CN104965096A - Multi-sample immunity-detecting reaction disc capable of automatically separating serum - Google Patents
Multi-sample immunity-detecting reaction disc capable of automatically separating serum Download PDFInfo
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- CN104965096A CN104965096A CN201510304821.9A CN201510304821A CN104965096A CN 104965096 A CN104965096 A CN 104965096A CN 201510304821 A CN201510304821 A CN 201510304821A CN 104965096 A CN104965096 A CN 104965096A
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Abstract
The invention discloses a multi-sample immunity-detecting reaction disc capable of automatically separating serum. In use of the multi-sample immunity-detecting reaction disc, blood is added into the reaction disc, then the reaction disc is put into a special detection instrument, and the special detection instrument drives the reaction disc to carry out centrifugal movement; under the action of centrifugal force, serum is automatically separated, the serum and a diluent in a dilution cup enter reaction chambers distributed at the periphery of the reaction disc, and a dry reagent sealed up in the reaction chambers in advance reacts with the serum and the diluent; and eventually, report results of each item in corresponding reaction chambers are obtained through the detection instrument. The multi-sample immunity-detecting reaction disc can automatically carry out serum separation and detection of indexes of immunity items, so labor force is greatly reduced, samples are prevented from contamination, and errors caused by improper operation are decreased accordingly; and the multi-sample immunity-detecting reaction disc can carry out reaction detection on a plurality of samples at the same time, so the function of batch detection is realized, and efficiency is improved compared with single-sample detection.
Description
Technical field
The present invention relates to a kind of immunity analysis instrument reaction tray, the multisample specifically relating to a kind of automatic separation of serum detects immune response dish.
Background technology
In field of immunoassay detection, when using blood sample to carry out immunoassay detection, before use blood sample carries out analysis detection, need blood sample to carry out being separated of serum and haemoglobin, routine techniques is deposited by blood sample reagent separate cold storage, utilized the equipment such as the pipettor of specialty will refrigerate reagent sucking-off during use by professional, then blood sample carried out being separated of serum and haemoglobin by manual operation, then the serum sample separated is injected in cuvette to be detected and mixes with the dilution in cuvette, last again by its situation of change of optical system detection and its content of mensuration or composition, this in advance by the method complex operation manually carrying out separation of serum, easily sample is polluted.
The serum of separator well and dilution is utilized to carry out the whole process of hybrid detection in addition, traditional method is that filling reagent and collecting sample need to use pipettor, transfer pipet lamp apparatus, generally need the liquid shifting equipment of two or more to complete testing process during detection, there is preliminary work spended time length, complex operation, be not easy to shortcomings such as carrying, easily pollute and make mistakes.
Therefore, need to propose a kind of novel immunity analysis instrument reaction tray for blood sample.
Summary of the invention
Goal of the invention: in order to overcome the deficiencies in the prior art, the invention provides a kind of can automatically separation of serum, the multisample that automatically can carry out the automatic separation of serum of immunoassay detection detects immune response dish.
