank sample are sequenced, and a control section (31) performing control for executing analysis of reagent blank according to the order of analysis thus determined.

Description

分析装置Analysis equipment
 本発明は、試料と、試料の分析項目に応じた種類の試薬とを混合し、試料および試薬の混合液の吸光度を測定することによって試料の分析を行う分析装置に関するものである。 The present invention relates to an analyzer for analyzing a sample by mixing a sample and a reagent of a type corresponding to the analysis item of the sample, and measuring the absorbance of the mixed solution of the sample and the reagent.
 従来、試料および試薬の混合液の吸光度を測定することによって試料の分析を行う分析装置では、所定の期間ごとに試薬ブランク分析を行って、ブランク試料(試料中の目的成分濃度が0の場合の試料)および試薬の混合液の測定波長における吸光度(試薬ブランク値)を求め、この試薬ブランク値を補正値として試料および試薬の混合液の吸光度の算出に用いる検量線を設定することで試料の分析における分析精度を維持している。 Conventionally, in an analyzer that analyzes a sample by measuring the absorbance of a mixed solution of the sample and the reagent, a reagent blank analysis is performed every predetermined period and a blank sample (when the target component concentration in the sample is 0) Analyze the sample by determining the absorbance (reagent blank value) at the measurement wavelength of the sample and reagent mixture, and using this reagent blank value as a correction value to set the calibration curve used to calculate the absorbance of the sample and reagent mixture Analysis accuracy is maintained.
 例えば、下記特許文献1には、任意に決めた時間に自動で試薬ブランク分析を行う分析装置が記載されている。この分析装置では、1種類のブランク試料を用いることによって試薬ブランク分析を行っている。 For example, Patent Document 1 below describes an analyzer that automatically performs a reagent blank analysis at an arbitrarily determined time. In this analyzer, reagent blank analysis is performed by using one type of blank sample.
特開昭59-182347号公報JP 59-182347 A
 ところで、試薬ブランク分析は、ブランク試料の種類によって異なる検量線が作成される場合がある。このような場合、分析項目においては、どのようなブランク試料を用いて試薬ブランク分析を行うかが重要である。例えば、アルブミン(ALB)の分析では、試薬ブランク分析に用いるブランク試料としてイオン交換水を用いるよりも、生理食塩水を用いるのがより適している。 By the way, in the reagent blank analysis, different calibration curves may be created depending on the type of blank sample. In such a case, in the analysis item, what kind of blank sample is used to perform the reagent blank analysis is important. For example, in the analysis of albumin (ALB), it is more suitable to use physiological saline than ion-exchanged water as a blank sample used for reagent blank analysis.
 しかしながら、分析項目ごとに最適な種類のブランク試料を用いて試薬ブランク分析を行うには、複数の種類のブランク試料を用意し、分析項目ごとにブランク試料を変えながら分析を行わなければならないため、試薬ブランク分析に費やす時間が増大してしまうという問題があった。 However, in order to perform reagent blank analysis using the optimal type of blank sample for each analysis item, it is necessary to prepare multiple types of blank samples and perform analysis while changing the blank sample for each analysis item. There was a problem that the time spent for reagent blank analysis would increase.
 この発明は、上記に鑑みてなされたものであって、試薬ブランク分析に費やす時間を増大させることなく、分析項目ごとに最適なブランク試料を用いた試薬ブランク分析を行うことができる分析装置を提供することを目的とする。 The present invention has been made in view of the above, and provides an analyzer capable of performing a reagent blank analysis using an optimal blank sample for each analysis item without increasing the time spent for reagent blank analysis. The purpose is to do.
 上述した課題を解決し、目的を達成するために、この発明にかかる分析装置は、試料と、該試料の分析項目に応じた種類の試薬とを混合し、前記試料および前記試薬の混合液の吸光度を測定することによって前記試料の分析を行う分析装置において、前記分析項目と、該分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶手段と、試薬ブランク分析の対象となる分析項目を受け付ける受付手段と、前記ブランク試料が収容される複数の試料容器を保持する保持手段と、前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得する取得手段と、前記取得手段が取得したブランク試料の種類に適合する分析項目を前記ブランク試料情報に基づいて抽出する抽出手段と、前記抽出手段が抽出した分析項目と前記受付手段が受け付けた分析項目とを照合する照合手段と、前記照合手段の照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する決定手段と、前記決定手段が決定した分析順に従って試薬ブランク分析を実行する制御を行う制御手段と、を備えたことを特徴とする。 In order to solve the above-described problems and achieve the object, an analyzer according to the present invention mixes a sample and a reagent of a type corresponding to an analysis item of the sample, and provides a mixture of the sample and the reagent. In an analyzer for analyzing the sample by measuring absorbance, blank sample information storage for storing blank sample information in which the analysis item is associated with a type of blank sample to be used for reagent blank analysis of the analysis item Each of the plurality of sample containers held by the holding means, holding means for receiving the analysis items to be subjected to the reagent blank analysis, holding means for holding the plurality of sample containers in which the blank samples are accommodated, and Acquisition means for acquiring the type of the blank sample accommodated by the apparatus, and analysis items suitable for the type of blank sample acquired by the acquisition means. Extraction means for extracting based on the sample information, collation means for collating the analysis item extracted by the extraction means and the analysis item accepted by the acceptance means, and analysis items matched by the collation of the collation means, Reagent blank analysis according to each analysis item is determined according to the analysis order determined by the determination means for determining the analysis order of the reagent blank analysis so that at least the analysis items using the same type of blank sample are continuous. And a control means for performing control.
 上述した課題を解決し、目的を達成するために、この発明にかかる分析装置は、試料と、該試料の分析項目に応じた種類の試薬とを混合し、前記試料および前記試薬の混合液の吸光度を測定することによって前記試料の分析を行う分析装置において、前記分析項目と、該分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶手段と、試薬ブランク分析の対象となる分析項目を受け付ける受付手段と、前記ブランク試料が収容される複数の試料容器を保持する保持手段と、前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得する取得手段と、前記受付手段が受け付けた分析項目に適合するブランク試料の種類を前記ブランク試料情報に基づいて抽出する抽出手段と、前記抽出手段が抽出したブランク試料の種類と前記取得手段が取得したブランク試料の種類とを照合する照合手段と、前記照合手段の照合によって合致したブランク試料の種類に適合する分析項目に対し、各分析項目に応じた試薬ブランクの分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する決定手段と、前記決定手段が決定した分析順に従って試薬ブランク分析を実行する制御を行う制御手段と、を備えたことを特徴とする。 In order to solve the above-described problems and achieve the object, an analyzer according to the present invention mixes a sample and a reagent of a type corresponding to the analysis item of the sample, and provides a mixture of the sample and the reagent. In the analyzer for analyzing the sample by measuring absorbance, blank sample information storage for storing blank sample information in which the analysis item is associated with the type of blank sample to be used for the reagent blank analysis of the analysis item Each of the plurality of sample containers held by the holding means, holding means for receiving an analysis item to be subjected to reagent blank analysis, holding means for holding a plurality of sample containers in which the blank sample is accommodated, and Acquiring means for acquiring the type of the blank sample accommodated by the apparatus, and the type of blank sample suitable for the analysis item received by the receiving means. Extraction means for extracting based on rank sample information, collation means for collating the type of blank sample extracted by the extraction means with the type of blank sample obtained by the acquisition means, and a blank matched by the collation of the collation means Determination means for determining the analysis order of the reagent blanks corresponding to each analysis item with respect to the analysis items suitable for the type of sample so that the analysis items using at least the same type of blank sample are continuous, and the determination means Control means for performing control to execute reagent blank analysis in accordance with the determined analysis order.
 また、この発明にかかる分析装置は、上記の発明において、前記取得手段は、前記ブランク試料の種類と該ブランク試料の種類ごとに定められる前記試料容器の保持位置とを対応付ける保持位置情報を記憶した保持位置情報記憶手段と、前記保持位置における前記試料容器の有無を検出する検出手段と、を備え、前記保持位置情報記憶手段が記憶する前記保持位置情報および前記検出手段によって検出された結果を用いることにより、前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得することを特徴とする。 Further, in the analysis apparatus according to the present invention, in the above invention, the acquisition unit stores holding position information that associates the type of the blank sample with the holding position of the sample container determined for each type of the blank sample. A holding position information storing means; and a detecting means for detecting the presence or absence of the sample container at the holding position, and using the holding position information stored in the holding position information storing means and the result detected by the detecting means. Thus, the type of the blank sample stored in each of the plurality of sample containers held by the holding means is obtained.
 また、この発明にかかる分析装置は、上記の発明において、前記保持位置情報記憶手段が記憶する前記保持位置情報に基づいて、前記ブランク試料の種類と前記保持位置とを対応させた情報を出力する出力手段を備えたことを特徴とする。 Moreover, the analyzer according to the present invention outputs information in which the type of the blank sample and the holding position are associated with each other based on the holding position information stored in the holding position information storage means in the above invention. An output means is provided.
 また、この発明にかかる分析装置は、上記の発明において、前記ブランク試料情報記憶手段は、前記ブランク試料情報として分析項目ごとのブランク試料の種類とともに該ブランク試料の使用量を記憶し、前記受付手段が受け付けた分析項目に応じた試薬ブランク分析に必要なブランク試料の種類ごとの使用量を前記ブランク試料情報記憶手段が記憶する前記ブランク試料情報に基づいて算出する算出手段を備え、前記出力手段は、前記算出手段が算出した前記ブランク試料の種類ごとの使用量を出力することを特徴とする。 Moreover, in the analysis apparatus according to the present invention, in the above invention, the blank sample information storage unit stores the amount of the blank sample used as the blank sample information together with the type of the blank sample for each analysis item, and the reception unit Comprises calculating means for calculating the amount used for each type of blank sample necessary for the reagent blank analysis according to the analysis item received based on the blank sample information stored in the blank sample information storage means, and the output means The use amount for each type of the blank sample calculated by the calculation means is output.
 また、この発明にかかる分析装置は、上記の発明において、前記取得手段は、前記試料容器に設けられ、該試料容器内の前記ブランク試料の種類を識別する識別情報を記録した記録手段から該識別情報を読み取ることによって前記ブランク試料の種類を取得することを特徴とする。 In the analysis apparatus according to the present invention, in the above invention, the acquisition unit is provided in the sample container, and the identification unit is configured to record the identification information for identifying the type of the blank sample in the sample container. The type of the blank sample is acquired by reading information.
