AUTOMATIC ANALYZER AND CONTROL METHOD THEREOF

Information

  • Patent Application
  • 20250138042
  • Publication Number
    20250138042
  • Date Filed
    December 21, 2022
    2 years ago
  • Date Published
    May 01, 2025
    a month ago
Abstract
Provided is an automatic analyzer and a control method thereof that are capable of preventing liquid leakage when a dispensing probe that aspirated air and a liquid in order rises. The automatic analyzer for analyzing a sample includes: a dispensing unit configured to dispense the sample and/or a reagent; and a control unit configured to control the dispensing unit. When a dispensing probe provided in the dispensing unit rises after aspirating air and a liquid in order, the control unit aspirates an amount of outside air corresponding to a length of expansion of the air through a tip of the dispensing probe.
Description
TECHNICAL FIELD

The present invention relates to an automatic analyzer and a control method thereof.


BACKGROUND ART

An automatic analyzer for analyzing a specific component included in a sample such as blood and urine provided by a patient includes a dispensing unit that dispenses the sample or a reagent by aspirating them from a sample container or a reagent container and discharging them into a reaction container. In regard to the dispensing unit, Patent Literature 1 discloses detecting an abnormity of aspirating the sample or air based on a detection signal output by a sensor that detects presence of liquid in a predetermined location in the dispensing unit when the sample or air is aspirated.


CITATION LIST
Patent Literature





    • Patent Literature 1: Japanese Unexamined Patent Application Publication No. 2015-10894





SUMMARY OF INVENTION
Technical Problem

However, Patent Literature 1 does not take into consideration liquid leakage when a dispensing probe having sequentially aspirated the air and the liquid rises. The automatic analyzer is intended to speed up an operation of each unit, for example, vertical movement of the dispensing probe, to reduce time required for an analysis. However, speed-up of the vertical movement may cause the liquid leakage from the dispensing probe having sequentially aspirated the air and the liquid, thereby lowering dispensing accuracy and analytical accuracy.


Therefore, it is an object of the present invention to provide an automatic analyzer capable of suppressing liquid leakage when a dispensing probe having sequentially aspirated air and liquid rises, and a control method thereof.


Solution to Problem

To achieve the aforementioned object, the present invention provides an automatic analyzer for analyzing a sample, the automatic analyzer including: a dispensing unit that dispenses the sample and/or reagent; and a control unit that controls the dispensing unit, in which the control unit causes an amount of external air corresponding to a length by which the air expands to be aspirated through a tip of a dispensing probe when the dispensing probe provided in the dispensing unit rises after sequentially aspirating the air and liquid.


In addition, the present invention provides a control method of an automatic analyzer for analyzing a sample, the method including: causing an amount of external air corresponding to a length by which the air expands to be aspirated through a tip of a dispensing probe when the dispensing probe provided in the dispensing unit that dispenses the sample or the reagent rises after sequentially aspirating the air and liquid.


Advantageous Effects of Invention

According to the present invention, it is possible to provide an automatic analyzer capable of suppressing liquid leakage when a dispensing probe having sequentially aspirated air and liquid rises, and a control method thereof.





BRIEF DESCRIPTION OF DRAWINGS


FIG. 1 is a schematic diagram showing an example of an overall configuration of an automatic analyzer.



FIG. 2 is a schematic diagram showing a configuration example of a dispensing unit.



FIG. 3 is a diagram showing an example of operations of the dispensing unit.



FIG. 4 is a diagram showing an expansion amount of air when a dispensing probe rises.



FIG. 5 is a diagram showing an example of a rising velocity and acceleration of the dispensing probe.



FIG. 6 is a diagram showing an example of operations of the dispensing unit when aspirating two kinds of liquids.



FIG. 7 is a diagram showing an expansion amount of air when a dispensing probe that aspirated the two kinds of liquids rises.





DESCRIPTION OF EMBODIMENTS

In the following, preferred embodiments of an automatic analyzer according to the present invention will be described with reference to accompanying drawings. It should be noted that, in the following description and the accompanying drawings, components having an identical functional configuration will not be described again by denoting those components with an identical reference numerals.


