CN206573581U - Detecting system for chemical illumination immunity analysis instrument - Google Patents
Detecting system for chemical illumination immunity analysis instrument Download PDFInfo
- Publication number
- CN206573581U CN206573581U CN201720113373.9U CN201720113373U CN206573581U CN 206573581 U CN206573581 U CN 206573581U CN 201720113373 U CN201720113373 U CN 201720113373U CN 206573581 U CN206573581 U CN 206573581U
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- Prior art keywords
- elisa plate
- plate
- pump
- detection system
- track
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- 238000004458 analytical method Methods 0.000 title abstract 2
- 238000005286 illumination Methods 0.000 title abstract 2
- 230000036039 immunity Effects 0.000 title abstract 2
- 239000000126 substance Substances 0.000 title abstract 2
- 238000002965 ELISA Methods 0.000 claims abstract description 59
- 239000000523 sample Substances 0.000 claims abstract description 58
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 17
- 238000001514 detection method Methods 0.000 claims description 56
- 238000003018 immunoassay Methods 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 12
- 239000013307 optical fiber Substances 0.000 claims description 10
- 238000004020 luminiscence type Methods 0.000 claims description 5
- 238000012360 testing method Methods 0.000 abstract description 6
- 238000002347 injection Methods 0.000 abstract description 5
- 239000007924 injection Substances 0.000 abstract description 5
- 238000000034 method Methods 0.000 description 12
- 230000005484 gravity Effects 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
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- Investigating Or Analysing Biological Materials (AREA)
Abstract
One kind is used for the detecting system of chemical illumination immunity analysis instrument (1), it is characterised in that including：Mechanical gripping arm (2), mechanical gripper (3), ELISA Plate (4), stock guide (5), pop one's head in (6), cover plate (7), pallet (8), projectile (9), first pump (10) and the second pump (11), wherein, the mechanical gripper (3) is placed in the top of the ELISA Plate (4), the stock guide (5) is placed in the export position of the ELISA Plate (4), the probe (6) is used for the luminous value for detecting the sample in the ELISA Plate (4), the cover plate (7) is placed in the upper surface location of the ELISA Plate (4), the pallet (8) is placed in the test position of the ELISA Plate (4), the projectile (9) is installed on the stock guide (5), first pump (10) and the second pump (11) are used for the different reagent of the ELISA Plate (4) injection.
Description
Technical Field
The utility model relates to a chemiluminescence immunoassay appearance field specifically relates to a detecting system for chemiluminescence immunoassay appearance.
Background
In the detection process of the chemiluminescence immunoassay analyzer, a reaction cup is usually placed in an enzyme label plate, and then a sample in the reaction cup is detected. Generally, a single reaction cup detection method or a multi-reaction cup detection method is adopted for detection, however, the detection efficiency of the single reaction cup is low, the existing multi-reaction cup needs manual assistance, meanwhile, the detected ELISA plate needs manual treatment, and the sample usually contains viruses, bacteria and the like, so that the treatment of the ELISA plate is time-consuming, labor-consuming and unsafe.
Therefore, it is necessary to develop a detection system with high detection efficiency, time and labor saving and safety.
SUMMERY OF THE UTILITY MODEL
The object of the present invention is to overcome the problems of the prior art by providing a detection system for a chemiluminescent immunoassay analyzer 1.
In order to achieve the above purpose, the utility model adopts the technical scheme that: a detection system for a chemiluminescent immunoassay analyzer 1 comprising:
a mechanical gripper arm 2, a mechanical gripper 3, an ELISA plate 4, a material guide plate 5, a probe 6, a cover plate 7, a tray 8, a propelling part 9, a first pump 10 and a second pump 11,
wherein,
the mechanical gripper arms 2 are used to control the movement of the mechanical gripper 3,
the mechanical hand grip 3 is arranged above the ELISA plate 4 and is used for transferring the position of the ELISA plate 4,
the material guide plate 5 is arranged at the leading-out position of the ELISA plate 4 and is used for leading out the ELISA plate 4,
the probe 6 is used for detecting the luminescence value of the sample in the ELISA plate 4,
the cover plate 7 is arranged on the upper surface of the ELISA plate 4 and is used for covering or exposing the tray 8,
a tray 8 is arranged at the detection position of the ELISA plate 4 and is used for accommodating the ELISA plate 4
The pushing piece 9 is arranged on the material guide plate 5, is used for pushing the ELISA plate 4,
the first pump 10 and the second pump 11 are used to inject different reagents into the microplate 4.
