CN109142768A - Automatic analysing apparatus and method of sample analysis - Google Patents

Abstract

The present invention relates to a kind of automatic analysing apparatus, it include: filling unit, including the first filling unit and the second filling unit, the first filling unit is for filling sample or sample and portion of reagent to reaction vessel, and the second filling unit is for filling reagent to reaction vessel；Reaction vessel feed unit, for storing and supply response container；Filling station needs to fill the reaction vessel of sample or/and reagent for receiving and carrying, and the filling station can move back and forth between the reaction vessel feed unit, the first filling unit and the second filling unit；And buanch unit, transfer reaction container between the different positions.Sample and reagent is made to fill the completion of unit cooperation by the first filling unit and second in this way, the filling movement for filling unit is completed in independent filling station, and final realization ensures the purpose of raising test speed on the basis of complete machine compact layout.

Description

Automatic analysing apparatus and method of sample analysis

Technical field

The present invention relates to in-vitro diagnosis apparatus fields, and in particular to a kind of automatic analysing apparatus and method of sample analysis.

Background technique

In recent years, the development and progress of clinical examination and automatic technology not only improves clinical laboratroy automation water It is flat, the efficiency of medical test is improved, the q&r of inspection result is also improved.However, with detection specimen amount Increase, clinical labororatory needs constantly to increase Large-Scale Automatic Measurement System to meet its detection demand, so as to cause laboratory Increasingly crowded and testing cost is constantly soaring.Thus, how under the pressure and challenge for facing medical insurance control expense, is promoted and examine effect Rate guarantees result and makes full use of existing lab resources and reduce testing cost expenditure, is one that clinical examination to be solved Pressing issues.

In order to express easily, herein automatically to exempt from in-vitro diagnosis (In-Vitro Diagnostics, abbreviation IVD) Epidemic disease analyzer is particularly column with luminescence immunoassay instrument, illustrates that the technical program and method, those skilled in that art are answered The understanding, the present invention program and method can also be used for other clinical examination automation equipments, such as fluorescence immunoassay device, electrochemistry It is immunized.Automatic immunity is by using enzyme label, group of the lanthanides based on the immunological response that antigen-antibody be combined with each other Rubidium marking or chemiluminescent agent labelled antigen antibody, are reacted by a series of Cascaded amplifications, by optical signal or electric signal and are divided Analysis object concentration etc. is associated, and analyzes the antigen or antibody to be measured in human sample, is mainly used in clinical laboratory, the third of hospital The mechanisms such as square independent laboratory, blood examination center quantify each analyte content in Human Fluids, sxemiquantitative or qualitative inspection It surveys, carries out the diagnosis of infectious disease, tumour, endocrine function, cardiovascular disease and prenatal and postnatal care and autoimmunity class disease etc.. Automatic lmunoassays analyzer is usually by the groups such as sampling unit, reaction member, supply and waste waste unit, system control unit At.Electrochemiluminescent immunoassay due to quantitative detection, high sensitivity, the advantages such as specificity is good, the range of linearity is wide, the degree of automation is high just The mainstream technology immune as current automation.Full-automatic illumination immunoassay is according to labeling method and luminescence system difference, again Including enzyme-catalyzed chemical luminescence, direct chemiluminescence, electrochemical luminescence etc..

With reference to attached drawing 1-3, luminescence immunoassay by test philosophy and mode generally can be divided into one-step method, delay one-step method, Two-step method etc., main testing procedure generally comprises filling sample and reagent, reactant are mixed, are incubated for, cleaning separates (Bound- Free, abbreviation B/F), plus signal reagent, measurement etc..It should be pointed out that in order to express easily, the present invention distinguished reagent and Signal reagent, incubation and signal are incubated for.Reagent and analysis project are " one-to-one correspondence " relationship, i.e., the corresponding tool of different analysis projects Body reagent formula, amount of reagent, in terms of it is general different.According to the difference of concrete analysis project, reagent is usually wrapped Multiple components are included, the reagent components such as such as common 2-5 component, including magnetic particle reagent, enzyme marking reagent, dilution.According to anti- Answer mode different, multiple reagent components of an analysis project can be filled disposably or multiple steps is divided to fill, substep The first reagent, the second reagent, third reagent etc. are defined as according to filling order when rapid filling.Signal reagent is for measuring signal It generates, usually one kind of common reagent, is the corresponding relationship of " one-to-many " with analysis project, i.e., different analysis projects shares Signal reagent.Incubation of the invention refer in particular to reaction vessel start cleaning separation before, in reactant reaction member constant temperature The process of the antigen-antibody binding reaction or biotin-labeled pentylamine association reaction that occur under environment, specifically, one-step method are incubated for one Secondary, to enter the primary incubation before cleaning separation, delay one-step method is incubated for twice, incubates including the first time before the second reagent of filling It educates and into second of incubation before cleaning separation, two-step method is incubated for twice, incubated including the first time before first time cleaning separation Educate and clean for second second of incubation before separation.And signal is incubated for the reaction vessel after referring to cleaning separation and signal examination is being added After agent, a period of time is reacted under isoperibol, makes the process of signal enhancing.According to the difference of reaction system and principle of luminosity, Not all test requires signal incubation, and the test for needing signal to be incubated for is generally enzymatic class chemiluminescence immune assay. Details are as follows for the corresponding testing procedure of different test patterns:

1) one-step method: referring to attached drawing 1, filling sample (S) and reagent (R), mixing (some test methods it is also not necessary to Mix, similarly hereinafter, repeat no more), it is incubated for (generally 5-60 minutes), cleaning separation is carried out after the completion of being incubated for, fill signal reagent, Signal is incubated for (generally 1-6 minutes), finally measures.It should be pointed out that due to the difference of the specific ingredient of signal reagent, some Luminescence system undesired signal is incubated for, and can directly be measured during filling signal reagent or after having filled signal reagent.Letter Number reagent can be one or more, and with reference to attached drawing 2, signal reagent includes the first signal reagent, second signal reagent.

2) be delayed one-step method: with one-step method the difference is that reagent fills in two times, needs to be incubated for twice, adding the first examination First time incubation is carried out after agent mixing, and the second reagent is added after the completion of being incubated for for the first time and is mixed.It is more than once compared with one-step method It is incubated for, fills reagent and mixing movement, remaining process is as one-step method.

3) two-step method: it is more than once cleaning separating step with delay one-step method difference, other steps are identical.

In order to realize above-mentioned process automation test, existing specific implementation technical solution is as follows:

The first prior art will be incubated for, cleaning separation and measurement separate separated layout, respectively by three rotational circles Disk completes corresponding function, and reaction vessel is completed to shift by mechanical gripping arm between different units takes place.The technical solution component and unit It is more, it is incubated for transfer position, cleaning separation transfer position and measurement transfer position and is dispersed on different disks, and apart from remote, reaction vessel It needs to shift between each transfer position, causes the problems such as volume is big, at high cost, motion path is more, control flow is complicated.

Second of prior art will be incubated for and measurement is arranged together composition and is incubated for measuring unit, and cleaning separation is by another One separate unit is completed, although the technical solution reduces a measurement disk, certain compared with the first existing scheme Be conducive to control package size and cost in degree, but equally exist the problem identical as the first technical solution.The technical side For case in order to realize flexible incubation time, incubation measuring unit control is complicated, is incubated for and measurement also can be restricted mutually in control, Not there is only cannot achieve high-speed automated test, it also cannot achieve flexible signal and being incubated for.

The third prior art will be incubated for, cleaning separation and measurement are real on an individual pen disk or discrimination shape track Existing, for the program in order to support longer incubation time, disk is other than cleaning separation and measurement position, it is also necessary to be arranged very much It is incubated for position, in this way in order to realize that high speed test, disk or discrimination shape track size needs are designed very big, manufacturing difficulty Greatly, at high cost, in addition, in order to realize delay one-step method and two-step method test, it is also necessary at least two sample charging mechanisms and at least two A washing separator structure, to increase material, processing, production cost and package size.On the other hand, which also limits Incubation time has been made, incubation time has been resulted in and fixes, goes out the problems such as result overlong time.In addition, the technical solution is not only difficult Dark room conditions needed for realizing measurement, need to increase additional tripper, also cannot achieve flexible signal and are incubated for.

Summary of the invention

For solve the problems, such as the generally existing disadvantage of the prior art and, the present invention, which provides, a kind of can make complete machine compact layout and to mention The automatic analysing apparatus and method of sample analysis of high test speed.