First Embodiment

An example of an overall configuration of an automatic analyzer is described using FIG. 1. The automatic analyzer is a device that analyzes a specific component included in a sample such as blood and urine provided by a patient, and has a disk 102, a dispensing unit 105, an incubator (reaction disk) 104, a measurement unit 106, a control unit 107, an input and output unit 108, and a storage unit 109. Each unit will be described below.


The disk 102 stores therein a sample container 100 that contains the sample and a reagent bottle 101 that contains a reagent, and carries the sample container 100 and the reagent bottle 101 to a location accessible by the dispensing unit 105.


The dispensing unit 105 dispenses the sample or the reagent from the sample container 100 or the reagent bottle 101 to a reaction cell 103 stored in the incubator 104. It should be noted that the sample and the reagent may be dispensed by a single dispensing unit 105 or the sample and the reagent may be dispensed separately by each of a plurality of dispensing units 105. More detailed configuration of the dispensing unit 105 will be described later using FIG. 2.


The incubator 104 stores therein the reaction cell 103 containing a liquid mixture of the sample and the reagent within a temperature range for reacting the liquid mixture, and carries the reaction cell 103 to a location accessible by the dispensing unit 105 and measurement unit 106. The liquid mixture in the reaction cell 103 is turned into a reaction liquid to be used for measurement by storing the reaction cell 103 within a predetermined temperature range.


The measurement unit 106 emits light to the reaction cell 103, measures the light from the reaction cell 103, and transmits a measurement signal to the control unit 107.


The control unit 107 is a computer that analyzes a specific component included in the sample based on the measurement signal transmitted from the measurement unit 106 and controls an operation of each unit.


The input and output unit 108 is a device that receives an input of data required for an analysis and displays a result of the analysis, such as a keyboard, a mouse, a touch panel, a liquid crystal display, and the like.


The storage unit 109 is a device that stores therein the data required for the analysis and the result of the analysis, such as an HDD (Hard Disk Drive), an SSD (Solid State Drive), and the like.


An example configuration of the dispensing unit 105 is described using FIG. 2. The dispensing unit 105 includes a shaft 201, an arm 202, a dispensing probe 203, a syringe pump 204, a tube 205 and an electromagnetic valve 206.


The shaft 201 is a hollow member extending in a vertical direction, which is vertically moved. The arm 202 is a hollow member extending in a horizontal direction, to which an upper end of the shaft 201 is attached at one end and the dispensing probe 203 is attached at the other end, and which is rotated around the shaft 201 serving as an axis of rotation. The rotation of the arm 202 moves the dispensing probe 203 to a position right above the sample container 100 or the reagent bottle 101.


The dispensing probe 203 is a small tubing to be inserted into the sample container 100 or the reagent bottle 101 by the vertical movement of the shaft 201, and its upper end is connected to the tube 205. The tube 205 connects the dispensing probe 203 and the syringe pump 204 through the arm 202 and the shaft 201.


The syringe pump 204 applies pressure to system water in the dispensing probe 203 by driving a plunger 207 to aspirate or discharge the sample or the reagent from a lower end of the dispensing probe 203. That is, the sample or the like is dispensed by the aspiration resulting from a negative pressure of the system water and by the discharge resulting from a positive pressure of the system water.


The electromagnetic valve 206 is disposed between a system water container 208 containing the system water and the syringe pump 204, and is closed while the sample or the like is being dispensed. When the dispensation is terminated, the electromagnetic valve 206 is opened, an inner wall of the dispensing probe 203 is washed by the system water supplied from the system water container 208, and the inside of the tube 205 is filled with the system water. That is, the tube 205 before dispensation is filled with the system water.


A case of aspirating the sample is described using FIG. 3 as an example of an operation of the dispensing unit 105 controlled by the control unit 107. It should be noted that the liquid to be aspirated is not limited to the sample, but may be the reagent.

