US20070002309A1 - Analyzer and analytic system - Google Patents

Analyzer and analytic system Download PDF

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Publication number
US20070002309A1
US20070002309A1 US11/477,281 US47728106A US2007002309A1 US 20070002309 A1 US20070002309 A1 US 20070002309A1 US 47728106 A US47728106 A US 47728106A US 2007002309 A1 US2007002309 A1 US 2007002309A1
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United States
Prior art keywords
light
analyzer
analyzer according
optical
reagent
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Abandoned
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US11/477,281
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English (en)
Inventor
Norimasa Yamamoto
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Sysmex Corp
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Sysmex Corp
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Assigned to SYSMEX CORPORATION reassignment SYSMEX CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: YAMAMOTO, NORIMASA
Publication of US20070002309A1 publication Critical patent/US20070002309A1/en
Priority to US12/655,734 priority Critical patent/US7916298B2/en
Abandoned legal-status Critical Current

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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/02—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
    • G01N35/025—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations having a carousel or turntable for reaction cells or cuvettes
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/251—Colorimeters; Construction thereof
    • G01N21/253—Colorimeters; Construction thereof for batch operation, i.e. multisample apparatus
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/255—Details, e.g. use of specially adapted sources, lighting or optical systems
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/27—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands using photo-electric detection ; circuits for computing concentration
    • G01N21/272—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands using photo-electric detection ; circuits for computing concentration for following a reaction, e.g. for determining photometrically a reaction rate (photometric cinetic analysis)
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00—Features of devices classified in G01N21/00
    • G01N2201/08—Optical fibres; light guides

Definitions

  • the present invention relates to an analyzer and an analytic system.
  • an analyzer applies light to a sample for obtaining the quantity of transmitted light or absorbance, and analyzes the sample on the basis of this optical information.
  • An analyzer of this type must optically measure a large number of samples at the same time.
  • An analyzer disclosed in Japanese Patent Laying-Open No. 2-284064 (1990) applies light emitted from a single light source to the overall incidence end of an optical fiber bundle, thereby introducing the light emitted from the light source into the optical fiber bundle.
  • This optical fiber bundle has a plurality of branched exit ends, for applying light components to a plurality of reaction vessels from the exit ends respectively.
  • this analyzer can optically measure a plurality of samples at the same time.
  • the number of samples optically measurable at the same time must be increased.
  • the analyzer branches light with a single optical fiber bundle as in the analyzer disclosed in the aforementioned Japanese Patent Laying-Open No. 2-284064, however, the area of the incidence end of the optical fiber bundle is increased as the number of branching is increased, to reduce the quantities of light components outgoing from the exit ends. Further, the surface of the incidence end of the optical fiber bundle is so planar that the quantities of light components transmitted through respective optical fiber members are dispersed unless the analyzer uniformly applies light to the surface of the incidence end.
  • an analyzer disclosed in Japanese Patent Laying-Open No. 10-170432 (1998) is so formed as to supply light emitted from a single light source portion (photoirradiator) to a plurality of terminal portions while applying the supplied light to samples set on the terminal portions respectively.
  • the light applied to the samples is incident upon a single array-type photoreceptor provided in common to the respective terminal portions. Therefore, the conventional analyzer disclosed in the aforementioned Japanese Patent Laying-Open No. 10-170432, supplying light to the terminal portions from the single light source portion, can be downsized.
  • the downsizeable conventional analyzer disclosed in the aforementioned Japanese Patent Laying-Open No. 10-170432 which is so formed as to detect light with the single array type photoreceptor, cannot simultaneously introduce light components from the terminal portions into the array type photoreceptor for performing measurement. Therefore, the conventional analyzer disclosed in the aforementioned Japanese Patent Laying-Open No. 10-170432 must introduce the light components from the terminal portions into the array-type photoreceptor with a time lag, to disadvantageously require a long time for measurement in the respective terminal portions.
  • An object of the present invention is to provide an analyzer and an analytic system improved in specimen treatment efficiency while attaining downsizing of the analyzer.
  • an analyzer comprises a plurality of detection areas in which containers including the samples are receivable, at least one optical source configured to emit at least one series of lights, and more than one splitter configured to split the at least one series of lights into a plurality of series of lights each guided to one of the plurality of the detection areas at which the sample is optically analyzed.
  • An analyzer comprises a photoirradiation portion simultaneously photoirradiating a plurality of storage vessels storing a plurality of measurement samples prepared by admixing a reagent with a plurality of samples respectively, a plurality of photodetection portions detecting a plurality of light components resulting from simultaneous photoirradiation on the plurality of storage vessels storing the plurality of measurement samples respectively and an analytic portion analyzing characteristics of the plurality of samples on the basis of the light components detected by the photodetection portions.
  • the photoirradiation portion includes a light source, a first light guide portion branching light emitted from the light source into a plurality of light components and guiding the plurality of light components to the plurality of measurement samples respectively and a second light guide portion branching light emitted from the light source into a plurality of light components and guiding the plurality of light components to the plurality of measurement samples respectively.
  • An analyzer comprises a photoirradiation portion simultaneously photoirradiating a plurality of storage vessels storing a plurality of measurement samples prepared by admixing a reagent with a plurality of samples respectively, a plurality of photodetection portions detecting a plurality of light components resulting from simultaneous photoirradiation on the plurality of storage vessels storing the plurality of measurement samples respectively and an analytic portion analyzing characteristics of the plurality of samples on the basis of the light components detected by the photodetection portions.
  • the photoirradiation portion includes a light source having a platelike filament and an optical fiber bundle including an incidence end formed by bundling ends of a plurality of optical fibers and a plurality of exit ends directed toward the plurality of storage vessels respectively so that light emitted from a first surface of the platelike filament is incident upon the incidence end.
  • An analytic system comprises a photoirradiator, a first analyzer including a first reagent mixing portion mixing a reagent into an analyte and a first photodetection portion detecting light obtained by applying light emitted from the photoirradiator to the analyte mixed with the reagent by the first reagent mixing portion, a second analyzer including a second reagent mixing portion mixing another reagent into another analyte and a second photodetection portion detecting light obtained by applying light emitted from the photoirradiator to the analyte mixed with the reagent by the second reagent mixing portion and analytic means analyzing characteristics of the analyte mixed with the reagent by the first reagent mixing portion on the basis of the light detected by the first photodetection portion while analyzing characteristics of the analyte mixed with the reagent by the second reagent mixing portion on the basis of the light detected by the second photo
  • FIG. 1 is a plan view showing the overall structure of an analytic system including an analyzer and an extension analyzer according to an embodiment of the present invention
  • FIG. 2 is a perspective view partially showing the analytic system including the analyzer and the extension analyzer according to the embodiment shown in FIG. 1 ;
  • FIG. 3 is a perspective view for illustrating the structure of a lamp unit included in the analyzer according to the embodiment shown in FIG. 1 ;
  • FIG. 4 is a schematic diagram showing the structure of the lamp unit included in the analyzer according to the embodiment shown in FIG. 3 ;
  • FIG. 5 is a plan view showing a filter portion of the lamp unit included in the analyzer according to the embodiment shown in FIG. 3 ;
  • FIG. 6 is a block diagram for illustrating the structure of a first optical information acquisitive portion of the analyzer according to the embodiment shown in FIG. 1 ;
  • FIG. 7 is a block diagram for illustrating the structure of a second optical information acquisitive portion of the analyzer according to the embodiment shown in FIG. 1 ;
  • FIG. 8 is a schematic diagram showing the structure of a detection portion of the second optical information acquisitive portion of the analyzer according to the embodiment shown in FIG. 7 ;
  • FIG. 9 is a block diagram for illustrating the components of the second optical information acquisitive portion and a control board of the analyzer according to the embodiment of the present invention.
  • FIG. 10 is a block diagram for illustrating the structures of the detection portion and a signal processing portion of the analyzer according to the embodiment of the present invention.
  • FIG. 11 is a diagram for illustrating the structure of a logger memory of the control board of the analyzer according to the embodiment of the present invention.
  • FIG. 12 is a circuit diagram showing the circuit structures of an amplification circuit and a differentiation circuit of the control board of the analyzer according to the embodiment of the present invention.
  • FIG. 13 is a flow chart showing the outline of a control method by a PC body of the analyzer according to the embodiment of the present invention.
  • FIG. 14 is a flow chart showing a method of calculating n clocks acquired by the PC body with a control portion in initialization shown at a step S 1 in FIG. 13 ;
  • FIG. 15 is a waveform diagram showing changes in the quantity of reference light and a differential signal of a reference signal employed in the method of calculating n clocks shown in FIG. 14 ;
  • FIG. 16 is a flow chart showing the details (subroutine) of analysis with the PC body at a step S 3 shown in FIG. 13 ;
  • FIG. 17 illustrates a signal processing method in the signal processing portion of the analyzer according to the embodiment of the present invention
  • FIG. 18 is a graph showing a coagulation curve created by the analytic system according to the embodiment of the present invention.
  • FIG. 19 is a flow chart for illustrating a method of data acquisition with the control portion of the analyzer according to the embodiment of the present invention.
  • FIG. 20 is a flow chart for illustrating a method of data acquisition with the PC body of the analyzer according to the embodiment of the present invention.
  • FIG. 21 is a flow chart showing processing of monitoring a time interval for detecting an origin slit in processing of monitoring rotation of the filter portion with the control portion of the analyzer according to the embodiment of the present invention
  • FIG. 22 is a waveform diagram showing the waveforms of a signal output from a sensor detecting slits of the rotating filter portion and an integral signal generated on the basis of the signal output from the sensor;
  • FIG. 23 is a flow chart showing processing of monitoring a time interval for detecting a pair of adjacent slits (the origin slit and/or normal slit(s)) in the processing of monitoring rotation of the filter portion with the control portion of the analyzer according to the embodiment of the present invention
  • FIG. 24 is a flow chart showing processing of monitoring the number of normal slits detected while the origin slit is detected twice in the processing of monitoring rotation of the filter portion with the control portion of the analyzer according to the embodiment of the present invention.