An aspect of of the present present invention provides a kind of automatic analysing apparatus, comprising:

Fill unit, including first filling unit and second filling unit, it is described first filling unit for fill sample, Or sample and portion of reagent, to reaction vessel, the second filling unit is for filling reagent to reaction vessel；

Reaction vessel feed unit, for storing and supply response container；

Filling station needs to fill the reaction vessel of sample or/and reagent for receiving and carrying, and the filling station can be Move back and forth between the reaction vessel feed unit, the first filling unit and the second filling unit；And

Buanch unit, between the different positions transfer reaction container.

According to another aspect of the present invention, a kind of method of sample analysis is provided, comprising:

Step is filled, comes filling station between reaction vessel feed unit, the first filling unit and the second filling unit Return is dynamic, and provides reaction vessel to filling station with reaction vessel feed unit, is added with the first filling unit into reaction vessel Enter sample or sample and portion of reagent, reagent is added into reaction vessel with the second filling unit；

Incubation step turns to be displaced into being incubated for twice including at least needs for reaction member to being incubated for by least one Reaction vessel is incubated for；

Separating step is cleaned, it is clear to the reaction vessel progress for turning to be displaced into reaction member by least one cleaning separation Separation is washed, to remove the ingredient being not associated in reactant；

Signal reagent step is filled, signal reagent is filled into reaction vessel,

Measuring process measures the reaction signal in reaction vessel by measuring device.

The present invention fills sample and reagent by the way that independent filling station is arranged, and filling station can supply single in reaction vessel Move back and forth between member, the first filling unit and the second filling unit, so that the reaction for receiving the supply of reactor feed unit is held Device, reception the first filling unit filling sample or sample and portion of reagent receive the second filling unit filling reagent.Make in this way Sample and reagent are completed by the first filling unit and the second filling unit cooperation, and the filling for filling unit is acted independent Filling station is completed, and final realization ensures the purpose of raising test speed on the basis of complete machine compact layout.

Detailed description of the invention

Fig. 1 is one-step method reaction pattern schematic diagram；

Fig. 2 is one-step method reaction pattern (another signal measurement mode) schematic diagram；

Fig. 3 is delay one-step method and two-step method reaction pattern schematic diagram；

Fig. 4 is the first embodiment schematic diagram of automatic analysing apparatus of the present invention；

Fig. 5 is one-step method test flow chart；

Fig. 6 is delay one-step method test flow chart；

Fig. 7 is two-step method test flow chart；

Fig. 8 is second of embodiment schematic diagram of automatic analysing apparatus of the present invention；

Fig. 9 is the third embodiment schematic diagram of automatic analysing apparatus of the present invention；

Figure 10 is the 4th kind of embodiment schematic diagram of automatic analysing apparatus of the present invention；

Figure 11 is the 5th kind of embodiment schematic diagram of automatic analysing apparatus of the present invention.

Specific embodiment

Below by specific embodiment combination attached drawing, invention is further described in detail.

A kind of automatic analysing apparatus of the invention, comprising: filling unit fills sample and/or reagent to reaction vessel, instead Unit is answered, be incubated for and cleans the reactant in separation reaction vessel, measuring device measures the reaction signal in reaction vessel, turns Move unit, between the different positions transfer reaction container, the reaction member includes a rotating device, on the rotating device Several reaction vessel positions are set, for carrying and fixing reaction vessel, at least one incubation is set on the reaction member and is turned Displacement and at least one cleaning separation transfer position, at least one of the reaction member are incubated for transfer position and at least one cleaning point From transfer position within the scope of the horizontal movement of buanch unit.

Reaction vessel provides reacting environment for the reaction of sample and reagent, can be various shape and construction reaction tube, Reaction cup, the reaction cup item of multiple chambers, reaction chip etc., it is generally disposable.The material of reaction vessel is usually plastics, Such as polystyrene.Reaction vessel can not also be coated with, can also deposit in advance in it in the preparatory envelope antigen of inner wall or antibody Put the magnetic bead or baton round being coated with.The storage and supply of reaction vessel are completed by reaction vessel feed unit.For the machine of simplifying Structure, reaction vessel feed unit preferably use walkthrough column, and reaction vessel is arranged in reaction vessel pallet, box or reaction in advance to be held On device frame, conduit, reaction vessel feed unit every time can convey whole disk, whole box reaction vessel or a row, a column reaction vessel To target position.Reaction vessel feed unit can be bin type in other embodiments, and reaction vessel can be poured at packet is at random In the feed bin of reaction vessel feed unit, then reaction vessel feed unit automatically gradually individually sorts reaction vessel, supply Reaction vessel is to buanch unit.

Reaction vessel can be completed in the transfer in apparatus of the present invention between different location by buanch unit.Buanch unit can be with It is any suitable can shift or the mechanism of mobile response container, currently preferred buanch unit mainly include driving machine The structures such as structure, horizontal movement machinery arm, pick-and-place mechanism.Pick-and-place mechanism is usually mechanical finger, can be horizontal with pick-and-place reaction vessel Movable machinery arm under driving mechanism driving can along X to, Y-direction, X be to Y-direction, radially, circumferentially, radially and circumferentially etc. directions are moved Dynamic pick-and-place mechanism, is moved to different location for the reaction vessel that pick-and-place mechanism grabs.Other than horizontal movement, buanch unit may be used also It moves up and down, reaction vessel is put into different position or is taken out from different positions.It is laid out according to test speed and complete machine Difference, settable one or more buanch unit.

Fill the filling that unit completes sample, reagent.Unit is filled generally by steel needle or disposable suction nozzle (Tip), filling Motion driving mechanism, syringe or topping-up pump, valve, fluid circuit and service sink (can also not have service sink when using Tip) Equal components are constituted.In order to complete to draw sample, reagent and its filling movement, unit is filled other than it can move up and down, may be used also With horizontal movement, horizontal movement usually has rotation, X to several forms of motion such as, Y-direction and combinations thereof.Filling unit can be one It is a, it had not only been loaded this but also reagent adding, can make complete machine structure more compact so lower with cost.In order to improve test speed, filling is single Member can also further comprise one or several sample filling units, one or several reagents filling unit, and sample fills unit only Sample or filling sample and portion of reagent are filled, reagent fills unit and fills reagent.

In order to facilitate the filling of filling unit, the present invention may also include filling station.Filling station is located at buanch unit and filling It can be moved in the motion range of unit or by horizontal movement in the motion range of buanch unit and filling unit.Filling station connects It receives and carrying buanch unit shifts the reaction vessel to come, receiving filling unit fills sample and reagent into reaction vessel.Add Reaction vessel position is arranged on station in note, needs to fill the reaction vessel of sample and reagent for placing.In order to keep sample and reagent mixed Close more evenly, reaction it is more abundant, while in order to simplify complete machine structure and reduce volume, the present invention is preferably mixed filling station is integrated Mechanism carries out ultrasonic mixing to the reaction vessel after each filling, deviation rotates or concussion mixes.It is of course also possible to will mix Mechanism, such as supersonic generator are integrated in filling unit, fill sample and while reagent or after the completion of filling acts by It fills the ultrasonic wave that unit generates and realizes mixing.Those skilled in that art are appreciated that filling station can not also integrate mixing machine Structure, mixing can also be completed by the suction movement of filling unit or impact force.

Reaction member carrying and fixed reaction vessel.Reaction member mainly includes attemperator, rotating device and cleaning point From device.Attemperator periphery usually has the heat-barrier materials such as heat-preservation cotton, usually wraps up or surround bottom, the periphery of rotating device And top, side or bottom inside can be equipped with heating device and sensor, top is generally the structures such as cover board, mentions for reaction member For constant-temperature incubation environment and prevent or reduce scattering and disappearing for reaction member heat.Certainly, in order to which heat transfer efficiency is higher, heating device It may be mounted on rotating device.Other than providing and being incubated for environment, the also sustainable and fixed cleaning separator of attemperator Magnetic field generation device provides magnetic field environment for cleaning separation.In addition, if measuring device is mounted on reaction member, heat preservation dress Setting not only can provide installation site for light measurer, dark room conditions needed for can also be achieved light measurer.Rotating device is best It is one, including driving, transmission mechanism and relevant control circuit etc., control and drive rotating device are every set time (ratio Such as a circulation or period) the fixed angle of rotation, it transfers the reaction vessel position certain position of advancing and (for example advances one Reaction vessel position).Be arranged on rotating device several independent holes, slot, bracket, pedestal or other be suitble to carry reaction vessel Structure is defined as reaction vessel position.Reaction vessel position can also fix reaction vessel other than carrying reaction vessel position.Herein " fixation " refers to that reaction vessel will not be moved or be slided in reaction vessel position, but can be with reaction vessel position together mass motion. Reaction vessel can in this way be bonded with reaction vessel position tighter, gap is smaller, not only contribute to reaction vessel heat transfer be incubated for and Precise positioning, rotary device structure can also more simplified, accommodates more reaction vessel positions, manufacturing cost it is lower, to have Effect solve it is certain it is mobile in reaction vessel position due to reaction vessel in the prior art caused by heat transfer efficiencys are poor, space is unrestrained Take, the disadvantages of structure is complicated and defect.Reactant other than carrying and fixing, in reaction member also incubation reaction container.It is right In the test for needing signal to be incubated for, reaction member of the invention can also be achieved signal incubation function.