Technical scheme: for achieving the above object, a kind of multisample of automatic separation of serum that provides of the present invention detects immune response dish, comprises reaction disk body, diluted cup and reaction disk cover, described diluted cup comprises first, second, 3rd diluted cup, described first, second, 3rd diluted cup is located in described reaction disk body respectively, and described reaction disk cover is connected with described reaction disk body, and described first, second, 3rd diluted cup is between described reaction disk cover and described reaction disk body, and described reaction disk body comprises the identical part of three structures and turning axle fixed orifice, and the part that three structures are identical is respectively first, second and Part III, described turning axle fixed hole position in described reaction disk body center, described first, second and Part III be evenly arranged in described reaction disk body, described first, second and the center line of Part III all through described turning axle fixed orifice position, the part that described structure is identical is provided with diluted cup storage chamber from inside to outside successively, dilution cushion chamber, the quantitative chamber of dilution, hybrid chamber and immunization program reaction zone, diluted cup storage chamber comprises first, second, 3rd diluted cup storage chamber, described dilution cushion chamber comprises first, second, 3rd dilution cushion chamber, the quantitative chamber of described dilution comprises first, second, the 3rd quantitative chamber of dilution, described hybrid chamber comprises first, second, 3rd hybrid chamber, described immunization program reaction zone comprises first, second, 3rd immunization program reaction zone, described immunization program reaction zone is evenly provided with several immunization program reaction chambers, and part one end that described structure is identical is provided with calibration hole from top to bottom successively, excess blood collecting chamber, serum disengagement chamber and blood sample storage chamber, described calibration hole is located at described immunization program reaction chamber side, and the part other end that described structure is identical is provided with dilution waste collection chamber, and described calibration hole comprises first, second, 3rd calibration hole, described excess blood collecting chamber comprises first, second, 3rd excess blood collecting chamber, described serum disengagement chamber comprises first, second, 3rd serum disengagement chamber, is provided with heat-sealing film bearing below described diluted cup storage chamber, and described diluted cup storage chamber side is provided with pilot hole, and described heat-sealing film bearing comprises first, second, 3rd sealer bearing, described pilot hole comprises first, second, 3rd pilot hole, described first, second, 3rd diluted cup is placed in described first respectively, second, in 3rd diluted cup storage chamber, described reaction disk cover comprises blood adding mouth, be positioned at the register pin of described blood adding mouth side and be positioned at the exhausr port of described register pin side, described register pin comprises first, second, 3rd register pin, described first, second, 3rd register pin is respectively with described first, second, 3rd pilot hole is connected and described reaction disk cover is connected with described reaction disk body.
Further, described diluted cup comprises cup and the heat-sealing film for sealing described cup rim of a cup, is provided with dilution, is provided with folded part above described heat-sealing film in described cup, and bottom and the described heat-sealing film bearing of described folded part are connected.
Further, described diluted cup storage chamber is connected by breach with described dilution cushion chamber, be connected by the first kapillary between described dilution cushion chamber with the quantitative chamber of described dilution, the quantitative chamber of described dilution is connected with described dilution waste collection chamber by the second kapillary, the quantitative chamber of described dilution is connected with described hybrid chamber by three capillary simultaneously, described hybrid chamber is connected with described immunization program reaction chamber by the 4th kapillary, described blood sample storage chamber is connected with described serum disengagement chamber by the 5th kapillary, described serum disengagement chamber is connected with described excess blood collecting chamber by the 6th kapillary, described serum disengagement chamber is connected with described hybrid chamber by the 7th kapillary simultaneously.
Further, the volume of described dilution cushion chamber is greater than the volume in the quantitative chamber of described dilution and is less than the volume in the quantitative chamber of described dilution and the volume sum in described dilution waste collection chamber, and the volume of described serum disengagement chamber is greater than the volume of described hybrid chamber and is less than the volume sum of described hybrid chamber and described excess blood collecting chamber.
Further, described three capillary is less than the distance of the quantitative chamber of described dilution to described reaction disk body center to the distance of described reaction disk body center, described 7th kapillary is less than the distance of described serum disengagement chamber to described reaction disk body center to the distance of described reaction disk body center, and described 8th kapillary is less than the distance of described hybrid chamber to described reaction disk body center to the distance of described reaction disk body center.
Further, be welded to connect by ultrasonic welding process between described reaction disk cover and described reaction disk body.
Further, the number of described immunization program reaction chamber is no less than 10.
Further, described folded part length 2 ~ 4cm larger than the length of described cup.
Beneficial effect: compared with the prior art, the advantage had is in the present invention:
1, the present invention can carry out serum separation and immunization program Indexs measure automatically, and the present invention carries separation of serum function, and saved the manual operation that serum is separated, greatly reduce labour, sample also can not receive pollution; The present invention when not needing other any auxiliary material, can complete and detecting the every immune indexes of human body, greatly reducing labour automatically, also correspondingly decreases the error produced because of misoperation;
2, responding in the present invention is all carry out in reaction tray, can not to environment, and each immunization program reacts the detection that also can not have influence on other;
3, the present invention can carry out reaction detection to multisample simultaneously, achieves the function of batch detection, improves efficiency than single pattern detection.