  • FIG. 25 is a plan view showing the overall structure of the analytic system including no extension analyzer according to the embodiment of the present invention.
  • FIGS. 1 to 12 The structure of an analytic system 1 according to the embodiment of the present invention is described with reference to FIGS. 1 to 12 .
  • the analytic system 1 is a system for optically measuring and analyzing the quantities and the degrees of activity of specific substances related to a blood coagulative/fibrinolytic function, employing blood plasma as a specimen.
  • the analytic system 1 optically measures the specimen with a coagulation time method.
  • the coagulation time method employed in this embodiment is a measuring method detecting the process of coagulation of the specimen as change of transmitted light.
  • the structure of the analytic system 1 can be varied with the scale of an institution where the system 1 is installed.
  • the analytic system 1 When installed in an institution having a relatively small number of specimens, for example, the analytic system 1 is constituted of an analyzer 3 and a transporter 200 for supplying specimens to the analyzer 3 , as shown in FIG. 25 .
  • the analytic system 1 When installed in an institution having a large number of specimens, on the other hand, the analytic system 1 is constituted of a transport mechanism portion 2 substituting for the transporter 200 , an analyzer 3 and an extension analyzer 4 .
  • the extension analyzer 4 added to the analytic system 1 extends the specimen throughput of the analytic system 1 .
  • the transport mechanism portion 2 shown in FIG. 1 has a function of transporting racks 151 each carrying a plurality of ( 10 in this embodiment) test tubes 150 storing specimens to suctional positions 2 a and 2 b (see FIG. 1 ) of the analyzer 3 and the extension analyzer 4 respectively, in order to supply the specimens to the analyzer 3 and the extension analyzer 4 .
  • This transport mechanism portion 2 has a rack set area 2 c for setting racks 151 carrying test tubes 150 storing untreated specimens and a rack storage area 2 d for storing racks 151 carrying test tubes 150 storing treated specimens.
  • the analyzer 3 and the extension analyzer 4 are so formed as to optically measure different specimens supplied from the transport mechanism portion 2 thereby acquiring optical information related to the supplied specimens respectively.
  • the analyzer 3 and the extension analyzer 4 optically measure specimens injected into cuvettes 152 (see FIG. 1 ) from the test tubes 150 located on the transport mechanism portion 2 respectively.
  • the analyzer 3 includes an information processing terminal 3 a , a lamp unit 5 and a control board 6 .
  • the analyzer 3 further includes a cuvette supply portion 20 , a rotary transport portion 30 , a specimen injection arm 40 , two reagent injection arms 50 , cuvette transfer portions 60 and 60 a , a first optical information acquisitive portion 70 and a second optical information acquisitive portion 80 .
  • the extension analyzer 4 also includes a control board 6 , a cuvette supply portion 20 , a rotary transport portion 30 , a specimen injection arm 40 , two reagent injection arms 50 , cuvette transfer portions 60 and 60 a , a first optical information acquisitive portion 70 and a second optical information acquisitive portion 80 identical to those provided on the analyzer 3 . These components are identically arranged in the analyzer 3 and the extension analyzer 4 .
  • the analyzer 3 includes the information processing terminal 3 a and the lamp unit 5 , while the extension analyzer 4 includes no such components.
  • the information processing terminal 3 a is electrically connected not only to the body of the analyzer 3 but also to the extension analyzer 4 through communication cables. In other words, the analyzer 3 and the extension analyzer 4 share the information processing terminal 3 a of the analyzer 3 in common.
  • the analyzer 3 and the extension analyzer 4 have functions of transmitting optical information acquired from specimens to the information processing terminal 3 a .
  • the information processing terminal 3 a is formed by a personal computer (PC), and includes a PC body 3 b , a display portion 3 c and a keyboard 3 d , as shown in FIG. 2 .
  • the PC body 3 b analyzes the characteristics of the specimens on the basis of signals (optical information) acquired by signal processing portions 111 and control portions 112 , described later, of the control boards 6 .
  • the PC body 3 b of the information processing terminal 3 a is so formed as to analyze times (coagulation times) required for the specimens to reach prescribed coagulation states from prescribed timing after reagents are mixed into the specimens.
  • the PC body 3 b includes a control portion (not shown) formed by a CPU, a ROM, a RAM, a hard disk etc.
  • the display portion 3 c is provided for displaying information such as results of analysis obtained in the PC body 3 b .
  • the analyzer 3 and the extension analyzer 4 are identical in structure to each other except that the extension analyzer 4 includes neither information processing terminal 3 a nor lamp unit 5 . Therefore, the structure of the analyzer 3 is described in the following.
  • the lamp unit 5 has a halogen lamp 11 serving as a light source, two mirrors 12 a and 12 b , two sets of condensing lenses 13 a to 13 c and 13 d to 13 f , a discoidal filter portion 14 , a motor 15 , a light transmission sensor 16 and two optical fiber members 17 a and 17 b .
  • the halogen lamp 11 , the mirror 12 b , the condensing lenses 13 d to 13 f and the optical fiber member 17 b constitute an optical system for the analyzer 3
  • the halogen lamp 11 , the mirror 12 a , the condensing lenses 13 a to 13 c and the optical fiber member 17 a constitute an optical system for the extension analyzer 4 .
  • the forward end of the optical fiber member 17 b is connected to the second optical information acquisitive portion 80 of the analyzer 3 .
  • the forward end of the optical fiber member 17 a is connected to the second optical information acquisitive portion 80 of the extension analyzer 4 only when the extension analyzer 4 is provided on the analytic system 1 .
  • the mirror 12 a , the condensing lenses 13 a to 13 c and the optical fiber member 17 a may not be provided on the lamp unit 5 when the extension analyzer 4 is not provided on the analytic system 1 .
  • the mirror 12 a and the condensing lenses 13 a to 13 c may be mounted on a mirror mounting portion 12 c and lens mounting portions 13 g to 13 i respectively when the extension analyzer 4 is added to the analytic system 1 .
  • the cost for the lamp unit 5 can be reduced when the extension analyzer 4 is not provided on the analytic system 1 .
  • the optical fiber members 17 a and 17 b are constituted of 21 optical fibers 17 c and 21 optical fibers 17 d respectively. Bundling members 17 e and 17 f bundle the 21 optical fibers 17 c and the 21 optical fibers 17 d respectively.
  • the halogen lamp 11 includes a platelike filament 11 a capable of emitting light components from both surfaces, as shown in FIG. 4 . Thus, the halogen lamp 11 is so formed as to emit light components of the same characteristics from both surfaces of the platelike filament 11 a .
  • the platelike filament 11 a having small dispersion in the quantity of light in a photoirradiation region thereof, is so employed as to stabilize the quantities of light components (transmitted light components or scattered light components) obtained by applying light components to measurement samples, thereby suppressing measurement errors.
  • the two mirrors 12 a and 12 b are provided for reflecting the light components emitted from the halogen lamp 11 and guiding the same to prescribed optical paths respectively.
  • the mirrors 12 a and 12 b are arranged on both sides of the filament 11 a , and located on positions correctly opposed to first and second surfaces of the filament 11 a respectively. Further, the mirrors 12 a and 12 b are inclined with respect to the filament 11 a , in order to change the traveling directions of the light components emitted from the filament 11 a by 90° respectively.
  • the mirrors 12 a and 12 b reflect the light components emitted from the first and second surfaces of the platelike filament 11 a of the halogen lamp 11 respectively.
  • the light components reflected by the mirrors 12 a 12 b form two optical paths.
  • the mirrors 12 a and 12 b are detachably mounted on the mirror mounting portion 12 c and another mirror mounting portion 12 d respectively, as shown in FIG. 3 .
  • the condensing lenses 13 a to 13 c are arranged on the path of the light component whose traveling direction is changed by the mirror 12 a in this order from the side closer to the mirror 12 a , as shown in FIG. 4 .
  • the two sets of condensing lenses 13 a to 13 c and 13 d to 13 f condense the two light components reflected by the mirrors 12 a and 12 b for guiding the same to the optical fiber members 17 a and 17 b respectively, as shown in FIG. 4 .
  • the two light components reflected by the mirrors 12 a and 12 b are condensed by the condensing lenses 13 a to 13 c and 13 d to 13 f respectively, transmitted through any ones of optical filters 14 b to 14 f and guided to the optical fiber members 17 a and 17 b respectively.
  • the condensing lenses 13 a to 13 c are detachably mounted on the lens mounting portions 13 g to 13 i respectively, as shown in FIG. 3 .
  • the condensing lenses 13 d to 13 f are also detachably mounted on corresponding lens mounting portions (not shown) respectively.
  • the filter portion 14 of the lamp unit 5 is rotatable about a shaft 14 a , as shown in FIG. 5 .
  • This filter portion 14 is constituted of a filter plate 14 g provided with five optical filters 14 b to 14 f having different light transmission characteristics (transmission wavelengths) and a filter plate holding member 14 h holding the filter plate 14 g to expose both surfaces of the optical filters 14 b to 14 f .
  • the filter plate 14 g is fixed to the filter plate holding member 14 h .
  • This filter plate 14 g is provided with five holes 14 i for receiving the optical filters 14 b to 14 f respectively.
  • the five optical filters 14 b , 14 c , 14 d , 14 e and 14 f having different light transmission characteristics (transmission wavelengths) are set in the five holes 14 i respectively.
  • the filter plate 14 g is further provided with a hole 14 j , which is blocked not to transmit light.