 この発明によれば、試料の分析項目と、該分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶手段と、試薬ブランク分析の対象となる分析項目を受け付ける受付手段と、前記ブランク試料が収容される複数の試料容器を保持する保持手段とを備えた分析装置が、前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得し、取得したブランク試料の種類に適合する分析項目を前記ブランク試料情報に基づいて抽出し、抽出した分析項目と前記受付手段が受け付けた分析項目とを照合し、照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定し、決定した分析順に従って試薬ブランク分析を実行する制御を行っているため、試薬ブランク分析に費やす時間を増大させることなく、分析項目ごとに最適なブランク試料を用いた試薬ブランク分析を行うことができる。 According to this invention, the blank sample information storage means for storing the blank sample information in which the analysis item of the sample and the type of the blank sample to be used for the reagent blank analysis of the analysis item are associated, and the target of the reagent blank analysis Each of the plurality of sample containers held by the holding means accommodates an analysis apparatus including a receiving means for receiving the analysis item and a holding means for holding the plurality of sample containers in which the blank samples are accommodated. The type of the blank sample is acquired, the analysis item that matches the type of the acquired blank sample is extracted based on the blank sample information, the extracted analysis item and the analysis item received by the reception unit are verified, and verification is performed. For analysis items that match each other, use at least the same type of blank sample in the reagent blank analysis order according to each analysis item. Since the analysis blanks are determined to be continuous and the reagent blank analysis is controlled in accordance with the determined analysis order, the optimal blank sample can be selected for each analysis item without increasing the time spent on the reagent blank analysis. The used reagent blank analysis can be performed.
図1は、この発明の実施の形態1にかかる分析装置の構成を示す模式図である。FIG. 1 is a schematic diagram showing the configuration of the analyzer according to the first embodiment of the present invention. 図2は、図1に示したブランク試料情報記憶部に記憶されたブランク試料情報を示す図である。FIG. 2 is a diagram showing blank sample information stored in the blank sample information storage unit shown in FIG. 図3は、図1に示した保持位置情報記憶部に記憶された保持位置情報を示す図である。FIG. 3 is a diagram showing the holding position information stored in the holding position information storage unit shown in FIG. 図4は、図1に示した分析装置による試薬ブランク分析処理の手順を示すフローチャートである。FIG. 4 is a flowchart showing the procedure of the reagent blank analysis process by the analyzer shown in FIG. 図5は、図1に示した出力部が出力する受付メニュー画面を示す図である。FIG. 5 is a diagram showing a reception menu screen output by the output unit shown in FIG. 図6は、図1に示した出力部が出力する保持位置情報画面を示す図である。FIG. 6 is a diagram illustrating a holding position information screen output by the output unit illustrated in FIG. 図7は、図1に示した抽出部が抽出した分析項目を示す図である。FIG. 7 is a diagram illustrating analysis items extracted by the extraction unit illustrated in FIG. 1. 図8は、図1に示した照合部の照合によって合致した分析項目を示す図である。FIG. 8 is a diagram illustrating analysis items that are matched by the collation performed by the collation unit illustrated in FIG. 1. 図9は、この発明の実施の形態2にかかる分析装置の構成を示す模式図である。FIG. 9 is a schematic diagram showing the configuration of the analyzer according to the second embodiment of the present invention. 図10は、図9に示した分析装置による試薬ブランク分析処理の手順を示すフローチャートである。FIG. 10 is a flowchart showing the procedure of the reagent blank analysis process by the analyzer shown in FIG. 図11は、図9に示した抽出部が抽出したブランク試料の種類を示す図である。FIG. 11 is a diagram showing types of blank samples extracted by the extraction unit shown in FIG. 図12は、図9に示した出力部が出力する使用量表示画面を示す図である。FIG. 12 is a diagram showing a usage amount display screen output by the output unit shown in FIG. 図13は、図9に示した照合部の照合によって合致したブランク試料の種類を示す図である。FIG. 13 is a diagram illustrating types of blank samples that are matched by collation performed by the collation unit illustrated in FIG. 9. 図14は、この発明の実施の形態3にかかる分析装置の構成を示す模式図である。FIG. 14 is a schematic diagram showing the configuration of the analyzer according to the third embodiment of the present invention. 図15は、図14に示した分析装置による試薬ブランク分析処理の手順を示すフローチャートである。FIG. 15 is a flowchart showing a procedure of reagent blank analysis processing by the analyzer shown in FIG. 図16は、図14に示した試料容器識別ラベルに記録されるコード番号とブランク試料の種類とを対応させた情報を示す図である。FIG. 16 is a diagram showing information in which the code number recorded on the sample container identification label shown in FIG. 14 is associated with the type of blank sample.
符号の説明Explanation of symbols
 1,2,3 分析装置
 10,60 測定部
 11  試料供給部
 11a 第1試料容器
 11b ラック
 11c 反応容器
 11f 試料容器識別ラベル
 12  試料保持部
 12a 第2試料容器
 13  反応槽
 13a ホイール
 14  試薬庫
 14a 試薬容器
 15  試料分注機構
 15a,16a ノズル
 15b,16b アーム
 16  試薬分注機構
 17  攪拌部
 18  測光部
 19  洗浄部
 20  容器有無検出部
 30,50,70  制御装置
 31,51,71  制御部
 32  入力部
 33  分析部
 34  出力部
 35,52,72  記憶部
 35a,52a ブランク試料情報記憶部
 35b 保持位置情報記憶部
 36,73 取得部
 37,53 抽出部
 38,54 照合部
 39,55 決定部
 56  算出部
 P1~Pn,p1~p5 位置
1, 2, 3 Analyzer 10, 60 Measuring unit 11 Sample supply unit 11a First sample vessel 11b Rack 11c Reaction vessel 11f Sample vessel identification label 12 Sample holder 12a Second sample vessel 13 Reaction tank 13a Wheel 14 Reagent chamber 14a Reagent Container 15 Sample dispensing mechanism 15a, 16a Nozzle 15b, 16b Arm 16 Reagent dispensing mechanism 17 Stirring unit 18 Photometric unit 19 Washing unit 20 Container presence / absence detecting unit 30, 50, 70 Control unit 31, 51, 71 Control unit 32 Input unit 33 Analyzing unit 34 Output unit 35, 52, 72 Storage unit 35a, 52a Blank sample information storage unit 35b Holding position information storage unit 36, 73 Acquisition unit 37, 53 Extraction unit 38, 54 Verification unit 39, 55 Determination unit 56 Calculation unit P 1 to P n , p 1 to p 5 positions
 以下、図面を参照して、この発明にかかる分析装置の好適な実施の形態を詳細に説明する。なお、この実施の形態によってこの発明が限定されるものではない。
(実施の形態1)
Hereinafter, preferred embodiments of an analyzer according to the present invention will be described in detail with reference to the drawings. The present invention is not limited to the embodiments.
(Embodiment 1)
 図1は、この発明の実施の形態1にかかる分析装置の構成を示す模式図である。分析装置1は、図1に示すように、測定部10および制御装置30を有する。測定部10は、検体等の試料と試薬とを反応容器11c内にそれぞれ分注し、反応容器11cで生じる反応を光学的に測定する。制御装置30は、測定部10を含む分析装置1全体の制御を行うとともに測定部10における測定データの分析を行う。分析装置1は、これら各部が連携することによって複数の試料の生化学分析を順次自動的に行う。 FIG. 1 is a schematic diagram showing the configuration of the analyzer according to the first embodiment of the present invention. As shown in FIG. 1, the analysis device 1 includes a measurement unit 10 and a control device 30. The measurement unit 10 dispenses a sample such as a specimen and a reagent into the reaction container 11c, and optically measures the reaction occurring in the reaction container 11c. The control device 30 controls the entire analyzer 1 including the measurement unit 10 and analyzes measurement data in the measurement unit 10. The analysis apparatus 1 automatically performs biochemical analysis of a plurality of samples sequentially in cooperation with each other.
 測定部10は、試料供給部11、試料保持部12、反応槽13、試薬庫14、試料分注機構15、試薬分注機構16、攪拌部17、測光部18、洗浄部19、および容器有無検出部20を有する。 The measurement unit 10 includes a sample supply unit 11, a sample holding unit 12, a reaction tank 13, a reagent storage 14, a sample dispensing mechanism 15, a reagent dispensing mechanism 16, a stirring unit 17, a photometric unit 18, a washing unit 19, and a container presence / absence A detection unit 20 is included.
 試料供給部11は、一般検体等の試料を収容した第1試料容器11aを保持したラック11bを搬送することによって、第1試料容器11aを試料吸引位置に搬送する。試料吸引位置に搬送された第1試料容器11a内の試料は、試料分注機構15によって、試料の分注位置に搬送された反応容器11c内に分注される。 The sample supply unit 11 transports the first sample container 11a to the sample suction position by transporting the rack 11b holding the first sample container 11a containing a sample such as a general specimen. The sample in the first sample container 11a conveyed to the sample suction position is dispensed by the sample dispensing mechanism 15 into the reaction container 11c conveyed to the sample dispensing position.
 試料保持部12は、保持位置Pv(v=1,…,n,…,30:nは自然数)に一般検体以外の各種試料(ブランク試料、緊急検体等)を収容する第2試料容器12aを保持するための凹状の収容部を有する。試料保持部12は、制御装置30の制御のもと、図示しない駆動機構が駆動することによって、試料保持部12の中心を通る鉛直線を回転軸として時計回りまたは反時計回りに回動自在であり、所定の第2試料容器12aを試料分注機構15による試料の吸引位置まで移送する。なお、試料保持部12は、30個の収容部を有するものを例示したが、これに限らず、複数の収容部を有していればよい。 The sample holder 12 is a second sample container 12a that accommodates various samples (blank samples, emergency samples, etc.) other than general samples at holding positions P v (v = 1,..., N,..., 30: n is a natural number). Has a concave accommodating portion. The sample holding unit 12 can be rotated clockwise or counterclockwise about a vertical line passing through the center of the sample holding unit 12 as a rotation axis by driving a driving mechanism (not shown) under the control of the control device 30. Yes, the predetermined second sample container 12a is transferred to the sample suction position by the sample dispensing mechanism 15. In addition, although the sample holding | maintenance part 12 illustrated what has 30 accommodating parts, it should just have not only this but a several accommodating part.