In order to allow reaction vessel to pass in and out reaction member, at least two transfer positions are set on reaction member.Shift position definition For it is within the scope of buanch unit horizontal movement, on reaction member reaction vessel pass in and out reaction member fixation position, not with The rotation of reaction vessel position and rotate.The reaction vessel position of different location, which can transfer and be navigated under the rotation of rotating device, to be turned Displacement receives reaction vessel or exits reaction vessel thereon so that reaction vessel completes subsequent corresponding function, for example enters Reaction member is incubated for or is transferred to other reaction vessel positions and carries out cleaning separation etc..According to the stage of reaction vessel disengaging and realization Major function it is different, transfer position can be divided into incubation transfer position and cleaning separation transfer position.The present invention will need to be incubated for anti- It answers container to enter reaction member, be incubated for after a certain period of time or be incubated for that the reaction vessel terminated is transferred out of that reaction member passed through turns Displacement is defined as being incubated for transfer position；It will be incubated for after a certain period of time or need to clean the reaction vessel of separation after being incubated for into instead It answers unit or/and completes to clean isolated reaction vessel and be transferred out of the transfer position that reaction member is passed through and be defined as cleaning separating to turn Displacement.At least one is arranged in the incubation transfer position of reaction member of the present invention, and the specific transfer position that is incubated for can be as needed only into not Out, only export but no import or not only go out again into reaction vessel, may be implemented so flexible incubation time and multiplicity complete machine be laid out.It needs , it is noted that the shortcomings that in order to solve the problems, such as the prior art and, pass through be incubated for transfer position pass in and out reaction member reaction vessel packet It includes and needs to be incubated for the primary, reaction vessel of incubation two or more times, can will need to be incubated for once, twice and more in this way Secondary reaction vessel first concentrates incubation, to reduce the size of reaction member and improve the space utilization rate of reaction member.Cleaning Separation transfer settable one of position, reaction vessel not only go out again into, can make in this way cleaning separator it is more compact, may also set up to It is one few, it in this way can more flexible arrangement cleaning separator.In short, shifting the setting of position on reaction member, solve existing The problem of technology transfer displacement is dispersed on multiple and different units and the reaction vessel being incubated for is needed to be scattered, can not only make Buanch unit motion path is less, apart from space that is shorter, and taking full advantage of reaction member, to keep complete machine control simpler It is single, smaller.

For reaction member other than above-mentioned function, cleaning separator thereon can also be achieved cleaning separation, anti-to remove Answer the ingredient being not associated in object.The cleaning separator of reaction member of the present invention includes magnetic field generation device and flushing machine.Magnetic Field generation device provides magnetic field environment, and the paramagnetic particle in reaction vessel is made to be adsorbed onto reaction vessel inner wall.Due in magnetic field Factors, the paramagnetic particle such as response time, moving distance and resistance be adsorbed onto reaction vessel inner wall and need the regular hour, lead to It was often differed for several seconds to tens seconds, in this way before drawing waste liquid (including unbonded ingredient) every time, reaction vessel is needed by magnetic Field a period of time.In a preferred embodiment of the present invention, magnetic field generation device can be mounted directly or be fixed on reaction member On attemperator, additional fixed mechanism not only can be saved, reduces cost, can also make magnet generation device closer to anti- Container position is answered, to reduce the adsorption time of paramagnetic particle, improves cleaning separative efficiency.Flushing machine includes imbibition and fluid injection dress It sets, aspirate the unbonded ingredient in reaction vessel and injects cleaning buffer solution into the reaction after suction.Liquid absorption device includes inhaling The imbibition portion of the suitable pumping liquid such as liquid needle, pipette or imbibition nozzle, imbibition portion are arranged in the top of reaction member, can pass through Reaction vessel on the drive disengaging reaction vessel position of driving mechanism, aspirates the unbonded ingredient in reaction vessel.Priming device Fluid injection portion including suitable row's fluid injection body such as injection needle, pipe, mouth, fluid injection portion are equally arranged in the reaction vessel position of reaction member Cleaning buffer solution is injected into the reaction vessel after suction in top.Rinse every time includes that an imbibition and primary injection cleaning are slow Fliud flushing and process, generally flush three times or four times, that is, carry out three times or four flushings, certain washing time can also be flexible and changeable. In order to keep cleaning more thorough, residual is less, also vortex mixer can be arranged in fluid injection position and mix reaction vessel or rushing when using fluid injection Power is hit, make paramagnetic particle resuspension simultaneously or after note cleaning buffer solution in note cleaning buffer solution and is dispersed in cleaning buffering In liquid.Reaction member rotating device transfers reaction vessel to when cleaning separator, and cleaning separator starts to reaction vessel Carry out cleaning separation.In addition, cleaning separator also further can fill mechanism by coupled signal reagent in order to streamline organizations, After reaction vessel completes cleaning separation, all or part of signal reagent is filled into it, for example fills the first, second whole letters Number reagent etc. only fills the first signal reagent etc., and remaining signal reagent can be filled in measurement.It can make full use of in this way The function of washing separator structure reduces organization volume and saves cost.

As seen from the above description, cleaning separator is arranged in above reaction member rotating device periphery or rotating device, Cleaning separation directly can be carried out to the reaction vessel on reaction member rotating device, it in this way can be to avoid the independent cleaning of setting Rotating device, such as independent cleaning separator disk or cleaning separation track are separated, component and complete machine mechanism has not only been simplified, has made whole Machine mechanism is more compact and cost is lower, it is thus also avoided that reaction vessel turns between independent cleaning separator and reaction member It moves, is simple and efficient complete machine control flow more, to improve treatment effeciency and reliability.

Measuring device measures the signal in reaction vessel.Signal is to generate after signal reagent is added in reaction vessel Electric signal, fluorescence signal or faint chemiluminescence signal etc..Measuring device includes dim light detector photomultiplier tube (PMT) Or other sensitive optoelectronic induction devices, the optical signal of measurement can be converted to electric signal, be sent to control centre.In addition, being Raising measurement efficiency and guarantee measurement consistency, measuring device can also further comprise that optical signal is collected and the optics such as calibration dress It sets.By taking faint chemiluminescence signal as an example, in order to avoid the interference of environment light, measuring device is in reaction vessel in the present invention There are three types of implementations for signal measurement.Measuring device is installed on reaction member in the first implementation, reacts reaction member The reaction signal in reaction vessel on container position measures.The reaction vessel on reaction member can be made full use of in this way Position, makes that complete machine is more compact, cost is lower.It include measurement darkroom and measurement position, measuring device installation in second of embodiment In on measurement darkroom, the signal in the reaction vessel on measurement position is measured.Position is measured in the level fortune of buanch unit In dynamic range or it is horizontally movable within the scope of the horizontal movement of the buanch unit.The third embodiment mainly includes measurement Disk, measurement darkroom and measuring device etc..Measuring plate includes holding by at least one circle reaction in the center of circle of the Measuring plate rotation center Device position, for carrying the reaction vessel for needing to measure.Reaction for the test for needing signal to be incubated for, in Measuring plate Container position can also be achieved signal incubation function.It, can be the reaction on any reaction vessel position thereon by the rotation of Measuring plate Container rotates to measuring device and measures, to realize that flexible signal is incubated for, improves the flexibility and efficiency of test.Measurement The periphery of Measuring plate is wrapped up or is enclosed in the measurement darkroom of unit, and closed dark room conditions are provided for measuring unit.Further, In order to realize some test signal incubation function, measure the also settable heating device of side or bottom and sensor in darkroom, Constant-temperature incubation environment is provided for measuring unit and prevents or reduces scattering and disappearing for reaction member heat.Certainly, more for heat transfer efficiency Height, heating device also may be mounted in Measuring plate.Measuring device can be connected or attached to measurement darkroom by generic way On, for example be mounted directly and be fixed on measurement darkroom or be connected on measurement darkroom by optical fiber, it in this way can be directly right The signal in reaction vessel on Measuring plate reaction vessel position measures, and treatment effeciency and reliability can be made higher.The present invention Measuring device can flexible topology according to the design needs, not only dark room conditions easy to accomplish, can also be achieved flexible signal and incubate It educates, solves the disadvantages of prior art darkroom structure is complicated, measuring device layout is difficult.

