Platelet aggregation analysis method, platelet aggregation analysis device, program for analyzing platelet aggregation, and platelet aggregation analysis system

Abstract

A measurement method of simply and quickly measuring platelet aggregation, is provided. The measurement method is a platelet aggregation analysis method, including: a step of adding a platelet-inducing substance and a calcium salt to a platelet-containing specimen; a step of stirring the platelet-containing specimen; and a step of acquiring measurement data of an electrical characteristic and/or viscoelasticity of the platelet-containing specimen.

Claims

1. A platelet aggregation analysis method, comprising: adding a platelet-inducing substance and a calcium salt to a first platelet-containing specimen; acquiring first measurement data of an electrical characteristic and/or viscoelasticity of the first platelet-containing specimen; acquiring second measurement data of the electrical characteristic and/or viscoelasticity of a second platelet-containing specimen to which the platelet-inducing substance is not added; and analyzing platelet aggregation, on a basis of the first measurement data of the electrical characteristic and/or the viscoelasticity of the first platelet-containing specimen, and the second measurement data of the electrical characteristic and/or viscoelasticity of the second platelet-containing specimen, wherein analyzing platelet aggregation includes extracting a characteristic point from the first and second measurement data and determining a difference between the first measurement data and the second measurement data at the extracted characteristic point and wherein a magnitude of the difference between the first measurement data and the second measurement data at the extracted characteristic point is indicative of an amount of platelet aggregation.

2. The platelet aggregation analysis method according to claim 1, wherein the measurement data of the electrical characteristic is a dielectric constant of the platelet-containing specimen.

3. The platelet aggregation analysis method according to claim 1, wherein the measurement data of the viscoelasticity is measurement data of the platelet-containing specimen according to a rheometer.

4. The platelet aggregation analysis method according to claim 1, wherein the platelet-containing specimen is blood or blood plasma.

5. The platelet aggregation analysis method according to claim 4, wherein the blood or the blood plasma is collected from a test subject dosed with an antiplatelet aggregation agent and/or an anticoagulation agent.

6. The platelet aggregation analysis method according to claim 1, further comprising stirring the platelet-containing specimen.

7. A platelet aggregation analysis device, comprising: a biological sample retention unit configured to retain a platelet-containing specimen; a medical agent supply unit configured to supply a platelet-inducing substance and/or a calcium salt to the platelet-containing specimen; a measurement unit configured to measure an electrical characteristic of the platelet-containing specimen; and an analysis unit configured to analyze platelet aggregation, on a basis of first measurement data of the electrical characteristic and/or the viscoelasticity, acquired from a first platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added and second measurement data of the electrical characteristic and/or viscoelasticity, acquired from a second platelet-containing specimen to which the platelet-inducing substance is not added, wherein analyzing platelet aggregation includes extracting a characteristic point from the first and second measurement data and determining a difference between the first measurement data and the second measurement data at the extracted characteristic point and wherein a magnitude of the difference between the first measurement data and the second measurement data at the extracted characteristic point is indicative of an amount of platelet aggregation.

8. The platelet aggregation analysis device according to claim 7, further comprising a stirring mechanism configured to stir the platelet-containing specimen.

9. A non-transitory computer readable medium storing instructions that, when executed by a computer, perform a method for analyzing platelet aggregation comprising: analyzing platelet aggregation, on a basis of first measurement data of an electrical characteristic and/or viscoelasticity, acquired from a first platelet-containing specimen to which a platelet-inducing substance and a calcium salt are added, and second measurement data of the electrical characteristic and/or viscoelasticity, acquired from a second platelet-containing specimen to which the platelet-inducing substance is not added, wherein analyzing platelet aggregation includes extracting a characteristic point from the first and second measurement data and determining a difference between the first measurement data and the second measurement data at the extracted characteristic point and wherein a magnitude of the difference between the first measurement data and the second measurement data at the extracted characteristic point is indicative of an amount of platelet aggregation.