 反応槽13は、図示しない保温部材と、ホイール13aとを有する。ホイール13aは、複数の反応容器11cを保持し、図示しない駆動機構によって回転して反応容器11cを周方向に移送する。反応槽13は、図示しない円盤状の蓋によって覆われており、ホイール13aの半径方向内側と外側とに配置される図示しない保温部材とともに、内部の温度を人間の体温程度に保温する保温槽を構成している。 The reaction tank 13 has a heat insulating member (not shown) and a wheel 13a. The wheel 13a holds a plurality of reaction vessels 11c and rotates by a drive mechanism (not shown) to transfer the reaction vessels 11c in the circumferential direction. The reaction tank 13 is covered with a disk-shaped lid (not shown), and a heat insulation tank that keeps the internal temperature at a human body temperature is provided along with a heat insulation member (not shown) disposed on the inside and outside in the radial direction of the wheel 13a. It is composed.
 試薬庫14は、反応容器11c内に分注される試薬が収容された試薬容器14aを着脱自在に複数収納する。試薬庫14は、制御装置30の制御のもと、図示しない駆動機構が駆動することによって、試薬庫14の中心を通る鉛直線を回転軸として時計回りまたは反時計回りに回動自在であり、所定の試薬容器14aを試薬分注機構16による試薬吸引位置まで移送する。 The reagent storage 14 detachably stores a plurality of reagent containers 14a in which reagents to be dispensed in the reaction container 11c are stored. The reagent storage 14 can be rotated clockwise or counterclockwise about a vertical line passing through the center of the reagent storage 14 as a rotation axis by driving a drive mechanism (not shown) under the control of the control device 30. The predetermined reagent container 14a is transferred to the reagent suction position by the reagent dispensing mechanism 16.
 試料分注機構15は、試料の吸引および吐出を行うノズル15aが先端部に取り付けられたアーム15bを有する。アーム15bは、鉛直方向への昇降および自身の基端部を通過する鉛直線を中心軸とする回転を自在に行う。試料分注機構15は、吸排シリンジまたは圧電素子を用いた吸排機構を有する。試料分注機構15は、試料供給部11の試料吸引位置に移送された第1試料容器11a内からノズル15aによって試料を吸引し、アーム15bを図中反時計回りに旋回させ、反応槽13上の試料吐出位置に搬送された反応容器11cに、試料を吐出する。 The sample dispensing mechanism 15 has an arm 15b to which a nozzle 15a for sucking and discharging a sample is attached at the tip. The arm 15b freely moves up and down in the vertical direction and rotates around a vertical line passing through its base end as a central axis. The sample dispensing mechanism 15 has an intake / exhaust mechanism using an intake / exhaust syringe or a piezoelectric element. The sample dispensing mechanism 15 sucks the sample from the first sample container 11a transferred to the sample suction position of the sample supply unit 11 by the nozzle 15a, rotates the arm 15b counterclockwise in the drawing, The sample is discharged into the reaction container 11c conveyed to the sample discharge position.
 試薬分注機構16は、試薬の吸引および吐出を行うノズル16aが先端部に取り付けられたアーム16bを有する。アーム16bは、鉛直方向への昇降および自身の基端部を通過する鉛直線を中心軸とする回転を自在に行う。試薬分注機構16は、図示しない吸排シリンジまたは圧電素子を用いた吸排機構を有する。試薬分注機構16は、試薬庫14上の所定位置に移送された試薬容器14a内の試薬をノズル16aによって吸引し、アーム16bを図中時計回りに旋回させ、反応槽13上の所定位置に搬送された反応容器11cに、試薬を吐出する。 The reagent dispensing mechanism 16 has an arm 16b to which a nozzle 16a for sucking and discharging the reagent is attached to the tip. The arm 16b freely moves up and down in the vertical direction and rotates around the vertical line passing through its base end as a central axis. The reagent dispensing mechanism 16 has an intake / exhaust mechanism using an unillustrated intake / exhaust syringe or piezoelectric element. The reagent dispensing mechanism 16 sucks the reagent in the reagent container 14a transferred to a predetermined position on the reagent storage 14 by the nozzle 16a, rotates the arm 16b clockwise in the drawing, and moves the arm 16b to the predetermined position on the reaction tank 13. The reagent is discharged into the transported reaction container 11c.
 攪拌部17は、反応容器11cに分注された試薬と試料の混合液の攪拌を行い、試料と試薬の反応を促進させる。 The stirring unit 17 stirs the mixed solution of the reagent and the sample dispensed in the reaction vessel 11c to promote the reaction between the sample and the reagent.
 測光部18は、所定の測定位置に移送された反応容器11cに光源18aから測定光を照射し、反応容器11c内の試料と試薬との混合液を透過した光を分光し、受光素子18bによる各波長光の強度測定を行うことによって、分析対象である試料と試薬との混合液に特有の波長の吸光度を測定する。 The photometry unit 18 irradiates the reaction vessel 11c, which has been transferred to a predetermined measurement position, with measurement light from the light source 18a, disperses the light transmitted through the mixture of the sample and the reagent in the reaction vessel 11c, and uses the light receiving element 18b. By measuring the intensity of each wavelength light, the absorbance at a wavelength peculiar to the mixed solution of the sample to be analyzed and the reagent is measured.
 洗浄部19は、図示しないノズルによって、測光部18による測定が終了した反応容器11c内の混合液を吸引して排出するとともに、洗剤や洗浄水等の洗浄液を注入および吸引することで洗浄を行う。 The cleaning unit 19 performs cleaning by sucking and discharging the mixed solution in the reaction vessel 11c that has been measured by the photometry unit 18 by using a nozzle (not shown) and injecting and sucking cleaning liquid such as detergent and cleaning water. .
 容器有無検出部20は、試料保持部12の近傍に配置される。容器有無検出部20は、検出手段として、保持位置Pvにおける第2試料容器12aの有無を検出する。容器有無検出部20は、例えば、光学的に第2試料容器12aの有無を検出する光センサによって実現される。容器有無検出部20は、第2試料容器12aを検出すると、検出信号を制御装置30に出力する。 The container presence / absence detection unit 20 is disposed in the vicinity of the sample holding unit 12. The container presence / absence detection unit 20 detects the presence / absence of the second sample container 12a at the holding position Pv as detection means. The container presence / absence detection unit 20 is realized by, for example, an optical sensor that optically detects the presence / absence of the second sample container 12a. The container presence / absence detection unit 20 outputs a detection signal to the control device 30 when detecting the second sample container 12a.
 制御装置30は、制御部31、入力部32、分析部33、出力部34、記憶部35、取得部36、抽出部37、照合部38、および決定部39を有する。制御部31は、CPU等によって実現され、分析装置1の各部の処理および動作を制御する。制御部31は、これらの各構成部位に入出力される情報について所定の入出力制御を行い、かつ、この情報に対して所定の情報処理を行う。 The control device 30 includes a control unit 31, an input unit 32, an analysis unit 33, an output unit 34, a storage unit 35, an acquisition unit 36, an extraction unit 37, a collation unit 38, and a determination unit 39. The control unit 31 is realized by a CPU or the like, and controls processing and operation of each unit of the analyzer 1. The control unit 31 performs predetermined input / output control on information input / output to / from each of these components, and performs predetermined information processing on this information.
 入力部32は、キーボードやマウス等によって実現され、試料数あるいは分析項目等の各種情報の入力が可能である。なお、入力部32は、受付手段として、試薬ブランク分析に対応する分析項目の入力を受け付ける。 The input unit 32 is realized by a keyboard, a mouse, or the like, and can input various information such as the number of samples or analysis items. The input unit 32 receives input of analysis items corresponding to reagent blank analysis as receiving means.
 分析部33は、測光部18によって測定された測定結果をもとに、試料内における検出対象物の濃度を求め、試料の成分分析等を行う。出力部34は、ディスプレイパネルやプリンタ等によって実現され、出力手段として、試料の分析データや警報等の各種情報を出力する。また、出力部34は、入力部32による試薬ブランク分析に対応する分析項目の入力を補助する情報の出力が可能である。 The analysis unit 33 obtains the concentration of the detection target in the sample based on the measurement result measured by the photometry unit 18, and performs component analysis of the sample. The output unit 34 is realized by a display panel, a printer, or the like, and outputs various types of information such as sample analysis data and alarms as output means. The output unit 34 can output information that assists the input of analysis items corresponding to the reagent blank analysis by the input unit 32.
 記憶部35は、ブランク試料情報記憶部35aおよび保持位置情報記憶部35bを有する。ブランク試料情報記憶部35aは、ブランク試料情報記憶手段として、試料の分析項目と、この分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶する。図2は、各分析項目Ai(i=1,…,m:mは自然数)に、分析項目Aiの試薬ブランク分析に用いるべきブランク試料の種類Bj(j=1,…,n:nは自然数)を対応させたブランク試料情報テーブル35a-1を示す図である。ブランク試料情報テーブル35a-1では、例えば、種類B1のブランク試料が、分析項目A1の試薬ブランク分析に用いるべきブランク試料として対応付けられていることを示す。 The storage unit 35 includes a blank sample information storage unit 35a and a holding position information storage unit 35b. The blank sample information storage unit 35a stores, as blank sample information storage means, blank sample information in which sample analysis items are associated with types of blank samples to be used for reagent blank analysis of the analysis items. FIG. 2 shows, for each analysis item A i (i = 1,..., M: m is a natural number), a blank sample type B j (j = 1,..., N: to be used for the reagent blank analysis of the analysis item A i. FIG. 11 is a diagram showing a blank sample information table 35a-1 in which n is a natural number). In the blank sample information table 35a-1, for example, indicates that the blank sample type B 1 is, it is associated as blank sample to be used for the reagent blank analysis of analysis items A 1.