In addition, in order to convey sample, storing reagent, the also settable sample supply unit of automatic analysis apparatus of the present invention, The units such as reagent storage unit.

Sample supply unit is for placing sample to be examined pipe and target sample pipe being delivered to suction sample bit.Sample conveying is single Member has three kinds of track sample introduction, sample disk sample introduction and fixed area sample introduction major ways, and sample tube is generally positioned on sample rack, often A sample rack generally places 5 or 10 sample tubes, and sample rack is placed on transmission rail, on sample disk or analytical equipment is consolidated Determine region.

Destination agent is simultaneously transferred to suction reagent position by reagent storage unit refrigeration reagent.Reagent storage unit generallys use examination Agent disk and fixating reagent memory block two ways, in order to guarantee the stability of reagent, reagent disc generally has refrigerating function, such as 4- 10℃.Several reagent container positions are generally set on reagent disc, for placing reagent container.Several are arranged in each reagent container Independent cavity, for storing different reagent components, such as magnetic particle reagent, enzyme marking reagent, dilution reagent component.

The first embodiment of automatic analysing apparatus of the present invention, with reference to Fig. 4.Automatic analysing apparatus 100 mainly includes sample This supply unit 30, reagent storage unit 40, filling unit 20, filling station 90, reaction vessel feed unit 70, buanch unit 50, reaction member 10 and measuring device 86 etc..The function and effect of each section is described separately as below.

Sample supply unit 30 is for placing sample to be examined pipe 31 and target sample pipe being delivered to suction sample bit.This implementation In example, sample supply unit 30 is sample disk, is placed on arc sample rack (not marking in figure) on sample disk, each arc sample Frame places 10 sample tubes 31.Sample disk can be driven by driving mechanism under the control of control centre target sample transferring to suction Sample bit inhales sample bit and is located at the press horizontal mobile range of filling unit 20 and the point of intersection of sample tube center circle.

Reagent storage unit 40, which refrigerates reagent container 41 and transfers to destination agent, inhales reagent position.In the present embodiment, examination Agent storage unit 40 is reagent disc, and 25 reagent positions are arranged, and can accommodating 25 reagent containers 41, (or kit, reagent bottle are table It states conveniently, hereinafter referred to as reagent bottle).In the present embodiment, 4 cavitys 41a, 41b, 41c, 41d are arranged in each reagent bottle 41, can use In reagent components such as storage magnetic particle reagent, enzyme marking reagent, dilutions.Reagent disc can be under the control of control centre by driving machine Structure, which drives to transfer in destination agent bottle, inhales reagent position, inhales reagent position and is located at filling unit horizontal motion range and reagent chamber center Round point of intersection, it is corresponding with corresponding 4 reagent components in the present embodiment, there are 4 suction reagent positions (not marking in figure).

Fill the filling that unit 20 completes sample, reagent.Fill the sample on unit horizontal motion range and sample disk 30 Position, the reagent position on reagent disc 40, the reaction vessel position in Measuring plate are intersected respectively, and point of intersection is respectively to inhale sample bit, inhale examination Agent position and filling position.In the present embodiment, filling unit is single sample charging mechanism, can do upper and lower and horizontal revolving motion, both fill Sample fills reagent again, can make complete machine structure more compact so lower with cost.In some embodiments, it fills on unit 20 also Can the mixing mechanisms such as integrated ultrasonic generator, ultrasonic mixing is carried out to the reaction vessel after each filling.

Filling station 90 is located under the horizontal movement track of buanch unit 50 and filling unit 20, receives and carry buanch unit 50 shift the reaction vessel to come, receiving filling unit 20 fills sample and reagent into reaction vessel.It is arranged on filling station anti- Container position is answered, for placing the reaction vessel for needing to be loaded this and reagent.In the present embodiment, mixing mechanism is integrated in filling station, Ultrasonic mixing is carried out to the reaction vessel after each filling or eccentric concussion mixes, preferably eccentric concussion mixes, and such technology is real Existing difficulty is lower, more compact structure.

The storage of reaction vessel feed unit 70 and offer reaction vessel.In the present embodiment, in order to make complete machine more it is compact and Cost is lower, and reaction vessel feed unit uses preparatory arranged type.Reaction vessel feed unit 70 includes two reaction vessel supports Disk is arranged a number of reaction vessel position on reaction vessel pallet, stores not used reaction vessel.Reaction vessel supply is single Within the scope of the horizontal movement of buanch unit 50, such buanch unit 50 can traverse on pallet on each reaction vessel position member 70 Not used reaction vessel, the test newly to start provides not used reaction vessel.

The transfer reaction container between the different location of automatic analysing apparatus 100 of buanch unit 50.In this implementation, transfer is single Member 50 is set as 1, can do three-dimensional motion, can make complete machine more compact lower with cost in this way.Buanch unit 50 includes X to fortune Dynamic mechanical arm 50b, Y-direction guide rail 50a, Y-direction movable machinery arm 50c and vertical movement mechanism and mechanical finger (not marked in figure) Etc. mechanisms.Buanch unit 50 can be simultaneously along X to, Y-direction horizontal moving mechanical finger, and horizontal movement range covers bounding rectangles 56 Interior range, can by 9 incubations of the reaction vessel on reaction vessel feed unit 70, reaction member 10 shift position (12a1-3, 12b1-3,12c1-3), 2 cleanings separation on reaction member 10 is shifted position (12d1 and 12d2), is lost between reaction vessel position 60 Transfer.Further, since position is shifted in multiple incubations on 50 motion range of buanch unit covering reaction member 10, buanch unit can be with Reaction vessel is put by different incubation transfer positions or goes out to answer container from different incubation transfer bit transitions flexible to realize Incubation time.

Reaction member 10 carries and fixes reaction vessel, incubation and cleans the reactant separated in reaction vessel.This implementation In example, the attemperator of reaction member 10 is pot body 12 and upper cover (not marking in figure), and rotating device is a reaction tray 11, clearly Washing separator is 16.12 side or bottom inboard having heaters of pot body and sensor surround the bottom and periphery of reaction tray 11, Constant-temperature incubation environment is provided for reaction member 10, prevents or reduces scattering and disappearing for 10 heat of reaction member.Environment is incubated in addition to providing Outside, pot body 12 also supports and fixes the magnetic field generation device of cleaning separator 16, provides magnetic field environment for cleaning separation.This reality It applies in example, the magnet generation device of cleaning separator 16 is permanent magnet device, can provide stronger and more stable magnetic in this way Field environment.The flushing machine for cleaning separator 16 includes liquid absorption device and priming device and mixing mechanism.Cleaning separation dress Set 16 can also coupled signal reagent filling mechanism, reaction vessel on 10 reaction vessel position of reaction member completes cleaning separation Afterwards, all or part of signal reagent is filled into it.

Measuring device 86 in the present embodiment is directly installed on the side of pot body 12, certainly also mountable in attemperator Upper lid on, can the reaction signal in the reaction vessel on the reaction vessel position directly to reaction tray 11 measure.In this way may be used To make full use of the reaction vessel position on reaction member, make that complete machine is more compact, cost is lower.