According to the utility model discloses, stock guide 5 has first track and second track, and first track is the horizontal orbit, and the second track is the landslide track.
According to the utility model discloses, the orbital both sides of second have the frame to prevent that ELIAS plate 4 on the second track from droing from the second track.
According to the utility model discloses, the luminous value of sample in the probe 6 passes through optical fiber detection ELIAS plate 4.
According to the utility model discloses, apron 7 passes through the connecting piece and is connected with the conveyer belt for apron 7 slides through the drive of conveyer belt.
According to the utility model discloses, first pump 10 and second pump 11 are connected with the application of sample needle respectively to inject different reagents into ELIAS plate 4 through this application of sample needle.
According to the utility model discloses, propulsion member 9 has promotion portion, pulling portion and motor.
According to the utility model, the pushing part of the pushing piece 9 is right-angled so as to frame the edge of the ELISA plate 4.
According to the utility model discloses, the pulling portion of propulsion member 9 is connected with the promotion portion and by the motor drive of propulsion member 9 to the promotion portion of pulling propulsion member 9.
According to the utility model discloses, set up the track at the lateral part of stock guide 5 for the pulling portion of propelling part 9 when being driven by the motor of propelling part 9, along the track motion.
Compared with the prior art, the beneficial effects of the utility model are that:
(1) use the utility model discloses a detecting system examines time measuring, because mechanical tongs can be accurate and shift the ELIAS plate fast for detection efficiency is high.
(2) The utility model discloses a detecting system is provided with the stock guide for the testing process labour saving and time saving is safe again.
(3) The utility model discloses a detecting system, simple structure, easy to operate.
Drawings
FIG. 1 is a perspective view of a chemiluminescent immunoassay analyzer; and
fig. 2 is a perspective view of a detection system according to the present invention.
Detailed Description
The invention is described below with reference to the drawings and examples.
FIG. 1 is a perspective view of a chemiluminescent immunoassay analyzer. Referring to fig. 1, a mechanical gripper arm 2, a mechanical gripper 3, an elisa plate 4 and a second track of the stock guide can be seen. As shown in figure 1, the mechanical gripper 3 is arranged above the ELISA plate 4 and is driven by the mechanical gripper arm 2, so that the ELISA plate 4 is transferred from the plate washing position to the detection position, then the ELISA plate 4 is transferred from the detection position to the lead-out position, and finally the ELISA plate 4 is led out through the guide plate 5.
Fig. 2 is a perspective view of a detection system according to the present invention. In fig. 2, the microplate 4 is placed in the tray 8, while the microplate to be removed is placed on the first track of the guide plate 5, and the cover plate 7 abuts against the entrance of the detection site (i.e., the exit of the detection site). As can be seen from fig. 2, the cover plate 7 is connected with the conveyor belt through a connecting piece, an optical fiber is arranged at the probe 6, the leading-out position is adjacent to the inlet of the detection position, the pulling part of the pushing part 9 is perpendicular to the right-angle surface of the pushing part, and the detection system is provided with two pumps, namely a first pump 10 and a second pump 11.