 保持位置情報記憶部35bは、保持位置情報記憶手段として、ブランク試料の種類と種類ごとに定められる第2試料容器12aの保持位置とを対応付ける保持位置情報を記憶する。図3は、保持位置P1~Pnと、保持位置P1~Pnに保持すべきブランク試料の種類B1~Bnとを対応させた保持位置情報テーブル35b-1を示す図である。保持位置情報テーブル35b-1は、例えば、保持位置P1に種類B1のブランク試料を保持すべきことを示す。なお、ブランク試料を保持する位置が連続して隣り合うものを例示したが、これに限らず、複数のブランク試料をブランク試料の種類ごとに予め決められた保持位置に保持できればよい。例えば、保持位置P1にブランク試料を保持させ、保持位置P2にブランク試料を保持させず、保持位置P3にブランク試料を保持させてもよい。 The holding position information storage unit 35b stores, as holding position information storage means, holding position information that associates the type of blank sample with the holding position of the second sample container 12a determined for each type. Figure 3 is a diagram showing a holding position P 1 ~ P n, the holding position P 1 ~ type B 1 ~ holding position information table 35b-1 that the B n in correspondence of the blank sample to be retained in the P n . Holding position information table 35b-1, for example, indicates that it should retain the blank sample type B 1 in the holding position P 1. In addition, although the example which the position which hold | maintains a blank sample adjoins continuously was illustrated, it is not restricted to this, What is necessary is just to be able to hold | maintain a several blank sample in the holding position predetermined for every kind of blank sample. For example, the blank sample may be held at the holding position P 1, and the blank sample may be held at the holding position P 3 without holding the blank sample at the holding position P 2 .
 記憶部35は、情報を磁気的に記憶するハードディスクと、分析装置1が処理を実行する際にこの処理にかかわる各種プログラムをハードディスクから読み出して電気的に記憶するメモリとを有する。記憶部35は、演算処理された吸光度等を含む試料の分析データを記憶する。 The storage unit 35 includes a hard disk that magnetically stores information, and a memory that electrically reads various programs related to this process from the hard disk when the analyzer 1 executes the process. The storage unit 35 stores analysis data of the sample including the absorbance and the like that have been subjected to arithmetic processing.
 取得部36は、取得手段として、試料保持部12によって保持された複数の第2試料容器12aの各々が収容するブランク試料の種類を取得する。取得部36は、保持位置情報記憶部35bが記憶する保持位置情報および容器有無検出部20によって検出された結果を用いることにより、試料保持部12によって保持された複数の第2試料容器12aの各々が収容するブランク試料の種類を取得する。 The acquisition unit 36 acquires the type of blank sample accommodated in each of the plurality of second sample containers 12a held by the sample holding unit 12 as an acquisition unit. The acquisition unit 36 uses each of the plurality of second sample containers 12a held by the sample holding unit 12 by using the holding position information stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20. The type of the blank sample accommodated by is acquired.
 抽出部37は、取得部36が取得したブランク試料の種類に適合する分析項目をブランク試料情報記憶部35aに記憶されたブランク試料情報に基づいて抽出する。 The extraction unit 37 extracts analysis items that match the type of blank sample acquired by the acquisition unit 36 based on the blank sample information stored in the blank sample information storage unit 35a.
 照合部38は、抽出部37が抽出した分析項目と入力部32が受け付けた分析項目とを照合する。 The collation unit 38 collates the analysis item extracted by the extraction unit 37 and the analysis item received by the input unit 32.
 決定部39は、照合部38の照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する。 The determination unit 39 determines the analysis order of the reagent blank analysis corresponding to each analysis item for the analysis items matched by the verification of the verification unit 38 so that the analysis items using at least the same type of blank sample are continuous. .
 以上のように構成された分析装置1では、順次搬送される複数の反応容器11cに対して、試薬分注機構16が、試薬容器14aから反応容器11cに試薬を分注し、試料分注機構15が、第1試料容器11aから反応容器11cに所定量の試料を分注する。続いて、攪拌部17が、反応容器11c内の試薬と試料とを攪拌して反応させた後、測光部18が、試薬と試料との混合液の吸光度測定を行う。その後、分析部33は、測光部18の測定結果を分析する演算を行い、試料の成分分析等を自動的に行う。また、洗浄部19が、測光部18による測定が終了した反応容器11cの洗浄・乾燥を行う。 In the analyzer 1 configured as described above, the reagent dispensing mechanism 16 dispenses a reagent from the reagent container 14a to the reaction container 11c with respect to the plurality of reaction containers 11c that are sequentially transported, and the sample dispensing mechanism. 15 dispenses a predetermined amount of sample from the first sample container 11a to the reaction container 11c. Subsequently, after the stirring unit 17 stirs and reacts the reagent and the sample in the reaction vessel 11c, the photometry unit 18 measures the absorbance of the mixed solution of the reagent and the sample. Thereafter, the analysis unit 33 performs an operation for analyzing the measurement result of the photometry unit 18 and automatically performs a component analysis of the sample. In addition, the cleaning unit 19 cleans and dries the reaction vessel 11 c that has been measured by the photometry unit 18.
 次に、図4に示したフローチャートを参照して、分析装置1が行う試薬ブランク分析処理について説明する。まず、分析装置1は、試薬ブランク分析に対応する分析項目の受け付けがあるか否かを判断する(ステップS101)。試薬ブランク分析に対応する分析項目の受け付けは、例えば、出力部34が出力する受付メニュー画面を用いて入力部32を介して行われる。 Next, the reagent blank analysis process performed by the analyzer 1 will be described with reference to the flowchart shown in FIG. First, the analyzer 1 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S101). The reception of the analysis item corresponding to the reagent blank analysis is performed via the input unit 32 using the reception menu screen output by the output unit 34, for example.
 図5は、出力部34が出力する試薬ブランク分析に対応する分析項目の受け付けを行うための受付メニュー画面の表示例である。操作者が、入力部32を介して受付メニュー画面34a上の分析項目A1~Amから所定の分析項目を選択し、登録することによって、試薬ブランク分析に対応する分析項目の受け付けが行われる。例えば、分析項目A1,A3,およびA4を登録する場合、操作者が、マウス等を介して受付メニュー画面34a上の各分析項目ボタン34a-3,34a-4,34a-5を選択した後、登録ボタン34a-1を選択することによって分析項目A1,A3,A4が受け付けられる。なお、ここでは、出力部34が出力する受付メニュー画面34aを用いて分析項目の受け付けを行う場合を例示したが、キーボードを介して、分析項目ごとに割り当てられたコードを入力するようにしてもよい。 FIG. 5 is a display example of a reception menu screen for receiving an analysis item corresponding to the reagent blank analysis output by the output unit 34. Operator selects a reception menu analysis item A 1 ~ A predetermined analysis item from m on the screen 34a through the input unit 32, by registering, receiving the analysis item corresponding to the reagent blank analysis is performed . For example, when registering analysis items A 1 , A 3 , and A 4 , the operator selects each analysis item button 34 a-3, 34 a-4, 34 a-5 on the reception menu screen 34 a via a mouse or the like. After that, the analysis items A 1 , A 3 , A 4 are accepted by selecting the registration button 34a-1. Here, the case where the analysis item is received using the reception menu screen 34a output by the output unit 34 is illustrated, but the code assigned to each analysis item may be input via the keyboard. Good.
 ステップS101で試薬ブランク分析に対応する分析項目の受け付けがある場合(ステップS101:Yes)、出力部34は、保持位置情報画面を出力する(ステップS102)。図6は、保持位置情報記憶部35bが記憶する保持位置情報に基づいて、出力部34がディスプレイパネルに出力する保持位置情報画面の表示例である。同図に示す保持位置情報画面34bは、例えば、受付メニュー画面34a上の保持位置ボタン34a-2を選択することにより出力される。保持位置情報画面34bは、保持位置P1に、種類B1のブランク試料を保持すべきことを示す。なお、保持位置ごとに保持すべきブランク試料の種類は予め定められているため、保持位置情報画面34bを出力しなくてもよい。一方、ステップS101で試薬ブランク分析に対応する分析項目の受け付けが行われなかった場合(ステップS101:No)、制御部31はこの判断処理を繰り返す。 When an analysis item corresponding to the reagent blank analysis is received in step S101 (step S101: Yes), the output unit 34 outputs a holding position information screen (step S102). FIG. 6 is a display example of a holding position information screen that the output unit 34 outputs to the display panel based on the holding position information stored in the holding position information storage unit 35b. The holding position information screen 34b shown in the figure is output, for example, by selecting the holding position button 34a-2 on the reception menu screen 34a. Holding position information screen 34b is a holding position P 1, it indicates that it should retain the blank sample type B 1. Since the type of blank sample to be held for each holding position is determined in advance, the holding position information screen 34b need not be output. On the other hand, when the analysis item corresponding to the reagent blank analysis is not received in step S101 (step S101: No), the control unit 31 repeats this determination process.
 ステップS102で出力部34が保持位置情報画面を出力した後、制御部31は、試料保持部12への第2試料容器12aのセットが完了したか否かを判断する(ステップS103)。このステップS103における判断は、例えば、セット完了を示す信号、すなわち試薬ブランク分析を開始する旨の信号が入力部32から制御部31に出力されたか否かによって行われる。 After the output unit 34 outputs the holding position information screen in step S102, the control unit 31 determines whether or not the setting of the second sample container 12a to the sample holding unit 12 is completed (step S103). The determination in step S103 is performed based on, for example, whether or not a signal indicating completion of setting, that is, a signal indicating that reagent blank analysis is started is output from the input unit 32 to the control unit 31.
 ステップS103で試料保持部12への第2試料容器12aのセットが完了した場合(ステップS103:Yes)、容器有無検出部20は、ブランク試料が保持される保持位置P1~Pnにおける第2試料容器12aの有無を検出する(ステップS104)。この検出は、試料保持部12が試料保持部12の中心を通る鉛直線を回転軸として時計回りまたは反時計回りに一周する間に行われる。一方、試料保持部12への第2試料容器12aのセットが完了していない場合(ステップS103:No)、出力部34は、この判断処理を繰り返す。 When the setting of the second sample container 12a to the sample holding unit 12 is completed in step S103 (step S103: Yes), the container presence / absence detection unit 20 performs the second operation at the holding positions P 1 to P n where the blank sample is held. The presence or absence of the sample container 12a is detected (step S104). This detection is performed while the sample holder 12 makes a round clockwise or counterclockwise with a vertical line passing through the center of the sample holder 12 as a rotation axis. On the other hand, when the setting of the second sample container 12a to the sample holding unit 12 is not completed (step S103: No), the output unit 34 repeats this determination process.