  • the holes 14 i and 14 j are provided at a prescribed angular interval (regular interval of 60° according to this embodiment) along the direction of rotation of the filter portion 14 .
  • the hole 14 j is a preliminary hole for receiving an additional filter when the analytic system 1 requires this filter.
  • the optical filters 14 b , 14 c , 14 d , 14 e and 14 f transmit light components having wavelengths of 340 nm, 405 nm, 575 nm, 660 nm and 800 nm respectively, while transmitting no light components of other wavelengths. Therefore, light components transmitted through the optical filters 14 b , 14 c , 14 d , 14 e and 14 f have wavelength characteristics of 340 nm, 405 nm, 575 nm, 660 nm and 800 nm respectively.
  • the filter plate holding member 14 h is so annularly formed that the filter plate 14 g is arranged on a central hole portion thereof.
  • the filter plate holding member 14 h is circumferentially provided with six slits at a regular interval (60°).
  • One of the six slits is an origin slit 14 k having a larger width than the remaining five slits 14 l along the direction of rotation of the filter plate holding member 14 h.
  • the origin slit 14 k and the normal slits 14 l are formed on intermediate angular positions (deviating from the holes 14 i and 14 j by 30°) between the adjacent holes 14 i and 14 j at the regular interval of 60°.
  • the motor 15 (see FIG. 3 ) is connected to the shaft 14 a of the filter portion 14 .
  • the motor 15 drives the filter portion 14 to rotate about the shaft 14 a.
  • the control board 6 controls the motor 15 to continuously rotate the filter portion 14 when the lamp unit 5 emits a light component transmitted through any of the optical filters 14 b to 14 f .
  • the five optical filters 14 b to 14 f having different light transmission characteristics and the blocked hole 14 j are intermittently successively arranged on paths of the light components condensed by the condensing lenses 13 a to 13 c (see FIG. 4 ) and the condensing lenses 13 d to 13 f (see FIG. 4 ) respectively.
  • the lamp unit 5 intermittently successively applies five types of light components having different wavelength characteristics.
  • the light transmission sensor 16 is provided for detecting passage of the origin slit 14 k and the normal slits 14 l following the rotation of the filter portion 14 , as shown in FIG. 3 .
  • the sensor 16 is so set as to hold the filter portion 14 between a light source and a photoreceptive portion.
  • This sensor 16 is provided in correspondence to a position passed by the origin slit 14 k and the normal slits 14 l.
  • the optical fiber members 17 a and 17 b are provided for guiding the light components received from the lamp unit 5 to measurement samples stored in the cuvettes 152 set on the second optical information acquisitive portions 80 of the analyzer 3 and the extension analyzer 4 respectively.
  • the optical fiber member 17 a is so set as to extend from the lamp unit 5 toward the second optical information acquisitive portion 80 of the extension analyzer 4 through an extension connecting terminal 7 provided on the extension analyzer 4 .
  • the optical fiber member 17 b is so set as to extend from the lamp unit 5 toward the second optical information acquisitive portion 80 of the analyzer 3 .
  • the single lamp unit 5 can supply light components to the second optical information acquisitive portions 80 of the analyzer 3 and the extension analyzer 4 respectively.
  • the cuvette supply portion 20 arranges the plurality of cuvettes 152 , randomly introduced by a user, one by one on a position 152 a .
  • the cuvette transfer portion 60 a transfers the cuvettes 152 , each arranged on the position 152 a , one by one to the rotary transport portion 30 .
  • the rotary transport portion 30 includes a discoidal table 30 a , which is provided with a plurality of holes 152 b for storing the cuvettes 152 and a plurality of holes 152 c for storing reagent vessels (not shown) storing reagents added to specimens stored in the cuvettes 152 .
  • the rotary transport portion 30 transports the cuvettes 152 and the reagent vessels by rotating the table 30 a.
  • the specimen injection arm 40 has a function of sucking specimens from the test tubes 150 transported to the suctional/injective position 2 a ( 2 b ) while injecting the sucked specimens into the cuvettes 152 transferred by the rotary transport portion 30 .
  • the reagent injection arms 50 are provided for injecting the reagents stored in the reagent vessels (not shown) placed on the rotary transport portion 30 into the cuvettes 152 held on the rotary transport portion 30 thereby mixing the reagents into the specimens stored in the cuvettes 152 .
  • the cuvette transfer portion 60 is provided for transferring the cuvettes 152 between the rotary transport portion 30 and a cuvette receiving portion 81 , described later, of the second optical information acquisitive portion 80 .
  • the first optical information acquisitive portion 70 is so formed as to acquire optical information from the specimens, in order to detect presence/absence, types and contents of interference substances (hemoglobin, chyle (lipid) and bilirubin) in the specimens not yet mixed with the reagents.
  • the first optical information acquisitive portion 70 acquires the optical information before the second optical information acquisitive portion 80 optically measures the specimens.
  • the first optical information acquisitive portion 70 includes a light-emitting diode (LED) 71 serving as a light source, a photoelectric conversion element 72 , a preamplifier 73 and a substrate 74 .
  • This first optical information acquisitive portion 70 acquires the optical information from the specimens by applying light components to the cuvettes 152 held on the rotary transport portion 30 .
  • the controller 74 c is so formed as to change the gain (amplification factor) of the amplifier 74 d in response to periodic change of the wavelength characteristics (430 nm, 565 nm and 627 nm) of the light components emitted from the light-emitting diode 71 . Further, the controller 74 c is electrically connected to the PC body 3 b , for transmitting the digital signals converted by the A-D converter 74 b to the PC body 3 b .
  • the PC body 3 b analyzes the digital signals received from the first optical information acquisitive portion 70 thereby obtaining absorbance values (intensity levels of transmitted light components) of the specimens stored in the cuvettes 152 with respect to the three light components emitted from the light-emitting diode 71 , while analyzing the presence/absence, types and contents of the interference substances in the specimens.
  • the PC body 3 b determines whether or not to measure the specimens with the second optical information acquisitive portion 80 and controls a method of analyzing detection signals from the second optical information acquisitive portion 80 and a method of displaying the results of analysis.
  • the second optical information acquisitive portion 80 has a function of warming the measurement samples prepared by adding the reagents to the specimens and detecting optical information from the measurement samples.
  • This second optical information acquisitive portion 80 is constituted of the cuvette receiving portion 81 and a detection portion 82 (see FIG. 7 ) arranged under the cuvette receiving portion 81 .
  • the cuvette receiving portion 81 is provided with the 20 receiving holes 81 a for receiving the cuvettes 152 and the reference light measurement hole 81 b for measuring reference light without receiving any cuvette 152 , as shown in FIG. 1 . Further, the cuvette receiving portion 81 has a built-in warming mechanism (not shown) for warming the cuvettes 152 received in the receiving holes 81 a.
  • the detection portion 82 is so formed as to optically measure the measurement samples stored in the cuvettes 152 received in the receiving holes 81 a .
  • the detection portion 82 is provided with collimator lenses 83 a , photoelectric conversion elements 84 a and preamplifiers 85 a in correspondence to the receiving holes 81 a receiving the cuvettes 152 respectively, and further provided with a reference light collimator lens 83 b , a reference light photoelectric conversion element 84 b and a reference light preamplifier 85 b in correspondence to the reference light measurement hole 81 b (see FIG. 1 ).
  • the collimator lenses 83 a are set between ends of the optical fibers 17 d ( 17 c ) guiding the light components received from the lamp unit 5 (see FIG. 1 ) and the corresponding receiving holes 81 a .
  • the collimator lenses 83 a are provided for parallelizing the light components received from the optical fibers 17 d ( 17 c ).
  • the photoelectric conversion elements 84 a are mounted on surfaces, closer to the receiving holes 81 a , of substrates 86 a opposite to the ends of the optical fibers 17 d ( 17 c ) through the receiving holes 81 a .
  • the preamplifiers 85 a are mounted on other surfaces of the substrates 86 a opposite to the receiving holes 81 a .
  • the photoelectric conversion elements 84 a have functions of detecting light components (hereinafter referred to as transmitted light components) transmitted through the measurement samples stored in the cuvettes 152 received in the receiving holes 81 a upon photoirradiation and outputting electric signals (analog signals) corresponding to the detected transmitted light components.
  • the preamplifiers 85 a of the detection portion 82 are provided for amplifying the electric signals (analog signals) received from the photoelectric conversion elements 84 a.
  • the reference light collimator lens 83 b , the reference light photoelectric conversion element 84 b , the reference light preamplifier 85 b and a reference light substrate 86 b provided on the detection portion 82 in correspondence to the reference light measuring hole 81 b are identical in structure to the collimator lenses 83 a , the photoelectric conversion elements 84 a , the preamplifiers 85 a and the substrates 86 a provided on the detection portion 82 in correspondence to the receiving holes 81 a respectively.
  • the reference light photoelectric conversion element 84 b is so formed as to directly receive a light component emitted from the corresponding optical fiber 17 d ( 17 c ) and transmitted through the reference light collimator lens 83 b as reference light.
  • the reference light photoelectric conversion element 84 b is so formed as to detect the reference light applied without through the cuvettes 152 storing the measurement samples and to output an electric signal (analog signal) corresponding to the detected reference light.
  • the control board 6 is arranged under the second optical information acquisitive portion 80 .
  • This control board 6 has a function of controlling operations of the analyzer 3 and the lamp unit 5 while processing and storing the optical information (electric signals) received from the second optical information acquisitive portion 80 .
  • the control board 6 is provided with the signal processing portion 111 , the control portion 112 , an amplification circuit 113 , a differentiation circuit 114 and a temperature controller 115 .
  • the signal processing portion 111 is provided for processing the signals output from the photoelectric conversion elements 84 a detecting the transmitted light components when the lamp unit 5 applies the light components to the measurement samples. As shown in FIG.