10. A platelet aggregation analysis system, comprising: a platelet aggregation analysis device including: a biological sample retention unit configured to retain a platelet-containing specimen; a medical agent supply unit configured to supply a platelet-inducing substance and/or a calcium salt to the platelet-containing specimen; a measurement unit configured to measure an electrical characteristic of the platelet- containing specimen; and an analysis unit configured to analyze platelet aggregation, on a basis of first measurement data of the electrical characteristic and/or viscoelasticity, acquired from a first platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, and second measurement data of the electrical characteristic and/or viscoelasticity, acquired from a second platelet-containing specimen to which the platelet-inducing substance is not added, wherein analyzing platelet aggregation includes extracting a characteristic point from the first and second measurement data and determining a difference between the first measurement data and the second measurement data at the extracted characteristic point and wherein a magnitude of the difference between the first measurement data and the second measurement data at the extracted characteristic point is indicative of an amount of platelet aggregation; and a display device configured to display an analysis result.

11. The platelet aggregation analysis system according to claim 10, wherein the platelet aggregation analysis device further comprises a stirring mechanism configured to stir the platelet-containing specimen.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a diagram illustrating a measurement flow in a platelet aggregation analysis method.

(2) FIG. 2 is a diagram illustrating the outline of a configuration of a platelet aggregation analysis device.

(3) FIG. 3 is a diagram illustrating an analysis flow performed according to a program for analyzing platelet aggregation.

(4) FIG. 4 is a diagram illustrating the outline of a configuration of a platelet aggregation analysis system.

(5) FIG. 5-1 is a graph showing a measurement result of a test body according to impedance aggregation measurement.

(6) FIG. 5-2 is a graph showing a measurement result of the test body according to a dielectric constant.

(7) FIG. 6-1 is a graph showing an example of an analysis result based on the measurement result according to the dielectric constant.

(8) FIG. 6-2 is a graph showing an example of the analysis result based on the measurement result according to the dielectric constant.

(9) FIG. 7-1 is a graph showing a correlative relationship between measurement data according to the dielectric constant and a measurement data parameter (AUC(U)) according to the impedance aggregation measurement.

(10) FIG. 7-2 is a graph showing a correlative relationship between the measurement data according to the dielectric constant and a measurement data parameter (Aggregation (AU)) according to the impedance aggregation measurement.

(11) FIG. 8 is a graph showing a dielectric clot strength of a platelet-inducing substance-added test body and a control sample.

(12) FIG. 9-1 is a graph showing a correlative relationship between data of the dielectric clot strength based on the dielectric constant and the measurement data parameter (AUC(U)) according to the impedance aggregation measurement.

(13) FIG. 9-2 is a graph showing a correlative relationship between the data of the dielectric clot strength based on the dielectric constant and the measurement data parameter (Aggregation (AU))) according to the impedance aggregation measurement.

MODE FOR CARRYING OUT THE INVENTION

(14) Hereinafter, a preferred mode for carrying out the present technology, will be described. Furthermore, the following embodiment indicates a representative embodiment of the present technology, and with this arrangement, the scope of the present technology is not narrowly interpreted. Furthermore, the description will be given in the following order.

(15) 1. Platelet Aggregation Analysis Method

(16) 2. Platelet Aggregation Analysis Device

(17) 3. Program for Analyzing Platelet Aggregation

(18) 4. Platelet Aggregation Analysis System

(19) 5. Example

(20) (1) Method

(21) (2) Result

(22) (3) Analysis Example 1

(23) (4) Analysis Example 2

(24) 6. Conclusion

1. Platelet Aggregation Analysis Method

(25) A platelet aggregation analysis method of the present technology, includes:

(26) Step A: a step of adding a platelet-inducing substance and a calcium salt to a platelet-containing specimen;

(27) Step B: a step of stirring the platelet-containing specimen; and

(28) Step C: a step of acquiring measurement data of an electrical characteristic and/or viscoelasticity of the platelet-containing specimen.

(29) In Step A, the platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, is stirred in Step B, and thus, the platelets activated by the platelet-inducing substance, are aggregated. In Step C, the platelet that reacted in Step B, does not contribute to a response, but the platelet that did not react, responds in a process of a blood coagulation reaction.