Accompanying drawing explanation
Fig. 1 is the part drawing of the multisample detection immune response dish of automatic separation of serum of the present invention.
Fig. 2 is the part drawing of reaction disk body of the present invention.
Fig. 3 is the part drawing of diluted cup of the present invention.
Fig. 4 is the part drawing of reaction disk cover of the present invention.
Embodiment
Below in conjunction with embodiment, the present invention is further described.
With reference to Fig. 1, the multisample of a kind of automatic separation of serum provided by the invention detects immune response dish, comprise reaction disk cover 3, reaction disk body 1 and three are deposited in described reaction disk body 1, dilution is equipped with in inside diluted cup 2, described diluted cup 2 is placed in described reaction disk body 1, described reaction disk cover 3 is connected with described reaction disk body 1, described diluted cup 2 comprises first, second, third diluted cup, and described first, second, third diluted cup three diluted cups lay respectively in the space of composition between described reaction disk body 1 and described reaction disk cover 3;
With reference to Fig. 2, described reaction disk body 1 adopts circular configuration, described reaction disk body 1 comprises the identical part of three structures and turning axle fixed orifice 112, the part that three structures are identical is respectively first, second and Part III, described turning axle fixed orifice 112 is positioned at the center position of described reaction disk body 1, described first, second and Part III be evenly arranged in described reaction disk body 1, described first, second and Part III be evenly arranged in described reaction disk body 1 around described turning axle fixed orifice 112, described first, second and the center line of Part III all through described turning axle fixed orifice 112 position, described first, second is fan-shaped with Part III and structure is identical, for one of them part, this part is provided with diluted cup storage chamber 111 from inside to outside successively, dilution cushion chamber 105, the quantitative chamber of dilution (104), hybrid chamber 103 and immunization program reaction zone, heat-sealing film bearing 113 is provided with below described diluted cup storage chamber 111, described diluted cup storage chamber 111 side is provided with pilot hole 114, described immunization program reaction zone is in the outermost edges of this part, described immunization program reaction zone is evenly provided with several immunization program reaction chambers 102, this part one end is provided with calibration hole 101 from top to bottom successively, excess blood collecting chamber 109, serum disengagement chamber 108 and blood sample storage chamber 107, wherein said calibration hole 101 is just in time positioned at described immunization program reaction chamber 102 side, this part other end is provided with dilution waste collection chamber 106, wherein said diluted cup storage chamber 111 is connected by breach with described dilution cushion chamber 105, be connected by the first kapillary between described dilution cushion chamber 105 with the quantitative chamber 104 of described dilution, the quantitative chamber of described dilution 104 is connected with described dilution waste collection chamber 106 by the second kapillary, the quantitative chamber of described dilution 104 is connected with described hybrid chamber 103 by three capillary simultaneously, described hybrid chamber 103 is connected with described immunization program reaction chamber 102 by the 4th kapillary, described blood sample storage chamber 107 is connected with described serum disengagement chamber 108 by the 5th kapillary, described serum disengagement chamber 108 is connected with described excess blood collecting chamber 109 by the 6th kapillary, described serum disengagement chamber 108 is connected with described hybrid chamber 103 by the 7th kapillary simultaneously, described hybrid chamber 103 is connected with described immunization program reaction chamber 102 by the 8th kapillary,
The volume of described dilution cushion chamber 105 is greater than the volume in the quantitative chamber of described dilution 104 and is less than the volume in the quantitative chamber of described dilution 104 and the volume sum in described dilution waste collection chamber 106, the volume of described serum disengagement chamber 108 is greater than the volume of described hybrid chamber 103 and is less than the volume sum of described hybrid chamber 103 and described excess blood collecting chamber 109, described three capillary is less than the distance of the quantitative chamber of described dilution 104 to described reaction disk body 1 center to the distance of described reaction disk body 1 center, described 7th kapillary is less than the distance of described serum disengagement chamber 108 to described reaction disk body 1 center to the distance of described reaction disk body 1 center, described 8th kapillary is less than the distance of described hybrid chamber 103 to described reaction disk body 1 center to the distance of described reaction disk body 1 center.