 ステップS104で保持位置P1~Pnにおける第2試料容器12aの有無を検出した後、取得部36は、試料保持部12に保持された第2試料容器12a内のブランク試料の種類を取得する(ステップS105)。具体的には、取得部36は、保持位置情報記憶部35bに記憶されたブランク試料の種類ごとに定められる第2試料容器12aの保持位置情報と、容器有無検出部20によって検出された結果を用いることにより、ブランク試料の種類を取得する。例えば、容器有無検出部20が保持位置P1に第2試料容器12aが有ることを検出した場合、保持位置P1に対応するブランク試料B1が第2試料容器12aに収容されているものとする。 After detecting the presence or absence of the second sample container 12a at the holding positions P 1 to P n in step S104, the acquiring unit 36 acquires the type of blank sample in the second sample container 12a held by the sample holding unit 12. (Step S105). Specifically, the acquisition unit 36 obtains the holding position information of the second sample container 12a determined for each type of blank sample stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20. By using it, the type of the blank sample is acquired. For example, as when the container presence detector 20 detects that the second sample container 12a is in the holding position P 1, the blank sample B 1 corresponding to the holding position P 1 is accommodated in the second sample vessel 12a To do.
 その後、抽出部37が、取得部36が取得したブランク試料の種類に適合する分析項目を抽出する(ステップS106)。この分析項目の抽出は、ブランク試料情報記憶部35aに記憶されたブランク試料情報に基づいて行う。図7は、抽出部37が抽出した分析項目の例を示す図である。図7は、取得部36がブランク試料の種類B1およびB2を取得した場合を示すものである。抽出部37は、種類B1のブランク試料に適合する分析項目として分析項目A1を抽出し、種類B2のブランク試料に適合する分析項目として分析項目A2~A5を抽出する。 Then, the extraction part 37 extracts the analysis item suitable for the kind of blank sample which the acquisition part 36 acquired (step S106). The analysis item is extracted based on the blank sample information stored in the blank sample information storage unit 35a. FIG. 7 is a diagram illustrating an example of analysis items extracted by the extraction unit 37. FIG. 7 shows a case where the acquisition unit 36 acquires the types B 1 and B 2 of the blank sample. The extraction unit 37 extracts the analysis item A 1 as an analysis item suitable for the type B 1 blank sample, and extracts the analysis items A 2 to A 5 as analysis items suitable for the type B 2 blank sample.
 その後、照合部38が、抽出部37が抽出した分析項目と入力部32が受け付けた分析項目(以下、受付分析項目と書く)とを照合する(ステップS107)。図8は、図7に示す抽出部37が抽出した分析項目A1~A5の中で照合部38の照合によって合致した分析項目を示す図である。図8は、ステップS101で受付分析項目がA1,A3およびA4の場合を示しており、図7に示す分析項目A1~A5の中で合致した分析項目A1,A3およびA4と、取得したブランク試料の種類との対応関係を示す。 Thereafter, the collation unit 38 collates the analysis item extracted by the extraction unit 37 with the analysis item received by the input unit 32 (hereinafter referred to as reception analysis item) (step S107). FIG. 8 is a diagram showing analysis items matched by collation by the collation unit 38 among the analysis items A 1 to A 5 extracted by the extraction unit 37 shown in FIG. Figure 8 is accepted analysis items in step S101 shows the case of A 1, A 3 and A 4, analysis item A 1, A 3 and that meet in the analysis item A 1 ~ A 5 shown in FIG. 7 and a 4, showing the correspondence between the type of the obtained blank sample.
 その後、制御部31は、受付分析項目の試薬ブランク分析を全て行うことが可能であるか否かを判断する(ステップS108)。この判断は、照合部38の照合によって合致した分析項目の試薬ブランク分析を行った場合に、受付分析項目の試薬ブランク分析を全て行うことが可能であるか否かによって判断される。 Thereafter, the control unit 31 determines whether or not it is possible to perform all of the reagent blank analysis of the received analysis items (step S108). This determination is made based on whether or not all the reagent blank analyzes of the received analysis items can be performed when the reagent blank analysis of the analysis items matched by the verification of the verification unit 38 is performed.
 受付分析項目の試薬ブランク分析を全て行うことが可能である場合(ステップS108:Yes)、決定部39は、照合部38の照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を決定する(ステップS109)。この分析順は、同一種類のブランク試料を使用する分析項目が連続するように決定する。図8に示すように、種類B2のブランク試料を使用する分析項目がA3およびA4である場合、分析項目A3およびA4の試薬ブランク分析が連続するように分析順を決定する。一方、受付分析項目の試薬ブランク分析を全て行うことが可能でない場合(ステップS108:No)、出力部34は、試薬ブランク分析処理に異常があることを示す異常情報を出力する(ステップS110)。その後、制御部31は、本処理を終了する。 When it is possible to perform all the reagent blank analysis of the received analysis items (step S108: Yes), the determination unit 39 performs the reagent blank analysis corresponding to each analysis item with respect to the analysis item matched by the collation of the collation unit 38. The analysis order is determined (step S109). This analysis order is determined so that analysis items using the same type of blank sample are continuous. As shown in FIG. 8, analysis item using the blank sample type B 2 be a A 3 and A 4, the reagent blank analysis of analysis items A 3 and A 4 determines the analysis order to continuously. On the other hand, when it is not possible to perform all the reagent blank analysis of the reception analysis item (step S108: No), the output unit 34 outputs abnormality information indicating that the reagent blank analysis process is abnormal (step S110). Then, the control part 31 complete | finishes this process.
 ステップS109で受付分析項目の試薬ブランク分析の分析順を決定した後、制御部31は、決定部39が決定した分析順に従って受付分析項目の試薬ブランク分析を分析装置1に実行させる(ステップS111)。その後、制御部31は、本処理を終了する。 After determining the analysis order of the reagent blank analysis of the reception analysis item in step S109, the control unit 31 causes the analyzer 1 to perform the reagent blank analysis of the reception analysis item according to the analysis order determined by the determination unit 39 (step S111). . Then, the control part 31 complete | finishes this process.
 この発明の実施の形態1では、試料の分析項目と、分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶部35aと、試薬ブランク分析の対象となる分析項目を受け付ける入力部32と、ブランク試料が収容される複数の第2試料容器12aを保持する試料保持部12とを備えた分析装置1が、試料保持部12によって保持された複数の第2試料容器12aの各々が収容するブランク試料の種類を取得し、取得したブランク試料の種類に適合する分析項目をブランク試料情報に基づいて抽出し、抽出した分析項目と入力部32が受け付けた分析項目とを照合し、照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定し、決定した分析順に従って試薬ブランク分析を実行する制御を行っているため試薬ブランク分析に費やす時間を増大させることなく、分析項目ごとに最適なブランク試料を用いた試薬ブランク分析を行うことができる。 In Embodiment 1 of the present invention, a blank sample information storage unit 35a for storing blank sample information in which a sample analysis item is associated with a type of blank sample to be used for a reagent blank analysis of the analysis item, and a reagent blank analysis The sample holding unit 12 holds the analyzer 1 including an input unit 32 that receives an analysis item that is a target of the sample and a sample holding unit 12 that holds a plurality of second sample containers 12a in which blank samples are stored. The type of blank sample accommodated in each of the plurality of second sample containers 12a is acquired, analysis items that match the acquired type of blank sample are extracted based on the blank sample information, and the extracted analysis items and input unit 32 are provided. The analysis order received is collated, and the analysis order of the reagent blank analysis according to each analysis item is set to at least the analysis item matched by the collation. The analysis items that use different types of blank samples are determined to be continuous, and the reagent blank analysis is controlled according to the determined order of analysis, so there is no increase in the time spent on reagent blank analysis. Reagent blank analysis using an optimal blank sample can be performed.
 また、実施の形態1では、出力部34が、保持位置情報記憶部35bが記憶する保持位置情報に基づいて、ブランク試料の種類と保持位置とを対応させた情報を出力するようにしているため、操作者は、試料保持部12への種類ごとのブランク試料のセットを確実に行うことができる。 In the first embodiment, the output unit 34 outputs information that associates the type of the blank sample with the holding position based on the holding position information stored in the holding position information storage unit 35b. The operator can reliably set the blank sample for each type in the sample holder 12.
(実施の形態2)
 次に、この発明の実施の形態2について説明する。図9は、この発明の実施の形態2にかかる分析装置の構成を示す模式図である。図9に示す分析装置2は、測定部10および制御装置50を有する。なお、実施の形態1と同一構成部分には同一符号を付している。制御装置50の制御部51は、抽出部53、照合部54、決定部55、算出部56を有する。また、記憶部52は、ブランク試料情報記憶部52aを有する。
(Embodiment 2)
Next, a second embodiment of the present invention will be described. FIG. 9 is a schematic diagram showing the configuration of the analyzer according to the second embodiment of the present invention. The analysis device 2 illustrated in FIG. 9 includes a measurement unit 10 and a control device 50. In addition, the same code | symbol is attached | subjected to the same component as Embodiment 1. FIG. The control unit 51 of the control device 50 includes an extraction unit 53, a collation unit 54, a determination unit 55, and a calculation unit 56. The storage unit 52 includes a blank sample information storage unit 52a.
 抽出部53は、入力部32が受け付けた分析項目(以下、受付分析項目と書く)に適合するブランク試料の種類を上述したブランク試料情報に基づいて抽出する。照合部54は、抽出部53が抽出したブランク試料の種類と取得部36が取得したブランク試料の種類とを照合する。決定部55は、照合部54の照合によって合致したブランク試料の種類に適合する分析項目に対し、各分析項目に応じた試薬ブランクの分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する。算出部56は、受付分析項目に応じた試薬ブランク分析に必要なブランク試料の種類ごとの使用量をブランク試料情報記憶部52aが記憶するブランク試料情報に基づいて算出する。ブランク試料情報記憶部52aは、ブランク試料情報として分析項目ごとのブランク試料の種類とともにブランク試料の使用量を記憶する。 The extraction unit 53 extracts the type of blank sample that matches the analysis item received by the input unit 32 (hereinafter referred to as reception analysis item) based on the blank sample information described above. The collation unit 54 collates the type of the blank sample extracted by the extraction unit 53 and the type of the blank sample acquired by the acquisition unit 36. For the analysis item that matches the type of the blank sample matched by the collation of the collation unit 54, the determination unit 55 sets the analysis order of the reagent blanks according to each analysis item to the analysis item that uses at least the same type of blank sample. Decide to be continuous. The calculation part 56 calculates the usage-amount for every kind of blank sample required for the reagent blank analysis according to a reception analysis item based on the blank sample information which the blank sample information storage part 52a memorize | stores. The blank sample information storage unit 52a stores the amount of the blank sample used together with the type of the blank sample for each analysis item as blank sample information.