According to the utility model discloses an embodiment, the utility model provides a detecting system for chemiluminescence immunoassay appearance 1 as shown in figure 2, it is including the detecting system who is used for chemiluminescence immunoassay appearance 1, its characterized in that includes: a mechanical gripper arm 2, a mechanical gripper 3, an ELISA plate 4, a material guide plate 5, a probe 6, a cover plate 7, a tray 8, a propelling part 9, a first pump 10 and a second pump 11,
wherein,
the mechanical gripper arms 2 are used to control the movement of the mechanical gripper 3,
the mechanical hand grip 3 is arranged above the ELISA plate 4 and is used for transferring the position of the ELISA plate 4,
the material guide plate 5 is arranged at the leading-out position of the ELISA plate 4 and is used for leading out the ELISA plate 4,
the probe 6 is used for detecting the luminescence value of the sample in the ELISA plate 4,
the cover plate 7 is arranged on the upper surface of the ELISA plate 4 and is used for covering or exposing the tray 8,
the tray 8 is arranged at the detection position of the ELISA plate 4 and is used for accommodating the ELISA plate 4,
the pushing piece 9 is arranged on the material guide plate 5, is used for pushing the ELISA plate 4,
the first pump 10 and the second pump 11 are used to inject different reagents into the microplate 4.
According to the utility model discloses an embodiment, stock guide 5 has first track and second track, and first track is the horizontal orbit, and the second track is the landslide track. Specifically, when the detected microplate 4 is transferred to the lead-out position, the detected microplate 4 first passes through the first track of the guide plate 5, and then passes through the second track of the guide plate 5. Since the first track of the guide plate 5 is a horizontal track, the microplate 4 moves on the first track by being pushed by the pushing portion of the pusher 9. However, when the microplate 4 moves on the second track, since the second track of the guide plate 5 is a slide track, the microplate 4 can slide on the second track only by the action of gravity, and is then guided out.
According to the utility model discloses an embodiment, the both sides of second track have the frame to prevent that ELIAS plate 4 on the second track from droing from the second track. Specifically, when the microplate 4 moves on the second rail, since the microplate 4 slides downward on the second rail by the action of gravity, frames need to be provided on both sides of the second rail to prevent the microplate 4 on the second rail from falling off from the side of the second rail.
According to the utility model discloses an embodiment, probe 6 passes through the luminous value of sample in the optic fibre detection ELIAS plate 4. Specifically, since the probe 6 has a large volume, when the probe 6 is directly used to detect a sample, the seal between the probe 6 and the sample is not tight, and the detected luminescence value of the sample is not accurate. Therefore, an optical fiber is required to be arranged between the probe 6 and the sample, and since the optical fiber is thin, when the probe 6 detects the sample through the optical fiber, the sealing can be carried out between the optical fiber head and the sample, and then the optical fiber transmits the optical signal emitted by the sample to the probe 6, in this case, the detected luminous value of the sample is accurate.
According to the utility model discloses an embodiment, apron 7 passes through the connecting piece and is connected with the conveyer belt for apron 7 slides through the drive of conveyer belt. Specifically, before the sample in the microplate 4 is detected, first, the detection position needs to be exposed, that is, the place where the cover plate 7 is close to the detection position, and the tray is at the entrance of the detection position (i.e., the exit of the detection position), at this time, there is no microplate 4 in the tray 8, then, the microplate 4 is transferred from the plate washing position to the entrance of the detection position by the mechanical gripper and the microplate 4 is put into the tray 8, and finally, the cover plate 7 is slid by the movement of the conveyor belt, so that the cover plate 7 covers the microplate 4 and is put in the dark box.
According to the utility model discloses an embodiment, first pump 10 and second pump 11 are connected with the application of sample needle respectively to inject different reagents into ELIAS plate 4 through this application of sample needle. The first pump 10 and the second pump 11 may be a micro pump or a peristaltic pump, respectively, as needed. Specifically, before the detection, since it is necessary to inject a reagent into the sample to make the sample emit light, a sample injection needle and a first pump 10 and a second pump 11 for supplying power to the injected sample are provided.