(30) The platelet-containing specimen that is an analysis target of the present technology, is not particularly limited, but examples of the platelet-containing specimen include the blood (the whole blood) from humans or mammals, blood plasma, artificial blood, and the like. In addition, the platelet-containing specimen may be a specimen collected from a test subject dosed with an antiplatelet aggregation agent, an anticoagulation agent, or both of the antiplatelet aggregation agent and the anticoagulation agent.

(31) The platelet-inducing substance used in Step A, is a substance of causing or suppressing the aggregation of the platelet. The platelet-inducing substance, for example, is collagen (COL), epinephrine, ristocetin, thrombin, thromboxane A2 (TAX2), thrombin receptor activating protein (TRAP), adenosine diphosphate (ADP), arachidonic acid (AA), serotonin, adrenaline, and noradrenaline.

(32) For example, in a case of the thrombin receptor activating protein (TRAP), an added concentration of the platelet-inducing substance (the final concentration at the time of being added to the specimen), is preferably greater than or equal to 1 μM and less than or equal to 100 μM, is more preferably greater than or equal to 3 μM and less than or equal to 80 μM, and is even more preferably greater than or equal to 5.4 μM and less than or equal to 62 μM.

(33) In a case of the adenosine diphosphate (ADP), the added concentration of the platelet-inducing substance is preferably greater than or equal to 0.1 μM and less than or equal to 100 μM, is more preferably greater than or equal to 0.5 μM and less than or equal to 30 μM, and is even more preferably greater than or equal to 1.0 μM and less than or equal to 12.5 μM.

(34) In a case of the arachidonic acid (AA), the added concentration of the platelet-inducing substance is preferably greater than or equal to 0.01 mM and less than or equal to 10 mM, is more preferably greater than or equal to 0.05 mM and less than or equal to 5.0 mM, and is even more preferably greater than or equal to 0.08 mM and less than or equal to 1.0 mM.

(35) The calcium salt (calcium chloride or the like) used in Step A, is a substance for solving an anticoagulation action due to the citric acid added to the test body at the time of collecting the blood, according to a calcium ion to be contained.

(36) An added concentration of the calcium chloride (a reagent concentration of the calcium chloride) is not particularly limited insofar as being a concentration having a platelet coagulation accelerating effect, and is preferably greater than or equal to 150 mM and less than or equal to 250 mM, is more preferably greater than or equal to 170 mM and less than or equal to 230 mM, and is even more preferably greater than or equal to 185 mM and less than or equal to 215 mM.

(37) In Step A, a timing when the platelet-inducing substance and the calcium salt are added to the platelet-containing specimen, is not particularly limited, and in the present technology, the platelet-inducing substance and the calcium salt can be simultaneously added. Then, in Step B described above, the platelet-containing specimen, the platelet-inducing substance, and the calcium salt are stirred, and then, in Step C, data of platelet coagulability is acquired.

(38) A stirring condition in Step B described above, is not particularly limited insofar as being a condition in which a platelet coagulation reaction of the platelet-containing specimen is not hindered, and for example, the stirring is performed at 37° C. A stirring rate and a strength are also not particularly limited, but it is preferable that the stirring rate and the strength are considered in advance according to a stirring method or the type of inducing substance. The stirring method is also not particularly limited, and examples of the stirring method include suction and discharge with a pipette, the use of a stirrer, and the like. It is known that 5 minutes is a rough standard as a time for the platelet to react with the platelet-inducing substance, and to be aggregated, according to the consideration of the present technology, but a stirring time is not particularly limited thereto, and is preferably 3 minutes to 6minutes. The stirring time is shortened or prolonged, according to the stirring method or the type of inducing substance .

(39) In Step C described above, the electrical characteristic and/or the viscoelasticity of the platelet-containing specimen, are measured.

(40) Here, examples of the electrical characteristic are capable of including a dielectric constant, impedance, admittance, capacitance, conductance, an electrical conductivity, a phase angle, and the like. In a case of the dielectric constant, the dielectric constant may be measured according to a measurement method of a coagulation process described in the specification of Japanese Patent No. 5691168 and the specification of Japanese Patent No. 5768422.