 次に、図10に示したフローチャートを参照して、分析装置2が行う試薬ブランク分析処理について説明する。まず、分析装置2は、試薬ブランク分析に対応する分析項目の受け付けがあるか否かを判断する(ステップS201)。試薬ブランク分析に対応する分析項目の受け付けは、実施の形態1と同様に、例えば、出力部34がディスプレイパネルに出力する受付メニュー画面34aを用いて入力部32を介して行う。 Next, the reagent blank analysis process performed by the analyzer 2 will be described with reference to the flowchart shown in FIG. First, the analyzer 2 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S201). The analysis item corresponding to the reagent blank analysis is received via the input unit 32 using the reception menu screen 34a output to the display panel by the output unit 34, for example, as in the first embodiment.
 ステップS201で試薬ブランク分析に対応する分析項目の受け付けがある場合(ステップS201:Yes)、抽出部53が、受付分析項目に適合するブランク試料の種類をブランク試料情報記憶部52aに記憶されたブランク試料情報に基づいて抽出する(ステップS202)。図11は、抽出部53が抽出したブランク試料の種類を示す図である。図11に示す場合、抽出部53は、受付分析項目A1に適合するブランク試料の種類として種類B1を抽出し、受付分析項目A3およびA4に適合するブランク試料の種類として種類B2を抽出する。一方、ステップS201で試薬ブランク分析に対応する分析項目の受け付けがない場合(ステップS201:No)、制御部51はこの判断処理を繰り返す。 When the analysis item corresponding to the reagent blank analysis is received in step S201 (step S201: Yes), the extraction unit 53 stores the blank sample type that matches the received analysis item in the blank sample information storage unit 52a. Extraction is performed based on the sample information (step S202). FIG. 11 is a diagram illustrating the types of blank samples extracted by the extraction unit 53. The case shown in FIG. 11, the extraction unit 53 extracts the type B 1 as a blank sample type conforming to the acceptance analysis item A 1, type B 2 as a blank kinds of samples conform to the accepted analysis item A 3 and A 4 To extract. On the other hand, when no analysis item corresponding to the reagent blank analysis is received in step S201 (step S201: No), the control unit 51 repeats this determination process.
 ステップS202でブランク試料の種類が抽出された後、算出部56は、受付分析項目に応じた試薬ブランク分析に必要なブランク試料の種類ごとの使用量を算出する(ステップS203)。この使用量の算出は、ブランク試料情報記憶部52aがブランク試料の種類とともに記憶するブランク試料の使用量に基づいて行う。その後、出力部34は、算出部56が算出したブランク試料の使用量を出力する(ステップS204)。図12は、ブランク試料の種類と保持位置P1~Pnとを対応させた情報に、さらに算出部56が算出した使用量をブランク試料の種類に対応させた使用量表示画面54aである。使用量表示画面54aは、種類B1のブランク試料10μLを保持位置P1に保持すべきことを示し、種類B2のブランク試料20μLを保持位置P2に保持すべきことを示す。なお、保持位置ごとのブランク試料の種類は予め定められているため、出力部34は、使用量をブランク試料の種類に対応させた情報のみ出力してもよい。 After the blank sample type is extracted in step S202, the calculation unit 56 calculates the usage amount of each blank sample type necessary for the reagent blank analysis according to the received analysis item (step S203). The calculation of the usage amount is performed based on the usage amount of the blank sample that the blank sample information storage unit 52a stores together with the type of the blank sample. Thereafter, the output unit 34 outputs the usage amount of the blank sample calculated by the calculation unit 56 (step S204). FIG. 12 is a usage amount display screen 54a in which the usage amount calculated by the calculation unit 56 is further associated with the type of blank sample in association with the information that associates the type of blank sample with the holding positions P 1 to P n . The usage amount display screen 54a indicates that 10 μL of the type B 1 blank sample should be held at the holding position P 1 , and indicates that 20 μL of the type B 2 blank sample should be held at the holding position P 2 . Since the type of blank sample for each holding position is determined in advance, the output unit 34 may output only information in which the amount used corresponds to the type of blank sample.
 ステップS204で出力部34がブランク試料の使用量を出力した後、制御部51は、試料保持部12への第2試料容器12aのセットが完了したか否かを判断する(ステップS205)。この試料保持部12への第2試料容器12aのセットが完了したか否かの判断は、実施の形態1と同様に、例えば、セット完了を示す信号、すなわち試薬ブランク分析を開始する旨の信号が入力部32から制御部51に出力されたか否かによって行われる。 After the output unit 34 outputs the usage amount of the blank sample in step S204, the control unit 51 determines whether or not the setting of the second sample container 12a to the sample holding unit 12 is completed (step S205). The determination as to whether or not the setting of the second sample container 12a to the sample holding unit 12 has been completed is, for example, a signal indicating the completion of setting, that is, a signal indicating the start of reagent blank analysis, as in the first embodiment. Is performed depending on whether or not is output from the input unit 32 to the control unit 51.
 ステップS205において試料保持部12への第2試料容器12aのセットが完了した場合(ステップS205:Yes)、容器有無検出部20は、ブランク試料が保持される保持位置P1~Pnにおける第2試料容器12aの有無を検出する(ステップS206)。この検出は、試料保持部12が試料保持部12の中心を通る鉛直線を回転軸として時計回りまたは反時計回りに一周する間に行われる。一方、試料保持部12への第2試料容器12aのセットが完了していない場合(ステップS205:No)、出力部34は、この判断処理を繰り返す。 When the setting of the second sample container 12a to the sample holding unit 12 is completed in step S205 (step S205: Yes), the container presence / absence detection unit 20 performs the second operation at the holding positions P 1 to P n where the blank sample is held. The presence or absence of the sample container 12a is detected (step S206). This detection is performed while the sample holder 12 makes a round clockwise or counterclockwise with a vertical line passing through the center of the sample holder 12 as a rotation axis. On the other hand, when the setting of the second sample container 12a to the sample holding unit 12 is not completed (step S205: No), the output unit 34 repeats this determination process.
 ステップS206で保持位置P1~Pnにおける第2試料容器12aの有無を検出した後、取得部36は、試料保持部12に保持された第2試料容器12a内のブランク試料の種類を取得する(ステップS207)。取得部36は、保持位置情報記憶部35bに記憶されたブランク試料の種類ごとに定められる第2試料容器12aの保持位置情報と、容器有無検出部20によって検出された結果とを用いて第2試料容器12a内のブランク試料の種類を取得する。 After detecting the presence or absence of the second sample container 12a at the holding positions P 1 to P n in step S206, the acquisition unit 36 acquires the type of blank sample in the second sample container 12a held by the sample holding unit 12. (Step S207). The acquisition unit 36 uses the holding position information of the second sample container 12a determined for each type of blank sample stored in the holding position information storage unit 35b and the result detected by the container presence / absence detection unit 20 to perform the second operation. The type of blank sample in the sample container 12a is acquired.
 その後、照合部54が、抽出部53が抽出したブランク試料の種類と取得部36が取得したブランク試料の種類とを照合する(ステップS208)。図13は、照合部54の照合によって合致したブランク試料の種類を示す図である。図13は、ステップS207で取得部36が種類B1のブランク試料のみ取得した場合を示すものであり、抽出部53が抽出した図11に示すブランク試料の種類B1,B2の中で合致したブランク試料の種類B1と、受付分析項目との対応関係を示す。 Thereafter, the collation unit 54 collates the type of the blank sample extracted by the extraction unit 53 with the type of the blank sample acquired by the acquisition unit 36 (Step S208). FIG. 13 is a diagram illustrating the types of blank samples that are matched by the collation by the collation unit 54. FIG. 13 shows a case where the acquisition unit 36 acquires only a blank sample of type B 1 in step S207, which matches among the types of blank samples B 1 and B 2 shown in FIG. 11 extracted by the extraction unit 53. the type B 1 of the blank sample, showing the correspondence between the reception analysis item.
 その後、制御部51は、受付分析項目の試薬ブランク分析を全て行うことが可能であるか否かを判断する(ステップS209)。この判断は、照合部54の照合によって合致したブランク試料の種類に適合する分析項目の試薬ブランク分析を行った場合に、受付分析項目の試薬ブランク分析を全て行うことが可能であるか否かによって判断される。受付分析項目の試薬ブランク分析を全て行うことが可能である場合(ステップS209:Yes)、決定部55は、照合部54の照合によって合致したブランク試料の種類に適合する分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を決定する(ステップS210)。この分析順は、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する。一方、受付分析項目の試薬ブランク分析を全て行うことが可能でない場合(ステップS209:No)、出力部34は、試薬ブランク分析処理に異常があることを示す異常情報を出力する(ステップS211)。その後、制御部51は、本処理を終了する。 Thereafter, the control unit 51 determines whether or not it is possible to perform all of the reagent blank analysis of the received analysis items (step S209). This determination is based on whether or not all the reagent blank analyzes of the reception analysis items can be performed when the reagent blank analysis of the analysis items matching the type of the blank sample matched by the verification of the verification unit 54 is performed. To be judged. When it is possible to perform all of the reagent blank analysis of the received analysis items (step S209: Yes), the determination unit 55 performs each analysis on the analysis item that matches the type of the blank sample matched by the collation of the collation unit 54. An analysis order of reagent blank analysis corresponding to the item is determined (step S210). This analysis order is determined so that analysis items using at least the same type of blank sample are continuous. On the other hand, when it is not possible to perform all the reagent blank analysis of the received analysis items (step S209: No), the output unit 34 outputs abnormality information indicating that the reagent blank analysis process is abnormal (step S211). Then, the control part 51 complete | finishes this process.