In the present embodiment, the reaction tray 11 of reaction member 10 can be arranged thereon with rotation center around center axis rotation as circle The heart four circle reaction vessel positions, certainly enclose number can change, but at least 2 circle, such as can be 2 circles, 3 circle, 5 circle or more Several reaction vessel positions are arranged in multi-turn etc., every circle, and the reaction vessel bit quantity of every circle can be the same or different, this implementation In example, 30 reaction vessel positions are arranged in every circle.Each reaction vessel position is the suitable hole slot of size in reaction tray, can accommodate one A reaction vessel, carrying and fixed reaction vessel, after reaction vessel puts corresponding reaction vessel position into, in reaction vessel position not It can occur mobile or slide.Incubation function is realized in reaction vessel position in reaction tray on three circle 11a, 11b, 11c, and receiving is being incubated The reaction vessel educated.Reaction vessel position on the 11d of outer ring mainly accommodate incubation terminate or be incubated for after a certain period of time will or Isolated reaction vessel is cleaned, it is main to realize cleaning separation and measurement function.In order to which reaction vessel can pass in and out reaction tray 11 not It with the reaction vessel position on circle and can be realized flexible incubation time, aperture, aperture institute be set on the upper lid of attemperator It is to shift position in position, is provided with 9 incubation transfer position 13a1-3,13b1-3,13c1-3 and 2 cleaning separation transfer positions altogether 13d1 and 13d2, wherein be incubated for transfer position 13a1-3,13b1-3,13c1-3 respectively correspond in reaction tray three circle 11a, 11b, 11c, respectively for the reaction vessel position on reaction vessel disengaging 11a, 11b, 11c；Cleaning separation transfer position 12d1 and 12d2 is corresponding Reaction tray outer ring 11d, for the reaction vessel position on reaction vessel disengaging 11d.The reaction tray angle fixed every set time rotation Degree, can rotate or rotate clockwise counterclockwise, for example every 30 seconds rotate 12 degree, reaction vessel position of advancing.Pass through reaction Disc spins, the reaction vessel on reaction vessel position can be transferred to incubation transfer position or cleaning separation transfer position.Reaction tray is each In the postrotational intermittent time, buanch unit can by reaction vessel from multiple incubations transfer position and cleaning separation transfer be displaced into, Remove reaction tray.Reaction vessel is turned after being displaced into reaction tray by incubation, starts the reaction vessel on 11a, 11b or 11c Position be incubated for, be incubated for terminate or be incubated for after a certain period of time again from be incubated for transfer bit transition come out.By being incubated for the disengaging reaction of transfer position The reaction vessel of disk includes being incubated for the primary, reaction vessel of incubation two or more times, can make full use of reaction tray in this way Space.It should be pointed out that reaction vessel three circle 11a, 11b, 11c can be completed to be incubated for inside, it is enterprising to be then transferred to outer ring 11d Row cleaning separation, can also inside three circle complete certain times incubation after, such as complete the most of the time incubation, be then transferred to Then outer ring 11d completes the incubation of remaining time during reaction tray is transferred to magnetic separating device.Former implementation In in three circles no setting is required many reaction vessel positions, so that it may support to complete the incubation of reaction vessel, outer ring is without additional anti- Answer container position for being incubated for, so as to which so that reaction tray is smaller, cost is lower.For latter implementation, citing is such as Under, if the reaction vessel of a test needs to be incubated for 25 minutes, can first three enclose on a circle or a few circles of 11a, 11b, 11c inside Incubation in the completion most of the time such as 24 minutes, is then transferred on the 11d of outer ring, completes before being transferred to cleaning separator remaining Incubation in 1 minute.This scheme has shared the function that part is incubated for due to outer ring, can suitably reduce the reaction vessels of interior three circle Bit quantity, can balance the quantity of Internal and external cycle reaction vessel position in this way, to optimize the size of reaction tray and make full use of reaction The inner space of disk.

Below by taking one-step method is tested as an example, in conjunction with attached Figure 4 and 5, sketch automatic analysing apparatus 100 measurement procedure and Step.After test starts,

Step 200 loads reaction vessel: buanch unit 50 is not used anti-from the transfer of reaction vessel feed unit 70 one It answers on container to the reaction vessel position of filling station 90,

Step 201 fills sample and reagent: filling unit 20 draws sample and examination from suction sample bit and suction reagent position respectively Agent is filled into the reaction vessel on filling station 90,

Step 202 mix: if desired mix, then mixing mechanism in reaction vessel sample and reagent mix.If It does not need to mix, then omits the step,

Step 203 is incubated for: the reaction vessel for having filled sample and reagent is passed through incubation from filling station 90 by buanch unit 50 Transfer position (one in 12a1-3,12b1-3,12c1-3) be transferred in reaction tray 11 on three circle 11a, 11b, 11c some is anti- Container position is answered, reaction vessel starts to be incubated in reaction tray.While reaction vessel is incubated for, every the set time with reaction tray 11 It is rotationally advancing 1 position.Incubation time is different because of specific test item, and generally 5-60 minutes,

Step 204 cleaning separation: it is incubated for and completes or be incubated for after a certain period of time, buanch unit 50 is by being incubated for transfer position (one in 13a1-3,13b1-3,13c1-3) reaction of three circle 11a, 11b or 11c out of reaction tray 11 is held by reaction vessel Device is displaced out, is separated by cleaning shift the reaction that reaction vessel is moved into 11 outer ring 11d of reaction tray by position (13d1 or 13d2) again Container position.Reaction tray 11 is rotationally advancing 1 position every the set time, transfers the reaction vessel on outer ring 11d reaction vessel position To cleaning separator 16.If reaction vessel has been incubated for completion, it is not required to continue to incubate on the 11d of outer ring during transfer It educates, is not completed if reaction vessel is incubated for, the incubation of remaining time is completed during being transferred to cleaning separator 16.Outside Enclose 11d reaction vessel position on reaction vessel through over cleaning separator 16 magnetic field when, by the flushing of cleaning separator 16 Mechanism and mixing mechanism mix up to completion cleaning separation reaction vessel completion imbibition, note cleaning buffer solution, cleaning,

Step 205 fills signal reagent: after the completion of cleaning separation, reaction tray 11 transfers on outer ring 11d reaction vessel position Reaction vessel leaves field region, from washing separator structure on the signal reagent mechanism for filling liquid that couples injected into reaction vessel entirely Portion or part signal reagent,

Step 206 signal is incubated for: if desired signal is incubated for, then transfers the reaction vessel on the 11d of outer ring in reaction tray 11 It is incubated for signal is completed during measuring device 86, if undesired signal is incubated for, which is omitted,

Step 207 measurement: after the reaction vessel for needing to measure is transferred to measuring unit 86 on the 11d of outer ring, if optionally It needs, injects all or part of signal reagent, the reaction signal in reaction vessel is measured by measuring device 86, measure As a result it is sent to the control centre of automatic analysing apparatus after processing,

Step 208 abandons reaction vessel: the reaction vessel that reaction tray 11 continues to transfer on the 11d of outer ring turns to cleaning separation It shifts (13d1 or 13d2), the reaction vessel after measurement is removed reaction tray by buanch unit 50, is transferred to and is abandoned reaction vessel hole 60 abandon.

With reference to attached drawing 4 and attached drawing 6, it is to walk in place of be delayed one-step method testing process and step and one-step method examination main difference Reagent is dispensed and is increased in two times primary incubation by rapid 301-305, other steps are similar with one-step method, is repeated no more.

Step 301 fills sample and the first reagent: filling unit 20 draws sample from suction sample bit and suction reagent position respectively It is filled into the reaction vessel on filling station 90 with the first reagent,

Step 302 mixes: if desired mixing, if desired mixes, then mixing mechanism is to the sample and reagent in reaction vessel It is mixed.If not needing to mix, the step is omitted,

Step 303 is incubated for for the first time: buanch unit 50 leads to the reaction vessel for having filled sample and reagent from filling station 90 Incubation transfer position (one in 13a1-3,13b1-3,13c1-3) is crossed to be transferred in reaction tray 11 on three circle 11a, 11b, 11c Some reaction vessel position, reaction vessel start to be incubated in reaction tray.While reaction vessel is incubated for, every the set time with anti- 11 should be coiled and be rotationally advancing 1 position.Incubation time is different because of specific test item, and generally 5-60 minutes,

Step 304 fills the second reagent: after being incubated for for the first time, buanch unit 50 is by reaction vessel by being incubated for transfer Reaction vessel bit transition of the position (one in 13a1-3,13b1-3,13c1-3) out of reaction tray 11 on three circle 11a, 11b, 11c On reaction vessel position on to filling station 90, filling unit 20 is filled on filling station 90 from reagent position the second reagent of absorption is inhaled In reaction vessel,

Step 305 mixes: if desired mixing, if desired mixes, then mixing mechanism is to the sample and reagent in reaction vessel It is mixed.If not needing to mix, the step is omitted,