According to an embodiment of the present invention, the propelling member 9 has a pushing portion, a pulling portion, and a motor. Specifically, since the pushing member 9 is used for pushing the microplate 4 on the first track of the material guide plate 5, a pushing portion for pushing the microplate 4, a pulling portion for pulling the pushing portion, and a motor for powering the pulling portion are provided on the pushing member 9.
According to the embodiment of the present invention, the pushing portion of the pushing member 9 is formed in a right angle shape so as to frame the edge of the microplate 4. Specifically, the pushing portion of the pushing member 9 plays a role of pushing the elisa plate 4 on the first track, and the pushing portion is designed to be right-angled, so that the pushing portion can frame one corner of the elisa plate 4 to prevent the elisa plate 4 from falling off from the first track when moving on the first track.
According to the embodiment of the present invention, the rail is provided at the side portion of the material guide plate 5, so that the pulling portion of the pushing member 9 moves along the rail when driven by the motor of the pushing member 9.
Use the utility model discloses a detecting system examines time measuring, because mechanical tongs can be accurate and shift the ELIAS plate fast for detection efficiency is high.
The utility model discloses a detecting system is provided with the stock guide for the testing process labour saving and time saving is safe again.
The utility model discloses a detecting system, simple structure, easy to operate.
The detection process of the detection system of the present invention will be described below. During the measurement, since it is possible to inject one reagent or two reagents into the sample to be measured and then measure the luminescence value of the sample as needed depending on the sample to be measured, two cases are shown here.
The first condition, when need pour into two kinds of reagents in to the reaction cup, the utility model discloses a detecting system's testing process as follows: the ELISA plate 4 added with the sample is transferred to a tray 8 at the inlet of a detection position through a mechanical gripper 3, then a cover plate 7 is slid, the ELISA plate 4 is placed in a dark box, the tray 8 is moved to inject a first reagent into a reaction cup in the ELISA plate 4 through a sample injection needle of a first pump 10, a second reagent is injected into the reaction cup in the ELISA plate 4 through the sample injection needle of a second pump 11, then the sample added with the reagent is detected through an optical fiber by using a probe 6, after the detection is finished, the tray 8 is moved to an outlet of the detection position, finally, the detected ELISA plate 4 is transferred to a lead-out position through the mechanical gripper 3, and therefore the ELISA plate 4 is firstly pushed by a pushing piece 9 on a guide plate 5 and then is moved through the action of gravity, and the ELISA plate 4 is led out. During this test, the injection of the two samples may be simultaneous or sequential, depending on the test conditions of the samples. The above process is a complete detection process, and in an actual experiment, the above process is repeated for many times.
In the second situation, when a reagent is injected into the reaction cup, the detection process of the detection system of the utility model is as follows: the ELISA plate 4 added with the sample is transferred to a tray 8 at the inlet of a detection position through a mechanical gripper 3, then a cover plate 7 is slid, the ELISA plate 4 is placed in a dark box, the tray 8 is moved to inject the reagent into a reaction cup in the ELISA plate 4 through a sample adding needle of a first pump 10 or a second pump 11, then the sample added with the reagent is detected through an optical fiber by using a probe 6, after the detection is finished, the tray 8 is moved to the outlet of the detection position, finally, the detected ELISA plate 4 is transferred to a lead-out position through the mechanical gripper 3, so that the ELISA plate 4 is firstly pushed by a pushing piece 9 on a material guide plate 5 and then is moved through the action of gravity, and the ELISA plate 4 is led out. The above process is a complete detection process, and in an actual experiment, the above process is repeated for many times.
In the embodiment shown, the detection system has two pumps, a first pump 10 and a second pump 11, however, in the detection system of the present invention, the detection system may also have one pump or more than two pumps. In addition, set up the track in the side of stock guide 5 for the pulling portion of propulsion piece 9 is along this orbital motion, however in the utility model discloses an among the detecting system, also can set up the track in the below of stock guide 5, and correspondingly set up on the pulling portion of propulsion piece 9 with the track assorted part of this below, make the pulling portion of propulsion piece 9 along the orbital motion of this below.