 ステップS211で、受付分析項目の試薬ブランク分析の分析順を決定した後、制御部51は、決定部55が決定した分析順に従って受付分析項目の試薬ブランク分析を分析装置2に実行させる(ステップS212)。その後、制御部51は、本処理を終了する。 In step S211, after determining the analysis order of the reagent blank analysis of the reception analysis item, the control unit 51 causes the analyzer 2 to execute the reagent blank analysis of the reception analysis item according to the analysis order determined by the determination unit 55 (step S212). ). Then, the control part 51 complete | finishes this process.
 この発明の実施の形態2では、分析装置2が、試料保持部12によって保持された複数の第2試料容器12aの各々が収容するブランク試料の種類を取得し、入力部32が受け付けた分析項目に適合するブランク試料の種類をブランク試料情報に基づいて抽出し、抽出したブランク試料の種類と取得したブランク試料の種類とを照合し、照合によって合致したブランク試料の種類に適合する分析項目に対し、各分析項目に応じた試薬ブランク分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定し、決定した分析順に従って試薬ブランク分析を実行する制御を行っているため、実施の形態1と同様に、試薬ブランク分析に費やす時間を増大させることなく、分析項目ごとに最適なブランク試料を用いた試薬ブランク分析を行うことができる。 In Embodiment 2 of the present invention, the analysis device 2 acquires the type of blank sample stored in each of the plurality of second sample containers 12a held by the sample holding unit 12, and the analysis item received by the input unit 32 The blank sample type that conforms to the criteria is extracted based on the blank sample information, the extracted blank sample type is collated with the acquired blank sample type, , Because the reagent blank analysis order according to each analysis item is determined so that at least the analysis items using the same type of blank sample are continuous, and the reagent blank analysis is performed according to the determined analysis order, As in the first embodiment, a reagent using an optimal blank sample for each analysis item without increasing the time spent for reagent blank analysis It is possible to perform the rank analysis.
 また、実施の形態2では、算出部56が、受付分析項目に応じた試薬ブランク分析に必要なブランク試料の種類ごとの使用量をブランク試料情報記憶部52aが記憶するブランク試料情報に基づいて算出し、出力部34が、ブランク試料の種類と保持位置P1~Pnとを対応させた情報に、さらに算出部56が算出した使用量をブランク試料の種類に対応させた情報を出力しているので、操作者は、試料保持部12への種類ごとのブランク試料のセットを確実に行うことができるとともに、使用量分だけのブランク試料をセットすることができる。 Moreover, in Embodiment 2, the calculation part 56 calculates based on the blank sample information which the blank sample information storage part 52a memorize | stores the usage-amount for every kind of blank sample required for the reagent blank analysis according to a reception analysis item. The output unit 34 outputs information in which the type of the blank sample is associated with the holding positions P 1 to P n and information in which the usage amount calculated by the calculation unit 56 is associated with the type of the blank sample. Therefore, the operator can reliably set the blank sample for each type in the sample holding unit 12 and can set the blank sample corresponding to the amount used.
 なお、実施の形態1の分析装置1が算出部56を有し、照合部38が、抽出部37が抽出した分析項目と受付分析項目とを照合した後に、算出部56がブランク試料の試薬ブランク分析での使用量を算出し、出力部34が、算出部56が算出した使用量をブランク試料の種類に対応させて出力するようにしてもよい。 The analysis apparatus 1 according to the first embodiment includes the calculation unit 56, and after the collation unit 38 collates the analysis item extracted by the extraction unit 37 with the received analysis item, the calculation unit 56 uses the reagent blank of the blank sample. The usage amount in the analysis may be calculated, and the output unit 34 may output the usage amount calculated by the calculation unit 56 according to the type of the blank sample.
(実施の形態3)
 次に、この発明の実施の形態3について説明する。図14は、この発明の実施の形態3にかかる分析装置の構成を示す模式図である。図14に示す分析装置3は、測定部60および制御装置70を有する。なお、実施の形態1と同一構成部分には同一符号を付している。測定部60は、試料容器識別ラベル読取部61を有し、制御装置70の制御部71は、保持位置情報記憶部35bを有さない記憶部72および取得部73を有する。また、ブランク試料は、第2試料容器12aでなく、例えば、5つの保持位置p1~p5を有するラック11bに保持した第1試料容器11aに収容される。
(Embodiment 3)
Next, a third embodiment of the present invention will be described. FIG. 14 is a schematic diagram showing the configuration of the analyzer according to the third embodiment of the present invention. The analysis device 3 illustrated in FIG. 14 includes a measurement unit 60 and a control device 70. In addition, the same code | symbol is attached | subjected to the same component as Embodiment 1. FIG. The measurement unit 60 includes a sample container identification label reading unit 61, and the control unit 71 of the control device 70 includes a storage unit 72 and an acquisition unit 73 that do not include the holding position information storage unit 35b. Further, the blank sample is accommodated not in the second sample container 12a but in, for example, the first sample container 11a held in the rack 11b having five holding positions p 1 to p 5 .
 試料容器識別ラベル読取部61は、試料供給部11の近傍に配置される。試料容器識別ラベル読取部61は、第1試料容器11aに設けられ、第1試料容器11a内のブランク試料の種類を識別する識別情報を記録した試料容器識別ラベル11fの識別情報を読み取り、読み取った識別情報を制御装置70に出力する。試料容器識別ラベル11fは、例えば、バーコード等によって実現される。試料容器識別ラベル読取部61は、例えば、第1試料容器11a内の検体の種類を識別するための情報が記録された情報記録媒体を読み取る装置を利用するとよい。 The sample container identification label reading unit 61 is disposed in the vicinity of the sample supply unit 11. The sample container identification label reading unit 61 is provided in the first sample container 11a, and reads and reads the identification information of the sample container identification label 11f in which the identification information for identifying the type of the blank sample in the first sample container 11a is recorded. The identification information is output to the control device 70. The sample container identification label 11f is realized by, for example, a barcode. The sample container identification label reading unit 61 may use, for example, an apparatus that reads an information recording medium on which information for identifying the type of specimen in the first sample container 11a is recorded.
 取得部73は、試料容器識別ラベル読取部61によって制御装置70に出力された試料容器識別ラベル11fに記録された識別情報により、ラック11bによって保持された複数の第1試料容器11aの各々が収容するブランク試料の種類を取得する。 The acquisition unit 73 accommodates each of the plurality of first sample containers 11a held by the rack 11b based on the identification information recorded on the sample container identification label 11f output to the control device 70 by the sample container identification label reading unit 61. The type of blank sample to be acquired is acquired.
 次に、図15に示したフローチャートを参照して、分析装置3が行う試薬ブランク分析処理について説明する。まず、分析装置3は、試薬ブランク分析に対応する分析項目の受け付けがあるか否かを判断する(ステップS301)。試薬ブランク分析に対応する分析項目の受け付けは、実施の形態1および2と同様に、例えば、出力部34がディスプレイパネルに出力する受付メニュー画面34aを用いて入力部32を介して行われる。 Next, a reagent blank analysis process performed by the analyzer 3 will be described with reference to the flowchart shown in FIG. First, the analyzer 3 determines whether or not an analysis item corresponding to the reagent blank analysis is received (step S301). The analysis item corresponding to the reagent blank analysis is received through the input unit 32 using the reception menu screen 34a output to the display panel by the output unit 34, for example, as in the first and second embodiments.
 ステップS301で試薬ブランク分析に対応する分析項目の受け付けがある場合(ステップS301:Yes)、制御部71は、試料供給部11へのラック11bのセットが完了したか否かを判断する(ステップS302)。このステップS302における判断は、例えば、セット完了を示す信号、すなわち試薬ブランク分析を開始する旨の信号が入力部32から制御部71に出力されたか否かによって行われる。一方、ステップS301で試薬ブランク分析に対応する分析項目の受け付けが行なわれなかった場合(ステップS301:No)、制御部71はこの判断処理を繰り返す。 When an analysis item corresponding to the reagent blank analysis is received in step S301 (step S301: Yes), the control unit 71 determines whether or not the setting of the rack 11b to the sample supply unit 11 is completed (step S302). ). The determination in step S302 is performed based on, for example, whether a signal indicating completion of setting, that is, a signal indicating that reagent blank analysis is started is output from the input unit 32 to the control unit 71. On the other hand, when the analysis item corresponding to the reagent blank analysis is not received in step S301 (step S301: No), the control unit 71 repeats this determination process.
 ステップS302で試料供給部11へのラック11bのセットが完了した場合(ステップS302:Yes)、試料容器識別ラベル読取部61は、ラック11bの保持位置p1~p5における第1試料容器11aに設けられた試料容器識別ラベル11fの識別情報を読み取る(ステップS303)。この読取は、試料供給部11によってラック11bが試料容器識別ラベル読取部61の近傍を搬送される間に行われる。一方、試料供給部11へのラック11bのセットが完了していない場合(ステップS302:No)、制御部71はこの判断処理を繰り返す。 When the setting of the rack 11b to the sample supply unit 11 is completed in step S302 (step S302: Yes), the sample container identification label reading unit 61 applies the first sample container 11a at the holding positions p 1 to p 5 of the rack 11b. The identification information of the provided sample container identification label 11f is read (step S303). This reading is performed while the rack 11 b is transported in the vicinity of the sample container identification label reading unit 61 by the sample supply unit 11. On the other hand, when the setting of the rack 11b to the sample supply unit 11 is not completed (step S302: No), the control unit 71 repeats this determination process.
 ステップS303で保持位置p1~p5における第1試料容器11aに設けられた試料容器識別ラベル11fの識別情報を読み取った後、取得部73は、ラック11bに保持された第1試料容器11a内のブランク試料の種類を取得する(ステップS304)。図16は、試料容器識別ラベル11fに記録される識別情報としてのコード番号とブランク試料の種類とを対応させた情報テーブル72-1を示す。取得部73は、記憶部72に記憶された情報テーブル72-1を用いて、試料容器識別ラベル読取部61が読み取ったコード番号から第1試料容器11a内のブランク試料の種類を取得する。 After reading the identification information of the sample container identification label 11f provided in the first sample container 11a at the holding positions p 1 to p 5 in step S303, the acquisition unit 73 stores the inside of the first sample container 11a held in the rack 11b. The type of blank sample is acquired (step S304). FIG. 16 shows an information table 72-1 in which code numbers as identification information recorded on the sample container identification label 11f are associated with the types of blank samples. Using the information table 72-1 stored in the storage unit 72, the acquisition unit 73 acquires the type of blank sample in the first sample container 11a from the code number read by the sample container identification label reading unit 61.