Because described reaction disk body 1 comprises three identical parts of structure, these three parts are respectively first, second, and third part, and structure in these three parts is identical, so described reaction disk body 1 comprises three calibration holes 101, is respectively first, second, third calibration hole; Three immunization program reaction zones: be respectively first, second, and third immunization program reaction zone; Three hybrid chambers 103, are respectively first, second, and third hybrid chamber; Three quantitative chambeies 104 of dilution, are respectively the first, second, third quantitative chamber of dilution; Three dilution cushion chambers 105, are respectively first, second, and third dilution cushion chamber; Three dilution waste collection chambeies 106, are respectively first, second, and third dilution waste collection chamber; Three blood sample storage chambers 107, are respectively first, second, and third blood sample storage chamber; Three serum disengagement chambers 108, are respectively first, second, third serum disengagement chamber; Three excess blood collecting chambers 109, are respectively first, second, and third excess blood collecting chamber; Three diluted cup storage chambers 111, be respectively first, second, third diluted cup storage chamber, described diluted cup storage chamber 111 side is provided with pilot hole 114, therefore described reaction disk body 1 also comprises three pilot holes, heat-sealing film bearing 113 is provided with below described diluted cup storage chamber 111, therefore described reaction disk body 1 also comprises three heat-sealing film bearings of place, described first, second, third, fourth, the 5th, the 6th, the 7th and the 8th kapillary comprises three articles respectively, and each is in the parts that correspond;
Above-mentioned is that the number of the immunization program reaction chamber 102 arranged in three immunization program reaction zones is no less than 10.
Described diluted cup 2 comprises first, second, third diluted cup, and described first, second, third diluted cup is placed in described first, second, third diluted cup storage chamber respectively, with reference to Fig. 3, described diluted cup 2 comprises cup 22 and the heat-sealing film 21 for sealing described sample cup 22 rim of a cup, dilution is provided with in described cup 22, the manufacturing process of described cup 2 is injected by quantitative dilution in described cup 22, then described heat-sealing film 21 is used to be sealed by the rim of a cup of described cup 22, reverse 23 is provided with above described heat-sealing film 21, described cup 22 is placed in described diluted cup storage chamber 111, again the bottom of described reverse 23 and described heat-sealing film bearing 113 are connected, be fixed on by the bottom of described reverse 23 like this in the heat-sealing film bearing 113 of reaction disk body 1, the volume of described diluted cup storage chamber 111 is greater than the volume of described diluted cup 2, make described diluted cup 2 fully can move in diluted cup storage part like this, the bottom of wherein said reverse 23 is provided with folded part, folded part refers to and is folded by certain length the bottom of heat-sealing film, the length of described folded part should remain on and just can ensure that heat-sealing film can not avulsed minimum length, described folded part 23 length 2 ~ 4cm larger than the length of described cup 22,
With reference to Fig. 4, described reaction disk cover 3 comprises blood adding mouth 32, be positioned at the register pin 33 of described blood adding mouth 32 side and be positioned at the exhausr port 31 of described register pin 33 side, described blood adding mouth 32 comprises first, second, 3rd blood adding mouth, described register pin comprises first, second, 3rd register pin, described exhausr port 31 comprises first, second and the 3rd exhausr port, described first, second, 3rd register pin and described first, second, 3rd pilot hole is connected and described reaction disk cover 3 is located mutually with described reaction disk body 1, last again by between described reaction disk cover 3 and described reaction disk body 1 by being welded to connect, described reaction disk cover 3 is connected by ultrasonic welding process with described reaction disk body 1, described like this diluted cup 2 is just in time between described reaction disk cover 3 and described reaction disk body 1, three each and every one adding mouths on described reaction disk cover 3 are also just in time positioned at above the rim of a cup of described diluted cup 2.