  • this signal processing portion 111 has three multiplexers (MUX) 111 a , three offset circuits 111 b , three amplifiers 111 c and three A-D conversion portions 111 d .
  • the first multiplexer 111 a , the first offset circuit 111 b , the first amplifier 111 c and the first A-D conversion portion 111 d constitute a signal processing line L 0 .
  • the signal processing portion 111 is also provided with signal processing lines L 1 and L 2 similar in structure to the signal processing line L 0 . In other words, the signal processing portion 111 is provided with the three signal processing lines L 0 to L 2 for processing the plurality of analog signals received from the detection portion 82 .
  • the multiplexers 11 a are connected to the plurality of preamplifiers 85 a (reference light preamplifier 85 b ). These multiplexers 111 a are so formed as to select the plurality of analog signals received from the plurality of photoelectric conversion elements 84 a (reference light photoelectric conversion element 84 b ) through the preamplifiers 85 a (reference light preamplifier 85 b ) one by one and to successively output the same to the offset circuits 111 b .
  • the offset circuits 111 b have functions of correcting the signals received from the multiplexers 111 a .
  • the offset circuits 111 b are supplied with offset values corresponding to the receiving holes 81 a and the reference light measurement hole 81 b employed for measurement respectively from the control portion 112 (see FIG. 9 ).
  • the offset circuits 111 b subtract these offset values from the signals corresponding to the transmitted light components received from the multiplexers 111 a , thereby correcting the signals corresponding to the transmitted light components received from the multiplexers 111 a.
  • the amplifiers 111 c have functions of amplifying the analog signals received from the offset circuits 111 b .
  • the control portion 112 controls the gains (amplification factors) of these amplifiers 111 c , to be switchable between low gains and high gains higher than the low gains.
  • Signals of the low gains (amplification factors) and the high gains (amplification factors) amplified by the amplifiers 111 c are input in the A-D conversion portions 111 d at different timings.
  • the A-D conversion portions 111 d connected to the amplifiers 111 c respectively, are provided for converting processed analog signals amplified to the signals (analog signals) of the low and high gains by the amplifiers 111 c to digital signals (data).
  • the A-D conversion portions 111 d output 48 data ( 16 data per A-D conversion portion 111 d ) corresponding to channels CH 0 to CH 47 respectively, as shown in FIG. 10 .
  • the data of 42 channels CH 0 to CH 41 correspond to data based on the electric signals obtained from the photoelectric conversion elements 84 a and the reference light photoelectric conversion element 84 b respectively.
  • the amplifiers 111 c of the signal processing portion 111 amplify 20 data obtained from 20 photoelectric conversion elements 84 a to 40 data with the low and high gains (amplification factors).
  • One of the amplifiers 111 c of the signal processing portion 111 see FIG.
  • the data of the channels CH 0 to CH 41 correspond to 42 data obtained by totalizing the aforementioned 40 data and the two data corresponding to the reference light.
  • the remaining six channels CH 42 to CH 47 are preliminary channels not used in this embodiment, and data of these channels CH 42 to CH 47 do not correspond to the electric signals from the photoelectric conversion elements 84 a and the reference light photoelectric conversion element 84 b.
  • the control portion 112 has functions of controlling the operations of the analyzer 3 and acquiring and storing the digital signals (data) received from the A-D conversion portions 111 d .
  • this control portion 112 includes a controller 112 a , the filter rotation monitoring portion 112 b , a motor controller 112 c , a multiplexer control portion 112 d , an offset interface 112 e , an amplifier interface 112 f , an A-D conversion portion interface 112 g , a logger memory 112 h , a set memory 112 i , a controller status register 112 j and a local bus interface 112 k.
  • the controller 112 a has a function of unifying various control operations with the control portion 112 .
  • the filter rotation monitoring portion 112 b is provided for monitoring whether or not the filter portion 14 of the lamp unit 5 normally rotates. This filter rotation monitoring portion 112 b is so formed as to receive the detection signals from the sensor 16 detecting passage of the origin slit 14 k (see FIG. 5 ) and the normal slits 141 following rotation of the filter portion 14 .
  • the filter rotation monitoring portion 112 b monitors whether or not the filter portion 14 normally rotates by monitoring the time intervals of the detection signals for the origin slit 14 k (see FIG. 5 ) and the normal slits 141 (see FIG.
  • the motor controller 112 c has a function of controlling the rotational frequency of the motor 15 rotating the filter portion 14 .
  • the multiplexer control portion 112 d has a function of controlling operations of the multiplexers 111 a . More specifically, the multiplexer control portion 112 d controls the operations of the plurality of multiplexers 111 a to select the analog signals at different times respectively.
  • the controller 112 a controls the amplifiers 111 c between the low and high gains through the amplifier interface 112 f , while controlling the amplifiers 111 c to amplify the signals received from the offset circuits 111 b . Further, the controller 112 a controls the A-D conversion portions 111 d to convert the signals (analog signals) received from the amplifiers 111 c to digital signals through the A-D conversion portion interface 112 g .
  • the logger memory 112 h receives and stores the digital signals (data) acquired by the A-D conversion portions 111 d through the A-D conversion portion interface 112 g and the controller 112 a . At this time, the controller 112 a controls operations of the A-D conversion portions 111 d through the A-D conversion portion interface 112 g , not to overlap the periods for outputting the digital signals respectively with each other.
  • the controller 112 a also has a function of switching that executing processing among the multiplexers 111 a , the offset circuits 111 b , the amplifiers 111 c and the A-D conversion portions 111 d of the signal lines L 0 to L 2 and the logger memory 112 h , so that the A-D conversion portion 111 d of another signal processing line L 1 , L 2 or L 0 performs conversion processing with the corresponding A-D conversion portion 116 d and the logger memory 112 h of the control portion 112 stores data while the multiplexer 111 a , the offset circuit 111 b and the amplifier 111 c of a prescribed signal processing line L 0 , L 1 or L 2 process the corresponding analog signals. This point is described later in more detail with reference to an analytic operation.
  • the logger memory 112 h is provided for storing the digital signals (data) corresponding to the analog signals output from the photoelectric conversion elements 84 a .
  • the logger memory 112 h is constituted of 32 areas 0 to 31 in units of 128 bytes.
  • the areas 0 to 31 store data corresponding to the light components transmitted through the five optical filters 14 b to 14 f (see FIG. 5 ) and data corresponding to the blocked hole 14 j respectively. Every rotation of the filter portion 14 results in data corresponding to the light components transmitted through the five optical filters 14 b to 14 f having different light transmission characteristics.
  • the logger memory 112 h (see FIG. 11 ) stores these data successively from the area 0 .
  • the logger memory 112 h stores “0” in every sixth area as the data corresponding to the hole 14 j .
  • the logger memory 112 h uses six areas every rotation (about 100 msec.) of the filter portion 14 . After using the areas 0 to 31 up to the final area 31 , the logger memory 112 h returns to the area 0 for overwriting data.
  • Each of the areas 0 to 31 of the logger memory 112 h has 128 addresses.
  • the area 0 has 128 addresses 000h to 00Fh, 010h to 01Fh, 020h to 02Fh, 030h to 03Fh, 040h to 04Fh, 050h to 05Fh, 060h to 06Fh and 070h to 07Fh.
  • the area 0 is so formed as to store the data of the aforementioned channels CH 0 to CH 47 (see FIG. 10 ) in the 96 addresses 00h to 05Fh.
  • Each of the data of the channels CH 0 to CH 47 is stored in two addresses.
  • the channels CH 42 to 47 output no data as hereinabove described, so that addresses corresponding to these channels CH 42 to 47 store no data.
  • the addresses 060h to 06Fh and 070h to 07Fh in the area 0 of the logger memory 112 h shown in FIG. 11 are preliminary addresses storing no data in this embodiment.
  • the area 0 stores filter numbers ( 0 to 4 ) in the final address 07Fh. These filter numbers ( 0 to 4 ) are employed for identifying the five optical filters 14 b to 14 f (see FIG. 5 ) respectively.
  • the optical filters 14 b to 14 f can be identified by detecting the timing of passage of the origin slit 14 k .
  • the area 0 stores the filter numbers ( 0 to 4 ) corresponding to the five optical filters 14 b to 14 f in the address 07Fh, thereby identifying the optical filter (one of 14 b to 14 f ) through which the light component corresponding to the data stored in the area 0 has been transmitted.
  • the set memory 112 i shown in FIG. 9 is provided for storing set values such as the offset values supplied to the offset circuits 111 b and the gains (amplification factors) supplied to the amplifiers 111 c .
  • the controller status register 112 j is provided for temporarily storing information such as whether or not the filter portion 14 normally rotates, presence/absence of errors in analog-to-digital conversion by the A-D conversion portions 111 d , the status of data acquisition by the PC body 3 b from the logger memory 112 h and presence/absence of an instruction for starting measurement from the PC body 3 b .
  • the control portion 112 has a function of transmitting the data (optical information) of the measurement samples stored in the logger memory 112 h to the PC body 3 b through the local bus interface 112 k and an interface 116 .
  • the amplification circuit 113 of the control board 6 shown in FIG. 9 has a function of receiving the signal output from the reference light photoelectric conversion element 84 b (see FIG. 10 ) through the reference light preamplifier 85 b and amplifying the received signal.
  • this amplification circuit 113 is constituted of two resistors 113 a and 113 b and an operational amplifier 113 c .
  • a first end of the resistor 113 a receives the signal corresponding to the reference light from the reference light preamplifier 85 b , while a second end thereof is connected to an inverted input terminal of the operational amplifier 113 c .
  • the resistor 113 b is connected between an output terminal and the inverted input terminal of the operational amplifier 113 c .
  • a non-inverted input terminal of the operational amplifier 113 c is grounded.