(41) In addition, the viscoelasticity can be measured by a rheometer. Examples of the rheometer include a rotation thrombo elastometry, a thrombo elastography, and ReoRox (Trademark). Examples of a commercially available device include a thrombo elastography (TEG (Registered Trademark)) blood coagulation analysis device (manufactured by Haemonetics Corporation), a rotation thrombo elastometry (ROTEM (Registered Trademark)) blood coagulation analysis device (TEM group, Basel, Switzerland), and the like.

(42) For example, a platelet-containing specimen to which the calcium salt is added but the platelet-inducing substance is not added, maybe used as a control sample at the time of measuring the platelet aggregation.

(43) The measurement data of the platelet-containing specimen is compared with measurement data acquired from the platelet-containing specimen that is the control sample described above, to which the platelet-inducing substance is not added, and thus, it is possible to analyze the platelet aggregation. The comparison, for example, can be performed by calculating a difference in the data, a ratio, and a difference in the area of a measurement waveform.

(44) Furthermore, as described above, there are various platelet-inducing substances such as TRAP, ADP, and AA, and the functions of such platelet-inducing substances in a coagulation system are different from each other.

(45) Therefore, in a case where a plurality of the same platelet-containing specimens is prepared, a plurality of platelet-inducing substances is selected, and different platelet-inducing substances and the calcium salt are respectively added to the platelet-containing specimens, and are stirred, and thus, the electrical characteristic and/or the viscoelasticity are measured, and data comparison is performed, it is possible to consider the platelet coagulability corresponding to the platelet-inducing substance. Further, the measurement result can be compared with a measurement result of the control sample in which a normal saline solution, a buffer solution, or the like, with less influence on the platelet, is used instead of the platelet-inducing substance.

(46) The platelet aggregation analysis method of the present technology, for example, can be performed according to a measurement flowchart illustrated in FIG. 1.

(47) First, the blood is collected from the test subject (S101). The platelet-inducing substance and the calcium salt are added to the whole blood (S102). Such an operation can be performed in one step. After the platelet-inducing substance and the calcium salt are added, the whole blood is stirred under a heating condition (S103). The stirring time, for example, is 5 minutes.

(48) Next, the blood coagulability measurement is performed (S104). The measurement can be performed in a non-stirring state. Such a step is non-disturbance coagulability measurement in which a natural blood coagulation process is measured without further adding an accelerating reagent or the like. In addition, the blood coagulability measurement may be temporally performed, or a time from when the measurement is started, may be designated, and the coagulability at the time point may be measured.

(49) Finally, the obtained measurement data is analyzed, and a platelet contribution portion in the blood coagulation is calculated (S105).

2. Platelet Aggregation Analysis Device

(50) A platelet aggregation analysis device of the present technology includes: a biological sample retention unit configured to retain a platelet-containing specimen; a medical agent supply unit configured to supply a platelet-inducing substance and/or a calcium salt to the platelet-containing specimen; a stirring mechanism configured to stir the platelet-containing specimen; and a measurement unit configured to measure an electrical characteristic of the platelet-containing specimen.

(51) The outline of the configuration of the platelet aggregation analysis device, is illustrated in FIG. 2.

(52) A biological sample retention unit 1 retains the platelet-containing specimen supplied from a biological sample supply unit 2, and performs the stirring with respect to the platelet-containing specimen, and the platelet-inducing substance and the calcium salt, supplied from the medical agent supply unit 3.

(53) A stirring mechanism 6 is operated to stir the platelet-containing specimen, the platelet-inducing substance, and the calcium salt, supplied to the biological sample retention unit 1. A stirring method is not particularly limited, and for example, the stirring can be performedby using an electric pipette, a stirrer, and a device with a stirring function.

(54) The stirring is performed for a constant time in order for the reaction of the platelet.

(55) A temperature control unit 4 and a time control unit 5 control the condition in the biological sample retention unit. For example, the temperature control unit 4 performs control such that the platelet-containing specimen is retained at a constant temperature. The time control unit 5 controls a time for which the platelet-containing specimen is retained in the biological sample retention unit 1, the stirring time, or the like.

(56) A driving mechanism 7 performs a driving operation of the temperature control unit 4 or the stirring mechanism 6, an operation relevant to the biological sample retention unit 1, such as transferring the platelet-containing specimen.