With reference to attached drawing 4 and attached drawing 7, it is to increase in place of two-step method testing process and step and delay one-step method examination main difference Add step 404, increase primary cleaning separation:

Step 404 cleaning separation: it is incubated for for the first time and completes or be incubated for for the first time after a certain period of time, buanch unit 50 is by incubating Educate transfer position (one in 13a1-3,13b1-3,13c1-3) by reaction vessel out of reaction tray 11 three circle 11a, 11b or 11c Reaction vessel be displaced out, again by cleaning separation transfer position (13d1 or 13d2) by reaction vessel move into 11 outer ring of reaction tray The reaction vessel position of 11d.Reaction tray 11 is rotationally advancing 1 position every the set time, transfers on outer ring 11d reaction vessel position Reaction vessel to cleaning separator 16.If reaction vessel has been incubated for completion, it is not required to during transfer on the 11d of outer ring Continue to be incubated for, not completed if reaction vessel is incubated for, completes remaining time during being transferred to cleaning separator 16 It is incubated for.Reaction vessel on the 11d reaction vessel position of outer ring through over cleaning separator 16 magnetic field when, by cleaning separator 16 Flushing machine and mixing mechanism to reaction vessel complete imbibition, note cleaning buffer solution, cleaning mix until complete for the first time it is clear Wash separation.For the first time cleaning separation after the completion of, buanch unit 50 by reaction vessel by be incubated for transfer position (13a1-3,13b1-3, One in 13c1-3) out of reaction tray 11 three circle 11a, 11b, 11c on reaction vessel bit transition to filling station 90 on it is anti- It answers on container, filling unit 20 is filled into the reaction vessel on filling station 90 from reagent position the second reagent of absorption is inhaled,

Other steps of two-step method are similar with delay one-step method, repeat no more.

It can be seen from the above descriptions that three circles are concentrated to be incubated for and complete or be incubated for including 100 elder generation of automatic analysing apparatus in the present embodiment Certain time is incubated for completion or the reaction vessel of incubation certain time is then transferred to outer ring and carries out the incubation of remaining time, completes Cleaning separation and measurement, transfer of the reaction vessel between different circles is by buanch unit by being arranged on reaction member at least One incubation transfer position and a cleaning separation transfer position are completed, and the independent cleaning separator disk of prior art use is not only saved It with survey CD, reduces package size and reduces costs, also simplified testing procedure and reduced the complexity and difficulty of control Degree, avoids transfer of the reaction vessel between multiple disks.In addition, the transfer position that reaction member is different by setting, it can be fine The quantity of adjustment, setting and balance Internal and external cycle reaction vessel position, not only may be implemented flexible incubation time, can also abundant benefit Keep complete machine structure more compact to further reduce the size of reaction member with the inner space of reaction tray, cost is lower, Testing efficiency is higher.

Second of embodiment of the invention, referring to Fig. 8.Sample supply unit 30, reagent storage unit in the present embodiment 40 are the same as example 1 or are similar to filling unit 20, repeat no more.In the present embodiment, buanch unit 50 is set as 1, can Two dimensional motion is done, can make complete machine more compact lower with cost in this way.Buanch unit 50 includes Y-direction guide rail 50a, Y-direction fitness machine The mechanisms such as tool arm 50b and vertical movement mechanism and mechanical finger (not marked in figure).Buanch unit 50 can be moved along Y-direction level Dynamic mechanical finger, horizontal movement range are one-dimensional linear region 56, can be by reaction vessel in reaction vessel feed unit 70, reaction 2 on unit 10 are incubated for transfer position (13b, 13c), 1 cleaning separation transfer position (13a) on reaction member 10, react single 1 measurement in member 10 shifts position (13d), loses and shift between reaction vessel position 60.Further, since 50 motion range of buanch unit It covers multiple incubations on reaction member 10 and shifts position, buanch unit can be shifted by different incubations and be shifted into reaction vessel Or go out to answer container from different incubation transfer bit transitions to realize flexible incubation time.Filling station 90 is main with embodiment one Difference is that it is horizontally movable, can be along X into horizontal movement to the horizontal movement of buanch unit 50.Reaction vessel There was only the water for being listed in buanch unit 50 in reaction vessel thereon in place of the main difference of feed unit 70 and embodiment one In flat motion range, for sustainable supply reaction vessel, reaction vessel feed unit 70 can be along X to horizontal movement, to make Each column reaction vessel thereon passes through the horizontal movement range of buanch unit 50, and such buanch unit 50 can traverse every on pallet Not used reaction vessel on a reaction vessel position, the test newly to start provide not used reaction vessel.Reaction member Main difference with embodiment one is in the arrangement of cleaning separator and the setting of transfer position.In the present embodiment, cleaning point From device 16 be arranged in reaction tray inner ring 11a, to by cleaning separate transfer position 13a enter it is anti-on reaction tray inner ring 11a Container is answered to carry out cleaning separation.Measuring device 86 is mounted on attemperator side, enters reaction to by measurement transfer position 13d The signal in reaction vessel on the 11d of disk outer ring measures.Centre two enclose 11b, 11c on reaction vessel positions to pass through be incubated for The reaction vessel that transfer position (13b, 13c) enters processing unit is incubated for.In the present embodiment, the level of corresponding buanch unit 50 Motion in one dimension range and reaction tray four enclose the crosspoint of the reaction vessel position on 11a, 11b, 11c, 11d, on reaction member by Cleaning separation transfer position 13a is set gradually from inside to outside, is incubated for the totally 4 transfer positions transfer position 13b and 13c, measurement transfer position 13d. This implementation is arranged in separator is cleaned on reaction member inner ring, and can not only be made cleaning separator more compact, be also reduced Temperature fluctuation, the interference for introducing environment light that cleaning separator may cause measurement etc. adversely affect.

Those skilled in the art are appreciated that the testing process of the present embodiment and step are similar to embodiment one, Therefore it only makes a brief description below.When test, filling station 90, into horizontal movement to 50 horizontal movement of buanch unit, turns along X Unit 50 is moved from the reaction vessel position that reaction vessel feed unit 70 shifts that a unused reaction vessel is put into filling station 90, Then filling station 90 moves under the horizontal movement track of filling unit 20, fills reaction vessel of the unit 20 on filling station 90 Sample and reagent are filled, after the completion of filling, the vortex mixer for being integrated in filling station 90 can be mixed reaction vessel.It has mixed At in rear or blending process, filling station 90 is again within the scope of horizontal movement to the horizontal movement of buanch unit 50.In this way, filling station The reaction vessel for needing to be incubated on 90 first encloses 11b, 11c by being incubated for transfer position 13b or 13c immigration intermediate two by buanch unit 50 In a circle, be incubated for and complete or be incubated for when needing to clean separation after a certain period of time again by buanch unit 50 by being incubated for transfer position 13b or 13c removes intermediate two circles 11b, 11c, again by cleaning separation transfer position 13a immigration inner ring 11a, in the rotation of reaction tray Under transfer, cleaning separation is carried out by cleaning separator 86, cleaning separation is completed, then is turned by buanch unit 50 by cleaning separation If desired plus the second reagent it shifts 13a and removes inner ring 11d, then reaction vessel is transferred to filling station 90 and completed by buanch unit 50 The filling of second reagent；If desired it measures, then outer ring 11d, reaction vessel is moved by measurement transfer position 13d by buanch unit 50 Under the rotation of reaction tray, it is transferred to measuring device and measures.