  • the multiplexers 111 a of the signal processing portion 111 (see FIG. 9 ) and the differentiation circuit 114 receive an output of the operational amplifier 113 c.
  • the differentiation circuit 114 of the control board 6 has a function of generating a differential signal of the signal (hereinafter referred to as a reference signal) corresponding to the reference light received from the amplification circuit 113 .
  • this differentiation circuit 114 is constituted of two resistors 114 a and 114 b , two capacitors 114 c and 114 d and an operational amplifier 114 e .
  • a first end of the resistor 114 a receives the reference signal from the amplification circuit 113 , while a second end thereof is connected to a first electrode of the capacitor 114 c .
  • a second electrode of the capacitor 114 c is connected to an inverted input terminal of the operational amplifier 114 e .
  • Both of the resistor 114 b and the capacitor 114 d are connected between an output terminal and the inverted input terminal of the operational amplifier 114 e .
  • a non-inverted input terminal of the operational amplifier 114 e is grounded.
  • the controller 112 a of the control portion 112 receives an output of the operational amplifier 114 e through a comparator (not shown).
  • the temperature controller 115 of the control board 6 show in FIG. 9 has a function of controlling the temperature of the cuvette receiving portion 81 (see FIG. 1 ) receiving the cuvettes 152 by controlling another warming mechanism (not shown) stored in the second optical information acquisitive portion 80 . As shown in FIG. 9 , the temperature controller 115 is so formed as to control warming with the warming mechanism (not shown) of the second optical information acquisitive portion 80 in response to a set temperature (about 37° C.) received from the PC body 3 b through the interface 116 .
  • the outline of control of the analyzer 3 with the PC body 3 b is now described with reference to FIGS. 2, 3 and 13 .
  • the analyzer 3 and the extension analyzer 4 are identical in control to each other, and hence the control of the analyzer 3 is described in the following.
  • the analytic system 1 starts the information processing terminal 3 a , the body of the analyzer 3 and the extension analyzer 4 by supplying power thereto.
  • the PC body 3 b Upon this power supply, the PC body 3 b performs initialization at a step S 1 shown in FIG. 13 . In this initialization, the PC body 3 b initializes software stored therein and performs processing of acquiring n clocks described later from the control portion 112 of the analyzer 3 .
  • the halogen lamp 11 of the lamp unit 5 Upon power supply to the body of the analyzer 3 , the halogen lamp 11 of the lamp unit 5 (see FIG. 3 ) applies light while the filter portion 14 starts continuously rotating at a rotational speed of 10 revolutions/sec. in the initialization at the step S 1 .
  • the halogen lamp 11 continuously applies light and the filter portion 14 continuously rotates until the body of the analyzer 3 is turned off.
  • the PC body 3 b accepts entry of specimen analysis information by the user.
  • the user inputs information in columns of specimen numbers and measurement items of a specimen analysis list output on the display portion 3 c of the information processing terminal 3 a (see FIG. 2 ) through the keyboard 3 d of the information processing terminal 3 a .
  • the PC body 3 b preserves the specimen analysis information.
  • the PC body 3 b instructs analysis, so that the analyzer 3 performs the analysis.
  • the PC body 3 b determines whether or not a shutdown instruction for the analytic system 1 has been received. When determining that no shutdown instruction for the analytic system 1 has been received at the step S 4 , the PC body 3 b returns to the step S 2 for accepting entry of another specimen analysis information by the user.
  • the PC body 3 b performs shutdown processing at a step S 5 . According to this shutdown processing, the analytic system 1 automatically enters an OFF-state, thereby completing the operation thereof.
  • the quantity of the reference light incident upon the reference light photoelectric conversion element 84 b (see FIG. 8 ) from the lamp unit 5 changes along a waveform shown as “QUANTITY OF REFERENCE LIGHT” during the continuous rotation of the filter portion 14 (see FIG. 3 ).
  • symbol ⁇ denotes a period when any one of the optical filters 14 b to 14 f of the rotating filter portion 14 is arranged on the path of the corresponding light component from the halogen lamp 11 in the lamp unit 5 (see FIG. 3 ).
  • the quantity of the reference light gradually increases.
  • the path of the corresponding light component from the halogen lamp 11 completely falls into the aforementioned one of the optical filters 14 b to 14 f , so that the quantity of the reference light is constant.
  • the quantity of the reference light starts to gradually decrease.
  • the quantity of the reference light reaches zero.
  • the reference light photoelectric conversion element 84 b converts the reference light to an electric signal, so that the reference light preamplifier 85 b and the amplification circuit 113 amplify this electric signal.
  • the amplification circuit 113 outputs a signal (hereinafter referred to as a reference signal) corresponding to the reference light, so that the differentiation circuit 114 receives this reference signal.
  • the differentiation circuit 114 generates a differential signal of the reference signal having a waveform shown as “DIFFERENTIAL SIGNAL OF REFERENCE SIGNAL” in FIG. 15 .
  • the control portion 112 receives this differential signal of the reference signal from the differentiation circuit 114 (see FIG. 9 ) through the comparator (not shown).
  • the control portion 112 detects a clock number N 1 at a point of time when the differential signal of the reference signal reaches a prescribed positive threshold (+). More specifically, the differential signal of the reference signal rises following increase of the quantity of the reference light, as shown in FIG. 15 .
  • the comparator (not shown) receiving the differential signal from the differentiation circuit 114 (see FIG. 9 ) outputs a pulse signal rising to a high level.
  • the controller 112 a of the control portion 112 receives this pulse signal, and detects the clock number N 1 at the point of time when the pulse signal has risen to the high level.
  • the controller 112 a detects the clock number N 1 at the point of time when the differential signal of the reference signal reaches the prescribed positive threshold (+).
  • the control portion 12 detects a clock number (N 2 ) at a point of time when the differential signal of the reference signal reaches a prescribed negative threshold ( ⁇ ). More specifically, the comparator (not shown) receiving the differential signal from the differentiation circuit 114 (see FIG. 9 ) outputs a pulse signal rising to a high level in response to the differential signal of the reference signal gradually falling and reaching the prescribed negative threshold ( ⁇ ).
  • the controller 112 a of the control portion 112 receives this pulse signal, and detects the clock number N 2 at the time when the pulse signal has risen to the high level. Thus, the controller 112 a of the control portion 112 detects the clock number N 2 at the time when the differential signal of the reference signal reaches the prescribed negative threshold ( ⁇ ).
  • the control portion 112 calculates the timing for starting acquiring the signals corresponding to the transmitted light components with the reference light not influenced by the measurement samples etc. As understood from FIG. 15 , the control portion 112 can acquire signals in a period where the quantities of the light components applied from the lamp unit 5 are stable by acquiring the signals corresponding to the light components transmitted through the measurement samples from the detection portion 82 for the period of m clocks with the multiplexers 111 a after n clocks calculated in the aforementioned manner from the clock N 1 .
  • the PC body 3 b instructs primary measurement.
  • the aforementioned first optical information acquisitive portion 70 measures interference substances in the specimens.
  • the PC body 3 b receives the optical information acquired by the first optical information acquisitive portion 70 through the controller 74 c.
  • the PC body 3 b analyzes the received optical information, and determines whether or not the primarily measured specimens are to be subjected to secondary measurement with the second optical information acquisitive portion 80 on the basis of the results of the analysis.
  • the PC body 3 b makes the display portion 3 c display a message indicating that it is difficult to perform reliable analysis due to remarkable influence by interference substances contained in these specimens (step S 28 ).
  • the PC body 3 b instructs suction of the specimens at a step S 23 .
  • the specimen injection arm 40 sucks the specimens from the cuvettes 152 held on the rotary transport portion 30 .
  • the PC body 3 b instructs preparation of measurement samples.
  • the specimen injection arm 40 injects the sucked specimens into the plurality of cuvettes 152 while the reagent injection arms 50 add the reagents for starting blood coagulation contained in the reagent vessels (not shown) to the specimens stored in the plurality of cuvettes 152 in the analyzer 3 .
  • the analyzer 3 prepares the measurement samples.
  • the cuvette transfer portion 60 moves the cuvettes 152 storing the measurement samples toward the receiving holes 81 a of the cuvette receiving portion 81 of the second optical information acquisitive portion 80 .
  • the PC body 3 b instructs secondary measurement.
  • the analyzer 3 starts secondary measurement of the measurement samples. This secondary measurement is now described in detail.
  • the lamp unit 5 intermittently successively applies the five types of light components having different wavelength characteristics (340 nm, 405 nm, 575 nm, 660 nm and 800 nm) respectively to the cuvettes 152 moved toward the receiving holes 81 a .
  • the light components transmitted through the cuvettes 152 are converted to digital data through the photoelectric conversion elements 84 a , the preamplifiers 85 a , the multiplexers 111 a , the offset circuits 111 b , the amplifiers 111 c and the A-D conversion portions 111 d and stored in the logger memory 112 h.
  • the three signal processing lines L 0 to L 2 constituted of the multiplexers 111 a , the offset circuits 111 b , the amplifiers 111 c and the A-D conversion portions 111 d partially parallelly process the electric signals with the multiplexers 111 a , the offset circuits 111 b , the amplifiers 111 c and the A-D conversion portions 111 d .
  • the signal processing line L 0 processes the corresponding electric signals with the multiplexer 111 a , the offset circuit 111 b and the amplifier 111 c
  • the signal processing line L 1 converts the corresponding electric signals with the A-D conversion portion 111 d and the logger memory 112 h (see FIG.
  • the signal processing line L 1 processes the corresponding electric signals with the multiplexer 111 a , the offset circuit 111 b and the amplifier 111 c
  • the signal processing line L 2 converts the corresponding electric signals with the A-D conversion portion 111 d and the logger memory 112 h (see FIG. 9 ) of the control portion 112 stores data in parallel with each other.