(57) A measurement unit 9 adds the platelet-inducing substance and/or the calcium salt to the platelet-containing specimen, and stirs them, and then, measures the dielectric constant. A rheometer may be used as the measurement unit 9.

(58) A measurement condition control unit 9 sets and adjusts a temperature condition or a measurement time condition suitable for the measurement method. In addition, the measurement condition control unit 9 controls a frequency used for measurement, a measurement interval, or the like, at the time of performing dielectric constant measurement in the measurement unit 8.

(59) An accuracy management unit 10 performs management of data such that a measurement difference, a background variation, or the like in the measurement unit 8 does not occur, monitoring of a state of each unit of the device, and the like.

(60) An analysis unit 11 analyzes the platelet contribution portion in the blood coagulation, on the basis of the measurement data of the dielectric constant or the viscoelasticity. The analysis can be performedby using a program for analyzing platelet aggregation, as described later.

(61) Furthermore, the analysis unit 11 may further include an output control unit configured to output an analysis result, a display device configured to display the analysis result, a storage unit configured to store the measurement data or the analysis result, and the like.

3. Program for Analyzing Platelet Aggregation

(62) A program for analyzing platelet aggregation to be used in the present technology, allowing a computer to execute: analyzing platelet aggregation, on the basis of measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which a platelet-inducing substance and a calcium salt are added, and measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which the platelet-inducing substance is not added.

(63) The program is provided in a storage medium.

(64) The platelet-containing specimen to which the platelet-inducing substance is not added, can be used as the control sample. For example, a specimen to which the calcium salt is added, and a specimen to which a normal saline solution or a buffer solution is added, can be a control sample. By preparing the control sample, it is possible to calculate the platelet contribution portion by comparing and considering a difference in data, occurring due to the presence or absence of the addition of the platelet-inducing substance.

(65) In FIG. 3, a flowchart of analysis performed by the program, is illustrated.

(66) A characteristic point is extracted (S302), from the data of the measurement result obtained by the measurement unit 9 of the platelet aggregation analysis device (S301). The characteristic point, for example, is a point at which the measurement result of the control sample and the specimen starts to be stable, a point at which a coagulation time of the platelet is set, and the like. The characteristic point, for example, can be a specific time that has elapsed after the platelet-inducing substance and/or the calcium salt are added to the platelet-containing specimen, and are stirred.

(67) A difference between measurement values of the platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, and the platelet-containing specimen to which the calcium salt is added, is calculated at the characteristic point (S303), and the result thereof is output.

(68) The magnitude of the difference is set to the effect of a platelet function (S304). That is, it is determined that the platelet function (aggregation) is high in the platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, as the difference is large.

4. Platelet Aggregation Analysis System

(69) The outline of a platelet aggregation analysis system of the present technology, is illustrated in FIG. 4.

(70) A platelet aggregation analysis system 40 includes the platelet aggregation analysis device 41 described above, and a display device 42 configured to display an analysis result of platelet aggregation.

(71) In the platelet aggregation analysis device 41, a computer with the program for analyzing platelet aggregation, can be incorporated.

(72) A display, a print-out device, or the like, provided in the computer, can be used as the display device 42.

(73) The platelet aggregation analysis device 41 may be configured to analyze not only the platelet aggregation of the platelet-containing specimen but also other blood coagulation system measurement items, or may also function as a blood coagulation system analysis device.

(74) In a case where the platelet aggregation analysis device 41 is used as the blood coagulation system analysis device according to the dielectric constant, and examples of a measurement item include blood coagulation (blood clot) , fibrin formation, fibrin clot formation, blood cake formation, rouleau formation, blood aggregation, sedimentation of red blood cells (erythrocyte sedimentation), blood cake retraction (involution), cythemolysis, fibrinolysis, and the like. When such items are analyzed, a program for analyzing such items is used instead of the program for analyzing platelet aggregation, described above.

(75) The display device 42 may include a warning unit. The warning unit sets in advance the range of a normal value in a state change of each blood, and generates a warning when the analysis result of the specimen is out of the range of the normal value. A warning method is not particularly limited, and for example, the warning can be generated by a display or a sound.