The using method of the described integrated immune reaction tray that the present invention proposes:
First blood sample to be measured is joined in blood sample storage chamber 107 by blood adding mouth 32;
The multisample of the automatic separation of serum then the present invention proposed detects immune response dish and puts into special detecting instrument, start detection instrument, the turning axle of then special detecting instrument can pass turning axle fixed orifice 112, thus whole reaction tray be fixed in special detecting instrument, and reaction tray can rotate along with the rotation of turning axle;
Under the effect of the centrifugal force brought at High Rotation Speed, volume due to diluted cup storage chamber 111 is greater than the volume of diluted cup 2, make diluted cup 2 fully can move in diluted cup storage part like this, therefore diluted cup 2 can away from rotation center, the pulling force that the reverse 23 of heat-sealing film 21 is certain because High Rotation Speed has simultaneously, therefore reverse 23 bottom folded part (namely heat-sealing film bottom by certain length fold) can be torn (and reaction tray not by the length of folded part under service condition because of remain on just can ensure heat-sealing film can not avulsed minimum length and can not be torn), because described diluted cup storage chamber 111 is connected by breach with described dilution cushion chamber 105, dilution in described diluted cup 2 enters in dilution cushion chamber 105 under the influence of centrifugal force, be connected by the first kapillary between described dilution cushion chamber 105 with the quantitative chamber 104 of described dilution, therefore dilution is entered in the quantitative chamber 104 of described dilution by described first kapillary and carries out quantitative work, because the quantitative chamber of described dilution 104 is connected with described dilution waste collection chamber 106 by the second kapillary, so unnecessary dilution can enter in described dilution waste collection chamber 106 by described second kapillary, the quantitative chamber of described dilution 104 is connected with described hybrid chamber 103 by three capillary simultaneously, so quantitative dilution is entered into described hybrid chamber 103 by described three capillary in the quantitative chamber of described dilution 104,
Meanwhile, because described blood sample storage chamber 107 is connected with described serum disengagement chamber 108 by the 5th kapillary, so the blood sample left in described storage chamber 107 can enter into described serum disengagement chamber 108 by described 5th kapillary, described serum disengagement chamber 108 is connected with described excess blood collecting chamber 109 by the 6th kapillary, so unnecessary blood sample can enter into described by described 6th kapillary, then the blood under the effect of larger centrifugal force in described serum disengagement chamber 108 can be separated into serum and red blood cell, and serum and red blood cell can be spaced from each other, until after serum is separated, reaction tray stops operating, under the effect not having centrifugal force, serum can be full of in kapillary, reaction tray is rotated further, under the influence of centrifugal force, because described serum disengagement chamber 108 is connected with described hybrid chamber 103 by the 7th kapillary, so serum can enter into described hybrid chamber 103 by described 7th kapillary, because described hybrid chamber 103 is connected with described immunization program reaction chamber 102 by the 4th kapillary, the dilution finally assembled in described hybrid chamber 103 and serum can enter into immunization program reaction chamber 102 described in each by described 4th kapillary,
The number of immunization program reaction chamber 102 is no less than 10 in embodiments of the present invention, is equipped with the dry type reagent corresponding with immunization program in immunization program reaction chamber;
Find the calibration hole 101 of immune response dish kind finally by the sensor in special detecting instrument, successively the material (dilution and serum) in each immunization program reaction chamber 102 is detected subsequently, obtain the concrete report of each immunization program.
The above is only the preferred embodiment of the present invention; be noted that for those skilled in the art; under the premise without departing from the principles of the invention, can also make some improvements and modifications, these improvements and modifications also should be considered as protection scope of the present invention.