  • the signal processing line L 2 processes the corresponding electric signals with the multiplexer 111 a , the offset circuit 111 b and the amplifier 111 c
  • the signal processing line L 0 converts the corresponding electric signals with the A-D conversion portion 111 d and the logger memory 112 h (see FIG. 9 ) of the control portion 112 stores data in parallel with each other.
  • the signal processing portion 111 partially parallelly processes the electric signals in units of 48 ⁇ sec. by successively using the three signal processing lines L 0 to L 2 , as shown in FIG. 17 . More specifically, the signal processing line L 0 performs switching to the channel CH 0 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c at a step 0 shown in FIG. 17 . At this step 0 , the signal processing lines L 1 and L 2 are in states waiting for stabilization of the corresponding electric signals (signal wait states), to process no electric signals. At a step 1 in FIG.
  • the signal processing line L 1 performs switching to the channel CH 6 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c .
  • the signal processing lines L 0 and L 1 are in states waiting for stabilization of the corresponding electric signals, to process no electric signals.
  • the signal processing line L 0 performs A-D conversion of the electric signal of the channel CH 0 with the A-D conversion portion 111 d
  • the logger memory 112 h stores data
  • the signal processing line L 2 performs switching to the channel CH 32 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c in parallel with each other.
  • the signal processing line L 1 is in a state waiting for stabilization of the corresponding electric signals, not to process the electric signals.
  • the signal processing line L 0 performs switching to the channel CH 1 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c , the signal processing line L 1 performs A-D conversion of the electric signal of the channel CH 16 with the A-D conversion portion 111 d and the logger memory 112 h stores data in parallel with each other.
  • the signal processing line L 2 is in a state waiting for stabilization of the corresponding electric signals, not to process the electric signals.
  • the signal processing line L 1 performs switching to the channel CH 117 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c , the signal processing line L 2 performs A-D conversion of the electric signal of the channel CH 32 with the A-D conversion portion 111 d and the logger memory 112 h stores data in parallel with each other.
  • the signal processing line L 0 is in a state waiting for stabilization of the corresponding electric signals, not to process the electric signals.
  • the signal processing lines L 0 to L 2 repetitively perform parallel processing similar to that through the aforementioned steps 2 to 4 up to a step 49 while switching the channels for signal processing.
  • the signal processing line L 2 performs switching to the channel CH 32 with the multiplexer 111 a , correction with the offset circuit 111 b and amplification with the amplifier 111 c .
  • the signal processing lines L 0 and L 1 are in states waiting for stabilization of the corresponding electric signals, not to process the electric signals.
  • All output signals of the multiplexers 111 a , the offset circuits 111 b and the amplifiers 111 c are unstable immediately after signal processing. According to this embodiment, the aforementioned periods for waiting for stabilization of the electric signals are so provided as to prevent such unstable signals from application to analysis of analytes.
  • the signal processing lines L 0 to L 2 process the electric signals of all channels CH 0 to CH 47 through the 51 steps 0 to 50 in the aforementioned manner.
  • the logger memory 112 h stores data in prescribed addresses, for specifying the optical filters and the channels transmitting the light components received from the halogen lamp 11 .
  • the logger memory 112 h transmits the data stored therein to the PC body 3 b at prescribed timing.
  • the PC body 3 b selects optical information (data) suitable for analysis from among 10 types of optical information (data) having different wavelength characteristics and different amplification rates received from the second optical information acquisitive portion 80 , i.e., among data of the low and high gains corresponding to the five types of optical filters 14 b to 14 f respectively, on the basis of the results of analysis of the optical information (data) from the first optical information acquisitive portion 70 acquired at the step S 22 and analyzes the optical information.
  • the PC body 3 b outputs the results of analysis of the measurement samples (coagulation curve and coagulation time shown in FIG. 18 in this embodiment) to the display portion 3 c.
  • step S 3 Data acquisition with the control portion 112 according to this embodiment is now described with reference to FIGS. 9, 13 , 15 , 17 and 19 .
  • the PC body 3 b instructs analysis (step S 3 ), in order to start this data acquisition.
  • the control portion 112 ( FIG. 9 ) waits for detection of the leading edge of the differential signal of the reference signal corresponding to N 1 in FIG. 15 .
  • the control portion 112 waits for a lapse of n clocks calculated in the initialization from the leading edge of the differential signal of the reference signal.
  • the control portion 112 starts acquiring digital data output from the three A-D conversion portions 111 d respectively.
  • the control portion 112 waits for a lapse of m clocks from the start of digital data acquisition. Upon the lapse of m clocks, the control portion 112 ends the digital data acquisition at a step S 35 .
  • the control portion 112 determines whether or not a prescribed time has elapsed from the time receiving the instruction for analysis from the PC body 3 b . The control portion 112 ends the data acquisition if the prescribed time has elapsed, while returning to the step S 31 if the prescribed time has not yet elapsed.
  • the PC body 3 b monitors whether or not the logger memory 112 h has newly stored data, and waits until the logger memory 112 h stores data for 100 msec. (corresponding to single rotation of the filter portion 14 ). More specifically, the PC body 3 b waits for transmission of a notice from the control portion 112 indicating that the logger memory 112 h has stored data for 100 msec.
  • the PC body 3 b acquires the data (partial time-series data) for 100 msec. through the interface 116 and the local bus interface 112 k . In other words, the PC body 3 b acquires data for 100 msec. corresponding to single rotation of the filter portion 14 stored in the areas 0 to 5 of the logger memory 112 h as shown in FIG. 11 .
  • the PC body 3 b determines whether or not the information processing terminal 3 a has accepted a shutdown instruction.
  • the PC body 3 b returns to the step S 40 .
  • the PC body 3 b ends the data acquisition.
  • the PC body 3 b acquires data from the six areas 6 to 11 of the logger memory 112 h subsequent to the areas 0 to 5 , from which the data have been acquired at the first time.
  • the PC body 3 b successively acquires data from the logger memory 112 h every six areas.
  • the PC body 3 b creates prescribed time-series data by combining partial time-series data subsequent to the time when the cuvettes 152 (see FIG. 1 ) storing the measurement samples have been received in the receiving holes 81 a of the second optical information acquisitive portion 80 among those acquired from the logger memory 112 h at the step S 41 in a time-series manner. Then, the PC body 3 b creates the coagulation curve shown in FIG. 18 on the basis of the created time-series data, and obtains the coagulation times of the measurement samples from the created coagulation curve.
  • the PC body 3 b obtains a time t when the intensity of the transmitted light components reaches 50%, i.e., the intermediate level between 100% and 0%, and calculates elapsed times from this time t as the coagulation times.
  • the display portion 3 c displays the coagulation times at the step S 27 (see FIG. 16 ), as described above.
  • the control portion 112 parallelly and continuously executes the following three monitoring operations during the rotation of the filter portion 14 .
  • the control portion 112 stops the filter portion 14 from rotating.
  • a method of monitoring the time interval for detecting the origin slit 14 k is described with reference to FIGS. 2, 3 , 9 , 21 and 22 .
  • the filter portion 14 of the lamp unit continuously uninterruptedly rotates while a power source of the analyzer 3 (see FIG. 2 ) is in an ON-state.
  • the filter rotation monitoring portion 112 b of the control portion 112 receives signals from the sensor 16 detecting the slits 14 k and 141 of the rotating filter portion 14 .
  • the sensor 16 outputs a signal rising to ON-states as shown in a waveform diagram of FIG. 22 .
  • the filter rotation monitoring portion 112 b determines whether or not the sensor 16 has detected any slit on the basis of the signal received from the sensor 16 .
  • the filter rotation monitoring portion 112 b repetitively determines whether or not the sensor 16 has detected passage of any slit at the step S 51 again.
  • the filter rotation monitoring portion 112 b of the control portion 112 determines whether or not this slit is the origin slit 14 k at a step S 52 .
  • the filter rotation monitoring portion 112 b makes this determination on the origin slit 14 k on the basis of a signal generated by a slit width counter (not shown) provided therein.
  • the slit width counter (not shown) generates an integral signal of the signal received from the sensor 16 as shown in FIG. 22 .
  • the ON-state period of the signal output from the sensor 16 upon detection of the origin slit 14 k is longer than the ON-state period of the signal output from the sensor 16 upon detection of any normal slit 14 l due to the width of the origin slit 14 k larger than those of the remaining normal slits 14 l .
  • the integral signal generated by the slit width counter (not shown) of the filter rotation monitoring portion 112 b rises up to a level higher than those of integral signals output upon detection of the normal slits 14 l .
  • the filter rotation monitoring portion 112 b sets a prescribed threshold between the levels of rise of the integral signals output upon detection of the origin slit 14 k and the normal slits 14 l , for determining that the slit detected by the sensor 16 is the origin slit 14 k when the corresponding integral signal reaches the prescribed threshold while determining that the slit detected by the sensor 16 is not the origin slit 14 k (but any of the normal slits 14 l ) when the corresponding integral signal does not reach the prescribed threshold.
  • the filter rotation monitoring portion 112 b When determining that the slit detected by the sensor 16 is not the origin slit 14 k at the step S 52 in FIG. 21 , the filter rotation monitoring portion 112 b returns to the step S 51 .
  • the filter rotation monitoring portion 112 b stores the time T 1 when the sensor 16 has detected the origin slit 14 k at a step S 53 .
  • the filter rotation monitoring portion 112 b determines whether or not the sensor 16 has detected another slit similarly to the aforementioned step S 51 .
  • the filter rotation monitoring portion 112 b When determining that the sensor 16 has detected no slit at the step S 54 , the filter rotation monitoring portion 112 b repetitively makes the determination at the step S 54 . When determining that the sensor 16 has detected another slit at the step S 54 , on the other hand, the filter rotation monitoring portion 112 b determines whether or not the slit detected by the sensor 16 is the origin slit 14 k , similarly to the aforementioned step S 52 .