The above embodiments are only used for further illustration of the present invention, and should not be construed as limiting the scope of the present invention. The modifications and variations of the present invention, which are not essential to the skilled in the art, are within the scope of the present invention.
Reference numerals
1 chemiluminescence immunoassay analyzer
2 mechanical gripper arm
3 mechanical gripper
4 enzyme label plate
5 stock guide
6 Probe
7 cover plate
8 tray
9 propelling part
10 first pump
11 second pump.
Claims (10)
1. A detection system for a chemiluminescent immunoassay analyzer (1), comprising:
a mechanical gripper arm (2), a mechanical gripper (3), an ELISA plate (4), a material guide plate (5), a probe (6), a cover plate (7), a tray (8), a propelling piece (9), a first pump (10) and a second pump (11),
wherein,
the mechanical gripper arm (2) is used for controlling the movement of the mechanical gripper (3),
the mechanical gripper (3) is arranged above the ELISA plate (4) and is used for transferring the position of the ELISA plate (4),
the material guide plate (5) is arranged at the leading-out position of the ELISA plate (4) and is used for leading out the ELISA plate (4),
the probe (6) is used for detecting the luminous value of the sample in the ELISA plate (4),
the cover plate (7) is arranged on the upper surface of the ELISA plate (4) and is used for covering or exposing the ELISA plate (4),
the tray (8) is arranged at the detection position of the ELISA plate (4) and is used for accommodating the ELISA plate (4),
the pushing piece (9) is arranged on the material guide plate (5) and is used for pushing the ELISA plate (4),
the first pump (10) and the second pump (11) are used for injecting different reagents into the ELISA plate (4).
2. The detection system according to claim 1, wherein the guide plate (5) has a first rail which is a horizontal rail and a second rail which is a landslide rail.
3. The detection system according to claim 2, characterized in that the second track is provided with rims on both sides thereof to prevent the microplate (4) on the second track from falling off the second track.
4. The detection system according to claim 1, characterized in that the probe (6) detects the luminescence value of the sample in the microplate (4) by means of optical fibers.
5. Detection system according to claim 1, characterized in that the cover plate (7) is connected to a conveyor belt by means of a connection such that the cover plate (7) is slid by the conveyor belt.
6. The detection system according to claim 1, wherein the first pump (10) and the second pump (11) are connected to a sample application needle, respectively, so as to inject different reagents into the microplate (4) through the sample application needle.
7. Detection system according to claim 1, characterized in that the pusher (9) has a pushing portion, a pulling portion and a motor.
8. The detection system according to claim 7, characterized in that the push portion is right-angled so as to frame the edge of the microplate (4).
9. Detection system according to claim 7, characterized in that the pulling portion is connected to the pushing portion and is driven by a motor of the pusher (9) so as to pull the pushing portion.
10. The detection system according to claim 7, wherein a rail is provided at a side of the guide plate (5) so that the pulling part moves along the rail when driven by a motor of the propelling member (9).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201720113373.9U CN206573581U (en) | 2017-02-07 | 2017-02-07 | Detecting system for chemical illumination immunity analysis instrument |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201720113373.9U CN206573581U (en) | 2017-02-07 | 2017-02-07 | Detecting system for chemical illumination immunity analysis instrument |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN206573581U true CN206573581U (en) | 2017-10-20 |
Family
ID=60058296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201720113373.9U Expired - Fee Related CN206573581U (en) | 2017-02-07 | 2017-02-07 | Detecting system for chemical illumination immunity analysis instrument |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN206573581U (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113311179A (en) * | 2021-06-29 | 2021-08-27 | 烟台艾德康生物科技有限公司 | Full-automatic luminous apparatus |
-
2017
- 2017-02-07 CN CN201720113373.9U patent/CN206573581U/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113311179A (en) * | 2021-06-29 | 2021-08-27 | 烟台艾德康生物科技有限公司 | Full-automatic luminous apparatus |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20171020 Termination date: 20200207 |