Claims (8)
1. the multisample of automatic separation of serum detects an immune response dish, it is characterized in that: comprise reaction disk body (1), diluted cup (2) and reaction disk cover (3), described diluted cup (2) comprises first, second, 3rd diluted cup, described first, second, 3rd diluted cup is located in described reaction disk body (1) respectively, and described reaction disk cover (3) is connected with described reaction disk body (1), and described first, second, 3rd diluted cup is positioned between described reaction disk cover (3) and described reaction disk body (1), described reaction disk body (1) comprises the identical part of three structures and turning axle fixed orifice (112), and the part that three structures are identical is respectively first, second and Part III, described turning axle fixed orifice (112) is positioned at described reaction disk body (1) center, and described first, second and Part III be evenly arranged in described reaction disk body (1), described first, second and the center line of Part III all through described turning axle fixed orifice (112) position, the part that described structure is identical is provided with diluted cup storage chamber (111) from inside to outside successively, dilution cushion chamber (105), the quantitative chamber of dilution (104), hybrid chamber (103) and immunization program reaction zone, diluted cup storage chamber (111) comprises first, second, 3rd diluted cup storage chamber, described dilution cushion chamber (105) comprises first, second, 3rd dilution cushion chamber, the quantitative chamber of described dilution (104) comprises first, second, the 3rd quantitative chamber of dilution, described hybrid chamber (103) comprises first, second, 3rd hybrid chamber, described immunization program reaction zone comprises first, second, 3rd immunization program reaction zone, described immunization program reaction zone is evenly provided with several immunization program reaction chambers (102), and part one end that described structure is identical is provided with calibration hole (101) from top to bottom successively, excess blood collecting chamber (109), serum disengagement chamber (108) and blood sample storage chamber (107), described calibration hole (101) is located at described immunization program reaction chamber (102) side, the part other end that described structure is identical is provided with dilution waste collection chamber (106), and described calibration hole (101) comprises first, second, 3rd calibration hole, described excess blood collecting chamber (109) comprises first, second, 3rd excess blood collecting chamber, described serum disengagement chamber (108) comprises first, second, 3rd serum disengagement chamber, described diluted cup storage chamber (111) below is provided with heat-sealing film bearing (113), described diluted cup storage chamber (111) side is provided with pilot hole (114), and described heat-sealing film bearing (113) comprises first, second, 3rd sealer bearing (113), described pilot hole (114) comprises first, second, 3rd pilot hole, described first, second, 3rd diluted cup is placed in described first respectively, second, in 3rd diluted cup storage chamber, described reaction disk cover (3) comprises blood adding mouth (32), be positioned at the register pin (33) of described blood adding mouth (32) side and be positioned at the exhausr port (31) of described register pin (33) side, described register pin (33) comprises first, second, 3rd register pin, described first, second, 3rd register pin is respectively with described first, second, 3rd pilot hole is connected and described reaction disk cover (3) is connected with described reaction disk body (1).
2. the multisample of automatic separation of serum according to claim 1 detects immune response dish, it is characterized in that: described diluted cup (2) comprises cup (22) and the heat-sealing film (21) for sealing described cup (22) rim of a cup, described cup is provided with dilution in (22), described heat-sealing film (21) top is provided with folded part (23), and bottom and the described heat-sealing film bearing (113) of described folded part (23) are connected.
3. the multisample of automatic separation of serum according to claim 1 detects immune response dish, it is characterized in that: described diluted cup storage chamber (111) is connected by breach with described dilution cushion chamber (105), described dilution cushion chamber (105) is connected by the first kapillary with between the quantitative chamber of described dilution (104), the quantitative chamber of described dilution (104) is connected with described dilution waste collection chamber (106) by the second kapillary, the quantitative chamber of described dilution (104) are connected with described hybrid chamber (103) by three capillary simultaneously, described hybrid chamber (103) is connected with described immunization program reaction chamber (102) by the 4th kapillary, described blood sample storage chamber (107) is connected with described serum disengagement chamber (108) by the 5th kapillary, described serum disengagement chamber (108) is connected with described excess blood collecting chamber (109) by the 6th kapillary, described serum disengagement chamber (108) is connected with described hybrid chamber (103) by the 7th kapillary simultaneously.
4. the multisample of automatic separation of serum according to claim 3 detects immune response dish, it is characterized in that: the volume of described dilution cushion chamber (105) is greater than the volume in the quantitative chamber of described dilution (104) and is less than the volume in the quantitative chamber of described dilution (104) and the volume sum of described dilution waste collection chamber (106), the volume of described serum disengagement chamber (108) is greater than the volume of described hybrid chamber (103) and is less than the volume sum of described hybrid chamber (103) and described excess blood collecting chamber (109).
5. the multisample of the automatic separation of serum according to claim 1 or 3 detects immune response dish, it is characterized in that: described three capillary is less than the distance of the quantitative chamber of described dilution (104) to described reaction disk body (1) center to the distance of described reaction disk body (1) center, described 7th kapillary is less than the distance of described serum disengagement chamber (108) to described reaction disk body (1) center to the distance of described reaction disk body (1) center, described 8th kapillary is less than the distance of described hybrid chamber (103) to described reaction disk body (1) center to the distance of described reaction disk body (1) center.