    • (a) The dispensing probe 203 is moved to the position right above the sample container 100 containing a sample 303 by the rotation of the arm 202. It should be noted that there is air 302 at a tip of the dispensing probe 203 for separating system water 301 and the sample 303.
    • (b) The dispensing probe 203 is inserted into the sample container 100 by descent of the shaft 201. It should be noted that the descent of the shaft 201 and the dispensing probe 203 is stopped when the lower end of the dispensing probe 203 comes below a liquid level of the sample 303. Whether the lower end of the dispensing probe 203 is below the liquid level of the sample 303 or not is determined on the basis of an output signal of a liquid level sensor not shown in the figure.
    • (c) The negative pressure is applied to the system water 301 by the syringe pump 204, and the sample 303 is aspirated from the lower end of the dispensing probe 203. It should be noted that, because the liquid level is lowered by the aspiration of the sample 303, the height of the dispensing probe 203 during the aspiration is adjusted so that the lower end is not exposed to the air.
    • (d) The dispensing probe 203 having aspirated a predetermined amount of the sample 303 starts to rise. When the dispensing probe 203 rises acceleratingly, because a downward inertia force acts on the aspirated sample 303, the air 302 may be expanded and a part of the aspirated sample 303 may be pushed out of the dispensing probe 203, resulting in a liquid leakage. Therefore, in the first embodiment, an aspiration for suppressing the liquid leakage starts as soon as the dispensing probe 203 starts to rise. An aspiration amount is controlled according to an expansion amount of the air 302. The expansion amounts of the air 302 will be described later using FIG. 4.
    • (e) The dispensing probe 203 continues to rise acceleratingly, and its lower end gets out of the liquid level. Because the inertia force continues to act on the aspirated sample 303 while the dispensing probe 203 rises acceleratingly, the aspiration for suppressing the liquid leakage is continued even after the lower end of the dispensing probe 203 gets out of the liquid level. It should be noted that the air is aspirated after the lower end of the dispensing probe 203 gets out of the liquid level.
    • (f) After the rising speed reaches its maximum speed, the dispensing probe 203 decreases the rising speed and stops at an upper limit point that is the height when the dispensing probe 203 is in a stand-by state. It should be noted that, because the air 302 does not expand during a period in which the rising speed is constant and the air 302 shrinks during a period in which the rising speed is decreased, no liquid leakage occurs during both periods. The period in which the rising speed is constant includes a period of the maximum speed and a stop period. That is, the air 302 does not expand or shrink with the dispensing probe 203 stopping at the upper limit point.


An expansion amount Δh of the air 302 is described using FIG. 4. When the dispensing probe 203 containing the system water 301, the air 302, and the sample 303 rises at an acceleration α, the downward inertia force is applied to the sample 303 to expand the air 302. Assuming the air 302 as an air spring with a spring constant k, a force kΔh generated by the expansion amount Δh is balanced with an inertia force mα acting on the sample 303 with a mass m, whereby the following formula is established.











k

Δ

h

-

m

α


=
0




(

formula


1

)







It should be noted that the spring constant k of the air spring can be represented by the following formula based on the Boyle-Charles Law and the Hooke's Law.









k
=


γ

(


A
2


p

)

/

V
a






(

formula


2

)







Here, γ is a polytropic index of the air 302, A is a cross-sectional area of the dispensing probe 203, P is a pressure of the air 302, and Va is a volume of the air 302. It should be noted that γ=1.4 holds true assuming a series of operations in the dispensing probe 203 as an adiabatic cycle. In addition, since the lower end of the dispensing probe 203 before being inserted into the sample container 100 is open to the atmosphere, the pressure P is an atmospheric pressure.


Moreover, the mass m of the sample 303 can be represented by the following formula using a density ρ and a volume Vm of the sample 303.









m
=

ρ


V
m






(

formula


3

)







Furthermore, a height hm of the sample 303 and a height ha of the air 302 can be represented by the following formula using the volume Vm of the sample 303 or the volume Va of the air 302 and a cross-sectional area A of the dispensing probe 203.










h
a

=


V
m

/
A





(

formula


4

)













h
a

=


V
a

/
A





(

formula


5

)







Solving (Formula 1) for Δh from (Formula 2) using (Formula 5), the following formula is obtained.