EXAMPLES

5. Example

(1) Method

(76) The venous blood of a normal subject was collected according to a normal method by using a commercially available vacuum blood collection tube in which a citric acid was included as an anticoagulation agent. The first one was discarded without being used, and the blood collected subsequent to the first one, was used for the following tests. In addition, the blood was collected, and then, was used after standing to still at a room temperature for approximately 30 minutes.

(77) In dielectric constant measurement, a blood coagulation system analysis device described in the specification of Japanese Patent No. 5691168 and the specification of Japanese Patent No. 5768422 (hereinafter, referred to as a “dielectric coagulometer β machine”), was used. In addition, in impedance aggregation measurement, a platelet function analysis device Multiplate was used.

(78) First, the whole blood of 200 ul was added to a dedicated cartridge for the dielectric coagulometer, into which a platelet-inducing substance and a calcium aqueous solution (0.215M Ca) were put, and was stirred at 37° C. for 5 minutes. In addition, a system to which a normal saline solution was added instead of the platelet-inducing substance, was produced as a control sample, and similarly, the stirring was performed.

(79) Here, adenosine diphosphate (ADP), an arachidonic acid (AA) , and collagen were used as the platelet-inducing substance.

(80) The number of test bodies was N=3.

(81) The blood coagulability measurement according to the dielectricconstant,usingthedielectriccoagulometer β machine, was performed with respect to the blood of the test body. In addition, the impedance aggregation measurement was performed by the platelet function analysis device Multiplate, and thus, an ADP test, an ASPI test, and a COL test were performed. All of the measurements were performed at a temperature of 37° C.

(82) In the method described above, a similar test of a normal subject different from the normal subject described above, was also performed a plurality of times, in order to confirm reproducibility.

(2) Result

(83) A measurement result of Multiplate that is a platelet aggregation analysis device of the technology of the related art, is shown in FIG. 5-1.

(84) A measurement result of the dielectric coagulometer β machine according to a dielectric constant at 10 MHz, is shown in FIG. 5-2.

(85) In a case where a time change of the assumed result in the dielectric coagulometer β machine, was compared between the addition of the normal saline solution (the control sample) and the addition of the platelet-inducing substance, it was known that a change occurred in an amplitude in a case where the platelet-inducing substance was added.

(86) Such a result correlated with a change in the measurement result of Multiplate, and thus, indicated that it was possible to measure a platelet aggregation reaction even in the dielectric coagulometer β machine.

(3) Analysis Example 1

(87) An example of the analysis method will be described, on the basis of the measurement result according to the dielectric constant in FIG. 5-2 described above.

(88) 20 minutes when the measurement waveform of the dielectric constant was sufficiently stabilized, was set to a consideration time (FIG. 6-1). A value obtainedby subtracting 1 from a standard value of the time (a minimum value standard), was set to 100 times (correction for not decreasing the value), and the value was defined as CF (FIG. 6-2).

(89) Furthermore, the consideration time is not limited to 20 minutes, and can be shortened to 15 minutes or 10 minutes insofar as a dielectric constant change is stabilized after a coagulation time CT is set. However, it was considered that in a test body in which CT was prolonged, it was necessary to change the definition of the consideration time, according to the CT. Accordingly, there may be a case where the consideration time is after 20 minutes.

(90) In addition, the consideration time can be relatively (dynamically) set with respect to CT without being fixed, and for example, can be CT+X minutes, CT×Y minutes, or a more complex function including CT.

(91) In addition, as shown in FIG. 6-2, a decrease in CF due to the addition of the platelet-inducing substance, was a portion (a platelet contribution portion) reflected by the platelet function, in particular, the aggregation, on the basis of CF of the normal saline solution (NaCl, the control sample), and in a case where the platelet aggregation function decreased or a case where the platelet function inhibitor agent was administered, it was assumed that CT was close to the reference value.

(92) For example, in a patient to whom clopidogrel that is an ADP route inhibitor agent, was administered, a difference from the reference value is small even in a case of adding ADP.