6. the multisample of automatic separation of serum according to claim 1 detects immune response dish, it is characterized in that: be welded to connect by ultrasonic welding process between described reaction disk cover (3) and described reaction disk body (1).
7. the multisample of automatic separation of serum according to claim 1 detects immune response dish, it is characterized in that: the number of described immunization program reaction chamber (102) is no less than 10.
8. the multisample of automatic separation of serum according to claim 1 detects immune response dish, it is characterized in that: described folded part (23) length 2 ~ 4cm larger than the length of described cup (22).
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| CN201510304821.9A CN104965096A (en) | 2015-06-04 | 2015-06-04 | Multi-sample immunity-detecting reaction disc capable of automatically separating serum |
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| CN201510304821.9A CN104965096A (en) | 2015-06-04 | 2015-06-04 | Multi-sample immunity-detecting reaction disc capable of automatically separating serum |
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| CN106554903A (en) * | 2016-11-14 | 2017-04-05 | 湖南圣湘生物科技有限公司 | A kind of medicament evenly mixing device and its using method |
| WO2017118128A1 (en) * | 2016-01-09 | 2017-07-13 | 深圳市贝沃德克生物技术研究院有限公司 | Device for comprehensively testing multiple serum markers |
| CN108444804A (en) * | 2018-05-11 | 2018-08-24 | 石家庄禾柏生物技术股份有限公司 | A kind of test reaction capsule with mixing structure |
| CN108646015A (en) * | 2018-05-05 | 2018-10-12 | 武汉芯生生物科技有限公司 | Integrated apparatus based on multiple check bits and analysis method |
| CN109030806A (en) * | 2018-05-05 | 2018-12-18 | 武汉芯生生物科技有限公司 | A kind of biochemical immunity analyzer and its working method |
| WO2021031776A1 (en) * | 2019-08-21 | 2021-02-25 | 成都斯马特科技有限公司 | Fully-automated chemiluminescence immunoassay method |
| CN112517093A (en) * | 2020-11-17 | 2021-03-19 | 四川大学 | Fish saliva automatic sample separation detection disc and detection method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2017118128A1 (en) * | 2016-01-09 | 2017-07-13 | 深圳市贝沃德克生物技术研究院有限公司 | Device for comprehensively testing multiple serum markers |
| CN106554903A (en) * | 2016-11-14 | 2017-04-05 | 湖南圣湘生物科技有限公司 | A kind of medicament evenly mixing device and its using method |
| CN106554903B (en) * | 2016-11-14 | 2019-10-08 | 湖南圣湘生物科技有限公司 | A kind of medicament evenly mixing device and its application method |
| CN108646015A (en) * | 2018-05-05 | 2018-10-12 | 武汉芯生生物科技有限公司 | Integrated apparatus based on multiple check bits and analysis method |
| CN109030806A (en) * | 2018-05-05 | 2018-12-18 | 武汉芯生生物科技有限公司 | A kind of biochemical immunity analyzer and its working method |
| CN109030806B (en) * | 2018-05-05 | 2024-02-06 | 武汉芯生生物科技有限公司 | Biochemical immunity analyzer and working method thereof |
| CN108444804A (en) * | 2018-05-11 | 2018-08-24 | 石家庄禾柏生物技术股份有限公司 | A kind of test reaction capsule with mixing structure |
| WO2021031776A1 (en) * | 2019-08-21 | 2021-02-25 | 成都斯马特科技有限公司 | Fully-automated chemiluminescence immunoassay method |
| CN113495087A (en) * | 2020-04-03 | 2021-10-12 | 深圳市帝迈生物技术有限公司 | POCT blood cell analyzer and detection method thereof |
| CN112517093A (en) * | 2020-11-17 | 2021-03-19 | 四川大学 | Fish saliva automatic sample separation detection disc and detection method thereof |
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Application publication date: 20151007 |
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| WD01 | Invention patent application deemed withdrawn after publication |