Δ

h

=


h
a



h
m


ρ


α
/

(

γ

P

)







(

formula


6

)







Moreover, a leakage rate ΔV of the sample 303 pushed out of the dispensing probe 203 by expansion of the air 302 is proportional to the acceleration α as indicated by the following formula.










Δ

V

=



A

Δ

h

+
C

=



V
a



V
m


ρ


α
/

(

γ

PA

)



+
C






(

formula


7

)







Here, C is a noise component including a viscous friction between the inner wall of the dispensing probe 203 and the sample 303, a vibration of the dispensing probe 203, and the like, which is preset according to a kind and an amount of the sample 303. It should be noted that C is a value sufficiently smaller than Va Vmρα/(γPA).


An example of a rising speed u and the acceleration α of the dispensing probe 203 is described using FIG. 5. In FIG. 5, a solid line indicates the rising speed u that continuously changes via maximum speed u_max since the dispensing probe 203 having aspirated the predetermined amount of the sample 303 starts to rise at a time t1 until it stops at the upper limit point at a time t6. Moreover, a dotted line indicates the acceleration α that continuously changes through an acceleration period between the time t1 and a time t3, a constant speed period between the time t3 and a time t4, and a deceleration period between the time t4 and the time t6. It should be noted that the acceleration α becomes its maximum value α_max at a time t2 and becomes its minimum value α_min at a time t5. It should also be noted that the maximum value α_max and the minimum value α_min of the acceleration α is specified by the maximum speed u_max of the dispensing probe 203 and the time (t6−t1) required for its rising.


Because the leakage rate ΔV of the sample 303 is proportional to the acceleration α as indicated by (Formula 7), in a case where the rising speed u and the acceleration α of the dispensing probe 203 change as shown in FIG. 5, the leakage rate ΔV reaches its maximum at the time t2. That is, it is possible to suppress the liquid leakage by aspirating from the dispensing probe 203 an amount of the external air corresponding to the leakage rate ΔV calculated by substituting α=α_max into (Formula 7).


In addition, because the liquid leakage occurs during the acceleration period between the time t1 and the time t3, the aspiration of the external air from the dispensing probe 203 may be limited to be within the acceleration period between the time t1 and the time t3. It is possible to make a range smaller in which the inner wall of the dispensing probe 203 contacts the aspirated sample 303 by limiting the aspiration of the external air within the acceleration period.


Second Embodiment

In the first embodiment, the description is given of a case of the dispensing probe 203 aspirating one kind of liquid, namely aspirating the sample 303 only. The liquid aspirated by the dispensing probe 203 is not limited to one kind but there may be a plurality of kinds. In a second embodiment, the description is given of a case in which the dispensing probe 203 aspirates two kinds of liquids. It should be noted that the difference from the first embodiment is that two kinds of liquids are aspirated by the dispensing probe 203 instead of one kind, and therefore description of other features is omitted.


A case of aspirating a second liquid 604 after aspirating a first liquid 602 is described using FIG. 6 as an example of an operation of the dispensing unit 105 controlled by the control unit 107.