(93) Further, it was confirmed that a CF value had a high correlation with Blood Concentration-Area under Time Curve (AUC(U)) that is a parameter obtained from Multiplate, and aggregation unit (Aggregation (AU)) (FIG. 7-1 and FIG. 7-2). In addition, intergradation of a correlation coefficient in a case where the consideration time is changed (t=5 min, 10 min, 15 min, and 20 min) is shown in Table 1 and Table 2. From Table 1 and Table 2, it is known that in a case where the consideration time is earlier than the determination of CT (t=5 min), the correlation becomes worse, and it is difficult to grasp the platelet contribution portion.

(94) TABLE-US-00001 TABLE 1 t = 5 min t = 10 min t = 15 min t = 20 min AUC(U) −0.32089 −0.86685 −0.87283 −0.86327 Aggregation(AU) −0.17799 −0.77917 −0.83382 −0.8191

(95) TABLE-US-00002 TABLE 2 t = 5 min t = 10 min t = 15 min t = 20 min AUC(U) 0.103 0.7514 0.7618 0.7452 Aggregation(AU) 0.0317 0.6071 0.6953 0.6709

(4) Analysis Example 2

(96) An example of another analysis method will be described, on the basis of the measurement result according to the dielectric constant in FIG. 5-2 described above.

(97) A dielectric clot strength (hereinafter, referred to as “DCS”) that is a unique parameter of the blood coagulability measurement according to the dielectric constant, was considered.

(98) DCS is a parameter that can be calculated on the basis of a decrease width from a peak of temporal measurement data measured at a specific frequency.

(99) Specifically, for example, a time when a change in the dielectric constant at a frequency of 10 MHz, is in the vicinity of the minimum value, is defined as a clot time (hereinafter, referred to as “CT”) , DCS is calculated from a dielectric constant difference when the coagulation is ended with respect to a dielectric constant at a CT time (an end point). The setting of the end point is changed, and thus, various DCS parameters can be calculated. Here, the end point was set to a point of the maximum gradient of 10% of an inclination of a dielectric constant change after CT was determined at 10 MHz.

(100) In FIG. 8, a graph of DCS of a test body to which calcium chloride and the platelet-inducing substance were added, and DCS of a control sample to which calcium chloride and sodium chloride (a normal saline solution) were added, is shown.

(101) In the graph of FIG. 8, a change similar to that of the graph of FIG. 6-2, was observed, and thus, it was known that information (the platelet contribution portion) reflected by the platelet function, in particular, the aggregation was capable of being obtained by calculating DCS.

(102) In addition, it was confirmedthat DCS hada high correlation with AUC(U) that is a parameter obtained from Multiplate, and Aggregation (AU) (FIG. 9-1 and FIG. 9-2).

(103) As described above, DCS is a parameter that can be calculated on the basis of a decrease width from a peak of temporal measurement data measured at a specific frequency (for example, 1 MHz) , and may be calculated by using a width of a change in a dielectric constant at 10 MHz, or the like.

6. Conclusion

(104) The present technology is, as a clinical examination having thrombosis in view, capable of measuring and analyzing the platelet aggregation in the whole blood that is a more excellent specimen.

(105) In addition, in the related art, when the platelet aggregation and the blood coagulability are measured, different measurement technologies are used for each measurement, and thus, separate measurement devices are required, but according to the present technology, it is possible to perform the platelet aggregation measurement and the measurement relevant to a coagulation factor, by the same device.

(106) For example, in a case where a plurality of measurement units configured to perform simultaneous measurement, is provided in the device of the present technology, the control sample to which the sodium salt is added, and the specimen to which the sodium salt and the platelet-inducing substance are added, are measured, and the platelet aggregation is examined, and simultaneously, a specimen to which an extrinsic and intrinsic coagulation accelerating agent is added, is measured, and thus, it is possible to examine the blood coagulability. According to such a device, it is possible to investigate a mutual relationship between the platelet aggregation and the blood coagulability.

(107) Further, the present technology is useful in monitoring of a patient who is dosed with an antiplatelet aggregation agent and/or an anticoagulation agent, monitoring of a blood state of a patient during an operation, or the like.