 その後、分析装置3は、分析装置1が行ったステップS106~S111の処理と同様の処理を行う(ステップS305~S310)。 Thereafter, the analysis device 3 performs the same processing as the processing of steps S106 to S111 performed by the analysis device 1 (steps S305 to S310).
 この発明の実施の形態3では、分析装置3が、ラック11bによって保持された複数の第1試料容器11aの各々が収容するブランク試料の種類を取得し、取得したブランク試料の種類に適合する分析項目をブランク試料情報に基づいて抽出し、抽出した分析項目と入力部32が受け付けた分析項目とを照合し、照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定し、決定した分析順に従って試薬ブランク分析を実行する制御を行っているため、実施の形態1および2と同様に、試薬ブランク分析に費やす時間を増大させることなく、分析項目ごとに最適なブランク試料を用いた試薬ブランク分析を行うことができる効果を奏するとともに、試料容器識別ラベル読取部61が、第1試料容器11a内のブランク試料の種類を識別するコード番号を記録した試料容器識別ラベル11fを保持位置p1~p5ごとに読み取るようにしているので、ラック11b内の任意の保持位置に第1試料容器11aを保持させたとしても、第1試料容器11a内のブランク試料の種類を取得することができる。 In Embodiment 3 of the present invention, the analysis device 3 acquires the type of blank sample accommodated in each of the plurality of first sample containers 11a held by the rack 11b, and analyzes that match the acquired type of blank sample. The items are extracted based on the blank sample information, the extracted analysis items and the analysis items received by the input unit 32 are collated, and the analysis order of the reagent blank analysis corresponding to each analysis item is performed on the analysis items matched by the collation. Is determined so that at least analysis items using the same type of blank sample are continuous, and the reagent blank analysis is performed in accordance with the determined analysis order. Therefore, as in the first and second embodiments, the reagent It is possible to perform reagent blank analysis using an optimal blank sample for each analysis item without increasing the time spent for blank analysis. Rutotomoni, sample container identification label reader 61, so as to read each sample vessel identification label 11f the holding position p 1 ~ p 5 which records the code number identifying the blank type of sample in the first sample vessel 11a Therefore, even if the first sample container 11a is held at an arbitrary holding position in the rack 11b, the type of blank sample in the first sample container 11a can be acquired.
 以上のように、本発明にかかる分析装置は、検体に対して異なる分析項目を自動で分析する医療用分析装置に有用である。 As described above, the analyzer according to the present invention is useful for a medical analyzer that automatically analyzes different analysis items for a specimen.

Claims (6)

  1.  試料と、該試料の分析項目に応じた種類の試薬とを混合し、前記試料および前記試薬の混合液の吸光度を測定することによって前記試料の分析を行う分析装置において、
     前記分析項目と、該分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶手段と、
     試薬ブランク分析の対象となる分析項目を受け付ける受付手段と、
     前記ブランク試料が収容される複数の試料容器を保持する保持手段と、
     前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得する取得手段と、
     前記取得手段が取得したブランク試料の種類に適合する分析項目を前記ブランク試料情報に基づいて抽出する抽出手段と、
     前記抽出手段が抽出した分析項目と前記受付手段が受け付けた分析項目とを照合する照合手段と、
     前記照合手段の照合によって合致した分析項目に対し、各分析項目に応じた試薬ブランク分析の分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する決定手段と、
     前記決定手段が決定した分析順に従って試薬ブランク分析を実行する制御を行う制御手段と、
     を備えたことを特徴とする分析装置。
    In an analyzer for analyzing a sample by mixing a sample and a reagent of a type corresponding to the analysis item of the sample, and measuring the absorbance of a mixed solution of the sample and the reagent,
    Blank sample information storage means for storing blank sample information in which the analysis item is associated with the type of blank sample to be used for the reagent blank analysis of the analysis item;
    Receiving means for receiving an analysis item to be subjected to reagent blank analysis;
    Holding means for holding a plurality of sample containers in which the blank sample is stored;
    Obtaining means for obtaining the type of the blank sample contained in each of the plurality of sample containers held by the holding means;
    An extraction means for extracting an analysis item suitable for the type of blank sample acquired by the acquisition means based on the blank sample information;
    Collating means for collating the analysis items extracted by the extracting means with the analysis items received by the accepting means;
    Determination means for determining the analysis order of the reagent blank analysis according to each analysis item so that the analysis items using at least the same type of blank sample are continuous for the analysis items matched by the verification of the verification means;
    Control means for performing control to execute reagent blank analysis according to the analysis order determined by the determination means;
    An analyzer characterized by comprising:
  2.  試料と、該試料の分析項目に応じた種類の試薬とを混合し、前記試料および前記試薬の混合液の吸光度を測定することによって前記試料の分析を行う分析装置において、
     前記分析項目と、該分析項目の試薬ブランク分析に用いるべきブランク試料の種類とを対応付けたブランク試料情報を記憶するブランク試料情報記憶手段と、
     試薬ブランク分析の対象となる分析項目を受け付ける受付手段と、
     前記ブランク試料が収容される複数の試料容器を保持する保持手段と、
     前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得する取得手段と、
     前記受付手段が受け付けた分析項目に適合するブランク試料の種類を前記ブランク試料情報に基づいて抽出する抽出手段と、
     前記抽出手段が抽出したブランク試料の種類と前記取得手段が取得したブランク試料の種類とを照合する照合手段と、
     前記照合手段の照合によって合致したブランク試料の種類に適合する分析項目に対し、各分析項目に応じた試薬ブランクの分析順を、少なくとも同種類のブランク試料を使用する分析項目が連続するように決定する決定手段と、
     前記決定手段が決定した分析順に従って試薬ブランク分析を実行する制御を行う制御手段と、
     を備えたことを特徴とする分析装置。
    In an analyzer for analyzing a sample by mixing a sample and a reagent of a type corresponding to the analysis item of the sample, and measuring the absorbance of a mixed solution of the sample and the reagent,
    Blank sample information storage means for storing blank sample information in which the analysis item is associated with the type of blank sample to be used for the reagent blank analysis of the analysis item;
    Receiving means for receiving an analysis item to be subjected to reagent blank analysis;
    Holding means for holding a plurality of sample containers in which the blank sample is stored;
    Obtaining means for obtaining the type of the blank sample contained in each of the plurality of sample containers held by the holding means;
    An extraction means for extracting the type of blank sample suitable for the analysis item received by the reception means based on the blank sample information;
    Collating means for collating the type of blank sample extracted by the extracting means and the type of blank sample acquired by the acquiring means;
    For analysis items that match the type of blank sample matched by the verification of the verification means, the analysis order of reagent blanks according to each analysis item is determined so that at least analysis items that use the same type of blank sample are continuous. A decision means to
    Control means for performing control to execute reagent blank analysis according to the analysis order determined by the determination means;
    An analyzer characterized by comprising:
  3.  前記取得手段は、
     前記ブランク試料の種類と該ブランク試料の種類ごとに定められる前記試料容器の保持位置とを対応付ける保持位置情報を記憶した保持位置情報記憶手段と、
     前記保持位置における前記試料容器の有無を検出する検出手段と、
     を備え、
     前記保持位置情報記憶手段が記憶する前記保持位置情報および前記検出手段によって検出された結果を用いることにより、前記保持手段によって保持された前記複数の試料容器の各々が収容する前記ブランク試料の種類を取得することを特徴とする請求項1または2に記載の分析装置。
    The acquisition means includes
    Holding position information storage means for storing holding position information that associates the type of the blank sample with the holding position of the sample container determined for each type of the blank sample;
    Detecting means for detecting the presence or absence of the sample container in the holding position;
    With
    By using the holding position information stored in the holding position information storage unit and the result detected by the detection unit, the type of the blank sample stored in each of the plurality of sample containers held by the holding unit is determined. The analyzer according to claim 1, wherein the analyzer is acquired.
  4.  前記保持位置情報記憶手段が記憶する前記保持位置情報に基づいて、前記ブランク試料の種類と前記保持位置とを対応させた情報を出力する出力手段を備えたことを特徴とする請求項3に記載の分析装置。 The output means which outputs the information which matched the kind of the said blank sample and the said holding position based on the said holding position information which the said holding position information storage means memorize | stores, The output means is characterized by the above-mentioned. Analysis equipment.
  5.  前記ブランク試料情報記憶手段は、前記ブランク試料情報として分析項目ごとのブランク試料の種類とともに該ブランク試料の使用量を記憶し、
     前記受付手段が受け付けた分析項目に応じた試薬ブランク分析に必要なブランク試料の種類ごとの使用量を前記ブランク試料情報記憶手段が記憶する前記ブランク試料情報に基づいて算出する算出手段を備え、
     前記出力手段は、前記算出手段が算出した前記ブランク試料の種類ごとの使用量を出力することを特徴とする請求項4に記載の分析装置。
    The blank sample information storage means stores the usage amount of the blank sample together with the type of blank sample for each analysis item as the blank sample information,
    Comprising calculating means for calculating the amount used for each type of blank sample necessary for reagent blank analysis according to the analysis item received by the receiving means based on the blank sample information stored in the blank sample information storing means,
    The analyzer according to claim 4, wherein the output unit outputs a usage amount for each type of the blank sample calculated by the calculation unit.
  6.  前記取得手段は、
     前記試料容器に設けられ、該試料容器内の前記ブランク試料の種類を識別する識別情報を記録した記録手段から該識別情報を読み取ることによって前記ブランク試料の種類を取得することを特徴とする請求項1または2に記載の分析装置。
    The acquisition means includes
    The blank sample type is obtained by reading the identification information from a recording means provided in the sample container and recording identification information for identifying the type of the blank sample in the sample container. 3. The analyzer according to 1 or 2.
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