    • (a) The dispensing probe 203 is moved by the rotation of the arm 202 to a position right above a container 605 that contains the second liquid 604. It should be noted that first air 601 and the first liquid 602 have been aspirated into the dispensing probe 203. In addition, there is second air 603 at the tip of the dispensing probe 203 for separating the first liquid 602 and the second liquid 604.
    • (b) The dispensing probe 203 is inserted into the container 605 by the descent of the shaft 201. It should be noted that the descent of the shaft 201 and the dispensing probe 203 is stopped when the lower end of the dispensing probe 203 comes below the liquid level of the second liquid 604. Whether the lower end of the dispensing probe 203 is below the liquid level of the second liquid 604 or not is determined on the basis of the output signal of the liquid level sensor, as in the first embodiment.
    • (c) The negative pressure is applied to the system water 301 by the syringe pump 204, and second liquid 604 is aspirated from the lower end of the dispensing probe 203. The height of the dispensing probe 203 during the aspiration is adjusted so that the lower end is not exposed to the air.
    • (d) The dispensing probe 203 having aspirated a predetermined amount of the second liquid 604 starts to rise. When the dispensing probe 203 rises acceleratingly, because a downward inertia force acts on the first liquid 602 and the second liquid 604, the first air 601 and the second air 603 may be expanded and a part of the aspirated second liquid 604 may be pushed out of the dispensing probe 203, resulting in a liquid leakage. Therefore, in the second embodiment, also, an aspiration for suppressing the liquid leakage starts as soon as the dispensing probe 203 starts to rise. The aspiration amount is controlled according to the expansion amounts of the first air 601 and the second air 603. The expansion amounts of the first air 601 and the second air 603 will be described later using FIG. 7.
    • (e) The dispensing probe 203 continues to rise acceleratingly, and its lower end gets out of the liquid level. Because the inertia force continues to act on the first liquid 602 and the second liquid 604 while the dispensing probe 203 rises acceleratingly, the aspiration for suppressing the liquid leakage is continued even after the lower end of the dispensing probe 203 gets out of the liquid level. It should be noted that the air is aspirated after the lower end of the dispensing probe 203 gets out of the liquid level.
    • (f) After the rising speed reaches its maximum speed, the dispensing probe 203 decreases the rising speed and stops at an upper limit point that is the height when the dispensing probe 203 is in a stand-by state. It should be noted that no liquid leakage occurs during the constant speed period and the deceleration period for the rising speed, as in the first embodiment.


An expansion amount Δha1 of the first air 601 and an expansion amount Δha2 of the second air 603 will be described using FIG. 7. When the dispensing probe 203 containing the first air 601, the first liquid 602, the second air 603, and the second liquid 604 rises at the acceleration α, the downward inertia force acts on the first liquid 602 and the second liquid 604 to expand the first air 601 and the second air 603. Assuming the first air 601 as an air spring with a spring constant k1, a force k1Δha1 generated by the expansion amount Δha1 of the first air 601 is balanced with an inertia force (m1+m2)α acting on the first liquid 602 with a mass m1 and the second liquid 604 with a mass m2, whereby the following formula is established.











k
1


Δ


h

a

1



-


(


m
1

+

m
2


)


α

-
0




(

formula


8

)







In addition, assuming the second air 603 as an air spring with a spring constant k1, a force k2Δha2 generated by the expansion amount Δha2 of the second air 603 is balanced with an inertia force m2α acting on the second liquid 604, whereby the following formula is established.












k
2


γ


h

a

2



-


m
2


α


=
0




(

formula


9

)







It should be noted that the spring constants k1 and k2 of the air springs is calculated using (Formula 2).


An expansion amount Δh pushing out the second liquid 604 is equal to a sum of Δha1 and Δha2 respectively calculated from (Formula 8) and (Formula 9), which is represented in the following formula.










Δ

h

=


Δ


h

a

1



+

Δ


h

a

2








(

formula


10

)







Furthermore, the leakage rate ΔV of the second liquid 604 pushed out of the dispensing probe 203 by expansion of the first air 601 and the second air 603 is represented in the following formula using (Formula 5) from (Formula 10) or (Formula 8) from (Formula 5).










Δ

V

=



A

Δ

h

+
C

=



{



V

a

1


(


V

m

1


+

V

m

2



)

+


V

a

2




V

m

2




}



ρα
/

(

γ

PA

)



+
C






(

formula


11

)







As indicated in (Formula 11), when aspirating two kinds of liquid, the leakage rate ΔV is also proportional to the acceleration α when the dispensing probe 203 rises. That is, even when aspirating a plurality of kinds of liquids, it is possible to suppress the liquid leakage by aspirating from the dispensing probe 203 an amount of the external air corresponding to the leakage rate ΔV calculated by substituting the maximum value of the acceleration α into (Formula 11). It is also possible to make the range smaller in which the aspirated liquid contacts the inner wall of the dispensing probe 203 by limiting the aspiration of the external air within the acceleration period.