The third embodiment of the invention, referring to Fig. 9.This implementation and one main difference of implementation are the arrangement of measuring device On.The present embodiment further includes measurement darkroom (not marking in figure) and the measurement position 82 independently of reaction member 10, measuring device 86 It is installed on measurement darkroom, the signal in the reaction vessel on measurement position 82 is measured.Measurement darkroom is measuring device 86 provide needed for dark room conditions, measure position 82 within the scope of the horizontal movement of buanch unit 50 or be horizontally movable described turn It moves within the scope of the horizontal movement of unit 50.It is protected from light in order to easy to accomplish, measurement position 82 can be made fixed position, reaction vessel Inlet and outlet setting " skylight " mechanism, usually closes the dark room conditions to guarantee measurement darkroom, and reaction vessel is opened when passing in and out；Measurement Position 82 also can be made shift position, and in order to be easy to be protected from light, measurement position 82 can be to push and pull in the form of drawer etc. far from or close to surveying Measure device 86.Certainly it measures position 82 and being protected from light structure can be other suitable implementations accordingly.In addition, signal reagent Filling can also be completed in measurement position 82.The embodiment can make measuring device 86 relatively independent, it is easier to realize close when measuring Dark room conditions are closed, and reaction member does not need to be arranged again the structure that requirement is protected from light specifically for measuring device 86.It is in the art general Logical technical staff is appreciated that other units of this implementation are the same as example 1 or similar, the testing process of the present embodiment and Step refers to Fig. 5, Fig. 6 and Fig. 7, reacts appearance in last filling signal reagent, measurement, discarding with the main difference of embodiment one Three steps of device, remaining is same or similar.Filling signal reagent step in the present embodiment can be in the anti-of reaction tray outer ring 11d It answers and is completed on container position, can also be completed in measurement position 82, the can also be completed on the reaction vessel position of reaction tray outer ring 11d The filling of one signal reagent completes the filling of second signal reagent in measurement position 82；Measuring process, buanch unit 50 will need to survey The reaction vessel of amount is by cleaning separation transfer position 13d1 or 13d2 from the reaction vessel bit transition of reaction tray outer ring 11d to measurement Position 82 measures the reaction signal in the reaction vessel for being located at measurement position 82 by measuring device 86；Abandon reaction vessel step Suddenly, the reaction vessel for completing measurement is transferred to discarding hole 60 from measurement position 82 and abandoned by buanch unit 50.

4th kind of embodiment of the invention, referring to Figure 10.The present embodiment is being also independently from a main difference is implemented The measurement darkroom 82 of reaction member 10 and Measuring plate 81, measuring device 86 are installed on measurement darkroom 82.In the present embodiment, filling It stands and (is not marked in figure) and can integrate the reaction vessel position that can make full use of Measuring plate 81 in Measuring plate 81 and its rotation calmly Bit function can save the independent filling station of setting in this way, save mechanism, complete machine cost can be made lower, structure is more tight It gathers.Mixing mechanism can be integrated in filling station, for carrying out ultrasonic mixing or concussion mixing to the reaction vessel after filling.Measuring plate It is arranged on 81 and encloses reaction vessel position 81a using Measuring plate rotation center as the one of the center of circle, for carries the reaction for needing to measure Container.Multiple reaction vessel positions are arranged in the present embodiment, and all or part of signal may be implemented and be incubated for.Measuring plate 81 rotates every time, The reaction vessel that either signal is incubated on position can be rotated to measuring device 86 to measure, to realize that flexible signal is incubated It educates, improves the flexibility and efficiency of test.In order to which reaction vessel passes in and out Measuring plate 81, the top setting measurement in measurement darkroom 82 turns Shift 82a.Position 82a is within the scope of the horizontal movement of buanch unit 50 for measurement transfer, and buanch unit 50 can will need to measure anti- Container is answered to remove by the cleaning separation transfer position 13d1 or 13d2 of reaction member 10 from reaction tray 11, by measurement transfer position 82a moves into Measuring plate 81.Measurement darkroom 82 package or the periphery for being enclosed in Measuring plate 81 provide darkroom ring for measuring device 86 Border, for the test that signal is incubated for, measurement 82 side or bottom of darkroom can choose setting heating device and sensor, for measurement Disk reaction vessel position 81a provides constant temperature signal and is incubated for environment.Measuring device 86 includes dim light detector photomultiplier tube (PMT), it is directly installed on measurement darkroom 82, to the faint chemiluminescence signal generated after addition signal reagent in reaction vessel It measures.In addition, the filling of signal reagent for convenience, 81 top of Measuring plate of the invention or the periphery for measuring darkroom 82, Also settable signal reagent fills mechanism (not marking in figure), and filling is complete in the reaction vessel on 81 reaction vessel position of Measuring plate Portion or part signal reagent.Those skilled in the art are appreciated that other units of this implementation are the same as example 1 Or it is similar, the testing process and step of the present embodiment refer to Fig. 5, Fig. 6 and Fig. 7, and the main difference with embodiment one is initial It loads reaction vessel, filling sample and reagent and last filling signal reagent, measurement, abandon three steps of reaction vessel Deng remaining is same or similar.Buanch unit 50 turns not used reaction vessel from reaction vessel feed unit 70 by measurement The reaction vessel position that 82a is moved into Measuring plate 81 is shifted, Measuring plate 81 rotates, and reaction vessel is transferred to filling station, filling is single Member 20 draws sample and reagent is filled into the reaction vessel on filling station, after the completion of filling, is integrated in the mixing of filling station Mechanism mixes the mixture in reaction vessel.After the completion of mixing, buanch unit 50 leads to the reaction vessel for completing measurement Measurement transfer position 82a is crossed to be incubated for from the reaction vessel bit transition in Measuring plate 81 to reaction member.Filling letter in the present embodiment Number reagent step can be completed on the reaction vessel position of reaction tray outer ring 11d, can also be in the reaction vessel in Measuring plate 81 Position is completed, and the filling of the first signal reagent can also be completed on the reaction vessel position of reaction tray outer ring 11d, in Measuring plate 81 Reaction vessel position complete second signal reagent filling；Measuring process, buanch unit 50 will need the reaction vessel measured to lead to Over cleaning separation transfer position 13d1 or 13d2 is displaced out from the reaction vessel of reaction tray outer ring 11d, is moved by measurement transfer position 82a Enter the reaction vessel position in Measuring plate 81, Measuring plate 81 rotates, and reaction vessel is transferred to measuring device 86, by measuring device 86 Reaction signal in reaction vessel is measured；Reaction vessel step is abandoned, buanch unit 50 holds the reaction for completing measurement Device is abandoned by measurement transfer position 82a from the reaction vessel bit transition in Measuring plate 81 to hole 60 is abandoned.

Automatic analysis apparatus of the present invention can also be expanded flexibly and is multiplexed to the maximum extent, realize the seriation of product. On the basis of example IV, in order to further enhance complete machine specifications parameter and test flux, meet the bigger terminal of specimen amount Customer demand, can be by increasing buanch unit and filling element number, suitably increase reaction member size or increase reaction list The modes such as first quantity are realized.It is the 5th kind of embodiment schematic diagram of automatic analysing apparatus of the present invention with reference to Figure 11.Sample is defeated The input mode for sending unit 30 to take track and sample rack can accommodate more multisample in this way, can add sample in real time, operation Also more convenient.Sample rack 32 and sample tube 31 thereon can be transported under the motion range of the first filling unit 21.Reagent Storage unit 40 increases reagent storage position, can place more reagent containers.Filling unit 20 includes the first filling unit 21 and second fill unit 22, first filling 21 filling samples of unit or filling sample and portion of reagent, the second filling unit 22 filling reagents can also increase more filling units certainly, improve the speed of this and reagent of sample-adding in this way.Reaction vessel supplies Bin type is used to unit 70, and reaction vessel can be at wrapping in the feed bin at random for pouring into reaction vessel feed unit 70, this side Formula can make the supply of reaction vessel it is more, faster, it is more convenient.The reaction tray 11 of reaction member 10 includes with reaction tray rotation center For the outer ring 11d reaction vessel position and interior zone 11a reaction vessel position of center of circle distribution.Reaction vessel on interior zone 11a Position is distributed at " honeycomb ", can make full use of the space in reaction tray 11 in this way, more reaction vessel positions are arranged, and accommodates More reaction vessels are incubated for, and promote test flux.For the reaction vessel position in reaction vessel disengaging reaction tray 11, reaction is single One incubation transition range 13a of setting (including position is shifted in 7 incubations) and cleaning separation transfer position 13d in member 10.Measure darkroom 82 With Measuring plate 81 and measuring device 86 can multiplexing embodiment four completely, but in order to improve testing efficiency, no longer setting filling Position.Setting measurement transfer position 82a on darkroom 82 is measured, passes in and out Measuring plate for reaction vessel.Buanch unit 50 includes independently doing The first buanch unit 51 and the second buanch unit 52 of three-dimensional motion, the first reaction vessel unit 51 is mainly in reaction member 10 It is incubated for transition range 13a and cleaning separation transfer position 13d, Measuring plate 81 and reaction vessel is abandoned and shifted between the positions such as hole 60b Reaction vessel, the second buanch unit 52 are mainly shifted in the incubation of reaction vessel feed unit 70, filling station 90, reaction member 10 Area 13a and cleaning separation transfer position 13d and reaction vessel abandon transfer reaction container between the 60b of hole.Ordinary skill Personnel are appreciated that, by being reasonably laid out and distributing, the transfer of reaction vessel can all pass through first between any two position Or second buanch unit or both be completed at the same time.Certainly, buanch unit can be 2 more than, and it is more to can according to need setting Buanch unit is to improve the efficiency and speed that reaction vessel shifts.For complete machine compact layout and improve test speed, this implementation Example fills sample and reagent by the way of independent filling station 90.Filling station 90 can add in reaction vessel feed unit 70, first Note unit 21, second fills to be moved back and forth between unit 22, receives reaction vessel, receiving that reaction vessel feed unit 70 supplies First filling unit 21 fills sample or sample and portion of reagent, receives the second filling filling reagent of unit 22.It can fill Stand on 90 or filling unit 20 on integrate mixing mechanism, the reaction vessel after filling sample or/and reagent is mixed.It mixes After the completion, the reaction vessel on filling station 90 is transferred to reaction member 10 by buanch unit 50.Those skilled in the art It is appreciated that the other units and example IV of this implementation are same or similar, the testing process and step of the present embodiment and implementation One main difference of example is that fill sample and reagent is completed by the first and second filling unit cooperations, reaction vessel transfer by First and second buanch unit cooperations are completed, and the filling movement for filling unit is completed in independent filling station, other movements It is the same as example 1 with process or similar, with reference to Fig. 5-Fig. 7, repeats no more.The embodiment compared with prior art, avoids Additional large-sized cleaning separator disk is easier to realize dark room conditions and flexible independently of the measuring device of reaction member Measurement, while the size of reaction member itself is decreased by the subregion of the different reaction vessel position of function, to make complete machine It is more compact, cost is lower, more efficient and better reliability.