(108) For example, in a case where only the platelet is activated by the platelet-inducing substance, DCS described above is a value lower than that of the control sample (the normal saline solution). This is a change according to platelet contribution, and indicates that the platelet function increases as DCS decreases due to the addition of the platelet-inducing substance. In addition, in a case where DCS is high (a high value) identical to or close to that of the control sample regardless of the addition of the platelet-inducing substance, it is possible to presume that the platelet function decreases or there is a possibility that an antiplatelet agent is administered.

(109) Furthermore, the present technology is capable of having the following configurations:

(110) [1] A platelet aggregation analysis method, including:

(111) a step of adding a platelet-inducing substance and a calcium salt to a platelet-containing specimen;

(112) a step of stirring the platelet-containing specimen; and

(113) a step of acquiring measurement data of an electrical characteristic and/or viscoelasticity of the platelet-containing specimen.

(114) [2] The platelet aggregation analysis method described in [1],

(115) in which the measurement data of the electrical characteristic is a dielectric constant of the platelet-containing specimen.

(116) [3] The platelet aggregation analysis method described in [1],

(117) in which the measurement data of the viscoelasticity is measurement data of the platelet-containing specimen according to a rheometer.

(118) [4] The platelet aggregation analysis method described in [1] or [2], further including:

(119) a step of analyzing platelet aggregation, on the basis of the measurement data of the electrical characteristic and/or the viscoelasticity of the platelet-containing specimen, and measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which the platelet-inducing substance is not added.

(120) [5] The platelet aggregation analysis method described in any one of [1] to [4],

(121) in which the platelet-containing specimen is blood or blood plasma.

(122) [6] The platelet aggregation analysis method described in [5],

(123) in which the blood or the blood plasma is collected from a test subject dosed with an antiplatelet aggregation agent and/or an anticoagulation agent.

(124) [7] A platelet aggregation analysis device, including:

(125) a biological sample retention unit configured to retain a platelet-containing specimen;

(126) a medical agent supply unit configured to supply a platelet-inducing substance and/or a calcium salt to the platelet-containing specimen;

(127) a stirring mechanism configured to stir the platelet-containing specimen; and

(128) a measurement unit configured to measure an electrical characteristic of the platelet-containing specimen.

(129) [8] A program for analyzing platelet aggregation, allowing a computer to execute:

(130) analyzing platelet aggregation, on the basis of measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which a platelet-inducing substance and a calcium salt are added, and measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which the platelet-inducing substance is not added.

(131) [9] The program for analyzing platelet aggregation described in [8],

(132) in which the analyzing includes comparing the measurement data of the electrical characteristic and/or the viscoelasticity, acquired from the platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, with the measurement data of the electrical characteristic and/or the viscoelasticity, acquired from the platelet-containing specimen to which the platelet-inducing substance is not added.

(133) [10] A platelet aggregation analysis system, including:

(134) a platelet aggregation analysis device including: a biological sample retention unit configured to retain a platelet-containing specimen; a medical agent supply unit configured to supply a platelet-inducing substance and/or a calcium salt to the platelet-containing specimen; a stirring mechanism configured to stir the platelet-containing specimen; and a measurement unit configured to measure an electrical characteristic of the platelet-containing specimen,

(135) a computer with a program for analyzing platelet aggregation being built in the platelet aggregation analysis device, the program allowing the computer to execute analyzing platelet aggregation, on the basis of measurement data of the electrical characteristic and/or viscoelasticity, acquired from the platelet-containing specimen to which the platelet-inducing substance and the calcium salt are added, and measurement data of an electrical characteristic and/or viscoelasticity, acquired from a platelet-containing specimen to which the platelet-inducing substance is not added; and

(136) a display device configured to display an analysis result.

REFERENCE SIGNS LIST

(137) 1 Biological sample retention unit 2 Biological sample supply unit 3 Medical agent supply unit 4 Temperature control unit 5 Time control unit 6 Stirring mechanism 7 Driving mechanism 8 Measurement unit 9 Measurement condition control unit 10 Accuracy management unit 11 Analysis unit 40 Platelet aggregation analysis system 41 Platelet aggregation analysis device 42 Display device