  • the filter rotation monitoring portion 112 b When determining that the slit detected by the sensor 16 is not the origin slit 14 k , the filter rotation monitoring portion 112 b returns to the step S 54 .
  • the filter rotation monitoring portion 112 b stores the time T(n) when the sensor 16 has detected the origin slit 14 k at a step S 56 . Referring to the time T(n), n represents the frequency of detection of the origin slit 14 k .
  • the filter rotation monitoring portion 112 b determines whether or not the time interval T 2 ⁇ T 1 calculated at the step S 57 is in the range of a prescribed time interval previously set as necessary for single rotation of the filter portion 14 .
  • the filter rotation monitoring portion 112 b When determining that the time interval T 2 ⁇ T 1 is not in the range of the prescribed time interval at the step S 58 , the filter rotation monitoring portion 112 b outputs error information indicating that the rotation of the filter portion 14 is abnormal to the controller status register 112 j through the controller 112 a at a step S 59 . At this time, the filter rotation monitoring portion 112 b stops the filter portion 14 from rotating. The controller status register 112 j temporarily stores the error information. Then, the controller status register 112 j transmits the error information stored therein to the PC body 3 b through the local bus interface 112 k and the interface 116 . Then, the PC body 3 b displays an error message indicating that the rotation of the filter portion 14 is abnormal on the display portion 3 c of the information processing terminal 3 a.
  • the filter rotation monitoring portion 112 b determines whether or not the control portion 112 has instructed a stop of rotation of the filter portion 14 at a step S 60 .
  • the filter rotation monitoring portion 112 b returns to the step S 54 .
  • the filter rotation monitoring portion 14 ends the monitoring operation on the rotation of the filter portion 14 .
  • the filter rotation monitoring portion 112 b repeats the series of steps S 54 to S 60 until the same determines that the control portion 112 has instructed a stop of rotation of the filter portion 14 at the step S 60 .
  • the filter rotation monitoring portion 112 b of the control portion 112 determines whether or not the sensor 16 has detected passage of any slit (the origin slit 14 k (see FIG. 5 ) or any of the normal slits 14 l ) on the basis of the corresponding signal from the sensor 16 , similarly to the step S 51 shown in FIG. 21 .
  • the filter rotation monitoring portion 112 b repeats the step S 61 .
  • the filter rotation monitoring portion 112 b stores the time t 1 when the sensor 16 has detected this slit at a step S 62 .
  • the filter rotation monitoring portion 112 b determines whether or not the sensor 16 has detected passage of another slit, similarly to the aforementioned step S 61 .
  • the filter rotation monitoring portion 112 b repeats the step S 63 .
  • the filter rotation monitoring portion 112 b stores the time t(n) when the sensor 16 has detected this slit at a step S 64 . Referring to the time t(n), n represents the frequency of detection of slits by the sensor 16 .
  • the filter rotation monitoring portion 112 b determines whether or not the time interval t 2 ⁇ t 1 calculated at the step S 65 is in the range of a prescribed time interval previously set as that between the times for detecting two adjacent slits respectively. This time interval is either a first time interval required for normal passage of the optical filter 14 e following passage of the optical filter 14 f or a second time interval required for normal passage of the optical filter 14 f following passage of the optical filter 14 b.
  • the filter rotation monitoring portion 112 b When determining that the time interval t 2 ⁇ t 1 is neither in the range of the aforementioned first time interval nor in the range of the aforementioned second time interval at the step S 66 , the filter rotation monitoring portion 112 b outputs error information indicating that the rotation of the filter portion 14 is abnormal to the controller status register 112 j through the controller 112 a at a step S 67 . At this time, the filter rotation monitoring portion 112 b stops the filter portion 14 from rotating. The controller status register 112 j temporarily stores the error information. Then, the controller status register 112 j transmits the error information stored therein to the PC body 3 b through the local bus interface 112 k and the interface 116 . Then, the PC body 3 b displays an error message indicating that the rotation of the filter portion 14 is abnormal on the display portion 3 c of the information processing terminal 3 a (see FIG. 2 ).
  • the filter rotation monitoring portion 112 b determines whether or not the control portion 112 has instructed a stop of rotation of the filter portion 14 at a step S 68 .
  • the filter rotation monitoring portion 112 b returns to the step S 63 .
  • the filter rotation monitoring portion 112 b ends the monitoring operation on the rotation of the filter portion 14 .
  • the filter rotation monitoring portion 112 b repeats the series of steps S 61 to S 68 until the same determines that the control portion 112 has instructed a stop of rotation of the filter portion 14 at the step S 68 .
  • the filter rotation monitoring portion 112 b of the control portion 112 determines whether or not the sensor 16 has detected any slit of the rotating filter portion 14 (see FIG. 15 ) on the basis of the corresponding signal from the sensor 16 , similarly to the step S 51 shown in FIG. 21 .
  • the filter rotation monitoring portion 112 b repeats the step S 71 .
  • the filter rotation monitoring portion 112 b determines whether or not the slit detected by the sensor 16 is the origin slit 14 k at a step S 72 , similarly to the step S 52 shown in FIG. 21 . When determining that the detected slit is not the origin slit 14 k at the step S 72 , the filter rotation monitoring portion 112 b returns to the step S 71 . When determining that the detected slit is the origin slit 14 k at the step S 72 , on the other hand, the filter rotation monitoring portion 112 b stores the information indicating that the sensor 16 has detected the origin slit 14 k at a step S 73 .
  • the filter rotation monitoring portion 112 b determines whether or not the sensor 16 has detected another slit, similarly to the aforementioned step S 71 .
  • the filter rotation monitoring portion 112 b repeats the step S 74 .
  • the filter rotation monitoring portion 112 b determines whether or not the detected slit is the origin slit 14 k at a step S 75 , similarly to the aforementioned step S 72 .
  • the filter rotation monitoring portion 112 b When determining that the detected slit is not the origin slit 14 k (but any of the normal slits 14 l ) at the step S 75 , the filter rotation monitoring portion 112 b counts the number of the slit (normal slit 141 ) detected at the step S 75 at a step S 76 . Thereafter the filter rotation monitoring portion 112 b returns to the step S 74 .
  • the filter rotation monitoring portion 112 b stores the information indicating that the sensor 16 has detected the origin slit 14 k at a step S 77 .
  • the filter rotation monitoring portion 112 b acquires the number of the normal slits 14 l counted at the step S 76 as that of the normal slits 14 l detected while the origin slit 14 k has been detected twice.
  • the filter rotation monitoring portion 112 b determines whether or not the number of the normal slits 14 l acquired at the step S 78 is a prescribed number ( 5 ).
  • the filter rotation monitoring portion 112 b When determining that the acquired number of the normal slits 14 l is not the prescribed number ( 5 ) at the step S 79 , the filter rotation monitoring portion 112 b outputs error information indicating that the rotation of the filter portion 14 is abnormal to the controller status register 112 j through the controller 112 a at a step S 80 . At this time, the filter rotation monitoring portion 112 b stops the filter portion 14 from rotating. The controller status register 112 j temporarily stores the error information. Then, the controller status register 112 j transmits the error information stored therein to the PC body 3 b through the local bus interface 112 k and the interface 116 . Then, the PC body 3 b displays an error message indicating that the rotation of the filter portion 14 is abnormal on the display portion 3 c of the information processing terminal 3 a.
  • the filter rotation monitoring portion 112 b determines whether or not the control portion 112 has instructed a stop of rotation of the filter portion 14 at a step S 81 .
  • the filter rotation monitoring portion 112 b returns to the step S 74 .
  • the filter rotation monitoring portion 14 ends the monitoring operation on the rotation of the filter portion 14 .
  • the filter rotation monitoring portion 112 b repeats the series of steps S 74 to S 81 until the same determines that the control portion 112 has instructed a stop of rotation of the filter portion 14 at the step S 81 .
  • the two optical fiber members 17 b and 17 a guide the light components emitted from the lamp unit 5 to the measurement samples provided on the analyzer 3 and the extension analyzer 4 respectively so that no individual lamp units may be provided for supplying light components to the measurement samples provided on the analyzer 3 and the extension analyzer 4 respectively, whereby the analytic system 1 can be downsized.
  • the analyzer 3 and the extension analyzer 4 are so separately provided that the analytic system 1 can parallelly treat various prescribed measurement samples (specimens) with the analyzer 3 and the extension analyzer 4 .
  • the analytic system 1 can improve specimen treatment efficiency in a case of acquiring optical information from a plurality of different measurement samples (specimens). Consequently, the analytic system 1 can improve specimen treatment efficiency while attaining downsizing.
  • the two optical fiber members 17 a and 17 b so branch the light components that the analytic system 1 can increase the quantities of light components emitted from exit end surfaces can be increased as compared with a case of branching light with a single optical fiber member.
  • the analytic system 1 guides the light components of the same characteristics emitted from the halogen lamp 11 to the measurement samples of the analyzer 3 and the extension analyzer 4 through the mirror 12 b , the condensing lenses 13 d to 13 f and the optical fiber member 17 b and through the mirror 12 a , the condensing lenses 13 a to 13 c and the optical fiber member 17 a respectively, whereby the analyzer 3 and the extension analyzer 4 can reduce the numbers of errors resulting from different characteristics of the light components applied to the measurement samples respectively.
  • the halogen lamp 11 of the lamp unit 5 formed by the platelike filament 11 a capable of emitting light components from both surfaces thereof, can apply light components of substantially identical characteristics (quantities of light components etc.) from both surfaces of the platelike filament 11 a , whereby the analytic system 1 can easily guide the light components of substantially identical characteristics emitted from both surfaces of the platelike filament 11 a to the measurement samples of the analyzer 3 and the extension analyzer 4 through the mirror 12 b , the condensing lenses 13 d to 13 f and the optical fiber member 17 b and through the mirror 12 a , the condensing lenses 13 a to 13 c and the optical fiber member 17 a respectively.