The embodiment of the invention also provides a kind of method of sample analysis, specifically include:

Step is filled, fills sample and/or reagent in the reaction vessel；

Incubation step turns to be displaced into being incubated for twice including at least needs for reaction member to being incubated for by least one Reaction

Container is incubated for；

Separating step is cleaned, it is clear to the reaction vessel progress for turning to be displaced into reaction member by least one cleaning separation It washes point

From to remove the ingredient being not associated in reactant；

Signal reagent step is filled, signal reagent is filled into reaction vessel,

Measuring process measures the reaction signal in reaction vessel by measuring device.

Further, further include transfer step, by buanch unit from it is described at least one be incubated for transfer position, at least one Reaction vessel is moved in and out the reaction member by cleaning separation transfer position；It further include mixing step, to anti-in reaction vessel Object is answered to mix.

The present invention realizes that the incubation of reactant in reaction vessel, cleaning separate centered on reaction member, on reaction member At least one is set and is incubated for transfer position and at least one cleaning separation transfer position, buanch unit can be incubated for transfer position and cleaning point Transfer reaction container between offing normal not only may be implemented flexibly to be incubated for, but also can solve and must use in the prior art Multiple washing separator structures realize the problem of two-step method test, sufficiently realize efficient cleaning separation.In addition, measuring device can root According to the needs that complete machine layout or structure are realized, flexible arrangement or arrangement, for example can be directly mounted on reaction member, be arranged only It on vertical position or is mounted in independent Measuring plate etc., solves in the prior art that measuring device arrangement is limited, measurement environment is easily dry The problems such as disturbing.The present invention improves the working efficiency of analytical equipment and reduces the realization difficulty of automation function, solves very well The technical problems such as current self-reacting device volume is big, detection speed is slow, at high cost, performance is poor have not only saved laboratory sky Between, testing efficiency is improved, and advantageously reduce expenses, mitigates testee's burden, finally saved a large amount of nature Resource and social resources.

Technical characteristic or operating procedure described in the embodiment of the present invention can be combined in any suitable manner. Those skilled in the art are readily appreciated that, the sequence of step or movement in the method for description of the embodiment of the present invention is can be with Change.Therefore, certain sequence is required unless otherwise indicated, and any sequence in attached drawing or detailed description is intended merely to Illustrative purpose, rather than necessary sequence.

It may include various steps in various embodiments of the present invention, these steps can be presented as can be by general or specialized meter The executable instruction of the machine that calculation machine (or other electronic equipments) executes.Optionally, these steps can be by including to hold The hardware element of the particular logic circuit of these steps of row executes or is combined by hardware, software and/or firmware and executed.

Above by specific embodiment, the present invention is described, but the present invention is not limited to these specific implementations Example.It will be understood by those skilled in the art that various modifications, equivalent replacement, variation etc. can also be done to the present invention, these transformation It, all should be within protection scope of the present invention without departing from spirit of the invention.In addition, " a reality described in the above many places Apply example " " the present embodiment " etc. indicate different embodiments, naturally it is also possible to it is completely or partially combined in one embodiment.

The embodiments described above only express several embodiments of the present invention, and the description thereof is more specific and detailed, but simultaneously Limitations on the scope of the patent of the present invention therefore cannot be interpreted as.It should be pointed out that for those of ordinary skill in the art For, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to guarantor of the invention Protect range.Therefore, the scope of protection of the patent of the invention shall be subject to the appended claims.

Claims (10)

1. a kind of automatic analysing apparatus characterized by comprising

Fill unit, including first filling unit and second filling unit, it is described first filling unit for fill sample or Sample and portion of reagent are to reaction vessel, and the second filling unit is for filling reagent to reaction vessel；

Reaction vessel feed unit, for storing and supply response container；

Filling station needs to fill the reaction vessel of sample or/and reagent for receiving and carrying, and the filling station can be described Move back and forth between reaction vessel feed unit, the first filling unit and the second filling unit；And

Buanch unit, between the different positions transfer reaction container.

2. automatic analysing apparatus according to claim 1, which is characterized in that water of the filling station in the buanch unit In flat motion range or it is horizontally movable within the scope of the horizontal movement of the buanch unit.

3. automatic analysing apparatus according to claim 1, which is characterized in that it further include mixing mechanism, the mixing mechanism It is integrated in the filling station, the mixing mechanism is used to mix the reactant in reaction vessel.

4. automatic analysing apparatus according to claim 1, which is characterized in that further include for being incubated for and cleaning separation reaction The reaction member of reactant in container, the reaction member include a rotating device, and reaction is arranged on the rotating device Container position, the reaction vessel position are arranged at least one incubation and turn for carrying and fixing reaction vessel on the reaction member Displacement and at least one cleaning separation transfer position, at least one of the reaction member are incubated for transfer position and at least one cleaning point From transfer position within the scope of the horizontal movement of buanch unit.

5. automatic analysing apparatus according to claim 4, which is characterized in that the reaction member further includes cleaning separation dress It sets, the cleaning separator carries out cleaning point to the reaction vessel for turning to be displaced into reaction member by the cleaning separation From to remove the ingredient being not associated in reactant.

6. automatic analysing apparatus according to claim 4, which is characterized in that turn to be displaced into reaction list by described be incubated for The reaction vessel of member, which includes at least, needs to be incubated for reaction vessel twice, and the reaction member turns to be shifted by described be incubated for The reaction vessel for entering reaction member is incubated for.

7. automatic analysing apparatus according to claim 4, it is characterised in that: the rotating device is reaction tray, described anti- The angle fixed every set time rotation should be coiled, the reaction vessel position is transferred to described being incubated for and shifts position or described clear Wash separation transfer position.

8. a kind of method of sample analysis characterized by comprising

Step is filled, makes filling station between reaction vessel feed unit, the first filling unit and the second filling unit to move back It is dynamic, and reaction vessel is provided to filling station with reaction vessel feed unit, sample is added into reaction vessel with the first filling unit Reagent is added into reaction vessel with the second filling unit for sheet or sample and portion of reagent；

Incubation step is incubated for turn reaction including at least needs incubation twice for being displaced into reaction member to by least one Container is incubated for；

Separating step is cleaned, cleaning point is carried out to the reaction vessel for turning to be displaced into reaction member by least one cleaning separation From to remove the ingredient being not associated in reactant；

Signal reagent step is filled, signal reagent is filled into reaction vessel, and

Measuring process measures the reaction signal in reaction vessel by measuring device.

9. method of sample analysis according to claim 8, it is characterised in that: further include transfer step, pass through buanch unit The reaction list is moved in and out from least one described incubation transfer position, at least one cleaning separation transfer position by reaction vessel Member.

10. method of sample analysis according to claim 8, it is characterised in that: further include mixing step, in reaction vessel Reactant mix.