It should be noted that the following formula is obtained by extending (Formula 11) to the leakage rate ΔV when aspirating n kinds of liquids.










Δ

V

=



{



V

a

1


(


V

m

1


+

V

m

2


+

+

V
mn


)

+

+


V
an



V
mn



}


ρ


α
/

(

γ

PA

)



+
C





(

formula


12

)







It can be seen from (Formula 11) and (Formula 12) that the volume of the first air 601 has a significant effect when aspirating a plurality of kinds of liquids using a single dispensing probe 203.


A plurality of embodiments of the present invention have been described above. The present invention is not limited to the above embodiments, but alterations may be made to components thereof without departing from the scope of the invention. Moreover, a plurality of components disclosed in the above embodiments may be combined as appropriate. Furthermore, some of the components may be removed from all the components described in the above embodiments.


LIST OF REFERENCE SIGNS






    • 100: sample container


    • 101: reagent bottle


    • 102: disk


    • 103: reaction cell


    • 104: incubator


    • 105: dispensing unit


    • 106: measurement unit


    • 107: control unit


    • 108: input and output unit


    • 109: storage unit


    • 201: shaft


    • 202: arm


    • 203: dispensing probe


    • 204: syringe pump


    • 205: tube


    • 206: electromagnetic valve


    • 207: plunger


    • 208: system water container


    • 301: system water


    • 302: air


    • 303: sample


    • 601: first air


    • 602: first liquid


    • 603: second air


    • 604: second liquid


    • 605: container




Claims
  • 1-7. (canceled)
  • 8. An automatic analyzer for analyzing a sample, the automatic analyzer comprising: a dispensing unit configured to dispense the sample; anda control unit configured to control the dispensing unit, whereinwhen a dispensing probe provided in the dispensing unit rises after aspirating a first air and a first liquid in order and then aspirating a second air and a second liquid in order, the control unit calculates an amount corresponding to a sum of a length of expansion of the first air and a length of expansion of the second air by assuming the first air and the second air as air springs, and aspirates the calculated amount of outside air through a tip of the dispensing probe.
  • 9. The automatic analyzer according to claim 8, wherein The control unit aspirates the outside air during an acceleration period when the dispensing probe rises.
  • 10. The automatic analyzer according to claim 8, wherein the control unit calculates an amount ΔV corresponding to the sum of the length of expansion of the first air and the length of expansion of the second air as ΔV={Va1(Vm1+Vm2)+Va2Vm2}ρα/(γPA)+C using an acceleration α when the dispensing probe rises, a volume Va1 of the first air, a volume Vm1 of the first liquid, a volume Va2 of the second air, a volume Vm2 of the second liquid, a density ρ of the first liquid and the second liquid, a polytropic index γ of the first air and the second air, a pressure P of the first air and the second air, a cross-sectional area A of the dispensing probe, and a noise component C.
  • 11. A control method of an automatic analyzer for analyzing a sample, the method comprising: when a dispensing probe provided in a dispensing unit that dispenses the sample or a reagent rises after aspirating a first air and a first liquid in order and then aspirating a second air and a second liquid in order, calculating an amount corresponding to a sum of a length of expansion of the first air and a length of expansion of the second air by assuming the first air and the second air as air springs, and aspirating the calculated amount of outside air through a tip of the dispensing probe.
  • 12. The automatic analyzer according to claim 8, wherein when the dispensing probe rises after aspirating air and liquid n times in order, the control unit calculates an amount ΔV corresponding to a sum of the lengths of expansion of n kinds of air as ΔV={Va1(Vm1+Vm2+ . . . +Vmn)+ . . . +VanVmn}ρα/(γPA)+C using an acceleration α when the dispensing probe rises, a volume Van of an nth air, a volume Vmn of an nth liquid, a density ρ of the liquid, a polytropic index γ of the air, a pressure P of the air, a cross-sectional area A of the dispensing probe, and noise component C.
Priority Claims (1)
Number Date Country Kind
2022-021935 Feb 2022 JP national
PCT Information
Filing Document Filing Date Country Kind
PCT/JP2022/047243 12/21/2022 WO