  • the analytic system temporarily stores the data output from the detection portion and the signal processing portion in the logger memory of the control portion so that the PC body successively acquires the partial time-series data of the prescribed period from the data stored in the logger memory in the aforementioned embodiment
  • the present invention is not restricted to this but the analytic system may alternatively directly output the data from the detection portion or the signal processing portion to the PC body without temporarily storing the data in the logger memory.
  • control portion calculates the timing ( n clocks) for starting signal acquisition on the basis of the differential signal of the reference signal and starts acquiring data upon a lapse of the calculated n clocks after the differential signal of the reference signal reaches the prescribed threshold in the aforementioned embodiment
  • the present invention is not restricted to this but the control portion may alternatively start data acquisition at previously set timing.
  • control portion starts data acquisition upon a lapse of n clocks from the leading edge of the differential signal of the reference signal corresponding to the reference light in the aforementioned embodiment
  • the present invention is not restricted to this but the control portion may alternatively start data acquisition upon a lapse of a prescribed period from the time when the sensor gas detected any slit.
  • the present invention is applied to the analyzer performing coagulation measurement in the aforementioned embodiment, the present invention is not restricted to this but may also be applied to an analyzer (analytic system) performing measurement, other than coagulation measurement, requiring employment of a plurality of light components having different wavelength characteristics.
  • the present invention may be applied to a biochemical analyzer (analytic system).
  • the present invention is not restricted to this but the information processing terminal and the body of the analyzer may alternatively be integrated with each other.
  • the analyzer is rendered extendable with the extension analyzer for treating a large number of specimens in the aforementioned embodiment, the present invention is not restricted to this but the analyzer may alternatively be rendered unextendable with any extension analyzer.
  • the analytic system employs the multiplexers selecting the signals one by one from the plurality of analog signals output from the plurality of photoelectric conversion elements and successively outputting the same to the offset circuits in the aforementioned embodiment
  • the present invention is not restricted to this but the analytic system may alternatively employ an analog signal selector simultaneously selecting at least two signals from the plurality of analog signals output from the plurality of photoelectric conversion elements.
  • the analytic system 1 bidirectionally emits light components from the filament 11 a of the halogen lamp 11 for introducing the first light component into the optical fiber member 17 a through the condensing lenses 13 a to 13 c while introducing the second light component into the optical fiber member 17 b through the condensing lenses 13 d to 13 f in the aforementioned embodiment
  • the present invention is not restricted to this but the analytic system 1 may alternatively be provided with two halogen lamps (light sources) for introducing a light component emitted from the first halogen lamp into the optical fiber member 17 a through the condensing lenses 13 a to 13 c while introducing a light component emitted from the second halogen lamp into the optical fiber member 17 b through the condensing lenses 13 d to 13 f.

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080245960A1 (en) * 2007-04-09 2008-10-09 Baker Hughes Incorporated Method and Apparatus to Determine Characteristics of an Oil-Based Mud Downhole
US20100148049A1 (en) * 2007-11-01 2010-06-17 Baker Hughes Incorporated Method of identification of petroleum compounds using frequency mixing on surfaces
US20100181472A1 (en) * 2007-04-09 2010-07-22 Baker Hughes Incorporated Method and Apparatus to Determine Characteristics of an Oil-Based Mud Downhole
US20100291667A1 (en) * 2009-05-14 2010-11-18 Sony Corporation Optical detector
US20150316564A1 (en) * 2012-12-03 2015-11-05 Tommy Forsell Blood Analyzing Device for Malaria Analysis
US20160349237A1 (en) * 2014-02-19 2016-12-01 Roche Diagnostics Operations, Inc. Method and device for assigning a blood plasma sample
US20170045539A1 (en) * 2015-08-11 2017-02-16 Shimadzu Corporation Automatic blood coagulation analysis device
EP3239713A1 (en) * 2016-04-28 2017-11-01 Sysmex Corporation Method for analyzing blood specimen, reagent and reagent kit for analyzing blood specimen, and blood specimen analyzer
CN107923853A (zh) * 2015-08-26 2018-04-17 株式会社日立高新技术 自动分析装置、自动分析系统和自动分析方法

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU229210B1 (en) 2011-11-16 2013-09-30 Diagon Kft Method and automatic device for in vitro diagnostic tests of blood clotting
JP6101655B2 (ja) * 2014-03-27 2017-03-22 シスメックス株式会社 分析装置
US20160238627A1 (en) 2015-02-13 2016-08-18 Abbott Laboratories Decapping and capping apparatus, systems and methods for use in diagnostic analyzers
JP6689597B2 (ja) 2015-11-27 2020-04-28 シスメックス株式会社 血液凝固分析装置
JP6813953B2 (ja) * 2016-02-29 2021-01-13 シスメックス株式会社 血液凝固分析装置および血液凝固分析方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5283178A (en) * 1989-05-03 1994-02-01 Abbott Laboratories Method of forming agglutinates in blood samples
US20050106745A1 (en) * 2003-09-19 2005-05-19 Agy Therapeutics, Inc. Combination of solubility and membrane permeability measurement methods for profiling of chemical compounds

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06100607B2 (ja) * 1984-07-20 1994-12-12 オリンパス光学工業株式会社 自動化学分析装置
JPS6188158A (ja) * 1985-09-03 1986-05-06 Olympus Optical Co Ltd 自動分析装置
JP2731229B2 (ja) 1989-04-25 1998-03-25 オリンパス光学工業株式会社 自動分析装置
JPH08315783A (ja) * 1995-05-17 1996-11-29 Olympus Optical Co Ltd ランプ
US5825478A (en) * 1996-11-15 1998-10-20 Wilcox; Steven Multifunctional photometer apparatus
JPH10170432A (ja) 1996-12-13 1998-06-26 Kubota Corp 分光分析装置
DE19752925C2 (de) * 1997-11-28 2003-11-27 Agfa Gevaert Ag Vorrichtung zum Auslesen von einer in einem Phosphorträger abgespeicherten Information und Röntgenkassette
US6608671B2 (en) * 1998-07-17 2003-08-19 Vertex Pharmaceuticals (San Diego) Llc Detector and screening device for ion channels
JP3380542B2 (ja) * 1998-07-27 2003-02-24 株式会社日立製作所 生体サンプルの分析方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5283178A (en) * 1989-05-03 1994-02-01 Abbott Laboratories Method of forming agglutinates in blood samples
US20050106745A1 (en) * 2003-09-19 2005-05-19 Agy Therapeutics, Inc. Combination of solubility and membrane permeability measurement methods for profiling of chemical compounds

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080245960A1 (en) * 2007-04-09 2008-10-09 Baker Hughes Incorporated Method and Apparatus to Determine Characteristics of an Oil-Based Mud Downhole
US20100181472A1 (en) * 2007-04-09 2010-07-22 Baker Hughes Incorporated Method and Apparatus to Determine Characteristics of an Oil-Based Mud Downhole
US20100148049A1 (en) * 2007-11-01 2010-06-17 Baker Hughes Incorporated Method of identification of petroleum compounds using frequency mixing on surfaces
US8487238B2 (en) 2007-11-01 2013-07-16 Baker Hughes Incorporated Method of identification of petroleum compounds using frequency mixing on surfaces
US20100291667A1 (en) * 2009-05-14 2010-11-18 Sony Corporation Optical detector
CN102890073A (zh) * 2009-05-14 2013-01-23 索尼公司 光学检测器
US8945911B2 (en) * 2009-05-14 2015-02-03 Sony Corporation Optical detector
US9651492B2 (en) * 2009-05-14 2017-05-16 Sony Corporation Optical detector
US9228950B2 (en) 2009-05-14 2016-01-05 Sony Corporation Optical detector
US9541552B2 (en) * 2012-12-03 2017-01-10 Tommy Forsell Blood analyzing device for malaria analysis
US20150316564A1 (en) * 2012-12-03 2015-11-05 Tommy Forsell Blood Analyzing Device for Malaria Analysis
US20160349237A1 (en) * 2014-02-19 2016-12-01 Roche Diagnostics Operations, Inc. Method and device for assigning a blood plasma sample
US9983192B2 (en) * 2014-02-19 2018-05-29 Roche Diagnostics Operations, Inc. Method and device for assigning a blood plasma sample
US10359416B2 (en) 2014-02-19 2019-07-23 Roche Diagnostics Operations, Inc. Method and device for assigning a blood plasma sample
US20170045539A1 (en) * 2015-08-11 2017-02-16 Shimadzu Corporation Automatic blood coagulation analysis device
US9746485B2 (en) * 2015-08-11 2017-08-29 Shimadzu Corporation Automatic blood coagulation analysis device
CN107923853A (zh) * 2015-08-26 2018-04-17 株式会社日立高新技术 自动分析装置、自动分析系统和自动分析方法
JPWO2017033562A1 (ja) * 2015-08-26 2018-08-16 株式会社日立ハイテクノロジーズ 自動分析装置、自動分析システム及び自動分析方法
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US10725028B2 (en) 2015-08-26 2020-07-28 Hitachi High-Tech Corporation Automatic analysis device, automatic analysis system, and automatic analysis method
EP3239713A1 (en) * 2016-04-28 2017-11-01 Sysmex Corporation Method for analyzing blood specimen, reagent and reagent kit for analyzing blood specimen, and blood specimen analyzer
US11150253B2 (en) 2016-04-28 2021-10-19 Sysmex Corporation Method for analyzing blood specimen, reagent and reagent kit for analyzing blood specimen, and blood specimen analyzer

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